Abstract
Background
During menopause, women experience a range of physiological changes, including reduction in skeletal muscle mass, bone mineral density, and an increase in fat mass. Although strength training and dietary strategies have individually been shown to counteract these changes, evidence for their combined effects is currently lacking. This review aims to investigate the combinatory effects on body composition, muscle strength, and bone mineral density.
Methods
Three databases (PUBMED, Web of Science, and SPORTDiscus) were screened following the PRISMA guidelines. The PEDro scale was utilized to evaluate methodological quality and potential bias risk. The analyzed outcome parameters were body composition, muscle strength, and bone mineral density.
Results
A total of 34 studies including postmenopausal women (N = 1,541) were identified; 31 of these had a PEDro score of 6 or higher. In general, body composition, muscle strength, and bone mineral density have been significantly altered through systematic strength training. Eleven studies focused on an additional calorie deficit (250-750 kcal/day) which enhanced the reduction of fat mass. Protein intake was examined in nine studies and has no significant additional effect on muscle strength and lean body mass with a minimal intake of 0.8 g/kg bodyweight. Only a few studies could be identified on other nutritional and supplementation strategies. A total of three studies were identified investigating strength training in conjunction with amino acid supplementation, four studies examining calcium and vitamin D, four studies on creatine, one study on zataria multiflora, one study on omega-3 supplementation and one study on shatavari.
Conclusion
Systematic strength training has been consistently demonstrated to improve body composition, strength capacity, and bone mineral density. However, the evidence supporting the effectiveness of additional nutritional and supplementation strategies remains inconclusive. While a calorie-restricted diet and adequate protein intake appear to promote favourable changes in body composition, the available data is still insufficient to derive specific and evidence-based recommendations regarding supplementation in conjunction with strength training. Moreover, research on additional nutritional and supplementation strategies remains inconsistent or scarce, underscoring the need for further studies to allow for more precise recommendations.
PROSPERO Registration Number CRD42023412915 (12th April 2023).
Supplementary Information
The online version contains supplementary material available at 10.1186/s40798-025-00954-2.
Keywords: Diet, Physical fitness, Postmenopausal women, Resistance training, Supplementation
Introduction
It is generally known that body composition, physical performance and functionality begin to decline steadily in the fourth decade of life [1]. In women, one of the most crucial phases in ageing is menopause, which usually occurs between the ages of 45 and 55 years [2]. Menopause is defined as 12 consecutive months of amenorrhea without surgical intervention or other causes. It marks the end of reproductive function [3]. This transition is characterized by several physiological and hormonal changes, most notably a reduction in estradiol and progesterone concentrations. These hormonal alterations contribute to a decline in skeletal muscle mass (SMM), muscle strength and bone mineral density (BMD) as well as an increase in fat mass (FM) [4–7]. It is estimated that about 3–10% of SMM is lost per decade of life after the third decade [1]. A decrease in SMM leads to reduced functionality and performance, which increases the risk of falls and fractures [8–10]. In this context, postmenopausal women with reduced SMM exhibit a 2.1-fold higher risk of falls and a 2.7-fold higher risk of fractures compared with those who have maintained SMM [11]. Overall, menopausal women are at an increased risk of developing osteoporosis and musculoskeletal disorders, including musculoskeletal pain and sarcopenic obesity [7, 12–14].
To maintain SMM and promote longevity, physical activity is an ideal prevention strategy to counteract the ageing process [15]. Systematic strength training (ST) in particular seems to be an ideal strategy to counteract the side effects of menopause. Recent reviews on postmenopausal women have shown that ST improves functionality, BMD [16, 17], and body composition. For example, Thomas et al. [8] found that ST achieved a small to moderate increase in lean body mass (LBM) [8]. Sá et al. [17] observed a reduction in FM when performing ST [17]. Regarding the effects of training frequency on BMD and body composition, however, the available data remains insufficient to draw definitive conclusions [16]. Concerning training duration, the meta-analysis by González-Gálvez et al [18] demonstrates that three training sessions per week with a duration of 60 min can improve strength in the lower and upper body [18].
In addition to physical activity, nutritional strategies are recognized crucial for promoting a healthy lifestyle. Although general dietary recommendations for postmenopausal women do not differ substantially from those for other populations [19], only a few specific guidance on nutrition and supplementation are available. A low-energy diet is recommended for postmenopausal women to counteract metabolic changes and high-fat accumulation [20]. Regarding minerals and vitamin D intake, current recommendations to preserve BMD suggest a daily calcium intake of 700 mg – 1500 mg/day and a vitamin D intake of 400–800 IU/day [21–24]. Further recommendations regarding supplementation specifically for postmenopausal women have not been established in the literature. Although evidence exists on physical activity and nutrition strategies in postmenopausal women, these two aspects are primarily considered separately. However, for a healthy lifestyle, physical activity should be combined with a balanced and nutritious diet. In younger adults, for example, studies demonstrated that the combination of ST and nutritional interventions is more effective on body composition than ST alone [25–27].
To date, no systematic review has examined the combined effects of ST and nutritional interventions in postmenopausal women. Accordingly, this review aims to identify and summarize the potential effects of ST in conjunction with dietary strategies. It will investigate the additive impact of nutritional interventions on body composition, muscle strength, and BMD within ST programs targeting postmenopausal women.
Methods
Information Source and Search
The literature search was independently completed by two researchers (JS and FW) following the PRISMA guidelines across PubMed, Web of Science, and SPORTDiscus [28]. The last search was conducted on August 5, 2025.
The study selection process, including the removal of exact duplicates, was managed using the current version of Rayyan.ai (Rayyan Systems Inc., Cambridge, USA). Any discrepancies during the selection process were resolved through consultation with a third reviewer (EI). In cases where the full text was unavailable online, the primary author and/or co-authors of the study were contacted via email by researcher FW. The systematic review was registered beforehand on PROSPERO on the April 12, 2023 (registration number: CRD42023412915).
The search strategy involved utilizing Medical Subject Headings (MeSH) and keywords, which were combined using Boolean operators (“AND”, “OR”). The used terms were: (postmenopaus*) AND ((strength*) OR (weight*) OR (resistance*) OR (barbell*) OR (machine*) OR (freeweight*)) AND ((*diet*) OR (nutrition*) OR (supple*) OR (*intake)) AND ((*performance) OR (fitness) OR (capacity) OR (muscle*) OR (lean body mass) OR (fat mass) OR (fat-free mass) OR (body composition) OR (body fat) OR (body mass) OR (BMI) OR (bone density)).
Selection Criteria
The eligibility criteria were established using the Patient-Intervention-Comparison-Outcome-Study-Timing (PICOST) scheme. Randomized, controlled study designs (RCTs) or controlled clinical trials written in either English or German were included in the screening process (S). The aspired study population comprised healthy postmenopausal (≥ 1 year without menstruation) women (P). The intervention required a structured ST program with a reproducible exercise intensity in combination with a diet or a dietary supplementation (I). The minimum intervention duration (T) was four weeks. Diet-and-exercise intervention groups were compared with diet-only, exercise-only, non-dieting, non-exercising control, or distinct diet-and-exercise intervention groups (C). Finally, only studies evaluating relevant outcomes on health parameters for body composition such as fat-free mass (FFM), LBM, SMM or FM, muscle strength or BMD were included (O). If there were multiple reports of the same study with the same sample size, the results were treated as a single study. Exclusion criteria included studies involving animal models, studies where male participants could not be distinguished, cohorts with a mean age greater than 65 years, participants using prescribed medication, or populations with pre-existing diseases other than obesity. Studies were also excluded if the full text could not be obtained despite attempts to contact the corresponding author.
Data Extraction
The extracted data included information on study design, participants, performed interventions including exercises and nutritional instructions, and relevant outcome parameters. When a study compared multiple treatments or included male participants, only outcomes relevant to the research question were considered. When parameters were presented exclusively in graphical form, PlotDigitizer was used to extract mean values and standard deviations (SD) or standard errors (SE) from the figures. The standard deviation and mean value of all parameters were assessed and used to calculate the correlation coefficient r [29]. In case the SD was not provided, it was calculated by using the SE and the sample size or the confidence interval, if reported. The used formulas were as follows [29, 30]:
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Quality Assessment and Risk of Bias
To evaluate the quality of all included studies the PEDro scale was used [31]. The PEDro scale includes eleven questions that address random and concealed allocation, blinding of participants, therapists and assessors, as well as quantity and quality of the outcome measures. Each question item was independently rated as (a) yes, (b) no, or (c) no information. Any discrepancies were discussed and subsequently resolved in consultation with a third researcher (EI).
Results
Study Selection
Initially, a total of 7540 hits were identified, as illustrated in the PRISMA 2020 flow diagram (Fig. 1) [28]. A total of 34 studies involving 1541 postmenopausal women with an average age ranging from 53.8 to 65.0 years were included. The duration of these studies varied, ranging from four weeks to four years. The included studies that were published between 1996 and 2025. The results of the individual studies were presented according to the original data reported by the authors, either in absolute values or in relative (percentage) terms. No conversions or modifications of the data (such as rounding or reduction of decimal places) were performed. The PEDro score of the included studies ranged from poor to excellent. One study was identified as poor (score 0–3), two studies as fair (score 4–5), eighteen as good (score 6–8) and thirteen studies were identified as excellent (score 9–10). Results are shown in Table 1: PEDro Scale.
Fig. 1.
PRISMA Flow diagram [28]
Table 1.
PEDro scale
| Study group (year) | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | Summe |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Aguiar et al. (2013) | a | a | a | a | a | a | a | a | a | a | a | 10 |
| Bagheri et al. (2021) | a | a | a | a | a | c | a | a | a | a | a | 9 |
| Bouchard et al. (2009) | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Brochu et al. (2009) | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Candow et al. (2021) | a | a | a | a | a | a | a | b | a | a | a | 9 |
| Chilibeck et al. (2015) | a | a | a | a | a | a | a | b | a | a | a | 9 |
| Cussler et al. (2005) | a | a | c | a | b | b | b | a | a | a | a | 6 |
| de Branco et al. (2019) | a | a | a | a | a | a | a | a | a | a | a | 10 |
| Drapeau et al. (2011) | a | a | a | a | b | b | b | b | a | a | a | 6 |
| Félix-Soriano et al. (2021) | a | a | a | a | a | b | a | b | a | a | a | 8 |
| Figueroa et al. (2013) 1 | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Figueroa et al. (2013) 2 | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Figueroa et al. (2015) | a | a | a | a | a | c | c | a | a | a | a | 8 |
| Ghanbari-Niaki et al. (2018) | a | a | a | a | a | c | c | a | a | a | a | 8 |
| Greed et al. (2025) | a | a | a | a | a | a | c | c | a | a | a | 8 |
| Haghighi et al. (2023) | a | a | a | a | a | a | a | a | a | a | a | 10 |
| Holm et al. (2008) | a | a | a | b | a | a | a | b | a | a | a | 8 |
| Ioannidou et al. (2024) | a | a | a | a | b | b | a | a | a | a | a | 8 |
| Isenmann et al. (2023) | a | a | a | a | a | b | b | b | a | a | a | 7 |
| Johannsmeyer et al. (2016) | a | a | a | a | a | a | a | a | a | a | a | 10 |
| Joseph et al. (2001) | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Kang et al. (2022) | a | a | a | a | a | c | a | a | a | a | a | 9 |
| Kerksick et al. (2020) | a | a | a | a | a | a | a | b | a | a | a | 9 |
| Maesta et al. (2007) | a | a | c | a | a | c | c | b | a | a | a | 7 |
| McNeil et al. (2015) | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Molina et al. (2015) | a | c | c | c | b | b | b | c | a | a | b | 2 |
| Orsatti et al. (2017) | a | a | a | a | a | a | a | b | a | a | a | 9 |
| Rossato et al. (2017) | a | a | a | a | a | a | b | b | a | a | a | 8 |
| Ryan et al. (1996) | a | b | b | b | b | b | b | a | a | a | a | 4 |
| Ryan et al. (2003) | a | c | c | a | b | b | b | b | a | a | a | 4 |
| Senechal et al. (2012) | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Shenoy et al. (2013) | a | a | a | a | b | b | b | a | a | a | a | 7 |
| Tayebi et al. (2019) | a | a | a | c | a | a | a | a | a | a | a | 9 |
| Weisgarber et al. (2015) | a | a | a | a | a | a | a | b | a | a | a | 9 |
a = yes; b = no; c = no information; 1 = eligibility criteria were specified; 2 = subjects were randomly allocated to groups; 3 = allocation was concealed; 4 = the groups were similar at baseline regarding the most important prognostic indicators; 5 = there was blinding of all subjects*; 6 = there was blinding of all therapists who administered the therapy*; 7 = there was blinding of all assessors who measured at least one key outcome*; 8 = measures of at least one key outcome were obtained from more than 85% of the subjects initially allocated to groups; 9 = all subjects for whom outcome measures were available received the treatment or control condition as allocated or, where this was not the case, data for at least one key outcome was analysed by “intention to treat”; 10 = the results of between-group statistical comparisons are reported for at least one key outcome; 11 = the study provides both point measures and measures of variability for at least one key outcome; *blinding regarding nutritional strategies
Study Designs
Six of the included studies compared a diet-only intervention with a diet-and-exercise intervention. Seventeen studies assessed the impacts of an exercise-only intervention versus a diet-and-exercise intervention. Three studies had a three-arm study design comparing exercise-only and diet-only interventions to a diet-and-exercise intervention. Data from two studies with a three-arm study design compared a diet-and-exercise intervention with a diet-only and a control intervention and three studies with a three-arm study design compared a diet-and-exercise intervention with an exercise-only and a control intervention. Eleven studies featured a four-arm study design comparing diet-and-exercise interventions with diet-only, exercise-only and control interventions, four studies compared distinct diet-and-exercise interventions, with one of them having an exercise-only control group. Finally, one study had a six-arm design with two different diet-and-exercise and two different exercise-only interventions and a diet-only and a control intervention.
Exercise Interventions
The included studies performed ST ranging from two to four times per week. The ST was performed with resistance bands, free weights, weight machines, or in the form of whole-body vibration (WBV) training.
Caloric Restriction Diet
Eleven studies [32–42] investigated the interaction of ST and different calorie-restrictive diets (CRD). The study periods ranged from four to twenty-six weeks. Most of the studies performed ST three times per week.
A total of five studies compared a CRD with ST to ST alone [32, 35, 36, 38, 42]. All studies showed significant differences between the groups with a significantly greater reduction in BW, body mass index (BMI), waist circumference (WC), FM and body fat (BF) percentage in the dieting groups. Besides, Bouchard et al. [32] observed a significant decline in leg extension exercises in both CRD groups (ST + CRD: 123 ± 31 kg to 108 ± 21 kg*; CRD: 104 ± 40 kg to 78 ± 33 kg*) but not in the ST group (94 ± 34 to 106 ± 29 kg) without CRD. Concerning LBM or SMM, Figueroa et al. [35, 36] detected a significant decline in the CRD groups (Figueroa et al. (2013) 1: 20.5 ± 1.0 kg to 19.5 ± 1.1 kg*; Figueroa et al. (2013) 2: 43.6 ± 1.6 kg to 42.3 to 1.8 kg*) without ST over time but not in the CRD groups with ST (Figueroa et al. (2013)1: 19.5 ± 0.8 kg to 19.1 ± 0.7 kg; Figueroa et al. (2013) 2: 42.4 ± 1.3 kg to 41.6 to 1.2 kg). However, in both studies, no significant group differences were observed. The other two studies did not show significant differences regarding LBM or muscle strength parameters between CRD groups [38, 42].
Nine studies [32–37, 39, 40, 42] compared a CRD alone versus a CRD in combination with ST. Five of these studies [33, 36, 37, 39, 40] found significant differences between the two groups. Two studies [36, 37] showed that the group combining CRD with training had a significantly greater increase in muscle strength parameters. Figueroa et al. demonstrated a significant increase and group effect in absolute muscle strength in the CRD + ST group (from 104 ± 5 kg to 129 ± 5 kg), compared with the CRD-only group (from 118 ± 8 kg to 111 ± 8 kg), which was similar to the effect observed in the ST-only group (113 ± 3 kg to 141 ± 8 kg) [36]. These effects are supported by observations from Joseph et al., who reported a significant difference between the groups in overall muscle strength (CRD + ST: ∆+23 ± 2 %; CRD: ∆+2 ± 2 %) [37].
Concerning FM, BF or circumferences, Bronchu et al. reported significant group differences with the combination of CRD and ST resulting in greater reductions in BF (CRD + ST: ∆ −3.7 ± 3.5 %; CRD: ∆−2.5 ± 2.7 %), trunk FM (CRD + ST: ∆−3.3 ± 2.6 kg; CRD: ∆−2.2 ± 2.5 kg), and hip circumference (HC; CRD + ST: ∆−7.5 ± 9.9 cm; CRD: ∆−4.5 ± 4.4 cm) compared with CRD alone [33]. McNeil et al. supported this findings, observing a significantly greater decline in FM in CRD + ST compared with CRD only (CRD + ST: ∆-6.1 ± 4.1 kg; CRD: ∆-3.9 ± 2.4 kg) [39]. Ryan et al. demonstrated a significant reduction in FM (33.1 ± 5.4 kg to 28.6 ± 4.6 kg) and BF (42.8 ± 3.4 % to 39.3 ± 3.7 %) following a CRD combined with ST [41]. In contrast to other studies, however, only participants with a BMI >27 kg/m² were instructed to follow the CRD, whereas the control group (BMI < 27 kg/m²) received no dietary guidance and consequently exhibited no significant changes in FM (22.2 ± 6.1 kg to 21.8 ± 6.3 kg) or BF ( 36.8 ± 5.0 % to 35.6 ± 6.1 %).
Furthermore, Joseph et al. [37] observed a significant decrease in SMM over time only in the CRD group as well as a significant between-group effect in SMM (CRD + ST: 17.9 ± 0.8 kg to 18.3 ± 0.8 kg; CRD: 16.0 ± 1.3 kg to 15.4 ± 1.3 kg). The remaining four studies [32, 34, 35, 42] did not detect any statistically significant differences between the CRD + ST and CRD only groups for body composition parameters.
With respect to BMD, only one study was identified [38]. Kerksick et al. [38] did not find any significant differences between the groups.
More detailed information is provided in Table 2.
Table 2.
Caloric restriction
| Author/ Date | Study design | Population | Training | Nutrition | Outcomes | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Bouchard et al. (2009) |
Randomized controlled double-blind study |
Total (n = 46) |
obese postmenopausal | Duration: 12 weeks | Body composition | Muscle strength | ||||||||
| BW (kg) |
BMI (kg/m2) |
FM (kg) |
LBM (kg) |
leg extension (lbs) |
one leg squat | |||||||||
| ST + CR (n = 12) | Ø 64.4 ± 4.5 years |
3/ week resistance training |
weight reduction by 0.5–1 kg/ week 1 h/ week NIS AHA diet |
77.5 ± 8.9 to 73.9 ± 9.2* r = -0.195 |
31.7 ± 2.6 to 30.2 ± 2.6* r = -0.277 |
33.8 ± 6.5 to 30.6 ± 6.6* r = -0.237 |
40.8 ± 3.2 to 40.5 ± 2.8 r = -0.050 |
123 ± 32 to 108 ± 21* r = -0.320 |
3.4 ± 2.6 to 6.4 ± 3.0*# r = 0.469 |
|||||
|
CR (n = 11) |
Ø 60.7 ± 4.6 years | no supervised training |
78.4 ± 10.8 to 74.4 ± 9.8* r = -0.190 |
31.9 ± 2.7 to 30.4 ± 2.3* r = -0.285 |
36.1 ± 7.4 to 32.9 ± 7.3* r = -0.213 |
39.2 ± 4.7 to 38.5 ± 4.1* r = -0.079 |
104 ± 40 to 78 ± 33* r = -0.331 |
2.5 ± 2.5 to 3.9 ± 4.3* r = 0.184 |
||||||
|
ST (n = 11) |
Ø 62.8 ± 3.7 years |
3/ week resistance training |
no prescribed diet |
78.5 ± 8.1 to 76.8 ± 8.2 r = -0.104 |
30.8 ± 2.2 to 30.7 ± 2.3 r = -0.022 |
34.4 ± 4.3 to 34.7 ± 5.1 r = 0.032 |
40.9 ± 4.3 to 41.1 ± 4.1 r = 0.024 |
94 ± 34 to 106 ± 29 r = 0.185 |
3.4 ± 1.7 to 7.0 ± 2.9*# r = 0.581 |
|||||
|
C (n = 12) |
Ø 62.5 ± 3.1 years | no supervised training |
80.1 ± 8.9 to 80.1 ± 9.4 r = 0 |
32.3 ± 2.4 to 32.6 ± 2.4 r = 0.062 |
36.9 ± 5.7 to 36.9 ± 5.8 r = 0 |
40.4 ± 4.1 to 40.1 ± 4.5 r = -0.035 |
113 ± 35 to 93 ± 35 r = -0.275 |
3.2 ± 3.0 to 3.4 ± 3.0 r = 0.033 |
||||||
|
main outcome: both CR groups (CR, ST + CR) significantly decreased BW, BMI, FM and leg extension strength over time (*) CR significantly decreased in LBM over time (*) One leg squat increased significantly in both ST groups (ST, ST + CR) compared to CR and C (#) |
||||||||||||||
|
Brochu et al. (2009) |
Randomized double-blind, controlled study |
Total (n = 107) |
overweight/obese postmenopausal women |
Duration: 26 weeks | body composition | |||||||||
|
BW (kg) |
BMI (kg/m2) |
WC (cm) |
HC (cm) |
BF (%) |
total FM (kg) |
trunk FM (kg) |
total LBM (kg) |
trunk LBM (kg) | ||||||
| ST + CR (n = 36) | Ø 57.2 ± 5.0 years |
3/ week resistance training |
CR: BRMR minus 500–800 kcal x 1.4 (PAF) 2/ month NIS AHA diet |
Baseline 84.1 ± 15.8 ∆ -5.8 ± 4.9* r = -0.509 |
Baseline 32.6 ± 4.9 ∆ -3.3 ± 1.9* r = -0.656 |
Baseline 97.1 ± 9.8 ∆ -5.6 ± 4.7* r = -0.512 |
Baseline 116.8 ± 13.1 ∆ -7.5 ± 9.9*# r = -0.354 |
Baseline 46.5 ± 4.9 ∆ -3.7 ± 3.3*# r = -0.489 |
Baseline 39.5 ± 10.5 ∆ -5.3 ± 4.3* r = -0.525 |
Baseline 19.3 ± 6.2 ∆ -3.3 ± 2.6*# r = -0.536 |
Baseline 42.1 ± 5.8 ∆ -0.4 ± 2.2* r = -0.091 |
Baseline 19.6 ± 5.1 ∆ +0.2 ± 1.6 r = 0.062 |
||
|
CR (n = 71) |
Ø 58.0 ± 4.7 years | no supervised training |
Baseline 83.6 ± 14.4 ∆ -5.1 ± 4.7 r = -0.477 |
Baseline 32.2 ± 4.6 ∆ -1.9 ± 1.8 r = -0.467 |
Baseline 95.7 ± 9.4 ∆ -4.3 ± 3.8* r = -0.492 |
Baseline 115.9 ± 10.4 ∆ -4.5 ± 4.4* r = -0.455 |
Baseline 45.0 ± 4.3 ∆ -2.5 ± 2.7* r = -0.420 |
Baseline 37.6 ± 8.6 ∆ -4.0 ± 3.5* r = -0.496 |
Baseline 17.8 ± 4.5 ∆ -2.2 ± 2.5* r = -0.403 |
Baseline 43.0 ± 7.2 ∆ -0.9 ± 2.4* r = -0.184 |
Baseline 19.7 ± 4.0 ∆ -0.6 ± 2.0 r = -0.148 |
|||
|
main outcome: The ST + CR group showed significantly greater decreases in HC, BF and trunk FM (#) |
||||||||||||||
|
Drapeau et al. (2011) |
Randomized controlled study |
Total (n = 46) |
overweight/obese postmenopausal | Duration: 26 weeks | body composition | no strength and bone mineral density parameters | ||||||||
|
BW (kg) |
BMI (kg/m2) |
BF (%) |
FM (kg) |
FFM (kg) |
subcutaneous fat (cm2) | visceral fat (cm2) | ||||||||
| ST + CR (n = 24) | Ø 58.0 ± 4.1 years |
3/ week resistance training |
CR: BRMR minus 500–800 kcal x 1.4 (PAF) 2/ month NIS AHA diet |
84.4 ± 15.1 to 77.7 ± 16.6 ∆ (relative %) -8.2 ± 5.0* r = -0.634 |
32.9 ± 4.9 to 30.3 ± 5.5 ∆ (relative %) -8.1 ± 5.0* r = -0.629 |
46.6 ± 4.2 to 42.3 ± 5.9 ∆ (relative %) -9.3 ± 8.3* r = -0.489 |
39.6 ± 10.0 to 33.6 ± 12.3 ∆ (relative %) -16.5 ± 11.5* r = -0.583 |
44.6 ± 6.3 to 44.1 ± 5.4 ∆ (relative %) -0.9 ± 4.7* r = -0.095 |
465.6 ± 92.9 to 406.8 ± 101.3 ∆ (relative %) -14.6 ± 8.0* r = -0.674 |
180.1 ± 57.9 to 146.9 ± 56.5 ∆ (relative %) -19.3 ± 10.3* r = -0.684 |
||||
|
CR (n = 22) |
Ø 58.5 ± 4.6 years | no supervised training |
82.5 ± 16.4 to 76.2 ± 15.7 ∆ (relative) -7.7 ± 3.8* r = -0.712 |
32.1 ± 5.5 to 29.7 ± 5.5 ∆ (relative) -7.7 ± 3.8* r = -0.712 |
44.3 ± 5.0 to 40.9 ± 6.6 ∆ (relative) -7.8 ± 7.9* r = -0.443 |
36.9 ± 10.0 to 31.9 ± 10.8 ∆ (relative) -14.7 ± 9.6* r = -0.608 |
45.8 ± 8.4 to 44.4 ± 7.2 ∆ (relative) -2.5 ± 5.3* r = -0.230 |
460.5 ± 122.7 to 407.1 ± 135.8 ∆ (relative) -12.6 ± 8.7* r = -0.587 |
175.8 ± 54.6 to 148.7 ± 55.3 ∆ (relative) -15.3 ± 15.3* r = -0.447 |
|||||
| No significant differences in between the groups | ||||||||||||||
|
Figueroa et al. (2013) 1 |
Randomized controlled study |
Total (n = 41) |
Obese postmenopausal | Duration: 12 weeks | body composition | No strength parameters | ||||||||
|
BW (kg) |
BMI (kg/m2) |
WC (cm) |
SMM (kg) |
SMM index (%) |
||||||||||
| ST + CR (n = 14) | Ø 54 ± 1 years |
3/ week low-intensity resistance training |
diet: approx. 1250 kcal/day portion controlled foods + recommended conventional foods |
86.8 ± 3.6 to 81.9 ± 3.5*# r = -0.181 |
32.7 ± 1.1 to 30.9 ± 0.9* r = -0.231 |
115 ± 3 to 110 ± 3* r = -0.217 |
19.5 ± 0.8 to 19.1 ± 0.7 r = -0.071 |
22.4 ± 0.6 to 23.4 ± 0.6* r = 0.217 |
||||||
|
CR (n = 14) |
Ø 55 ± 1 years | no supervised training |
92.2 ± 3.7 to 86.5 ± 3.6*# r = -0.204 |
35.1 ± 1.0 to 32.8 ± 1.1*# r = -0.280 |
118 ± 3 to 111 ± 3*# r = -0.298 |
20.5 ± 1.0 to 19.5 ± 1.1*# r = -0.126 |
22.3 ± 0.4 to 22.7 ± 0.6 r = 0.101 |
|||||||
|
ST (n = 13) |
Ø 54 ± 1 years |
3/ week low-intensity resistance training |
no prescribed diet |
88.7 ± 4.6 to 86.5 ± 4.1 r = -0.070 |
32.6 ± 1.0 to 31.8 ± 1.1 r = -0.105 |
116 ± 4 to 115 ± 4 r = -0.035 |
20.7 ± 1.0 to 21.5 ± 1.3 r = 0.094 |
23.4 ± 0.8 to 24.3 ± 0.8 r = 0.154 |
||||||
|
main outcome: the CR group had a significant decrease in BW, BMI, WC compared to ST (#), but also a significant decrease in SMM over time (*) the ST + CR group had a significant decrease only in BW compared to ST (#) and a significant increase in SMM index over time (*) - no significant differences in between the CR and ST + CR group |
||||||||||||||
|
Figueroa et al. (2013) 2 |
Randomized controlled study |
Total (n = 41) |
overweight/obese postmenopausal | Duration: 12 weeks | body composition | muscle strength | ||||||||
|
BW (kg) |
total FM (kg) |
trunk FM (kg) |
total LM (kg) |
arm LM (kg) |
leg LM (kg) |
Absolute (kg) |
Relative (kg/kg BW) |
|||||||
| ST + CR (n = 14) | Ø 54 ± 1 years |
3/ week low-intensity resistance training |
diet: approx. 1250 kcal/day portioncontrolled foods + recommended conventional foods |
86.7 ± 2.7 to 81.9 ± 2.5*# r = -0.239 |
41.9 ± 2.0 to 37.5 ± 2.0*# r = -0.282 |
22.1 ± 1.1 to 19.6 ± 1.2*# r = -0.278 |
42.4 ± 1.3 to 41.6 ± 1.2 r = -0.085 |
4.6 ± 0.2 to 4.5 ± 0.2 r = -0.067 |
14.9 ± 0.6 to 14.6 ± 0.5 r = -0.072 |
104 ± 5 to 129 ± 5*# r = 0.556 |
7.1 ± 0.4 to 8.8 ± 0.3* r = 0.533 |
|||
|
CR (n = 13) |
Ø 54 ± 1 years | no supervised training |
89.0 ± 4.4 to 83.4 ± 4.6*# r = -0.170 |
44.1 ± 2.9 to 39.7 ± 3.1*# r = -0.199 |
23.5 ± 1.7 to 20.8 ± 1.5*# r = -0.227 |
43.6 ± 1.6 to 42.3 ± 1.8* r = -0.105 |
4.8 ± 0.3 to 4.7 ± 0.3 r = -0.046 |
15.6 ± 0.8 to 14.6 ± 0.9*# r = -0.160 |
118 ± 8 to 111 ± 8 r = -0.120 |
7.6 ± 0.6 to 7.3 ± 0.6 r = -0.069 |
||||
|
ST (n = 14) |
Ø 54 ± 1 years |
3/ week low-intensity resistance training |
no prescribed diet |
88.4 ± 4.6 to 86.9 ± 4.3 r = -0.045 |
41.3 ± 3.2 to 40.2 ± 2.7 r = -0.072 |
20.2 ± 1.8 to 20.0 ± 1.6 r = -0.016 |
44.0 ± 2.1 to 44.2 ± 2.3 r = 0.012 |
4.6 ± 0.2 to 4.7 ± 0.3 r = 0.050 |
15.8 ± 0.9 to 16.1 ± 1.1 r = 0.039 |
113 ± 3 to 141 ± 8*# r = 0.471 |
7.3 ± 0.4 to 8.8 ± 0.8* r = 0.278 |
|||
|
main outcome: The CR and the ST + CR group had a significantly greater decrease in BW, total and trunk FM compared to ST group (#) Both ST groups had a significantly greater increase in absolute, relative strength compared to CR group (only)(#) |
||||||||||||||
|
Joseph et al. (2001) |
Randomized double-blind, controlled study |
Total (n = 19) |
overweight/obese postmenopausal women |
Duration: 4 weeks | body composition | muscle | ||||||||
|
BW (kg) |
BMI (kg/m2) |
WC (cm) |
waist to hip ratio |
BF (%) |
FM (kg) |
FFM (kg) |
SMM (kg) |
total body strength (%) |
||||||
| ST + CR (n = 10) | Ø 65 ± 2 years |
3/ week resistance training |
CR: 750 kcal less per day |
78.2 ± 2.1 to 75.0 ± 2.2* r = -0.229 |
29.4 ± 0.9 to 28.2 ± 0.9* r = -0.206 |
90.9 ± 2.1 to 88.2 ± 2.2* r = -0.195 |
0.81 ± 0.02 to 0.80 ± 0.02 r = -0.079 |
47.0 ± 1.4 to 44.6 ± 1.4* r = -0.262 |
36.9 ± 1.9 to 33.7 ± 1.9* r = -0.257 |
41.2 ± 0.6 to 41.3 ± 0.7 r = 0.024 |
17.9 ± 0.8 to 18.3 ± 0.8 r = 0.079 |
∆ +23 ± 2*# r = 0.866 |
||
|
CR (n = 9) |
Ø 61 ± 2 years | no supervised training |
80.8 ± 2.6 to 78.8 ± 2.7* r = -0.185 |
30.4 ± 1.0 to 29.3 ± 1.0* r = -0.180 |
97.3 ± 2.7 to 93.3 ± 2.2* r = -0.259 |
0.86 ± 0.02 to 0.85 ± 0.01 r = -0.096 |
47.2 ± 1.4 to 45.2 ± 1.6* r = -0.216 |
38.3 ± 2.1 to 35.3 ± 2.2* r = -0.226 |
42.5 ± 1.3 to 42.4 ± 1.3 r = -0.013 |
16.0 ± 1.3 to 15.4 ± 1.3*# r = -0.077 |
∆ +2 ± 2 r = 0.164 |
|||
|
main outcome: the ST + CR group showed a significantly greater increase in muscle strength and preserved SMM (#) |
||||||||||||||
|
Kerksick et al. (2020) |
Randomizedcontrolled double-blind study |
Total (n = 128) |
obese/overweight postmenopausal women (50–75 years) |
Duration: 14 weeks | body composition | muscle strength | bone mineral density | |||||||
|
BW (kg) |
FM (kg) |
FFM (kg) |
BF (%) |
bench press 1RM (kg) |
bench press volume (kg) |
leg press 1RM (kg) |
leg press volume (kg) |
bone mineral content (g) |
||||||
| ST + CRP (n = 50) |
3/ week resistance training (30 min.) |
CR (week 2–10:) 1600 kcal/day with high protein (55%) |
94.6 ± 17.5 to 90.8 ± 17.0* r = -0.109 |
42.4 ± 11.0 to 38.9 ± 10.8* r = -0.159 |
46.0 ± 7.0 to 45.6 ± 6.7 r = -0.029 |
47.4 ± 4.5 to 45.4 ± 4.9* r = -0.208 |
27.9 ± 6.2 to 31.5 ± 6.9* r = 0.264 |
183 ± 98 to 174 ± 78 r = -0.050 |
139.7 ± 36.3 to 158.5 ± 34.9* r = 0.255 |
1726 ± 1034 to 1658 ± 690 r = -0.037 |
1770 ± 292 to 1775 ± 308 r = 0.008 |
|||
| ST + CRC (n = 48) |
CR (week 2–10:) 1600 kcal/day with high carbohydrates (55%) |
90.5 ± 17.3 to 85.4 ± 16.0* r = -0.151 |
39.1 ± 10.4 to 35.5 ± 10.6* r = -0.221 |
44.7 ± 7.0 to 44.2 ± 6.7 r = -0.036 |
46.3 ± 4.0 to 44.0 ± 5.1* r = -0.240 |
28.2 ± 6.1 to 30.9 ± 6.1* r = 0.216 |
166 ± 92 to 146 ± 57 r = -0.123 |
142.4 ± 32.1 to 151.5 ± 37.8* r = 0.128 |
1472 ± 854 to 1275 ± 647 r = -0.127 |
1748 ± 248 to 1731 ± 223 r = -0.036 |
||||
|
ST (n = 30) |
no prescribed diet |
84.5 ± 11.3 to 84.1 ± 12.1 r = -0.017 |
36.5 ± 8.1 to 35.9 ± 7.8 r = -0.094 |
42.0 ± 4.0 to 43.1 ± 4.6* r = 0.127 |
46.0 ± 4.7 to 44.4 ± 4.2* r = -0.176 |
26.8 ± 5.0 to 29.5 ± 4.5* r = 0.272 |
151 ± 44 to 173 ± 60 r = 0.200 |
149.8 ± 48.6 to 164.2 ± 43.7* r = 0.154 |
1530 ± 951 to 1782 ± 1192 r = 0.115 |
1681 ± 260 to 1667 ± 240 r = -0.028 |
||||
|
main outcome: No significant differences between both CR groups The CRC and the CRP group showed a significantly greater decrease in FM compared to the control (*) Control group significant increase in FFM over time (*) |
||||||||||||||
|
McNeil et al. (2015) |
Randomized double-blind, controlled study |
Total (n = 83) |
overweight/obese postmenopausal women Ø 58.1 ± 4.8 years |
Duration: 26 weeks | body composition | No strength and bone mineral density parameters | ||||||||
|
BW (kg) |
FM (kg) |
FFM (kg) |
||||||||||||
| ST + CR (n = 28) |
3/ week resistance training |
CR: BRMR minus Ø 633 kcal x 1.4 (PAF) |
81.5 ± 11.2 to 74.8 ± 10.9 ∆ -6.7 ± 4.5* r = -0.597 |
37.9 ± 7.3 to 31.8 ± 8.1 ∆ -6.1 ± 4.1*# r = -0.597 |
43.6 ± 5.5 to 43.0 ± 4.2 ∆ -0.5 ± 2.3* r = -0.108 |
|||||||||
|
CR (n = 65) |
no supervised training |
83.5 ± 14.5 to 78.6 ± 18.3 ∆ -4.8 ± 6.7* r = -0.463 |
37.8 ± 8.8 to 33.9 ± 9.2 ∆ -3.9 ± 2.4* r = -0.476 |
45.6 ± 7.3 to 44.7 ± 6.2 ∆ -0.9 ± 2.4* r = -0.184 |
||||||||||
|
main outcome: the ST + CR training group showed a significant greater decrease in FM than CR group |
||||||||||||||
|
Ryan et al. (1996) |
non-randomized |
Total (n = 13) |
overweight/obese postmenopausal | Duration: 16 weeks | body composition | muscle strength | ||||||||
|
BW (kg) |
BMI (kg/m2) |
FM (kg) |
FFM (kg) |
BF (%) |
biceps flexion (Nm) |
triceps extension (Nm) |
leg extension (Nm) |
leg flexion (Nm) |
||||||
| ST + CR (n = 6) |
Ø 58 ± 2 years BMI > 27 kg/m2 |
3/ week resistance training |
weight reduction by approx. 0.25–0.5 kg/week 1/week NIS AHA diet |
78.5 ± 6.1 to 74.3 ± 5.8* r = -0.330 |
30.3 ± 3.1 to 28.7 ± 2.9 r = 0.391 |
33.1 ± 5.4 to 28.6 ± 4.6* r = -0.409 |
43.3 ± 1.0 to 44.2 ± 1.5 r = 0.200 |
42.8 ± 3.4 to 39.3 ± 3.7* r = -0.442 |
25 ± 10 to 36 ± 15* r = 0.410 |
33 ± 7 to 52 ± 10* r = 0.540 |
63 ± 24 to 95 ± 22* r = 0.565 |
40 ± 15 to 64 ± 15* r = 0.632 |
||
|
ST (n = 7) |
Ø 58 ± 2 years BMI < 27 kg/m2 |
AHA diet |
61.8# ± 7.9 to 61.9# ± 7.9 r = 0.006 |
23.2 ± 2.4# to 23.2 ± 2.4 r = 0.0 |
22.2 ± 6.1# to 21.8 ± 6.3 r = -0.040 |
37.6 ± 2.4# to 38.4 ± 3.2# r = 0.142 |
36.8 ± 5.0# to 35.6 ± 6.1 r = -0.107 |
18 ± 11 to 34 ± 13* r = 0.558 |
34 ± 11 to 44 ± 11* r = 0.273 |
63 ± 8 to 86 ± 21* r = 0.528 |
34 ± 11 to 57 ± 11* r = 0.736 |
|||
|
main outcome: The ST + CR group showed a significant decrease in BW, BMI, FM and BF over time (*) - no significant differences in strength parameters |
||||||||||||||
|
Ryan et al. (2003) |
Randomized double-blind, controlled study |
Total (n = 24) |
overweight/obese postmenopausal | Duration: 26 weeks | body composition | no muscle strength and bone mineral density parameter | ||||||||
|
BW (kg) |
BMI (kg/m2) |
WC (cm) |
waist to hip ratio |
FM (kg) |
FFM (kg) |
BF (%) |
||||||||
| ST + CR (n = 9) | Ø 57 ± 2 years |
3/ week resistance training |
CR: 250–350 kcal less per day AHA diet |
87.1 ± 13.9 to 81.4 ± 12.6* r = -0.210 |
32.1 ± 4.4 to 30.1 ± 4.4* r = -0.112 |
93.7 ± 10.1 to 90.4 ± 10.4* r = -0.161 |
0.81 ± 0.1 to 0.81 ± 0.1 r = 0.0 |
40.7 ± 9.5 to 35.6 ± 8.5* r = -0.268 |
45.5 ± 6.3 to 44.4 ± 5.7* r = -0.075 |
46.9 ± 5.1 to 43.9 ± 5.1* r = -0.284 |
||||
|
CR (n = 15) |
Ø 56 ± 1 years | no supervised training | ||||||||||||
|
main outcome: no significant differences between the groups for body composition and data were not shown separately |
||||||||||||||
|
Senechal et al. (2012) |
Randomizedcontrolled double-blind study |
Total (n = 38) |
obese postmenopausal women Ø 62.6 ± 4.1 years (54–74 years) |
Duration: 12 weeks | body composition | muscle strength | ||||||||
|
BW (kg) |
WC (cm) |
BF (%) |
total FM (kg) |
trunk FM (kg) |
LBM (kg) |
isometric leg strength (Nm) |
||||||||
| ST + CR (n = 9) |
3/ week resistance training |
weight reduction by 0.5–1 kg/ week 1 h/ week NIS AHA diet |
Pre 77.5 ± 7.7 ∆ -3.8 ± 1.8*# r = -0.726 |
Pre 96.6 ± 7.9 ∆ -5.3 ± 5.7* r = -0.422 |
Pre 44.4 ± 4.1 ∆ -2.2 ± 1.8*# r = -0.521 |
Pre 32.5 ± 5.9 ∆ -3.1 ± 1.8*# r = -0.653 |
Pre 16.9 ± 2.7 ∆ -2.0 ± 1.3*# r = -0.610 |
Pre 40.1 ± 2.7 ∆ -0.4 ± 0.9 r = -0.217 |
Pre 114.4 ± 20.2 ∆ -11.2 ± 17.9 r = -0.299 |
|||||
|
CR (n = 9) |
no supervised training |
Pre 78.7 ± 11.7 ∆ -4.3 ± 2.7*# r = -0.623 |
Pre 99.1 ± 7.2 ∆ -6.1 ± 3.9* r = -0.616 |
Pre 47.8 ± 2.3 ∆ -1.8 ± 1.3*# r = -0.569 |
Pre 36.2 ± 6.7 ∆ -3.2 ± 2.0*# r = -0.625 |
Pre 17.3 ± 2.4 ∆ -1.3 ± 1.1* r = -0.509 |
Pre 39.3 ± 5.2 ∆ -0.8 ± 1.2 r = -0.316 |
Pre 82.4 ± 23.6 ∆ -17.6 ± 24.9 r = -0.333 |
||||||
|
ST (n = 10) |
3/ week resistance training |
no prescribed diet |
Pre 77.5 ± 7.7 ∆ 0.5 ± 1.7# r = 0.145 |
Pre 99.8 ± 7.1 ∆ -0.7 ± 4.9 r = -0.071 |
Pre 45.4 ± 2.4 ∆ -0.6 ± 1.5 r = -0.196 |
Pre 33.8 ± 4.2 ∆ -0.2 ± 1.4 r = -0.071 |
Pre 17.3 ± 3.5 ∆ +0.2 ± 1.6 r = 0.062 |
Pre 40.6 ± 4.0 ∆ +0.5 ± 1.0 r = 0.243 |
Pre 82.3 ± 19.8 ∆ +19.8. ± 37.5 r = 0.255 |
|||||
|
C (n = 10) |
no supervised training |
Pre 77.5 ± 7.2 ∆ -0.7 ± 1.4 r = -0.243 |
Pre 99.5 ± 6.4 ∆ -1.7 ± 0.3 r = -0.094 |
Pre 47.5 ± 3.5 ∆ -0.1 ± 1.3 r = -0.038 |
Pre 35.6 ± 5.3 ∆ -0.1 ± 1.2 r = -0.042 |
Pre 18.0 ± 3.1 ∆ -0.2 ± 1.3 r = -0.077 |
Pre 39.0 ± 3.1 ∆ -0.1 ± 1.0 r = -0.050 |
Pre 102.7 ± 26.2 ∆ -13.6 ± 38.4 r = -0.174 |
||||||
|
main outcome: the CR group and ST + CR showed a significantly greater decline in BW, BF and total FM compared to control group (#) the CR group showed a significantly greater decline in BW and total FM (#) and the ST + CR group in BF%, total and trunk FM compared to ST group (#) - no significant difference between CR and ST + CR |
||||||||||||||
High-protein Diet and Protein Supplementation
Nine of the included studies [43–51] examined the effect of protein supplementation in combination with ST. Various protein sources and strategies were identified, including whey protein (10 to 40 g/serving) on training days [43–45, 50], daily soy protein supplementation (25 to 40 g/ serving) [46, 47, 49] and a general high-protein diet ranging from 1.2 to 1.8 g/kg bodyweight (kgBW) [48, 51]. The duration of the studies ranged from 8 to 24 weeks. All studies implemented ST with two, three or four sessions per week. When reported, the control groups also consumed 0.7–0.9 g of protein/kgBW.
Orsatti et al. [47] was the only study to report a significant between-group difference the groups group receiving daily soy protein supplementation (P + ST) and the ST group receiving placebo. The P + ST group showed significantly greater increase in bench press (P + ST: ∆+12.2 kg [8.5–15.9]; ST: ∆+6.9 kg [4.5–9.4]), knee extension (P + ST: ∆+6.5 kg [4.7–8.2]; ST: ∆+3.9 kg [2.2–5.5]) and total load (P + ST: ∆+23.6 kg [19.0-28.7]; ST: ∆+15.7 kg [11.1–20.4]) compared with the placebo group. Nevertheless, both groups exhibited significant improvements in all strength parameters, with high effect sizes, over the 16-week intervention. Holm et al. [44] reported a significant increase over time in LBM (42.3 ± 4.8 kg to 43.1 ± 4.8 kg) and quadriceps strength (∆+14 ± 4%) in P + ST, although no significant between-group differences were observed (ST: LBM: 42.9 ± 3.3 kg to 43.3 ± 3.3 kg; quadriceps strength: ∆+8 ± 4%). All the other studies did not detect any significant group differences between the protein-supplemented and the training controls for any outcome parameters.
Detailed information is provided in Table 3.
Table 3.
Protein
| Author/ Date | Category | Study design | Population | Training | Nutrition | Outcomes | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
de Branco et al. (2019) |
Protein timing |
Randomized parallel group, double blind study |
Total (n = 34) |
Postmenopausal Ø 60.9 ± 6.7 years |
Duration: 8 weeks | Body composition | Muscle strength | ||||||||||
|
BW (kg) |
BMI (kg/m2) |
SMM index (kg/m2) |
total LM (kg) |
Total FM (kg) |
Bench press (kg) |
leg extension (kg) |
Handgrip strength (kg) | ||||||||||
|
ST + P immediately (n = 17) |
Ø 60.5 years (57.7–63.3) |
3/ week resist. training |
immediately after exercise: 30 g of whey protein after 6 h: 30 g of carbohydrate |
69.3 [62.6–76.6] to 69.6 [62.7–77.3] r = 0.011 |
27.9 [25.2–30.8] to 28.1 [25.4–31.1]* r = 0.018 |
6.9 [6.4–7.5] to 7.1 [6.6–7.6]* r = 0.098 |
37.3 [35.0-39.7] to 38.1 [35.9–40.5]* r = 0.088 |
29.4 [24.5–35.4] to 29.3 [24.4–35.3] r = -0.005 |
29.2 [27.1–31.3] to 33.8 [31.4–36.6]* r = 0.444 |
30.0 [26.5–33.8] to 33.8 [31.0–37.0]* r = 0.278 |
27.0 [25.6–28.5] to 28.3 [26.5–30.2]* r = 0.195 |
||||||
|
ST + P 6 h post (n = 17) |
Ø 61.4 years (58.0–65.0) |
immediately after exercise: 30 g of carbohydrate after 6 h: 30 g of whey protein |
70.9 [65.6–76.7] to 71.8 [66.2–77.9] r = 0.058 |
27.6 [25.7–29.7] to 27.8 [25.8–29.9]* r = 0.026 |
6.8 [6.4–7.3] to 7.0 [6.6–7.5]* r = 0.114 |
38.2 [36.0-40.5] to 38.8 [36.5–41.3]* r = 0.066 |
30.6 [27.2–34.5] to 30.5 [27.0-34.3] r = -0.007 |
29.3 [26.2–32.7] to 34.8 [31.3–38.8]* r = 0.372 |
30.7 [26.5–35.7] to 33.3 [29.4–37.8] r = 0.150 |
27.4 [24.8–30.2] to 29.3 [26.6–32.1] r = 0.176 |
|||||||
| Main outcome: no significant differences between groups | |||||||||||||||||
|
Holm et al. (2008) |
Protein supplement |
Randomizedcontrolled double-blind study |
Total (n = 29) |
postmenopausal women |
Duration: 24 weeks | body composition | muscle | bone mineral density | |||||||||
| SMM (quadriceps) |
FM (kg) |
LBM (kg) |
quadriceps strength (%) |
total body (g/mm3) |
Femoral (g/mm3) |
Lumbar (g/mm3) |
|||||||||||
| Proximal (mm2) |
Mid (mm2) |
Distal (mm2) |
|||||||||||||||
|
ST + P (n = 13) |
Ø 55 ± 1 years |
3/ week resist. training |
after exercise: 10 g of protein (whey protein), 31 g of carbohydrate, 1 g of fat, 5 g of vitamin D and 250 mg of calcium |
2894 ± 108 to 3071 ± 124* r = 0.218 |
5099 ± 103 to 5386 ± 124* r = 0.346 |
4307 ± 189 to 4622 ± 202* r = 0.144 |
21.1 ± 4.7 to 20.6 ± 4.7 r = -0.051 |
42.3 ± 4.8 to 43.1 ± 4.8* r = 0.079 |
∆ +14 ± 4* r = 0.437 |
1.113 ± 0.027 to 1.116 ± 0.027 r = 0.015 |
0.953 ± 0.051 to 0.978 ± 0.043 r = 0.073 |
1.084 ± 0.053 to 1.108 ± 0.049* r = 0.065 |
|||||
|
ST (n = 16) |
Ø 55 ± 1 years |
after exercise: 6 g of carbohydrate and 12 mg of calcium |
3380 ± 121 to 3566 ± 140* r = 0.143 |
5565 ± 197 to 5838 ± 196* r = 0.431 |
4442 ± 158 to 4630 ± 166* r = 0.174 |
26.5 ± 10.2 to 25.8 ± 10.2 r = -0.033 |
42.9.1 ± 3.3 to 43.3 ± 3.3 r = 0.065 |
∆ +8 ± 4 r = 0.267 |
1.117 ± 0.022 to 1.122 ± 0.023 r = 0.028 |
0.943 ± 0.028 to 0.930 ± 0.024 r = -0.062 |
1.043 ± 0.032 to 1.068 ± 0.038* r = 0.088 |
||||||
| Main outcome: no significant differences between the groups | |||||||||||||||||
|
Isenmann et al. (2023) |
Protein supplement |
Randomized single-blind study |
Total (n = 24) |
postmenopausal women |
Duration: 10 weeks | body composition | muscle strength | ||||||||||
|
BW (kg) |
BMI (kg/m2) |
FFM (kg) |
SMM (kg) |
FM (kg) |
left handgrip (kg) |
right handgripp (kg) |
squat 1RM (kg) |
bench press 1RM (kg) |
|||||||||
|
mST + P (n = 10) |
Ø 54.3 ± 4.7 years |
2/ week moderate-intensity resistance training |
after exercise: carbohydrate/ protein rich meal (one of three options, 30.7–38.4 g protein and 45.5–50.9 g carbohydrates) |
70.4 ± 8.4 to 70.0 ± 8.3 r = -0.023 |
25.5 ± 2.5 to 25.4 ± 2.3 r = -0.032 |
48.1 ± 3.9 to 47.0 ± 4.4 r = -0.128 |
27.8 ± 2.2 to 27.6 ± 2.7 r = -0.037 |
22.8 ± 7.3 to 23.1 ± 6.1 r = -0.019 |
31.5 ± 3.8 to 31.0 ± 3.5 r = -0.077 |
33.3 ± 3.6 to 33.1 ± 4.5 r = -0.026 |
36.8 ± 21.5 to 60.7 ± 18.9* r = 0.507 |
27.1 ± 2.9 to 33.1 ± 5.5* r = 0.539 |
|||||
|
lST + P (n = 12) |
Ø 55.6 ± 2.9 years |
2/ week low-intensity resistance training |
69.7 ± 7.9 to 69.6 ± 8.3 r = -0.007 |
25.1 ± 2.9 to 25.1 ± 3.1 r = 0.010 |
49.2 ± 4.6 to 48.5 ± 4.0 r = -0.085 |
29.8 ± 3.2 to 28.8 ± 2.1 r = -0.178 |
20.5 ± 3.9 to 21.3 ± 4.9 r = 0.094 |
27.2 ± 5.1 to 28.7 ± 4.4 r = 0.159 |
29.8 ± 5.9 to 29.8 ± 4.7 r = -0.004 |
35.5 ± 9.2 to 62.7 ± 15.9* r = 0.703 |
27.5 ± 3.2 to 33.4 ± 3.6* r = 0.654 |
||||||
| Main outcome: no significant differences between the groups | |||||||||||||||||
| Ioannidou et al. (2024) | High-Protein Diet | Randomized Controlled Trial |
Total (n = 55) |
postmenopausal (58.2 ± 5.6 years) |
Duration: 12 weeks | body composition | Muscle strength | No bone mineral density parameter | |||||||||
|
BW (kg) |
FFM (kg) |
SMM (kg) |
FM (kg) |
Hand grip strength (kg) |
squat 1RM (kg) |
deadlift 1RM (kg) |
|||||||||||
|
ST + P (n = 15) |
Ø 57.0 ± 6.1 years |
3/ week resistance training |
1.7 g/kgBW/day |
71.6 ± 8.9 to 72.3 ± 9.1 ∆ +1.3 ± 6.7 r = 0.040 |
47.3 ± 5.5 to 48.6 ± 5.9 ∆ +1.3 ± 1.6* r = 0.110 |
19.8 ± 3.3 to 21.2 ± 3.5 ∆ +1.4 ± 0.9*# r = 0.200 |
25.9 ± 8.5 to 24.4 ± 8.4 ∆ -1.5 ± 2.0*# r = -0.090 |
29.5 ± 2.8 to 34.2 ± 3.3 ∆ +4.7 ± 2.4*# r = 0.610 |
47.5 ± 12.1 to 77.5 ± 20.3 ∆ +30.0 ± 14.2*# r = 0.650 |
56.4 ± 13.0 to 77.2 ± 13.3 ∆ +20.8 ± 10.3*# r = 0.620 |
|||||||
|
ST (n = 12) |
Ø 57.6 ± 5.1 years |
3/ week resistance training |
no specific introduction 0.9 g/kgBW/day |
68.1 ± 7.6 to 68.4 ± 8.1 ∆ +0.3 ± 0.9 r = 0.02 |
49.9 ± 8.1 to 50.6 ± 8.3 ∆ +0.6 ± 2.6 r = 0.04 |
20.6 ± 3.4 to 21.8 ± 3.8 ∆ +1.2 ± 1.3*# r = 0.160 |
23.2 ± 8.1 to 20.8 ± 7.4 ∆ -2.4 ± 2.9*# r = -0.15 |
29.8 ± 3.8 to 33.4 ± 3.6 ∆ +3.6 ± 3.0*# r = 0.39 |
42.7 ± 12.1 to 76.7 ± 12.1 ∆ +34.0 ± 12.0*# r = 0.81 |
48.3 ± 10.3 to 70.4 ± 8.4 ∆ +22.1 ± 7.6*# r = 0.76 |
|||||||
| P (n = 14) | Ø 56.8 ± 5.4 years | no specific intervention | 1.8 g/kgBW/day |
65.3 ± 7.7 to 66.5 ± 8.2 ∆ +1.2 ± 2.4 r = 0.080 |
46.2 ± 3.3 to 46.5 ± 2.8 ∆ +0.3 ± 2.2 r = 0.050 |
20.1 ± 1.7 to 20.1 ± 1.5 ∆ +0.0 ± 1.5 r = 0.000 |
18.9 ± 5.7 to 19.9 ± 6.0 ∆ +0.9 ± 1.8 r = 0.088 |
28.4 ± 2.8 to 30.0 ± 3.3 ∆ +1.7 ± 3.9* r = 0.249 |
57.2 ± 14.5 to 64.7 ± 17.1 ∆ +7.5 ± 5.4*# r = 0.230 |
54.9 ± 10.7 to 60.5 ± 11.0 ∆ +5.5 ± 7.7*# r = 0.25 |
|||||||
| C (n = 14) | Ø 60.7 ± 4.8 years | no specific intervention |
no specific intervention 0.7 g/kgBW/day |
73.0 ± 11.5 to 72.4 ± 11.4 ∆ -0.6 ± 1.4 r = -0.029 |
44.6 ± 7.9 to 43.8 ± 7.6 ∆ -0.8 ± 1.5 r = -0.049 |
19.6 ± 3.3 to 19.2 ± 3.5 ∆ -0.4 ± 1.0 r = -0.06 |
29.1 ± 9.9 to 29.2 ± 9.4 ∆ +0.2 ± 1.7 r = 0.009 |
29.2 ± 5.4 to 28.0 ± 6.5 ∆ -1.1 ± 2.2 r = -0.007 |
40.8 ± 16.5 to 40.4 ± 14.1 ∆ -0.4 ± 3.85 r = -0.008 |
44.8 ± 13.6 to 45.4 ± 13.4 ∆ +0.5 ± 3.9 r = 0.019 |
|||||||
| main outcome: -in comparison to the non-exercising control groups (P, C): The training groups (ST + P, ST) showed significant increases in all strength parameters and in SMM (#) and a significant reduction in FM (#) - in comparison to the control group (C): The diet group (P) showed a significant increase in squat and deadlift strength (#) No significant difference between the training groups (ST + P, ST) | |||||||||||||||||
|
Maesta et al. (2007) |
Daily Soy Protein |
Randomized controlled double-blind study |
Total (n = 46) |
postmenopausal | Duration: 16 weeks | body composition | No strength and bone mineral density parameters | ||||||||||
|
BMI (kg/m2) |
WC (cm) |
SMM (kg) |
BF (%) |
||||||||||||||
|
ST + P (n = 14) |
Ø 57.6 ± 6.7 years |
3/ week resistance training |
Daily: 25 g of soy protein (containing 50 mg of isoflavones) form: powder to be incorporated into 200mL of skimmed milk |
27.8 ± 4.0 to 28.1 ± 4.0 ∆ +0.3 ± 0.5 r = 0.287 |
90.9 ± 9.1 to 89.6 ± 10.1 ∆ -1.3 ± 0.9* r = -0.585 |
19.7 ± 3.3 to 21.0 ± 3.6 ∆ +1.3 ± 0.9* r = 0.585 |
32.2 ± 6.3 to 31.9 ± 6.8 ∆ -0.3 ± 4.4 r = -0.034 |
||||||||||
| P (n = 10) | Ø 61.3 ± 5.3 years | no supervised training |
27.2 ± 5.3 to 26.9 ± 5.1 ∆ -0.3 ± 0.7 r = -0.210 |
91.8 ± 14.4 to 91.3 ± 14.4 ∆ -0.6 ± 1.3 r = -0.225 |
18.3 ± 2.4 to 18.8 ± 2.5 ∆ +0.5 ± 1.0 r = 0.243 |
30.8 ± 7.0 to 29.1 ± 4.0 ∆ -1.8 ± 3.6 r = -0.243 |
|||||||||||
|
ST (n = 11) |
Ø 60.7 ± 7.1 years |
3/ week resistance training |
Daily: 25 g of maltodextrine form: powder to be incorporated into 200mL of skimmed milk |
27.7 ± 4.4 to 28.3 ± 4.9 ∆ 0.6 ± 1.3 r = 0.225 |
90.5 ± 9.8 to 88.3 ± 10.2 ∆ -2.1 ± 2.0* r = -0.465 |
17.8 ± 2.5 to 19.2 ± 2.8 ∆ +1.3 ± 1.2* r = 0.476 |
33.3 ± 8.3 to 32.9 ± 8.7 ∆ 0-0.3 ± 0.8 r = -0.184 |
||||||||||
| C (n = 11) | Ø 57.9 ± 6.9 years | no supervised training |
26.6 ± 3.6 to 26.6 ± 3.8 ∆ 0.0 ± 0.5 r = -0.030 |
92.0 ± 7.9 to 91.6 ± 9.3 ∆ -0.4 ± 3.1 r = -0.064 |
17.8 ± 2.7 to 18.6 ± 2.9 ∆ +0.7 ± 1.2 r = 0.280 |
31.7 ± 5.9 to 30.3 ± 5.7 ∆ -1.4 ± 3.5 r = -0.196 |
|||||||||||
| No significant differences between the two training groups | |||||||||||||||||
|
Orsatti et al. (2017) |
Daily Soy Protein |
Randomized controlled study |
Total (n = 32) |
postmenopausal women |
Duration: 16 weeks | Body composition | Muscle strength | No bone mineral density | |||||||||
| SMM | bench press | lat. pull down | Knee extension | total loads | |||||||||||||
|
ST + P (n = 16) |
Ø 56.8 ± 6.6 years |
3/ week resistance training |
Daily: 25 g of soy protein (containing 50 mg of isoflavones) form: powder to be incorporated into 200mL of skimmed milk |
19.5 ± 3.1 to 20.7 ± 3.5 ∆ +1.2 [0.7–1.7] r = 0.539 |
33.4 ± 7.1 to 45.5 ± 8.8 ∆ +12.2 [8.5–15.9]*# r = 0.669 |
30.3 ± 6.7 to 35.7 ± 5.5 ∆ 5.7[4.1–7.4]* r = 0.677 |
28.1 ± 6.8 to 34.7 ± 6.7 ∆ +6.5 [4.7–8.2]*# r = 0.703 |
91.8 ± 16.1 to 115.5 ± 15.7 ∆ +23.6 [19.0-28.7]*# r = 0.814 |
|||||||||
|
ST (n = 16) |
Ø 58.8 ± 8.9 years |
Daily: 25 g of maltodextrin form: powder to be incorporated into 200mL of skimmed milk |
18.0 ± 2.4 to 19.5 ± 2.7 ∆ +1.5 [1.0-1.9] r = 0.624 |
29.1 ± 7.6 to 36.0 ± 8.5 ∆ +6.9 [4.5–9.4]* r = 0.601 |
27.6 ± 6.3 to 32.0 ± 6.7 ∆ +4.4 [2.7–6.2]* r = 0.557 |
26.0 ± 5.3 to 29.6 ± 5.2 ∆ +3.9 [2.2–5.5]* r = 0.534 |
82.6 ± 17.5 to 96.8 ± 19.3 ∆ +15.7 [11.1–20.4]* r = 0.669 |
||||||||||
| Main outcome: - in comparison to the ST group: The ST + P group showed a significant increase in three of the four strength parameters compared to control (being bench press, knee extension and total of loads) (#) | |||||||||||||||||
|
Rossato et al. (2017) |
High-Protein Diet |
Randomized parallel-group, single-blind study |
Total (n = 23) |
Postmenopausal women |
Duration: 10 weeks | body composition | muscle strength | ||||||||||
|
Total LM (kg) |
Leg LM (kg) |
Trunk LM (kg) |
Total FM (kg) |
Leg extension | Bench press | ||||||||||||
| ST + high P (n = 12) | Ø 63.4 ± 7.6 years |
3/ week resistance training |
1.2 g protein /kg/day with both groups instructed to ingest similar amounts of protein after training (20–30 g) |
37.1 ± 6.2 to 38.4 ± 6.5 ∆ +1.3 ± 0.7* r = 0.259 |
12.7 ± 2.9 to 13.2 ± 3.2 ∆ +0.5 ± 0.5* r = 0.063 |
15.8 ± 7.2 to 15.7 ± 7.2 ∆ 0.0 ± 0.7 r = 0.000 |
28.6 ± 11.6 to 28.3 ± 11.4 ∆ -0.3 ± 1.1 r = 0.135 |
75.3 ± 14.8 to 84.7 ± 14.6* r = 0.137 |
32.2 ± 6.3 to 34.3 ± 7.9* r = 0.383 |
||||||||
| ST + low P (n = 11) | Ø 63.0 ± 8.6 years |
0.8 g protein /kg/day with both groups instructed to ingest similar amounts of protein after training (20–30 g) |
37.6 ± 6.2 to 38.8 ± 6.5 ∆ +1.3 ± 0.8* r = 0.210 |
12.7 ± 2.6 to 13.1 ± 2.7 ∆ 0.4 ± 0.8* r = 0.110 |
15.3 ± 5.3 to 15.2 ± 0.5 ∆ -0.2 ± 0.8 r = 0.124 |
28.0 ± 9.4 to 27.7 ± 10.4 ∆ -0.3 ± 1.5 r = -0.100 |
71.1 ± 15.8 to 77.8 ± 22.2* r = 0.192 |
33.0 ± 4.9 to 35.6 ± 5.6* r = 0.177 |
|||||||||
| Main outcome: no significant differences between groups | |||||||||||||||||
|
Shenoy et al. (2013) |
Daily Soy Protein |
Randomized controlled study |
Total (n = 60) |
postmenopausal women (45–65 years) |
Duration: 12 weeks | Muscle strength | bone mineral density | No body composition parameters | |||||||||
| Isokinetic strength (peak torque) | Maximum power | Radial | Tibial | ||||||||||||||
|
knee flexors (Nm) |
knee extensors (Nm) |
elbow flexors (Nm) |
elbow extensors (Nm) |
knee flexors (Nm) | |||||||||||||
|
ST + P (n = 20) |
Ø 54.10 ± 6.9 years |
4/ week resistance training |
Daily: 40 g of soy protein form: powder to be incorporated into 200–250 ml of milk twice a day |
38.9 ± 17.6 to 129.1 ± 47.5*# r = 0.811 |
43.1 ± 17.9 to 106.6 ± 24.2*# r = 0.833 |
19.7 ± 8.9 to 60.1 ± 9.8*# r = 0.707 |
24.5 ± 10.6 to 58.2 ± 7.7*# r = 0.872 |
18.8 ± 8.5 to 64.0 ± 10.8*# r = 0.919 |
3904.9 ± 113.1 to 4369.4 ± 85.3*# r = 0.920 |
3652.5 ± 106.8 to 4333.3 ± 90.3*# r = 0.961 |
|||||||
| P (n = 20) | Ø 54.55 ± 5.2 years | no supervised training | no supplement |
34.6 ± 13.7 to 50.4 ± 17.8* r = 0.449 |
49.1 ± 22.4 to 66.9 ± 26.9* r = 0.449 |
25.1 ± 14.4 to 37.0 ± 16.0* r = 0.363 |
25.7 ± 12.7 to 36.1 ± 13.4* r = 0.369 |
18.6 ± 11.2 to 32.5 ± 11.9* r = 0.517 |
3944.1 ± 57.0 to 4122.6 ± 96.0* r = 0.759 |
3705.5 ± 120.5 to 3985.5 ± 113.1* r = 0.701 |
|||||||
| C (n = 20) | Ø 54.05 ± 7.1 years |
33.9 ± 13.9 to 36.6 ± 13.5* r = 0.097 |
33.9 ± 13.9 to 14.0 ± 47.5* r = 0.122 |
20.0 ± 9.1 to 19.6 ± 8.5 r = -0.026 |
24.8 ± 7.8 to 24.2 ± 7.4 r = -0.043 |
20.2 ± 10.8 to 20.6 ± 11.7 r = 0.018 |
3875.5 ± 108.3 to 3868.5 ± 119.4 r = -0.031 |
3738.1 ± 126.5 to 3747.9 ± 130.4 r = 0.038 |
|||||||||
| Main outcome: - In comparison to the nutrition (P) and the control (C) group: The training intervention (ST + P) showed a significantly greater increase in all parameters (#) - in comparison to the control (C) group: the non-exercising protein (P) group showed a significant increase in isokinetic strength parameters and BMD parameters (*) | |||||||||||||||||
|
Weisgarber et al. (2015) |
Protein supplement |
Randomized double-blind within subject study |
Total (n = 12) |
postmenopausal women Ø 57 ± 4.7 years |
Duration: 10 weeks | body composition | muscle strength | ||||||||||
| SMM | LM |
biceps curls (kg) |
leg extension (kg) |
triceps extension (kg) |
leg curl (kg) |
||||||||||||
|
knee flexors (cm) |
knee extensors (cm) |
elbow flexors (cm) |
elbow extensors (cm) |
arm (g) | leg (g) | ||||||||||||
|
ST + P (n = 12) |
4/ week resist. training with training: 2/ week the right side of the body 2/ week the left side |
2/week: following each exercise: 40 g of whey protein (consumed in 4 × 10 g) |
4.4 ± 0.7 to 4.6 ± 0.6 ∆ +3.0 ± 6.6% r = 0.222 |
3.2 ± 1.0 to 3.4 ± 0.8 ∆ +6.4 ± 13.7% r = 0.227 |
2.4 ± 0.5 to 2.6 ± 0.6 ∆ +3.2 ± 9.7%* r = 0.163 |
3.3 ± 0.8 to 3.7 ± 0.6 ∆ +17.2 ± 24.3%* r = 0.334 |
1847.3 ± 419.0 to 1920 ± 419.4 r = 0.087 |
6067.3 ± 975.8 to 6228.9 ± 1082.1 r = 0.078 |
18.2 ± 3.9 to 1920 ± 419.4 ∆ +34.5 ± 32.6%* r = 0.468 |
59.7 ± 15.3 to 65.2 ± 9.9* ∆ +7.6 ± 11.2%* r = 0.321 |
11.0 ± 1.7 to 20.5 ± 4.2* ∆ +87.7 ± 24.4%* r = 0.874 |
61.8 ± 11.9 to 60.1 ± 7.4 ∆ +0.7 ± 17.0% r = -0.021 |
|||||
| ST (n = 12) |
2/ week: following each exercise: Placebo: 30 g of maltodextrin and 10 g of sucrose |
4.6 ± 0.7 to 4.6 ± 0.6 ∆ +1.7 ± 10.9% r = 0.078 |
3.3 ± 1.0 to 3.6 ± 0.85 ∆ +2.2 ± 14.8% r = 0.074 |
2.5 ± 0.5 to 2.6 ± 0.4* ∆ +12.0 ± 16.5%* r = 0.342 |
3.3 ± 0.4 to 3.7 ± 0.5* ∆ +15.2 ± 15.2%* r = 0.452 |
1808.3 ± 341.9 to 1853.0 ± 337.9 r = 0.065 |
6162.7 ± 923.5 to 6186.4 ± 1080.3 r = 0.012 |
19.0 ± 4.4 to 22.5 ± 4.1* ∆ +22.6 ± 30.1%* r = 0.351 |
61.0 ± 16.1 to 66.2 ± 13.5* ∆ +9.3 ± 30.1%* r = 0.171 |
11.0 ± 1.7 to 20.2 ± 5.2* ∆ +83.8 ± 28.7%* r = 0.825 |
61.5 ± 12.2 to 62.5 ± 7.1* ∆ +1.9 ± 13.7% r = 0.069 |
||||||
| No significant differences between groups | |||||||||||||||||
Amino Acids
In total, three studies [52–54] examined the effect of different amino acids in combination with ST. Two studies examined L-citrulline (LCi), and one focused on branched-chain amino acids (BCAA) supplementation [52–54]. Figueroa et al. [53] reported no significant differences in body composition or muscle strength between ST with and without LCi supplementation. However, the group that received both ST and 6 g of LCi per day showed a significant increase in appendicular lean mass index (from 7.6 ± 0.3 to 7.9 ± 0.3) over time, whereas neither the training-only group (8.1 ± 0.3 to 8.2 ± 0.3) nor the supplementation-only group (7.4 ± 0.3 to 7.5 ± 0.3) demonstrated significant changes. [53] Moreover, Kang et al. [54] reported that the group receiving ST combined with LCi (10 g/day) showed a significantly greater increase in leg curl strength (ST + LCi: 21.8 ± 4.7 kg to 28.7 ± 6.5 kg; ST: 19.8 ± 3.1 kg to 23.8 ± 3.8 kg) and leg lean mass (ST + LCi: 13.4 ± 2.2 kg to 14.0 ± 2.5 kg; ST: 12.6 ± 1.6 kg to 12.4 ± 1.6 kg) compared with the ST-only group. In contrast Bagheri et al. [4, 52, 53]
Table 4.
Amino acids
| Author/Date | Category | Study design | Population | Training | Nutrition | Outcomes | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Bagheri et al (2021) |
BCAA | Randomized placebo-controlled, double blind study |
Total (n = 30) |
Postmenopausal women (50–60 years) Ø 56 ± 3.7 years |
Duration: 8 weeks | Body composition | Muscle strength | |||||||||||||
| BW (kg) | BMI (kg/m2) | SMM (kg) | BF (%) | Leg press kg) | Chest press (kg) | Quadriceps Strength (kg) | Right Handgrip | Left Handgrip | ||||||||||||
|
ST + BCAA (n = 10) |
3/week resist. training |
On exercise days: 9 g of BCAA that contained 4.5 g of leucine, 2.25 g of isoleucine and 2.25 g of valine in capsule form |
71.1 ± 5.1 to 72.6 ± 5.1* r = 0.165 |
28.8 ± 1.9 to 29.5 ± 1.9* r = 0.181 |
24.3 ± 3.2 to 26.3 ± 3.5* r = 0.285 |
43.0 ± 4.4 to 39.7 ± 8.2* r = -0.226 |
∆ + 5.0° | ∆ + 4.4° |
36.5 ± 5.4 to 40.4 ± 5.7* r = 0.331 |
21.6 ± 2.5 to 25.5 ± 2.5*# r = 0.615 |
20.7 ± 2.5 to 25.6 ± 3.5*# r = 0.617 |
|||||||||
|
ST (n = 10) |
No supervised training |
On exercise days: isocaloric and isovolumetric placebo capsule of identical appearance |
71.1 ± 5.1 to 72.6 ± 5.1* r = 0.145 |
27.8 ± 1.6 to 28.4 ± 1.3* r = 0.200 |
21.6 ± 1.9 to 23.0 ± 2.2* r = 0.321 |
42.9 ± 6.3 to 40.9 ± 3.2* r = 0.180 |
∆ + 3.4° | ∆ + 3.6° |
35.0 ± 7.0 to 38.8 ± 5.7* r = 0.283 |
21.9 ± 2.8 to 24.0 ± 3.2* r = 0.328 |
21.2 ± 3.5 to 23.6 ± 3.2* r = 0.336 |
|||||||||
|
C (n = 10) |
70.1 ± 5.1 to 69.8 ± 5.1 r = -0.029 |
28.0 ± 1.9 to 28.0 ± 1.9 r = 0.000 |
21.1 ± 2.5 to 21.1 ± 1.9 r = 0.000 |
40.7 ± 7.6 to 40.7 ± 9.5 r = 0.00 |
–- | –- |
39.4 ± 5.4 to 37.3 ± 6.3* r = -0.175 |
20.7 ± 2.8 to 20.5 ± 2.5* r = -0.038 |
19.8 ± 2.2 to 18.7 ± 3.5 r = -0.177 |
|||||||||||
| Main outcome: no significant differences between the groups °no exact data published that is necessary to calculate r | ||||||||||||||||||||
|
Figueroa et al (2015) |
L-Citrulline | Randomized parallel group controlled study | Total (n = 41) |
overweight postmenopausal women |
Duration: 8 weeks | Body composition | Muscle strength | |||||||||||||
|
BW (kg) |
BMI (kg/m2) |
BF (%) |
leg LM (kg) |
arm LM (kg) |
appendicular LM index |
leg strength (kg) |
arm strength (kg) |
|||||||||||||
| WBV + LCi (n = 13) | Ø 58 ± 3 years |
3/ week whole-body vibration training |
6 g/d LCi form: capsules |
88.3 ± 11.7 to 89.1 ± 12.4 r = 0.033 |
33.8 ± 3.9 to 34.1 ± 4.3 r = 0.036 |
47.1 ± 1.3 to 46.2 ± 1.4* r = -0.353 |
15.1 ± 2.7 to 16.0 ± 2.7 r = 0.164 |
4.6 ± 0.7 to 4.7 ± 0.9 r = 0.047 |
7.6 ± 0.3 to 7.9 ± 0.3* r = 0.347 |
233 ± 51 to 316 ± 95* r = 0.654 |
55 ± 13 to 56 ± 13 r = 0.023 |
|||||||||
| WBV (n = 14) | Ø 58 ± 4 years | Placebo containing maltodextrin |
89.5 ± 10.6 to 90.0 ± 11.3 r = 0.023 |
35.0 ± 3.4 to 35.1 ± 4.0 r = 0.013 |
46.9 ± 1.4 to 46.0 ± 1.3* r = -0.406 |
15.9 ± 3.0 to 16.0 ± 2.6 r = 0.018 |
5.0 ± 0.9 to 5.0 ± 1.0 r = 0.000 |
8.1 ± 0.3 to 8.2 ± 0.3 r = 0.045 |
238 ± 72 to 316 ± 95* r = 0.414 |
58 ± 16 to 59 ± 16 r = 0.016 |
||||||||||
| LCi (n = 14) | Ø 58 ± 4 years | no supervised training |
6 g/d LCi form: capsules |
83.8 ± 8.4 to 84.4 ± 7.9 r = 0.037 |
32.7 ± 3.1 to 33.1 ± 2.8 r = 0.067 |
46.7 ± 1.3 to 46.7 ± 1.3 r = 0.000 |
14.8 ± 1.6 to 14.9 ± 1.9 r = 0.028 |
4.6 ± 0.7 to 4.7 ± 0.9 r = 0.061 |
7.4 ± 0.3 to 7.5 ± 0.3 r = 0.045 |
227 ± 56 to 238 ± 55 r = 0.099 |
56 ± 7 to 57 ± 8 r = 0.033 |
|||||||||
| Main outcome: - in comparison to LCi: the WBV group showed a significant greater increase in leg muscle strength (#) the WBV + LCi group showed a significant greater increase in leg LM and leg muscle strength (#) - no significant differences between the training groups | ||||||||||||||||||||
|
Kang et al (2022) |
L-Citrulline | Randomized, parallel-group, double blind, controlled study | Total (n = 24) | Postmenopausal women (50–75 years) | Duration: 4 weeks | Body composition | Muscle strength | |||||||||||||
| BW (kg) | BMI (kg/m2) | WC (cm) | Visceral FM (kg) | BF (%) | Arm LM (kg) | Leg LM (kg) |
Leg press (kg) |
LEG extension (kg) | Leg curl (kg) | Calf raise (kg) | ||||||||||
| ST + LCi (n = 13) | Ø 62 ± 2 years | 3/ week slow-velocity low-intensity resistance training |
10 g/d LCi form: capsules |
72.3 ± 10.1 to 72.5 ± 10.5 r = 0.010 |
29.6 ± 3.9 to 29.5 ± 4.3 r = -0.012 |
91.5 ± 10.4 to 90.8 ± 8.6 r = -0.036 |
0.84 ± 0.5 to 0.81 ± 0.5 r = -0.031 |
42.9 ± 5.0 to 42.0 ± 3.9 r = -0.097 |
4.3 ± 0.8 to 4.3 ± 0.8 r = 0.013 |
13.4 ± 2.2 to 14.0 ± 2.5*# r = 0.126 |
96.4 ± 35.0 to 109.6 ± 32.5* r = 0.192 |
20.9 ± 5.4 to 27.7 ± 7.5* r = 0.450 |
21.8 ± 4.7 to 28.7 ± 6.5*# r = 0.511 |
84.4 ± 29.9 to 102.6 ± 38.9* r = 0.250 |
||||||
| ST (n = 11) | Ø 63 ± 1 year | Placebo containing maltodextrin |
72.2 ± 12.0 to 72.4 ± 12.4 r = 0.063 |
29.2 ± 6.1 to 29.4 ± 6.1 r = 0.016 |
93.6 ± 14.8 to 92.6 ± 14.5 r = -0.032 |
1.2 ± 0.7 to 1.15 ± 0.8 r = -0.037 |
29.6 ± 3.9 to 29.5 ± 4.3 r = 0.015 |
4.1 ± 0.7 to 4.1 ± 0.7 r = 0.007 |
12.6 ± 1.6 to 12.4 ± 1.6 r = -0.060 |
88.1 ± 33.2 to 100.2 ± 30.7* r = 0.177 |
19.6 ± 4.7 to 27.3 ± 7.3* r = 0.498 |
19.8 ± 3.1 to 23.8 ± 3.8* r = 0.476 |
78.6 ± 18.7 to 94.4 ± 16.1* r = 0.395 |
|||||||
| Main outcome: ST + LC showed a significantly greater increase in leg LM and leg curl strength than ST only group (#) | ||||||||||||||||||||
Calcium and Vitamin D
Four studies [38, 55–57] investigated the effects of ST in combination with calcium and/or vitamin D supplementation. In three of these studies [38, 55, 57] the participants received 800–1000 mg of calcium/day and two of these also included a daily dose of 400 IU of vitamin D. Haghighi et al. [56] administered 50,000 IU of vitamin D every two weeks without calcium supplementation. All participants in the exercising groups performed ST three times per week. The study periods ranged from 12 weeks to four years.
The four-year longitudinal study by Cussler et al. [55–57] demonstrated that daily supplementation of 1000 mg calcium and 400 IU vitamin D was associated with a significant percentage reduction in BMD in the lumbar region (∆-1.75 %) after one year. In contrast, no decrease was observed in the ST group, which exhibited significant increases in BMD in both the lumbar region (∆-1.15 %) and the femur (∆-2.57 %). In contrast, Kerksick et al. [38] and Haghighi et al. [56] did not show any significant differences between the exercising groups. Only in comparison to the non-exercising groups, Haghighi et al. [56] showed a significantly greater increase in all four muscle strength parameters in the training groups.
Detailed information are provided in Table 5.
Table 5.
Calcium and Vitamin D
| Author/Date | Study design | Population | Training | Nutrition | Outcomes | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Cussler et al (2005) |
Randomized controlled study | Total (n = 167) |
Postmenopausal women Ø 56.15 ± 4.4 years |
Duration: 4 years aiming for: 3/ week resistance training | Body composition | Bone mineral density | No strength parameters | |||||||
|
BW (kg) |
LBM (kg) |
BF (%) |
Femur trochanter (g/cm2) | Femur neck (g/cm2) | Lumbar spine (g/cm2) | Total body (g/cm2) | ||||||||
| RT + Ca high exercise frequency | Highest exercise frequency (average: 70% of the time) | Aiming for: 800 mg/day of calcium |
∆ + 0.9 ± 3.1 r = 0.144 |
∆ 0.9 ± 1.2# r = 0.351 |
∆ -0.5 ± 2.8# r = -0.089 |
∆ + 0.014 ± 0.033# r = 0.202 |
∆ + 0.004 ± 0.037 r = 0.054 |
∆ + 0.022 ± 0.046# r = 0.233 |
∆ 0.000 ± 0.018# r = 0.000 |
|||||
|
RT + Ca middle exercise frequency |
Middle exercise frequency (average: 30%) |
∆ -0.6 ± 5.3# r = -0.057 |
∆ + 0.1 ± 1.6# r = 0.031 |
∆ -0.7 ± 4.3# r = -0.081 |
∆ -0.003 ± 0.041# r = -0.037 |
∆ -0.005 ± 0.047 r = -0.053 |
∆ -0.007 ± 0.055# r = -0.064 |
∆ -0.014 ± 0.026# r = -0.260 |
||||||
|
RT + Ca low exercise frequency |
Lowest exercise frequency including 23 controls (average: 5%) |
∆ + 2.4 ± 4–8# r = 0.243 |
∆ + 0.4 ± 1.5 r = 0.132 |
∆ + 1.7 ± 3.4# r = 0.243 |
∆ -0.007 ± 0.036# r = -0.097 |
∆ -0.005 ± 0.042 r = -0.059 |
∆ -0.010 ± 0.046# r = -0.108 |
∆ -0.011 ± 0.027# r = -0.200 |
||||||
| All groups | All exercise frequencies | < 800mg/d actual supplemental calcium intake |
∆ -1.8 ± 0.9%° r = -0.707 |
∆ -1.4 ± 0.8%° r = -0.659 |
∆ -2.2 ± 0.6%° r = -0.808 |
∆ -2.5 ± 0.3%° r = -0.972 |
||||||||
| > 800mg/d actual supplemental calcium intake |
∆ + 1.3 ± 1.3%° r = -0.447 |
∆ + 1.2 ± 1.4%° r = -0.394 |
∆ + 0.1 ± 1.3%° r = -0.038 |
∆ -1.5 ± 0.5%° r = -0.832 |
||||||||||
| Main outcome: - in comparison to group middle and low frequency: group high frequency shwoed a significantly greater increase in LBM and BMD (FT, LS and TB) - in comparison to group low frequency: group high frquency and middle showed a significantly decrease in BF and group middle a significantly decrease in BW -in comparison to a high calcium intake: the low group (< 800mg calcium/d) showed a significantly decrease in BMD (FT and TB) °no exact data published that is necessary to calculate r | ||||||||||||||
| Haghighi et al. (2024) | Randomized, double-blind, placebo-controlled study | Total (n = 44) | Postmenopausal | Duration: 12 weeks | Body composition | Muscle strength | No bone mineral density parameter | |||||||
|
BW (kg) |
BMI (kg/m2) |
leg press (kg) |
chest press (kg) |
lower body (cm) |
upper body (cm) |
|||||||||
| RT + VitD (n = 11) | Ø 55.4 ± 3.8 years | 3/ week resistance training |
Every two weeks: 50.000 IU vitamin D |
69.7 ± 8.0 to 69.2 ± 7.5 r = -0.032 |
28.6 ± 3.1 to 28.4 ± 2.9 r = -0.033 |
31.1 ± 12.8 to 53.1 ± 9.1*# r = 0.694 |
20.7 ± 8.0 to 34.9 ± 5.7*# r = 0.705 |
17.3 ± 5.5 to 18.1 ± 4.2*# r = 0.080 |
256 ± 34 to 298 ± 34*# r = 0.525 |
|||||
| RT (n = 11) | Ø 55.4 ± 0 years |
Placebo containing rice flour |
74.4 ± 7.8 to 72.5 ± 5.9* r = -0.134 |
29.8 ± 3.7 to 29.1 ± 2.8* r = -0.104 |
44.5 ± 10.0 to 63.7 ± 16.0*# r = 0.566 |
21.6 ± 5.7 to 38.6 ± 5.7*# r = 0.831 |
15.0 ± 4.5 to 18.5 ± 6.7*# r = 0.284 |
260 ± 68 to 322 ± 35*# r = 0.466 |
||||||
| VitD (n = 11) | Ø 57.4 ± 4.8 years | No supervised training | every two weeks: 50.000 IU vitamin D |
69.0 ± 12.8 to 68.0 ± 11.5 r = -0.039 |
29.9 ± 5.0 to 29.5 ± 4.5 r = -0.042 |
27.7 ± 5.9 to 28.4 ± 7.5 r = 0.051 |
20.7 ± 4.9 to 23.4 ± 8.0 r = 0.190 |
14.9 ± 2.0 to 14.2 ± 3.3 r = -0.121 |
226 ± 28 to 230 ± 28 r = 0.071 |
|||||
| C (n = 11) | Ø 55.8 ± 4.7 years | Placebo containing rice flour |
75.0 ± 13.9 to 75.1 ± 13.4 r = 0.004 |
30.1 ± 5.3 to 30.1 ± 5.2 r = 0.003 |
33.1 ± 3.6 to 34.1 ± 14.7 r = 0.038 |
27.2 ± 7.0 to 29.0 ± 7.7 r = 0.121 |
13.2 ± 5.1 to 13.1 ± 5.4 r = -0.010 |
243 ± 40 to 241 ± 38 r = -0.026 |
||||||
| Main outcome: -in comparison to VitD and C: both RT groups showed a significantly greater increase in all four muscle strength parameters (#) no significant differences between the two training groups | ||||||||||||||
|
Kerksick et al (2020) |
Randomized, controlled double-blind study | Total (n = 128) |
Obese/ overweight postmenopausal Women (50—75 years) |
Duration: 14 weeks | Body composition | Muscle strength | Bone mineral density | |||||||
|
BW (kg) |
FM (kg) |
FFM (kg) |
BF (%) |
Bench press 1RM (kg) | Bench press LV |
Leg press 1RM (kg) |
Leg press LV |
BMC (g) |
||||||
| RT + Ca (n = 47) | 3/ week resistance training (30 min.) | 800 mg/d calcium |
92.7 ± 14.6 to 88.4 ± 13.3* r = -0.152 |
41.2 ± 9.9 to 38.3 ± 9.9* r = -0.145 |
44.9 ± 5.2 to 44.4 ± 5.5 r = -0.049 |
47.4 ± 4.6 to 45.7 ± 5.2* r = -0.170 |
27.6 ± 5.6 to 29.3 ± 5.0* r = 0.158 |
142 ± 56 to 155 ± 59 r = 0.063 |
140.3 ± 31.5 to 150.8 ± 33.8* r = 0.158 |
1535 ± 738 to 1415 ± 581 r = -0.089 |
1745 ± 239 to 1761 ± 250 r = 0.033 |
|||
| RT + Ca + D (n = 42) | 800 mg/d calcium, 400 IU/d vitamin D, 300 mg magnesium, 7.5 mg zinc, 2 mg copper and 2 mg manganese |
90.4 ± 20.8 to 86.9 ± 20.2* r = 0.085 |
39.5 ± 12.8 to 35.9 ± 12.5* r = -0.141 |
44.6 ± 7.9 to 44.8 ± 7.8 r = 0.013 |
46.2 ± 5.0 to 43.6 ± 5.3* r = -0.244 |
27.6 ± 7.0 to 31.3 ± 6.5* r = 0.250 |
169 ± 71 to 161 ± 73 r = -0.055 |
141.3 ± 45.9 to 157.7 ± 40.1* r = 0.186 |
1531 ± 844 to 1644 ± 1014 r = 0.060 |
1755 ± 299 to 1732 ± 298 r = -0.038 |
||||
| RT (n = 39) |
Placebo: 800 mg maltodextrin |
88.5 ± 13.4 to 85.7 ± 12.8* r = -0.106 |
38.2 ± 7.5 to 35.5 ± 7.4* r = -0.178 |
44.1 ± 6.5 to 44.1 ± 6.1 r = 0.000 |
46.2 ± 3.4 to 44.3 ± 3.7* r = -0.258 |
28.2 ± 4.6 to 32.1 ± 6.7* r = 0.312 |
206 ± 119 to 176 ± 71 r = -0.143 |
148.8 ± 34.0 to 164.6 ± 40.2* r = 0.206 |
1720 ± 1284 to 1563 ± 860 r = 0.069 |
1719 ± 272 to 1698 ± 238 r = -0.041 |
||||
| Main outcome no significant differences between the groups | ||||||||||||||
|
Molina et al (2015) |
Randomized, controlled study | Total (n = 34) | Postmenopausal | Duration: 1 year | Boner mineral density | No strength and bone mineral density parameters | ||||||||
|
Femoral (%) |
LUMBAR (%) |
|||||||||||||
| RT + Ca (n = 7) | Ø 56.6 ± 6.5 years | 3/ week resistance training | 1000 mg/d Calcium and 400 IU/d of Vitamin D | ∆ + 2.57* | ∆ + 1.15* | |||||||||
| Ca (n = 27) | Ø 60.1 ± 10.9 years | no supervised training | ∆ -1.68 | ∆ -1.75* | ||||||||||
| Main outcome: - In comparison to the Ca group: the RT + Ca group showed a significant increase in both BMD parameters (*) | ||||||||||||||
Creatine Monohydrate
The effects of creatine monohydrate were investigated in four studies [58–61] Two studies went for one year and the other two for 12 weeks, all of them performing ST three times per week. Three studies supplied a daily dose of 0.1 g of creatine/kgBW to the intervention group [58, 59, 61] and one study 5 g of creatine per day [60].
Aguiar et al. showed, after 12 weeks of ST, a greater increase in all muscle strength parameters in the creatine group in comparison to the control group (bench press Cr: Δ+14.3 ± 6.7 %, CO: Δ+9.2 ± 4.4 %; knee extension Cr: Δ+8.6 ± 2.7 %, CO Δ+4.7 ± 1.8 %; biceps curls Cr: Δ+22.3 ± 7.1 %, CO Δ+13.5 ± 3.9 %) [60]. The body composition parameters FFM and SMM likewise only significantly increased in the creatine group but not in control without significant interaction effect. No significant differences were observed for the other body composition parameters. The only comparable outcome parameter of the other 12-week study of Johannsmeyer et al., lat pull down strength, significantly increased in both groups with no differences between the groups. After one year, Candow et al. [58] reported that the supplemented training group showed a significant group difference in lower leg muscle density. The ST group receiving creatine exhibited a significant increase compared with the exercising control group (ST + Cr: 70 [62–67] to 73 [62–67] mg/cm3; ST: 69 [62–64, 68, 69] to 70 [62–64, 68, 69] mg/cm3). Furthermore, in the study by Chilibeck et al. [59] the exercising group demonstrated a significantly greater decline in femoral neck BMD than the supplemented group. For all other parameters related to body composition, muscle strength and BMD no significant differences were observed across the year-long studies.
Detailed information is provided in Table 6.
Table 6.
Creatine
| Author/Date | Study design | Population | Training | Nutrition | Outcomes | |||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Aguiar et al (2013) |
Randomized, controlled study | Total (n = 18) | Postmenopausal women | Duration: 12 weeks | Body composition | Muscle strength | No BMD parameters | |||||||||||||||||||||
| Body mass (kg) |
FM (kg) |
BF (%) |
FFM (kg) |
SMM (kg) |
bench press (kg) | knee extension (kg) | biceps curl (kg) | |||||||||||||||||||||
|
ST + Cr (n = 9) |
Ø 64 ± 4 years |
3/ week resistance training |
5 g/d Creatine monohydrate form: capsules |
60.5 ± 9.4 to 61.2 ± 9.6 r = 0.037 |
25.4 ± 7.4 to 25.0 ± 7.4 r = -0.027 |
41.3 ± 5.6 to 40.1 ± 5.7 r = -0,106 |
35.1 ± 2.3 to 36.2 ± 2.5* r = 0.223 |
15.5 ± 1.5 to 16.1 ± 1.4* r = 0.202 |
Δ + 14.3 ± 6.7%*#° | Δ + 8.6 ± 2.7%*#° | Δ + 22.3 ± 7.1%*#° | |||||||||||||||||
|
ST (n = 9) |
Ø 65 ± 6 years | Placebo containing maltodextrin |
57.1 ± 7.3 to 57.4 ± 7.5 r = 0,02 |
22.4 ± 5.8 to 22.6 ± 6.4 r = 0.016 |
38.8 ± 6.6 to 38.9 ± 7.4 r = 0.007 |
34.7 ± 4.0 to 34.7 ± 3.8 r = 0.000 |
15.4 ± 2.6 to 15.5 ± 2.5 r = 0.02 |
Δ + 9.2 ± 4.4%*° | Δ + 4.7 ± 1.8%*° | Δ + 13.5 ± 3.9%*° | ||||||||||||||||||
|
Main outcome: - in comparison to ST: the ST + Cr group showed a significantly greater increase in all muscle strength parameters (#) and only the ST + Cr group a significant increase in FFM and SMM (*) °no further data published that is necessary to calculate r |
||||||||||||||||||||||||||||
|
Candow et al (2021) |
Randomized controlled study |
Total (n = 22) | Postmenopausal women (> 49 years) | Duration: 1 year | Body composition | Bone mineral density |
No strength parameters |
|||||||||||||||||||||
| Forearm SMM (mm2) |
Forearm muscle density (mg/cm3) |
Lower leg SMM (mm2) | Lower leg muscle density (mg/cm3) |
Distal radius (mg/cm3) |
Radial shaft (mg/cm3) | Distal tibia (mg/cm3) | Tibial shaft (mg/cm3) | |||||||||||||||||||||
| ST + Cr (n = 10) |
3/ week resistance training |
0.1g/kg/d Creatine monohydrate form: powder |
2661 (2274–3048) to 2782 (2426–3138)* r = 0.115 |
74 (73–75) to 74 (73–75) r = 0.000 |
6198 5501–6896) to 6023 (5313–6732)* r = -0.089 |
70 (68–73) to 71 (68–73)# r = 0.142 |
285 (253–317) to 279 (248–311) r = -0.138 |
1110 (1088–1132) to 1114 (1091–1137) r = 0.027 |
274 (253–295) to 272 (252–293)* r = -0.025 |
1081 (1059–1102) to 1082 (1061–1103) r = -0.024 |
||||||||||||||||||
|
ST (n = 12) |
Placebo containing maltodextrin |
2956 (2603–3309) to 3000 (2675–3324)* r = 0.041 |
74 (73–75) to 74 (73–75) r = 0.000 |
7071 6406–7736) to 6680 (6003–7356)* r = -0.182 |
69 (66–71) to 68 (66–70) r = -0.137 |
283 (254–312) to 277 (248–305) r = -0.031 |
1108 (1088–1129) to 1103 (1082–1124) r = -0.025 |
284 (264–304) to 281 (262–301)* r = 0.016 |
1068 (1048–1089) to 1074 (1054–1094) r = 0.044 |
|||||||||||||||||||
| Main outcome: the ST + Cr group showed a significant increase in lower leg muscle density compared to ST only (#) | ||||||||||||||||||||||||||||
|
Chilibeck et al (2015) |
Randomized, controlled study | Total (n = 33) | Postmenopausal women | Duration: 1 year | Body composition | Muscle strength | Bone mineral density | |||||||||||||||||||||
|
LBM (kg) |
Triceps SMM (thickness) (cm) | Quadriceps SMM (thickness) (cm) | Gastrocnemius SMM (thickness) (cm) |
Bench press (kg) |
Squat press (kg) |
Femoral neck (mg/cm3) |
Total hip (mg/cm3) |
Lumbar spine (mg/cm3) |
Total body (mg/cm3) |
|||||||||||||||||||
| ST + Cr (n = 15) | Ø 57 ± 4 years |
3/ week resistance training |
0.1g/kg/d Creatine monohydrate form: powder |
∆ -1.0 (-2.1 to 0.8)* r = -0.224 |
∆ + 0.3 (-0.1 to 0.7)* r = 0.186 |
∆ + 0.2 (-0.3 to 0.6) r = 0.101 |
∆ + 0.5 (-0.1 to 1.2)* r = 0.206 |
∆ + 18 (10 to 25)* r = 0.495 |
∆ + 54 (29 to 79)* r = 0.480 |
∆ -0.010 (-0.025 to 0.005) r = -0.166 |
∆ -0.015 (-0.037 to 0.007)* r = -0.170 |
∆ + 0.005 (-0.017 to 0.028) r = 0.057 |
∆ -0.008 (-0.018 to 0.002) r = -0.198 |
|||||||||||||||
|
ST (n = 18) |
Ø 57 ± 7 years | Placebo containing maltodextrin |
∆ -1.3 (-2.3 to -0.3)* r = -0.288 |
∆ + 0.4 (0 to 0.8)* r = 0.225 |
∆ + 0.3 (-0.1 to 0.8) r = 0.171 |
∆ + 0.5 (-0.1 to 1.1)* r = 0.189 |
∆ + 11 (5 to 18)* r = 0.390 |
∆ + 50 (29 to 71)* r = 0.482 |
∆ -0.030 (-0.044 to 0.017)# r = -0.444 |
∆ -0.016 (-0.036 to 0.004)* r = -0.182 |
∆ -0.007 (-0.027 to 0.014) r = -0.081 |
∆ + 0.002 (-0.007 to 0.012) r = 0.051 |
||||||||||||||||
| Main outcome: the ST group showed a significantly greater decrease in femoral neck BMD than ST + Cr group | ||||||||||||||||||||||||||||
|
Johanns meyer et al. (2016) |
Randomized, controlled study | Total (n = 14) | Postmeno-pausal women | Duration: 12 weeks | Muscle strength | Body composition and other muscle strength parameters were not differentiated between males and females | ||||||||||||||||||||||
| Lat. pull down (kg) | ||||||||||||||||||||||||||||
|
ST + Cr (n = 7) |
Ø 58 ± 3 years | 3/ week resistance training |
0.1 g/kg/d Creatine monohydrate form: powder |
39.3 ± 5.9 to 45.8 ± 7.2 r = 0.439* |
||||||||||||||||||||||||
| ST (n = 7) | Ø 57.6 ± 5 years | Placebo containing maltodextrin |
38.2 ± 9.7 to 45.6 ± 10.6 r = 0.342* |
|||||||||||||||||||||||||
| No significant differences between groups | ||||||||||||||||||||||||||||
Zataria Multiflora
The effects of Zataria multiflora (Z) supplementation in combination with strength training were examined in two studies involving postmenopausal women over an eight-week period [70, 71]. Ghanbari-Niaki et al. observed a significant group difference in SMM and FM between ST + Z and control group, but not when compared ST only or Z only. The ST + Z group showed a reduction in FM from 21.0 ± 1.4 kg to 18.0 ± 1.1 kg compared with 20.1 ± 2.1 kg to 17.0 ± 1.9 kg in the ST group and from 19.9 ± 1.9 kg to 18.6 ± 1.4 kg in the Z group. In addition, both training groups showed a significant increase in SMM over time whereas no significant change was observed in the Z only group (ST + Z: 28.0 ± 1.9 kg to 29.6 ± 1.9 kg; ST: 26.8 ± 2.8 kg to 28.4 ± 2.2 kg; Z: 26.5 ± 2.5 kg to 26.8 ± 2.1 kg) [72]. Tayebi et al. reported similar results for BF and SMM. A significant decrease in BF over time was observed for ST + Z at both training intensities (35 % and 55 %) as well as in the Z only group without training. Moreover, significant group differences were found between each training group and the control group, whereas no differences were detected between the training groups. In addition, only the training groups exercising at an intensity of 55 % showed a significant increase in SMM over time [71].
Detailed information is provided in Table 6.
Omega-3 Fatty Acids (“Fish Oil”)
Only one study has investigated the combined effects of ST and omega-3 fatty acid (FO) supplementation. Felix-Soriano et al. [73] evaluated the effects of FO supplementation combined with ST performed twice per week. Participants received a daily dose of 1650 mg docosahexaenoic acid (DHA) and 150 mg eicosapentaenoic acid (EPA) alongside a Mediterranean diet. Over the 16-week intervention, no significant differences were observed between the two training groups; significant differences were only noted in comparison with the non-exercising groups (see Sect. 3.10). Both training groups showed significant increases in muscle strength in the upper body (ST + FO: ∆+0.11 ± 0.05 kg/kg LBM; ST: ∆+0.08 ± 0.06 kg/kg LBM, FO: ∆+0.02 ± 0.03 kg/kg LBM; C: ∆+0.02 ± 0.03 kg/kg LBM), lower body (ST + FO: ∆+1.0 ± 0.8 kg/kg LBM; ST: ∆+0.8 ± 0.6 kg/kg LBM, FO: ∆+0.3 ± 0.4 kg/kg LBM; C: ∆+0.0 ± 0.3 kg/kg LBM), and in lower limb muscle quality (ST + FO: ∆+2.0 ± 1.3 kg/kg LBM; ST: ∆+1.3 ± 1.2 kg/kg LBM, FO: ∆+0.4 ± 0.8 kg/kg LBM; C: ∆-0.4 ± 0.8 kg/kg LBM), compared with the control group. A significant decrease in BMC over time was observed in the FO and control groups, but not in either training groups (ST + FO: ∆-1.4 ± 32.8 g; ST: ∆ -1.4 ± 30.3 g, FO: ∆-17.5 ± 20.2 g; C: ∆-27.6 ± 17.4 g).
Detailed information is provided in Table 7.
Table 7.
Others
| Author/Date | Category | Study design | Population | Training | Nutrition | Outcomes | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Felix-Soriano et al (2021) |
Fish oil |
Randomized, parallel-group, double blind, controlled study |
Total (n = 71) |
Overweight/obese postmenopausal women 55–70 years |
Duration: 16 weeks | Body composition | Muscle strength | Bone mineral density | ||||||||||||||
|
BW (kg) |
WC (cm) |
Waist to hip ratio |
BF (%) |
Visceral FM (kg) |
LBM (%) |
CHEST press 1RM (kg/kg LBM) | Leg press 1RM (kg/kg LBM) | Lower limbs muscle quality | BMC (g) | |||||||||||||
| ST + FO (n = 16) | Ø 58.13 ± 3.14 years |
2/ week resistance training |
Omega-3 fish oil: 1650 mg/d DHA + 150 mg/d EPA form: capsules + Mediterranean diet |
Pre 80.6 ± 6.6 ∆ -2.7 ± 3.5* r = -0.361 |
Pre 93.9 ± 7.7 ∆ -4.0 ± 3.7* r = -0.476 |
Pre 0.83 ± 0.06 ∆ -0.02 ± 0.03 r = -0.316 |
Pre 46.7 ± 2.9 ∆ -2.1 ± 2.4* r = -0.404 |
Pre 1.2 ± 0.5 ∆ -0.1 ± 0.2* r = -0.252 |
Pre 50.5 ± 2.7 ∆ -2.0 ± 2.3* r = 0.395 |
Pre 0.44 ± 0.05 ∆ + 0.11 ± 0.05*# r = 0.729 |
Pre 2.0 ± 0.3 ∆ + 1.0 ± 0.8*# r = 0.563 |
Pre 10.9 ± 1.3 ∆ + 2.0 ± 1.3*# r = 0.595 |
Pre 2240.3 ± 258.4 ∆ -1.4 ± 32.8 r = -0.021 |
|||||||||
|
ST (n = 20) |
Ø 58.95 ± 3.46 years |
Placebo containing olive oil form: capsules + Mediterranean diet |
Pre 77.8 ± 7.9 ∆ -2.2 ± 2.4* r = -0.420 |
Pre 92.7 ± 5.5 ∆ -3.01 ± 1.8* r = -0.641 |
Pre 0.84 ± 0.06 ∆ -0.00 ± 0.04 r = 0.0 |
Pre 47.1 ± 4.0 ∆ -1.8 ± 1.5* r = -0.508 |
Pre 1.3 ± 0.5 ∆ -0.1 ± 0.2* r = -0.292 |
Pre 50.2 ± 3.8 ∆ -1.7 ± 1.4* r = 0.511 |
Pre 0.45 ± 0.08 ∆ + 0.08 ± 0.09*# r = 0.430* |
Pre 2.2 ± 0.4 ∆ + 0.8 ± 0.6*# r = 0.561 |
Pre 12.0 ± 1.8 ∆ + 1.3 ± 1.2*# r = 0.476* |
Pre 2156.1 ± 231.2 ∆ -1.4 ± 30.3 r = 0.023 |
||||||||||
|
FO (n = 15) |
Ø 58.0 ± 2.78 years | no supervised training |
Omega-3 fish oil + Mediterranean diet |
Pre 80.3 ± 8.5 ∆ -2.7 ± 2.5* r = -0.473 |
Pre 95.0 ± 7.6 ∆ -3.2 ± 2.9* r = -0.472 |
Pre 0.85 ± 0.06 ∆ -0.01 ± 0.01* r = -0.447 |
Pre 45.6 ± 2.4 ∆ -1.6 ± 1.3* r = -0.508 |
Pre 1.4 ± 0.4 ∆ -0.1 ± 0.1* r = -0.366 |
Pre 51.5 ± 2.2 ∆ -1.5 ± 1.3* r = 0.509 |
Pre 0.44 ± 0.10 ∆ + 0.02 ± 0.03* r = 0.358 |
Pre 2.3 ± 0.5 ∆ + 0.3 ± 0.4* r = 0.408 |
Pre 11.9 ± 2.2 ∆ + 0.4 ± 0.8* r = 0.238 |
Pre 2366.3 ± 332.8 ∆ -17.5 ± 20.2* r = -0.398 |
|||||||||
|
C (n = 20) |
Ø 58.75 ± 3.39 years |
Placebo + Mediterranean diet |
Pre 76.7 ± 5.0 ∆ -2.7 ± 2.9* r = -0.411 |
Pre 93.1 ± 4.5 ∆ -3.5 ± 2.6* r = -0.550 |
Pre 0.84 ± 0.04 ∆ -0.01 ± 0.01* r = -0.447 |
Pre 47.4 ± 3.4 ∆ -2.3 ± 1.1* r = -0.706 |
Pre 1.3 ± 0.4 ∆ -0.2 ± 0.2* r = -0.466 |
Pre 49.8 ± 3.2 ∆ -2.0 ± 1.0* r = 0.715 |
Pre 0.44 ± 0.08 ∆ + 0.02 ± 0.03 r = 0.289 |
Pre 2.2 ± 0.4 ∆ 0.0 ± 0.3 r = 0.051 |
Pre 11.6 ± 3.4 ∆ -0.4 ± 0.8 r = -0.252 |
Pre 2152.7 ± 308.1 ∆ -27.6 ± 17.4* r = -0.622 |
||||||||||
| Main outcome: - in comparison to the FO and C group: the training groups significantly prevented BMD reduction and the training groups showed a significantly greater increase in muscle strength and muscle quality - no significant differences between the training groups | ||||||||||||||||||||||
|
Ghanbari-Niaki et al (2018) |
Zataria multiflora |
Randomized, parallel-group, double blind, controlled study |
Total (n = 48) |
Postmenopausal women |
Duration: 8 weeks | Body composition | No strength and bone mineral density parameters | |||||||||||||||
|
BW (kg) |
BMI (kg/m2) |
FM (%) |
SMM (kg) |
|||||||||||||||||||
|
ST + Z (n = 12) |
Ø 53.8 ± 6.0 years |
3/ week resistance training |
500 mg/d Z. multiflora |
69.9 ± 5.7 to 67.0 ± 4.0* r = -0.275 |
27.6 ± 2.7 to 26.4 ± 2.1* r = -0.237 |
21.0 ± 1.4 to 18.0 ± 1.1*# r = -0.762 |
28.0 ± 1.9 to 29.0 ± 1.9* r = 0.278 |
|||||||||||||||
|
ST (n = 12) |
Ø 58.03 ± 4.7 years | Placebo containing wheat flour |
67.1 ± 7.2 to 64.3 ± 5.6* r = -0.209 |
26.6 ± 3.1 to 25.5 ± 2.3*# r = -0.194 |
20.1 ± 2.1 to 17.0 ± 1.9*# r = -0.599 |
26.8 ± 2.8 to 28.4 ± 2.2* r = 0.299 |
||||||||||||||||
|
Z (n = 12) |
Ø 54.4 ± 3.9 years | No supervised training | 500 mg/d Z. multiflora |
66.4 ± 10.9 to 65.9 ± 5.1* r = -0.026 |
25.6 ± 2.2 to 25.4 ± 1.6# r = -0.051 |
19.9 ± 1.9 to 18.6 ± 1.4*# r = -0.356 |
26.5 ± 2.5 to 26.8 ± 2.1 r = 0.064 |
|||||||||||||||
|
C (n = 12) |
Ø 56.5 ± 4.2 years | Placebo containing wheat flour |
68.7 ± 13.3 to 68.7 ± 4.7 r = 000 |
27.9 ± 2.2 to 27.9 ± 1.8 r = 000 |
20.6 ± 1.7 to 20.5 ± 1.6 r = -0.030 |
27.6 ± 2.5 to 27.6 ± 2.3 r = 000 |
||||||||||||||||
| Main outcome: - in comparison with C: The Z and ST group has a significant difference in BMI and FM compared to C group (#) ST + Z group has a significant difference in FM compared to C group (#) -in comparison to Z: ST + Z group showed a significantly greater decrease in FM and a significantly greater increase in SMM (#) -no significant differences between the training groups | ||||||||||||||||||||||
|
Tayebi et al (2019) |
Zataria multiflora |
Randomized, parallel-group, double blind, controlled study |
Total (n = 72) |
Postmenopausal women |
Duration: 8 weeks | Body composition | No strength and bone mineral density parameters | |||||||||||||||
|
BW (kg) |
BMI (kg/m2) |
BF (%) |
SMM (kg) |
|||||||||||||||||||
|
ST 55 + Z (n = 12) |
Ø 53.8 ± 6 years |
3/ week resistance training intensity: 55% of 1RM |
500 mg/d Z. multiflora |
69.9 ± 5.7. to 67.0 ± 4.0* r = -0.275 |
27.6 ± 2.7 to 26.4 ± 2.1* r = -0.237 |
21.0 ± 1.4 to 18.0 ± 1.1*# r = -0.762 |
28.0 ± 1.9 to 29.5 ± 1.9 + # r = 0.367 |
|||||||||||||||
|
ST 55 (n = 12) |
Ø 58.0 ± 4.7 years | Placebo |
67.1 ± 7.2 to 64.3 ± 4.0* r = -0.209 |
27.6 ± 2.7 to 25.6 ± 2.3* r = -0.194 |
20.1 ± 1.4 to 18.0 ± 1.1*# r = -0.599 |
26.8 ± 2.8 to 28.4 ± 2.2* r = 0.299 |
||||||||||||||||
|
ST 35 + Z (n = 12) |
Ø 55.8 ± 4.5 years |
3/ week resistance training intensity: 35% of 1RM |
500 mg/d Z. multiflora |
66.8 ± 6.5 to 64.4 ± 5.0* r = -0.199 |
27.6 ± 2.7 to 26.6 ± 1.9* r = -0.204 |
20.0 ± 1.9 to 17.5 ± 1.4*# r = -0.591 |
26.7 ± 2.6 to 27.8 ± 2.0 r = 0.227 |
|||||||||||||||
|
ST 35 (n = 12) |
Ø 57.7 ± 3.6 years | Placebo |
69.3 ± 6.7 to 67.5 ± 3.9 r = -0.153 |
27.8 ± 2.9 to 27.0 ± 1.7 r = -0.157 |
20.7 ± 2.0 to 18.7 ± 1.2*# r = -0.498 |
27.7 ± 2.7 to 28.7 ± 1.6 r = 0.208 |
||||||||||||||||
|
Z (n = 12) |
Ø 54.4 ± 3.9 years | no supervised training | 500 mg/d Z. multiflora |
66.4 ± 6.4 to 65.9 ± 5.1 r = -0.043 |
25.6 ± 2.2 to 25.4 ± 1.6 r = -0.051 |
19.9 ± 1.9 to 18.6 ± 1.4* r = -0.356 |
26.5 ± 2.5 to 26.8 ± 2.1 r = 0.064 |
|||||||||||||||
|
C (n = 12) |
Ø 56.5 ± 4.2 years | Placebo |
68.7 ± 5.9 to 68.7 ± 4.7 r = 0.000 |
27.9 ± 2.2 to 27.9 ± 1.8 r = 0.000 |
20.6 ± 1.7 to 20.5 ± 1.6 r = -0.030 |
27.6 ± 2.5 to 27.6 ± 2.3 r = 0.0 |
||||||||||||||||
| Main outcome no significant differences were observed between the groups with the same training intensity | ||||||||||||||||||||||
| Greed et al. (2025) | Shatavari |
Randomized, parallel-group, double blind, controlled study |
Total (n = 22) | Postmenopausal women | Duration: 8 weeks | Muscle strength | No body composition and bone mineral density parameter | |||||||||||||||
|
Knee extension (kg) |
Leg press (kg) |
Hand grip strength (kg) |
||||||||||||||||||||
| SH (n = 12) | Ø 62.7 ± 5.3 years | 2/ week resistance training | 1000mg/d Shatavari |
59.8 ± 3.5 to 73.8 ± 12.3* r = 0.538 |
138.7 ± 14.0 to 206.3 ± 42.1* r = 0.673 |
22.9 ± 3.8 to 24.1 ± 4.6 r = 0.140 |
||||||||||||||||
| PL (n = 11) | Placebo |
59.8 ± 9.2 to 70.3 ± 12.5* r = 0.424 |
121.0 ± 29.5 to 180.2 ± 47.5* r = 0.580 |
25.9 ± 4.4 to 26.9 ± 4.8 r = 0108 |
||||||||||||||||||
| Main outcome no significant differences were observed between the groups | ||||||||||||||||||||||
AHA = American Heart Association; BCAA = branched-chain amino acids; BF% = Body Fat Percentage; BMD = Bone Mineral Density; BMI = Body Mass Index; BRMR = Baseline Resting Metabolic Rate; BW = Body Weight; C = Control; Ca = Calcium; CR = Caloric Restriction; Cr = Creatine; FFM = Fat Free Mass; FM = Fatt Mass; FO = Fish Oil; HC = Hip Circumference; LBM = Lean Body Mass; LCi = L-Citrulline; SMM = Skeletal Muscle Mass; SH = shatavari; NIS = Nutritional Information Session; P = Protein; PAF = Physical Activity Factor; ST = Strength Training; VitD = Vitamin D; WBV = Whole-body vibration; WC = Waist Circumference; Z = Zataria multiflora; 1RM = One-Repetition-Maximum; r = Pearson correlation coefficient r; * = significant time change; # = significant differences in comparison to other group
Shatavari
The potential performance-enhancing effect of Shatavari extract was conducted in one study by Greed et al. [68] Participants consumed a daily dose of 1000 mg of Shatavari extract over eight weeks, while performing ST twice per week. No significant differences were observed between the Shatavari and the placebo groups for all strength-related parameters. Body composition and BMD were not assessed.
Detailed information is provided in Table 7.
Strength Training vs. Non-exercising Control
When comparing exercising and non-exercising groups, several significant differences were observed, except in control groups following caloric restriction. Bagheri et al. [52] reported significant increases in BW and BMI in the training groups compared with the non-exercising controls, whereas Ghanbari-Niaki et al. [70] observed significant decreases relative to the unchanged control group. All other included studies did not report comparable effects. Regarding body composition parameters, all studies including the two mentioned above showed similar effects with a significant reduction in BF [52, 55, 71], FM [51, 70] and WC [46] and a significant increase in SMM [46, 51, 52, 70, 71] or LBM [55] compared with non-exercising control groups. In terms of muscle strength, all ST groups demonstrated significant improvements compared to the control groups. Eight studies [32, 42, 49, 51–53, 56, 73] assessed a total of seven different exercises for the lower body while five studies [49, 51, 52, 56, 73] evaluated five different exercises for the upper body.
Finally, four studies [49, 55, 57, 73] showed significant differences in BMD. All ST groups showed a greater increase compared to the non-exercising control groups.
More detailed information is provided in Tables 2, 3, 4, 5, 6 and 7.
Discussion
This systematic review aimed to examine the additive effects of nutritional strategies in combination with ST on body composition, strength capacity, and BMD in postmenopausal women with an average age below 65 years. In total, 34 studies comprising 1,541 participants were identified and analyzed. The interventions included CRD (n = 11), high-protein diets (n = 3), protein supplementation (n = 6), and the use of amino acids (n = 3), calcium (n = 3), vitamin D (n = 3), creatine (n = 4), omega-3 fatty acids (n = 1), zataria multiflora (n = 2) and shatavari (n = 1).
Benefits of Strength Training and Dose Responses
ST generally exerts a significant positive influence on body composition, strength capacity, and BMD. Systematic ST has been shown to reduce FM or BF and increase SMM or LBM. Regarding training frequency, initial evidence from one study suggests that performing two sessions per week with free weights at low (50–60% of 1-RM) to moderate intensities (70–80% of 1-RM) over a 10-week period may be insufficient to elicit significant changes in body composition [45]. In comparison, the same training protocol demonstrated an increase in FFM and SMM in premenopausal women [45]. In contrast, Félix-Soriano et al. [73] reported a significant increase in LBM following a 16-week training intervention with two sessions per week. These findings, however, should be interpreted with caution, as a similar increase was also observed in the control group that did not participate in ST. [73] However, regarding strength capacity, one study found that performing ST twice per week led to significant improvements in squat and bench press strength in postmenopausal women, comparable to those observed in premenopausal women [45].
Studies implementing three or four training sessions per week showed significant improvements in body composition, muscle strength and BMD [32, 33, 36, 37, 39, 41, 43, 44, 46–52, 55–57, 70, 71]. Concerning training intensity, individual studies suggest that higher intensities may elicit a greater effect than lower intensities [55, 71]. However, definitive conclusions on dose-response relationships cannot be drawn due to the limited number of studies and lack of formal statistical analyses. Current reviews on the effects of ST alone also report inconsistent findings. A meta-analysis by González-Gálvez et al. [18] indicated that three 60 min training sessions per week, significantly improved lower and upper body strength in postmenopausal women. However, these findings were not corroborated by Thomas et al. [8] and Borde et al. [69] Notably, Borde et al. [69] observed significant changes in muscle morphology with only two training sessions per week. Comparisons between younger and older adults further suggests that younger individuals derive greater benefits from higher training frequencies than older individuals.
Regarding the effects of ST on BMD, a meta-analysis by Shojaa et al. [16] reported that even one training session per week is sufficient to increase BMD. However, the authors noted several limitations, including that some studies failed to observe significant differences in BMD across varying training frequencies. In contrast, other studies have consistently demonstrated significantly greater improvements in lumbar and hip BMD when training frequencies of two or more sessions per week are employed [16].
Caloric Restriction
Sarcopenic obesity is considered a potential risks associated with menopause [14], and dietary interventions may represent a logical strategy to enhance the beneficial effects of ST on body composition. A meta-analysis by Cheng et al. [62] further demonstrated that dietary interventions were more effective than exercise alone in reducing BW and body composition parameters in peri- and postmenopausal women. In this review similar effects were observed when combining CRD and ST. An additional daily calorie deficit between 250 and 750 kcal significantly contributes to reduction in body composition, such as BMI, FM or BF parameters [32, 35, 36, 38, 42]. Furthermore, compared CRD alone LBM, including SMM, can be maintained through ST [32–36]. ST also increases daily energy expenditure, meaning that participants in CRD + ST interventions experience a greater actual energy deficit than the prescribed 250 kcal. The continuous activation of SMM can further enhance long-term energy expenditure, thereby promoting FM reduction while preserving SMM [63].
Regarding muscle strength, combining ST with CRD may reduce strength gains when the caloric deficit is excessive, as demonstrated in two studies targeting a weight loss of 0.5–1 kg/week [32, 42]. Furthermore, the additional benefits of ST on body composition parameters appear diminished under excessive caloric restriction, particularly when the deficit is not individualized according to initial BW [32–36, 42].
In terms of BMD, the study of Kerskick et al. [38] (PEDro: 9) showed no significant effects of a CRD (1600 kcal/day) on BMD. In contrast a previous investigation by Svendsen et al. [64] observed a significant decrease in BMD in postmenopausal women after CRD combined with concurrent training. Examining the intervention groups’ calorie intake, the groups reduced their daily energy intake by more than 800 kcal/day (daily intake diet: ~1093 kcal/day; diet + exercise: ~1051 kcal/day), which may be insufficient to preserve BMD. These findings suggest that an excessively restrictive CRD can attenuate the beneficial effects of training and lead to a significant reduction in BMD. Likewise, Seimon et al. [65] reported a greater decrease in total hip BMD in postmenopausal women subjected to severe energy restriction (65–75% of estimated energy expenditure) compared with those under moderate restriction (25–35% of estimated energy expenditure). Collectively, these findings indicate that excessively restrictive CRD may reduce BMD, even when physical activity is systematically implemented.
Protein
Proteins are macronutrients that are metabolized into amino acids within the body [66]. Amino acid availability serves as a key regulatory factor in muscle protein metabolism with improvements in muscular strength and body composition resulting from ST, depending on a predominance of protein anabolism over catabolism [67]. Accordingly, protein intake following exercise can maximize protein synthesis and offset protein catabolism [74]. Consistent with this, studies with healthy adults demonstrated that protein supplementation enhances muscle strength and hypertrophy when combined with ST [25].
When evaluating the effects of protein supplementation, distinctions must be made regarding the form and timing of intake. In this review, three studies provided protein supplementation only immediately after each exercise session [44, 45, 50]. Notably, one of these studies [45] implemented ST only twice per week, which may explain the absence of significant effects, as discussed previously. Additionally, Weisgarber et al. [50] employed a within-participants design alternating between placebo and whey protein supplementation per day of exercise while participants performed unilateral ST. No significant differences were observed between sides of the body of the same participants. The only comparable study by Holm et al. [44] likewise did not reveal significant differences between the two exercising groups overall, but did report a significant time-related increase in LBM and muscle strength in the supplemented training group. When total protein intake was examined, the supplemented group consumed an average of 1.1 g/kgBW/day throughout the intervention, compared with 0.9 g/kgBW/day in the non-supplemented group. Similarly, regarding protein timing, no significant differences were observed between consuming the same amount of protein immediately after exercise or six hours later [43]. This finding is consistent by a meta-analysis of Wirth et al. [75], which reported no additional benefits of a specific protein timing on LBM and muscle strength.
Regarding plant-based protein source, three studies provided daily soy protein supplementation [46, 47, 49]. Of these Shenoy et al. [49] (PEDro: 7) compared the supplemented training group only with non-exercising groups, precluding conclusions about the additional effects of protein supplementation in combination with ST. Maesta et al. [46] (PEDro: 7) did not observe significant differences between the training groups overall, although the supplemented training group demonstrated higher effect sizes for reductions in WC and increases in SMM. Notably, total daily protein intake was not reported in any group. In contrast, Orsatti et al. [47] (PEDro: 9) reported a significantly greater increase in three of four strength parameters in the supplemented training group which consumed an average of 1.4 g/kgBW/day compared with 1.0 g/kgBW/day in the non-supplemented training group.
Additionally, Ioannidou et al. [51] (PEDro: 8) demonstrated that a high-protein diet al.one, providing at least 2.5 g/kg FFM (1.8 g/kgBW/day), significantly improved strength parameters. When combined with ST, the high-protein group (1.7 g/kgBW/day) exhibited greater absolute gains in SMM (ST + P: ∆+1.4 ± 0.9 kg; ST alone: ∆+1.2 ± 1.3 kg), although these differences did not reach statistically significance and should be interpreted with caution. The authors also reported a significant ALT enzyme activity with the high-protein diet. While, there is currently no evidence of adverse effects of a high-protein diet in younger populations, further research in older women is needed to draw definitive conclusions [76, 77]. Current meta-analyses by Kuo et al. [78] support an additive effect of a high-protein diet and are consistent with the current recommendations of the International Society of Sports Nutrition [77]. However, among postmenopausal women, only two high-quality studies (PEDro: 8 and 9) have investigated a high-protein diet (>1.4 g/kgBW/day) in combination with ST, and the evidence from previous studies does not yet clearly confirm benefits in this population [47, 51].
Amino Acids
Amino acids can be classified as proteinogenic or non-proteinogenic. Proteinogenic amino acids acts as substrates for protein biosynthesis in animal cells, whereas non-proteinogenic amino acids do not participate in this process [79]. In postmenopausal women, supplementation with proteinogenic BCAAs does not appear to provide additional benefits for body composition or muscle strength when total daily protein intake is comparable between groups [52]. Although enhanced post-exercise muscle recovery has been reported in high-intensity endurance athletes and trained males [72, 80], such effects have not been observed in this population.
While LCi, a non-proteinogenic amino acid, may mechanistically increase nitric oxide bioavailability and improve muscle oxygenation [72, 81–84],only two small high-quality RCTs (PEDro: 8 and 9) in postmenopausal women have been conducted. The study of Kang et al. suggests an additional increase in LM und strength parameters in supplemented, strength-trained women. Figuerora et al. showed no significant differences between the supplemented and non-supplemented strength-trained women, however the performed ST was WBV. The results may therefore be limited by the effectiveness of this training method. [53, 54] Current evidence in postmenopausal women is apparently insufficient to provide clear recommendations and should be considered preliminary. Further studies are warranted to allow more definitive conclusions.
Calcium and Vitamin D
Vitamin D and calcium are essential for maintaining bone health, and deficiencies in either represent significant risk factor for osteoporosis development [85]. Vitamin D is primarily synthesized in human skin upon exposure to sunlight, but modern lifestyle patterns often limit sun exposure, making dietary sources (e.g., vitamin D2) increasingly important [86]. Once metabolized and activated, vitamin D (1,25-dihydroxyvitamin D) enhances calcium absorption in the intestine, stimulates calcium uptake by osteoblasts, and promotes osteoclast maturation [87, 88]. Calcium constitutes a major structural component of bone (~ 99%) and also plays essential roles in cellular signaling, nerve impulse transmission, and muscle contraction. Inadequate daily calcium intake forces the mobilization of calcium from bone, and prolonged deficiency can lead to decreased BMD [88–90].
Regarding the influence of calcium and vitamin D in combination with ST in postmenopausal women, four studies (PEDro: 2, 6, 9, 10) were identified in this review. The findings indicate that a calcium application exceeding 800 mg/day has no additive effects on body composition, strength capacity and BMD [38, 55–57]. However, the study by Cussler et al. [21–23, 55, 56]. However, a precise minimum effective dosage below 800 mg/day cannot currently be established for postmenopausal women. Nonetheless, existing evidence suggests that ST remains the primary factor in preserving BMD in this population.
Concerning vitamin D supplementation combined with ST, no significant effects were observed on body composition, strength capacity, or BMD [38, 56, 57] These results are consistent with previous research indicating that chronic vitamin D supplementation does not significantly influence BMD [24] and are further supported by studies examining combined calcium and vitamin D supplementation in premenopausal women [38]. Based on the limited data on calcium and vitamin D supplementation combined with ST, it appears that supplementation of both substances has no additive effect on body composition, strength and BMD. Importantly, however, a daily calcium intake of at least~800 mg/day appears necessary, as lower intakes may contribute to reductions in BMD [55].
Creatine Monohydrate
Creatine supplementation may mechanistically reduce muscle fatigue and improve performance by prolonging the energy contribution of the phosphocreatine system [91–93] and has been shown to be beneficial in enhancing strength, LBM and BMD in other populations, such as younger and older adults [58, 94–98]. Evidence in especially postmenopausal women however, is limited to four small, high-quality RCTs (PEDro: 9–10) [58–61]. No clear effects on body composition, strength, or BMD were observed [58, 59, 61]. Potential explanations for the lack of observed effects, besides the limited data available, may include that also in other populations only small to moderate effects could be achieved through creatine supplementation [94, 98–103]. Furthermore, two included studies in this review lasted at least one year and therefore it is plausible that ST was not structured into systematic macrocycles. Consequently, participants may have engaged in continuous, unsystematic training, thereby limiting potential adaptive responses. Recent reviews investigating creatine supplementation in women were also unable to draw definitive conclusions regarding postmenopausal populations [104, 105]. These considerations underscore the need for further research on structured, intensive ST combined with creatine supplementation to clarify its potential benefits in postmenopausal women.
Zararia Multiflora
For supplementing Zataria multiflora only two studies [70, 71] (PEDro: 8 and 9) were identified. Zataria multiflora is a plant used in traditional Iranian medicine, which is rich in antioxidative compounds, including thymol and carvacrol [106]. Previous research indicates that Zataria multiflora supplementation exhibits concentration-dependent radical-scavenging activity against 1,1-diphenyl-2-picryl-hydrazyl free radicals [107]. However, when examining the potential additive effects of Zataria multiflora supplementation in postmenopausal women undergoing ST, no significant differences were observed between the supplemented and non-supplemented exercise groups [70, 71].
Omega-3 Fatty Acids (“Fish Oil”)
Only one study [73] (PEDro: 8) investigated the additional effects of FO supplementation in postmenopausal women performing ST, which limits the generalizability of its findings. The omega-3 fatty acids EPA and DHA have been shown to reduce mitochondrial oxidant emissions, enhance muscle protein synthesis, and improve anabolic responses to exercise in older adults aged 65 and above [108]. In older women, omega-3 supplementation has been associated with increases in SMM and muscle strength in several studies [109–112]. However, in the present no significant differences were observed between the supplemented and non-supplemented exercises group. Further studies specifically targeting postmenopausal women are needed to enable more definitive recommendations and to confirm the findings of previous research in this population.
Shatavari
Shatavari is an Ayurvedic herb rich in phytoestrogens and a bioactive compounds, traditionally used to support female reproductive health [113–115]. Recent studies have investigated its potential effects on skeletal muscle function [116–118]. A RCT involving postmenopausal women demonstrated that six weeks of Shatavari supplementation (1000 mg/day) improved handgrip strength and increased myosin regulatory light chain phosphorylation in the vastus lateralis muscle, indicating enhanced myosin contractile function [117]. In the context of ST and Shatavari supplementation, one study was identified [68] (PEDro: 8). An 8-week supplementation regimen (1000 mg/day) did not induce significant increase in strength compared with ST alone, and effects on body composition and BMD were not evaluated. Consequently, no clear conclusions or recommendations can currently be made regarding these outcomes.
Limitations
In addition to the important and novel findings of the review, there are also some limitations. Although a total of 34 studies were identified, the evidence regarding individual dietary strategies in combination with ST is severely limited. No studies on different dietary habits such as intermittent fasting, plant-based diet, or paleo diet in combination with ST could be identified. Similarly, only a few studies were conducted on the use of various dietary supplements such as amino acids, creatine, calcium or vitamin D in postmenopausal women with ST. Consequently, no clear recommendations or statements can be made. Furthermore, the study designs and training protocols of the identified studies are highly heterogeneous, making comparisons very challenging. In addition to the heterogeneous study designs, only a very limited number of studies have investigated the long-term effects of supplementation, with the majority of trials lasting no longer than 12 weeks. Furthermore, the definition of postmenopausal women was somewhat nonspecific across studies. Regarding study quality, most investigations achieved a PEDro score of 6 or higher, indicating a high methodological standard. Only the study by Molina et al. [57] and the two investigations by Ryan et al. [40, 41] scored below 6.
In addition, some studies included combined strength and endurance training along with various dietary strategies making it difficult to isolate the specific effects of strength training or dietary interventions. Consequently, these studies were not included in the review. Nevertheless combining strength and endurance exercise is essential for maintaining overall health and promoting longevity and is therefore equally recommended by the World Health Organization [119]. However, ST has been shown to be fundamentally important for maintaining or improving body composition, muscle strength and BMD. An exact dose-response relationship, however, cannot be determined, as this depends on a various factors such as training intensity, weekly volume, frequency, duration of the intervention and the level of supervision provided to participants.
Conclusion
The present systematic review aimed to examine the effects of nutritional strategies in combination with ST on body composition, strength capacity and BMD in postmenopausal women. A total of 34 studies were identified. The evidence indicates that postmenopausal women should engage in structured and systematic ST. However, an exact dose-response relationship cannot be determined. For reducing BW and FM a CRD with a deficit of 250–750 kcal/day can be a beneficial strategy. A daily protein intake should be at least 0.8 g/kgBW/day to maintain LBM and muscle strength during CRD. The recommended amount can be attained through the consumption of high-protein foods, protein supplements or amino acids. The evidence on a high-protein diet (> 1.4 g/kgBW/day) in combination with ST in postmenopausal women is limited, making it impossible to draw definitive conclusions regarding potential additive or adverse effects. Regarding the use of dietary supplements in conjunction with ST, the limited number of available studies precludes drawing definitive conclusions. Consequently, the present findings and observations should be interpreted as exploratory. Therefore, further systematic investigations exploring diverse nutritional and supplementation strategies are required to generate more precise insights and develop evidence-based recommendations. A key consideration in all studies should be the implementation of structured and supervised training protocols to ensure sufficient training stimuli and accurately assessing potential additive effects.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
The authors would like to thank the working groups of the included studies for sending the free texts.
Abbreviations
- AHA
American Heart Association
- BCAA
Branched-chain amino acids
- BF
Body fat
- BF%
Body fat percentage
- BMI
Body Mass Index
- BMD
Bone mineral density
- BRMR
Baseline resting metabolic rate
- BW
Body Weight
- CRD
Calorie-restrictive diets
- DHA
Docosahexaenoic acid
- EFSA
European Food Safety Association
- EPA
Eicosapentaenoic acid
- FFM
Fat-free mass
- FM
Fat mass
- FO
Omega-3-fatty acids
- kgBW
Kilogram bodyweight
- kgBW/d
Kilogram bodyweight per day
- LCi
L-citrulline
- LBM
Lean body mass
- Mdiff
mean of the difference before and after the intervention
- MeSH
Medical Subject Headings
- P
Protein
- PRISMA
Preferred Reporting Items for Systematic Reviews and Meta-Analysis
- RCTs
Randomized, controlled study designs
- SD
Standard deviation
- SDdiff
Standard deviation of the difference before and after the intervention
- SE
Standard error
- SMM
Skeletal muscle mass
- ST
Strength training
- WC
Waist circumference
- Z
Zataria multiflora
Author Contributions
JS contributed to data collection and data reduction. FW contributed to data collection and interpretation of the results. EI and WB participated in the design of the study and interpretation of the results. PD and SG contributed data and participated in the interpretation of the results. All authors contributed to the manuscript writing.
Funding
Open Access funding enabled and organized by Projekt DEAL. No funding was received for the conduct of this research or for the publication of this article.
Available of Data and Materials
Data described in the manuscript, code book, and analytic code will be made available upon request pending.
Declarations
Consent for Publication
All authors agree to the publication of the data and the contents of the manuscript.
Competing Interests
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Volpi E, Nazemi R, Fujita S. Muscle tissue changes with aging. Curr Opin Clin Nutr Metab Care. 2004;7(4):405–10. 10.1097/01.mco.0000134362.76653.b2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Hale GE, Robertson DM, Burger HG. The perimenopausal woman: endocrinology and management. J Steroid Biochem Mol Biol. 2014;142:121–31. 10.1016/j.jsbmb.2013.08.015. [DOI] [PubMed] [Google Scholar]
- 3.Sapre S, Thakur R. Lifestyle and dietary factors determine age at natural menopause. J mid-life Health. 2014;5(1):3–5. 10.4103/0976-7800.127779. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Messier V, Rabasa-Lhoret R, Barbat-Artigas S, Elisha B, Karelis AD, Aubertin-Leheudre M. Menopause and sarcopenia: A potential role for sex hormones. Maturitas. 2011;68(4):331–6. 10.1016/j.maturitas.2011.01.014. [DOI] [PubMed] [Google Scholar]
- 5.Mohammad Rahimi GR, Smart NA, Liang MTC, Bijeh N, Albanaqi AL, Fathi M, Niyazi A, Mohammad Rahimi N. The impact of different modes of exercise training on bone mineral density in older postmenopausal women: A systematic review and Meta-analysis research. Calcif Tissue Int. 2020;106(6):577–90. 10.1007/s00223-020-00671-w. [DOI] [PubMed] [Google Scholar]
- 6.Janssen I, Powell LH, Kazlauskaite R, Dugan SA. Testosterone and visceral fat in midlife women: the study of women’s health across the Nation (SWAN) fat patterning study. Obes (Silver Spring Md). 2010;18(3):604–10. 10.1038/oby.2009.251. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Finkelstein JS, Brockwell SE, Mehta V, Greendale GA, Sowers MR, Ettinger B, Lo JC, Johnston JM, Cauley JA, Danielson ME, Neer RM. Bone mineral density changes during the menopause transition in a multiethnic cohort of women. J Clin Endocrinol Metab. 2008;93(3):861–8. 10.1210/jc.2007-1876. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Thomas E, Gentile A, Lakicevic N, Moro T, Bellafiore M, Paoli A, Drid P, Palma A, Bianco A. The effect of resistance training programs on lean body mass in postmenopausal and elderly women: a meta-analysis of observational studies. Aging Clin Exp Res. 2021;33(11):2941–52. 10.1007/s40520-021-01853-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.O’Bryan SJ, Giuliano C, Woessner MN, Vogrin S, Smith C, Duque G, Levinger I. Progressive resistance training for concomitant increases in muscle strength and bone mineral density in older adults: A systematic review and Meta-Analysis. Sports Med (Auckland N Z). 2022;52(8):1939–60. 10.1007/s40279-022-01675-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Rosenberg IH, Sarcopenia. Origins and clinical Relevance1. J Nutr. 1997;127(5):S990–1. 10.1093/jn/127.5.990S. [DOI] [PubMed] [Google Scholar]
- 11.Sjöblom S, Suuronen J, Rikkonen T, Honkanen R, Kröger H, Sirola J. Relationship between postmenopausal osteoporosis and the components of clinical sarcopenia. Maturitas. 2013;75(2):175–80. 10.1016/j.maturitas.2013.03.016. [DOI] [PubMed] [Google Scholar]
- 12.Ji M-X, Yu Q. Primary osteoporosis in postmenopausal women. Chronic Dis Translational Med. 2015;1(1):9–13. 10.1016/j.cdtm.2015.02.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Gulati M, Dursun E, Vincent K, Watt FE. The influence of sex hormones on musculoskeletal pain and osteoarthritis. Lancet Rheumatol. 2023;5(4):e225–38. 10.1016/S2665-9913(23)00060-7. [DOI] [PubMed] [Google Scholar]
- 14.Khadilkar SS. Musculoskeletal disorders and menopause. J Obstet Gynecol India. 2019;69(2):99–103. 10.1007/s13224-019-01213-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Reimers CD, Knapp G, Reimers AK. Does physical activity increase life expectancy? A review of the literature. J Aging Res. 2012;2012(243958). 10.1155/2012/243958. [DOI] [PMC free article] [PubMed]
- 16.Shojaa M, von Stengel S, Kohl M, Schoene D, Kemmler W. Effects of dynamic resistance exercise on bone mineral density in postmenopausal women: a systematic review and meta-analysis with special emphasis on exercise parameters. Osteoporos Int J Established as Result Cooperation between Eur Foundation Osteoporos Natl Osteoporos Foundation USA. 2020;31(8):1427–44. 10.1007/s00198-020-05441-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Sá KMM, da Silva GR, Martins UK, Colovati MES, Crizol GR, Riera R, Pacheco RL, Martimbianco ALC. Resistance training for postmenopausal women: systematic review and meta-analysis. Menopause (New York N Y). 2023;30(1):108–16. 10.1097/GME.0000000000002079. [DOI] [PubMed] [Google Scholar]
- 18.González-Gálvez N, Moreno-Torres JM, Vaquero-Cristóbal R. Resistance training effects on healthy postmenopausal women: a systematic review with meta-analysis. Climacteric J Int Menopause Soc 2024:1–9, 10.1080/13697137.2024.2310521 [DOI] [PubMed]
- 19.Arnett DK, Blumenthal RS, Albert MA, Buroker AB, Goldberger ZD, Hahn EJ, Himmelfarb CD, Khera A, Lloyd-Jones D, McEvoy JW, Michos ED, Miedema MD, Muñoz D, Smith SC, Virani SS, Williams KA, Yeboah J, Ziaeian B. 2019 ACC/AHA guideline on the primary prevention of cardiovascular disease: A report of the American college of Cardiology/American heart association task force on clinical practice guidelines. Circulation. 2019;140(11):e596–646. 10.1161/CIR.0000000000000678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Ko S-H, Kim H-S. Menopause-Associated lipid metabolic disorders and foods beneficial for postmenopausal women. Nutrients. 2020;12(1). 10.3390/nu12010202. [DOI] [PMC free article] [PubMed]
- 21.Salmon J. Excerpts from dietary reference values for food energy and nutrients for the united kingdom: introduction to the guide and summary tables. Nutr Rev. 1992;50(3):90–3. 10.1111/j.1753-4887.1992.tb01280.x. [DOI] [PubMed] [Google Scholar]
- 22.Ross AC, Taylor CL, Yaktine AL, Del Valle HB, editors. Dietary Reference Intakes for Calcium and Vitamin D. Washington (DC); 2011. [PubMed]
- 23.North American Menopause Society. The role of calcium in peri- and postmenopausal women: 2006 position statement of the North American menopause society. Menopause (New York N Y). 2006;13(6):862–77. 10.1097/01.gme.0000243566.25205.0b. quiz 878 – 80. [DOI] [PubMed] [Google Scholar]
- 24.Yao P, Bennett D, Mafham M, Lin X, Chen Z, Armitage J, Clarke R. Vitamin D and calcium for the prevention of fracture: A systematic review and Meta-analysis. JAMA Netw Open. 2019;2(12):e1917789. 10.1001/jamanetworkopen.2019.17789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Morton RW, Murphy KT, McKellar SR, Schoenfeld BJ, Henselmans M, Helms E, Aragon AA, Devries MC, Banfield L, Krieger JW, Phillips SM. A systematic review, meta-analysis and meta-regression of the effect of protein supplementation on resistance training-induced gains in muscle mass and strength in healthy adults. Br J Sports Med. 2018;52(6):376–84. 10.1136/bjsports-2017-097608. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Burke R, Piñero A, Coleman M, Mohan A, Sapuppo M, Augustin F, Aragon AA, Candow DG, Forbes SC, Swinton P, Schoenfeld BJ. The effects of creatine supplementation combined with resistance training on regional measures of muscle hypertrophy: A systematic review with Meta-Analysis. Nutrients. 2023;15(9). 10.3390/nu15092116. [DOI] [PMC free article] [PubMed]
- 27.Xie Y, Gu Y, Li Z, He B, Zhang L. Effects of different exercises combined with different dietary interventions on body composition: A systematic review and network Meta-Analysis. Nutrients. 2024;16(17). 10.3390/nu16173007. [DOI] [PMC free article] [PubMed]
- 28.Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, Shamseer L, Tetzlaff JM, Akl EA, Brennan SE, Chou R, Glanville J, Grimshaw JM, Hróbjartsson A, Lalu MM, Li T, Loder EW, Mayo-Wilson E, McDonald S, McGuinness LA, Stewart LA, Thomas J, Tricco AC, Welch VA, Whiting P, Moher D. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ (Clinical Res ed). 2021;372:n71. 10.1136/bmj.n71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Cohen J. Statistical power analysis for the behavioral sciences. 2nd ed. Hillsdale, N.J.: L. Erlbaum Associates; 1988. [Google Scholar]
- 30.Barde MP, Barde PJ. What to use to express the variability of data: standard deviation or standard error of mean? Perspect Clin Res. 2012;3(3):113–6. 10.4103/2229-3485.100662. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.PEDro. April : Physiotherapy Evidence Database. PEDro Scale. Available at: https://pedro.org.au/english/resources/pedro-scale/. Accessed 16 2024.
- 32.Bouchard DR, Soucy L, Sénéchal M, Dionne IJ, Brochu M. Impact of resistance training with or without caloric restriction on physical capacity in obese older women. Menopause (New York N Y). 2009;16(1):66–72. 10.1097/gme.0b013e31817dacf7. [DOI] [PubMed] [Google Scholar]
- 33.Brochu M, Malita MF, Messier V, Doucet E, Strychar I, Lavoie J-M, Prud’homme D, Rabasa-Lhoret R. Resistance training does not contribute to improving the metabolic profile after a 6-month weight loss program in overweight and obese postmenopausal women. J Clin Endocrinol Metab. 2009;94(9):3226–33. 10.1210/jc.2008-2706. [DOI] [PubMed] [Google Scholar]
- 34.Drapeau S, Doucet E, Rabasa-Lhoret R, Brochu M, Prud’homme D, Imbeault P. Improvement in insulin sensitivity by weight loss does not affect hyperinsulinemia-mediated reduction in total and high molecular weight adiponectin: a MONET study. Appl Physiol Nutr metabolism = Physiologie Appliquee Nutr Et Metab. 2011;36(2):191–200. 10.1139/h10-106. [DOI] [PubMed] [Google Scholar]
- 35.Figueroa A, Arjmandi BH, Wong A, Sanchez-Gonzalez MA, Simonavice E, Daggy B. Effects of hypocaloric diet, low-intensity resistance exercise with slow movement, or both on aortic hemodynamics and muscle mass in obese postmenopausal women. Menopause (New York N Y). 2013;20(9):967–72. 10.1097/GME.0b013e3182831ee4. [DOI] [PubMed] [Google Scholar]
- 36.Figueroa A, Vicil F, Sanchez-Gonzalez MA, Wong A, Ormsbee MJ, Hooshmand S, Daggy B. Effects of diet and/or low-intensity resistance exercise training on arterial stiffness, adiposity, and lean mass in obese postmenopausal women. Am J Hypertens. 2013;26(3):416–23. 10.1093/ajh/hps050. [DOI] [PubMed] [Google Scholar]
- 37.Joseph LJ, Trappe TA, Farrell PA, Campbell WW, Yarasheski KE, Lambert CP, Evans WJ. Short-term moderate weight loss and resistance training do not affect insulin-stimulated glucose disposal in postmenopausal women. Diabetes Care. 2001;24(11):1863–9. 10.2337/diacare.24.11.1863. [DOI] [PubMed] [Google Scholar]
- 38.Kerksick CM, Roberts MD, Campbell BI, Galbreath MM, Taylor LW, Wilborn CD, Lee A, Dove J, Bunn JW, Rasmussen CJ, Kreider RB. Differential impact of calcium and vitamin D on body composition changes in Post-Menopausal women following a restricted energy diet and exercise program. Nutrients. 2020;12(3). 10.3390/nu12030713. [DOI] [PMC free article] [PubMed]
- 39.McNeil J, Schwartz A, Rabasa-Lhoret R, Lavoie J-M, Brochu M, Doucet É. Changes in leptin and peptide YY do not explain the greater-than-predicted decreases in resting energy expenditure after weight loss. J Clin Endocrinol Metab. 2015;100(3):E443–52. 10.1210/jc.2014-2210. [DOI] [PubMed] [Google Scholar]
- 40.Ryan AS, Nicklas BJ, Berman DM, Elahi D. Adiponectin levels do not change with moderate dietary induced weight loss and exercise in obese postmenopausal women. Int J Obes Relat Metabolic Disorders J Int Association Study Obes. 2003;27(9):1066–71. 10.1038/sj.ijo.0802387. [DOI] [PubMed] [Google Scholar]
- 41.Ryan AS, Pratley RE, Goldberg AP, Elahi D. Resistive training increases insulin action in postmenopausal women. J Gerontol A. 1996;51(5):M199–205. 10.1093/gerona/51a.5.m199. [DOI] [PubMed] [Google Scholar]
- 42.Sénéchal M, Bouchard DR, Dionne IJ, Brochu M. The effects of lifestyle interventions in dynapenic-obese postmenopausal women. Menopause (New York N Y). 2012;19(9):1015–21. 10.1097/gme.0b013e318248f50f. [DOI] [PubMed] [Google Scholar]
- 43.de Branco FMS, Carneiro MAS, Rossato LT, Nahas PC, Teixeira KRC, de Oliveira GN, Orsatti FL, de Oliveira EP. Protein timing has no effect on lean mass, strength and functional capacity gains induced by resistance exercise in postmenopausal women: A randomized clinical trial. Clin Nutr. 2020;39(1):57–66. 10.1016/j.clnu.2019.01.008. [DOI] [PubMed] [Google Scholar]
- 44.Holm L, Olesen JL, Matsumoto K, Doi T, Mizuno M, Alsted TJ, Mackey AL, Schwarz P, Kjaer M. Protein-containing nutrient supplementation following strength training enhances the effect on muscle mass, strength, and bone formation in postmenopausal women. J Appl Physiol (Bethesda Md 1985). 2008;105(1):274–81. 10.1152/japplphysiol.00935.2007. [DOI] [PubMed] [Google Scholar]
- 45.Isenmann E, Kaluza D, Havers T, Elbeshausen A, Geisler S, Hofmann K, Flenker U, Diel P, Gavanda S. Resistance training alters body composition in middle-aged women depending on menopause - A 20-week control trial. BMC Womens Health. 2023;23(1):526. 10.1186/s12905-023-02671-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Maesta N, Nahas EAP, Nahas-Neto J, Orsatti FL, Fernandes CE, Traiman P, Burini RC. Effects of soy protein and resistance exercise on body composition and blood lipids in postmenopausal women. Maturitas. 2007;56(4):350–8. 10.1016/j.maturitas.2006.10.001. [DOI] [PubMed] [Google Scholar]
- 47.Orsatti FL, Maestá N, de Oliveira EP, Nahas Neto J, Burini RC, Nunes PRP, Souza AP, Martins FM, Nahas EP. Adding soy protein to milk enhances the effect of resistance training on muscle strength in postmenopausal women. J Diet Supplements. 2018;15(2):140–52. 10.1080/19390211.2017.1330794. [DOI] [PubMed] [Google Scholar]
- 48.Rossato LT, Nahas PC, de Branco FMS, Martins FM, Souza AP, Carneiro MAS, Orsatti FL, de Oliveira EP. Higher protein intake does not improve lean mass gain when compared with RDA recommendation in postmenopausal women following resistance exercise protocol: A randomized clinical trial. Nutrients. 2017;9(9). 10.3390/nu9091007. [DOI] [PMC free article] [PubMed]
- 49.Shenoy S, Bedi R, Sandhu JS. Effect of soy isolate protein and resistance exercises on muscle performance and bone health of osteopenic/osteoporotic post-menopausal women. J Women Aging. 2013;25(2):183–98. 10.1080/08952841.2013.764252. [DOI] [PubMed] [Google Scholar]
- 50.Weisgarber KD, Candow DG, Farthing JP. Whey protein and high-volume resistance training in postmenopausal women. J Nutr Health Aging. 2015;19(5):511–7. 10.1007/s12603-015-0454-7. [DOI] [PubMed] [Google Scholar]
- 51.Ioannidou P, Dóró Z, Schalla J, Wätjen W, Diel P, Isenmann E. Analysis of combinatory effects of free weight resistance training and a high-protein diet on body composition and strength capacity in postmenopausal women - A 12-week randomized controlled trial. J Nutr Health Aging. 2024;28(10):100349. 10.1016/j.jnha.2024.100349. [DOI] [PubMed] [Google Scholar]
- 52.Bagheri R, Forbes SC, Candow DG, Wong A. Effects of branched-chain amino acid supplementation and resistance training in postmenopausal women. Exp Gerontol. 2021;144:111185. 10.1016/j.exger.2020.111185. [DOI] [PubMed] [Google Scholar]
- 53.Figueroa A, Alvarez-Alvarado S, Ormsbee MJ, Madzima TA, Campbell JC, Wong A. Impact of L-citrulline supplementation and whole-body vibration training on arterial stiffness and leg muscle function in obese postmenopausal women with high blood pressure. Exp Gerontol. 2015;63:35–40. 10.1016/j.exger.2015.01.046. [DOI] [PubMed] [Google Scholar]
- 54.Kang Y, Dillon KN, Martinez MA, Maharaj A, Fischer SM, Figueroa A. Combined L-Citrulline supplementation and slow velocity Low-Intensity resistance training improves leg endothelial Function, lean Mass, and strength in hypertensive postmenopausal women. Nutrients. 2022;15(1). 10.3390/nu15010074. [DOI] [PMC free article] [PubMed]
- 55.Cussler EC, Going SB, Houtkooper LB, Stanford VA, Blew RM, Flint-Wagner HG, Metcalfe LL, Choi J-E, Lohman TG. Exercise frequency and calcium intake predict 4-year bone changes in postmenopausal women. Osteoporos Int J Established as Result Cooperation between Eur Foundation Osteoporos Natl Osteoporos Foundation USA. 2005;16(12):2129–41. 10.1007/s00198-005-2014-1. [DOI] [PubMed] [Google Scholar]
- 56.Haghighi AH, Shojaee M, Askari R, Abbasian S, Gentil P. The effects of 12 weeks resistance training and vitamin D administration on neuromuscular joint, muscle strength and power in postmenopausal women. Physiol Behav. 2024;274:114419. 10.1016/j.physbeh.2023.114419. [DOI] [PubMed] [Google Scholar]
- 57.Molina E, Ducaud P, Bustamante I, León-Prados JA, Otero-Saborido FM, Gonzalez-Jurado JA. Variación en la densidad mineral ósea inducida por ejercicio en mujeres posmenopáusicas / Variation of Bone Mineral Density Induced by Exercise in Postmenopausal Women pp. 527–541. rimcafd 2015; 59(2015):527–41. 10.15366/rimcafd2015.59.008
- 58.Candow DG, Chilibeck PD, Gordon JJ, Kontulainen S. Efficacy of creatine supplementation and resistance training on area and density of bone and muscle in older adults. Med Sci Sports Exerc. 2021;53(11):2388–95. 10.1249/MSS.0000000000002722. [DOI] [PubMed] [Google Scholar]
- 59.Chilibeck PD, Candow DG, Landeryou T, Kaviani M, Paus-Jenssen L. Effects of creatine and resistance training on bone health in postmenopausal women. Med Sci Sports Exerc. 2015;47(8):1587–95. 10.1249/MSS.0000000000000571. [DOI] [PubMed] [Google Scholar]
- 60.Aguiar AF, Januário RSB, Junior RP, Gerage AM, Pina FLC, do Nascimento MA, Padovani CR, Cyrino ES. Long-term creatine supplementation improves muscular performance during resistance training in older women. Eur J Appl Physiol. 2013;113(4):987–96. 10.1007/s00421-012-2514-6. [DOI] [PubMed] [Google Scholar]
- 61.Johannsmeyer S, Candow DG, Brahms CM, Michel D, Zello GA. Effect of creatine supplementation and drop-set resistance training in untrained aging adults. Exp Gerontol. 2016;83:112–9. 10.1016/j.exger.2016.08.005. [DOI] [PubMed] [Google Scholar]
- 62.Cheng C-C, Hsu C-Y, Liu J-F. Effects of dietary and exercise intervention on weight loss and body composition in obese postmenopausal women: a systematic review and meta-analysis. Menopause (New York N Y). 2018;25(7):772–82. 10.1097/GME.0000000000001085. [DOI] [PubMed] [Google Scholar]
- 63.D Cameron J, Sigal RJ, Kenny GP, Alberga AS, Prud’homme D, Phillips P, Doucette S, Goldfield G. Body composition and energy intake - skeletal muscle mass is the strongest predictor of food intake in obese adolescents: the HEARTY trial. Appl Physiol Nutr metabolism = Physiologie Appliquee Nutr Et Metab. 2016;41(6):611–7. 10.1139/apnm-2015-0479. [DOI] [PubMed] [Google Scholar]
- 64.Svendsen OL, Hassager C, Christiansen C. Effect of an energy-restrictive diet, with or without exercise, on lean tissue mass, resting metabolic rate, cardiovascular risk factors, and bone in overweight postmenopausal women. Am J Med. 1993;95(2):131–40. 10.1016/0002-9343(93)90253-l. [DOI] [PubMed] [Google Scholar]
- 65.Seimon RV, Wild-Taylor AL, Keating SE, McClintock S, Harper C, Gibson AA, Johnson NA, Fernando HA, Markovic TP, Center JR, Franklin J, Liu PY, Grieve SM, Lagopoulos J, Caterson ID, Byrne NM, Sainsbury A. Effect of weight loss via severe vs moderate energy restriction on lean mass and body composition among postmenopausal women with obesity: the TEMPO diet randomized clinical trial. JAMA Netw Open. 2019;2(10):e1913733. 10.1001/jamanetworkopen.2019.13733. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Pasini E, Corsetti G, Aquilani R, Romano C, Picca A, Calvani R, Dioguardi FS. Protein-Amino Acid Metabolism Disarrangements: The Hidden Enemy of Chronic Age-Related Conditions. Nutrients 2018; 10(4). 10.3390/nu10040391 [DOI] [PMC free article] [PubMed]
- 67.Tipton KD, Wolfe RR. Exercise, protein metabolism, and muscle growth. Int J Sport Nutr Exerc Metab. 2001;11(1):109–32. 10.1123/ijsnem.11.1.109. [DOI] [PubMed] [Google Scholar]
- 68.Greed E, Pritchard J, Struszczak L, Bozbaş E, Ek G, Acheson J, Winney B, Qadir A, Wong KK-L, Bowtell J, O’Leary M. Shatavari supplementation during eight weeks of resistance training increases training load, enhances skeletal muscle contractility and alters the skeletal muscle proteome in older women. Front Nutr. 2024;11:1498674. 10.3389/fnut.2024.1498674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Borde R, Hortobágyi T, Granacher U. Dose-Response relationships of resistance training in healthy old adults: A systematic review and Meta-Analysis. Sports Med (Auckland N Z). 2015;45(12):1693–720. 10.1007/s40279-015-0385-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Ghanbari-Niaki A, Saeidi A, Ahmadian M, Gharahcholo L, Naghavi N, Fazelzadeh M, Mahjoub S, Myers S, Williams A. The combination of exercise training and Zataria multiflora supplementation increase serum Irisin levels in postmenopausal women. Integr Med Res. 2018;7(1):44–52. 10.1016/j.imr.2018.01.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Tayebi SM, Saeidi A, Fashi M, Pouya S, Khosravi A, Shirvani H, Ahmadian M, Abderrahman AB, Hackney AC, Zouhal H. Plasma retinol-binding protein-4 and tumor necrosis factor-α are reduced in postmenopausal women after combination of different intensities of circuit resistance training and Zataria supplementation. Sport Sci Health. 2019;15(3):551–8. 10.1007/s11332-019-00544-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 72.Gonzalez AM, Trexler ET. Effects of citrulline supplementation on exercise performance in humans: A review of the current literature. J Strength Conditioning Res. 2020;34(5):1480–95. 10.1519/JSC.0000000000003426. [DOI] [PubMed] [Google Scholar]
- 73.Félix-Soriano E, Martínez-Gayo A, Cobo MJ, Pérez-Chávez A, Ibáñez-Santos J, Palacios Samper N, Goikoetxea Galarza I, Cuervo M, García-Unciti M, González-Muniesa P, Lorente-Cebrián S, Moreno-Aliaga MJ. Effects of DHA-Rich n-3 fatty acid supplementation and/or resistance training on body composition and cardiometabolic biomarkers in overweight and obese Post-Menopausal women. Nutrients. 2021;13(7). 10.3390/nu13072465. [DOI] [PMC free article] [PubMed]
- 74.Walker DK, Dickinson JM, Timmerman KL, Drummond MJ, Reidy PT, Fry CS, Gundermann DM, Rasmussen BB. Exercise, amino acids, and aging in the control of human muscle protein synthesis. Med Sci Sports Exerc. 2011;43(12):2249–58. 10.1249/MSS.0b013e318223b037. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75.Wirth J, Hillesheim E, Brennan L. The role of protein intake and its timing on body composition and muscle function in healthy adults: A systematic review and Meta-Analysis of randomized controlled trials. J Nutr. 2020;150(6):1443–60. 10.1093/jn/nxaa049. [DOI] [PubMed] [Google Scholar]
- 76.Remer T, Kalotai N, Amini AM, Lehmann A, Schmidt A, Bischoff-Ferrari HA, Egert S, Ellinger S, Kroke A, Kühn T, Lorkowski S, Nimptsch K, Schwingshackl L, Zittermann A, Watzl B, Siener R. Protein intake and risk of urolithiasis and kidney diseases: an umbrella review of systematic reviews for the evidence-based guideline of the German nutrition society. Eur J Nutr. 2023;62(5):1957–75. 10.1007/s00394-023-03143-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Antonio J, Ellerbroek A, Silver T, Vargas L, Tamayo A, Buehn R, Peacock CA. A High Protein Diet Has No Harmful Effects: A One-Year Crossover Study in Resistance-Trained Males. Journal of nutrition and metabolism 2016; 2016:9104792. 10.1155/2016/9104792 [DOI] [PMC free article] [PubMed]
- 78.Kuo Y-Y, Chang H-Y, Huang Y-C, Liu C-W. Effect of Whey protein supplementation in postmenopausal women: A systematic review and Meta-Analysis. Nutrients. 2022;14(19). 10.3390/nu14194210. [DOI] [PMC free article] [PubMed]
- 79.Hou Y, Wu G. Nutritionally essential amino Acids. Advances in nutrition (Bethesda. Md). 2018;9(6):849–51. 10.1093/advances/nmy054. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Hellsten Y, Nyberg M, Jensen LG, Mortensen SP. Vasodilator interactions in skeletal muscle blood flow regulation. J Physiol. 2012;590(24):6297–305. 10.1113/jphysiol.2012.240762. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Figueroa A, Wong A, Jaime SJ, Gonzales JU. Influence of L-citrulline and watermelon supplementation on vascular function and exercise performance. Curr Opin Clin Nutr Metab Care. 2017;20(1):92–8. 10.1097/MCO.0000000000000340. [DOI] [PubMed] [Google Scholar]
- 82.Maréchal G, Gailly P. Effects of nitric oxide on the contraction of skeletal muscle. Cell Mol Life Sci CMLS. 1999;55(8–9):1088–102. 10.1007/s000180050359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 83.Schwedhelm E, Maas R, Freese R, Jung D, Lukacs Z, Jambrecina A, Spickler W, Schulze F, Böger RH. Pharmacokinetic and pharmacodynamic properties of oral L-citrulline and L-arginine: impact on nitric oxide metabolism. Br J Clin Pharmacol. 2008;65(1):51–9. 10.1111/j.1365-2125.2007.02990.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.van’t Hof RJ, Ralston SH. Nitric oxide and bone. Immunology. 2001;103(3):255–61. 10.1046/j.1365-2567.2001.01261.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Fischer V, Haffner-Luntzer M, Amling M, Ignatius A. Calcium and vitamin D in bone fracture healing and post-traumatic bone turnover. Eur Cells Mater. 2018;35:365–85. 10.22203/eCM.v035a25. [DOI] [PubMed] [Google Scholar]
- 86.Wyskida M, Wieczorowska-Tobis K, Chudek J. Prevalence and factors promoting the occurrence of vitamin D deficiency in the elderly. Postepy Hig Med Dosw(Online). 2017;71(0):198–204. 10.5604/01.3001.0010.3804. [DOI] [PubMed] [Google Scholar]
- 87.Botelho J, Machado V, Proença L, Delgado AS, Mendes JJ. Vitamin D deficiency and oral health: A comprehensive review. Nutrients. 2020;12(5). 10.3390/nu12051471. [DOI] [PMC free article] [PubMed]
- 88.Song L. Calcium and bone metabolism indices. Adv Clin Chem. 2017;82:1–46. 10.1016/bs.acc.2017.06.005. [DOI] [PubMed] [Google Scholar]
- 89.Rossini M, Adami S, Bertoldo F, Diacinti D, Gatti D, Giannini S, Giusti A, Malavolta N, Minisola S, Osella G, Pedrazzoni M, Sinigaglia L, Viapiana O, Isaia GC. Guidelines for the diagnosis, prevention and management of osteoporosis. Reumatismo. 2016;68(1):1–39. 10.4081/reumatismo.2016.870. [DOI] [PubMed] [Google Scholar]
- 90.Reid IR. Osteoporosis: evidence for vitamin D and calcium in older people. Drug Ther Bull. 2020;58(8):122–5. 10.1136/dtb.2019.000063. [DOI] [PubMed] [Google Scholar]
- 91.Volek JS, Kraemer WJ, Bush JA, Boetes M, Incledon T, Clark KL, Lynch JM. Creatine supplementation enhances muscular performance during high-intensity resistance exercise. J Am Diet Assoc. 1997;97(7):765–70. 10.1016/S0002-8223(97)00189-2. [DOI] [PubMed] [Google Scholar]
- 92.Bird SP. Creatine supplementation and exercise performance: a brief review. J Sports Sci Med. 2003;2(4):123–32. [PMC free article] [PubMed] [Google Scholar]
- 93.Williams MH, Branch JD. Creatine supplementation and exercise performance: an update. J Am Coll Nutr. 1998;17(3):216–34. 10.1080/07315724.1998.10718751. [DOI] [PubMed] [Google Scholar]
- 94.Candow DG, Forbes SC, Chilibeck PD, Cornish SM, Antonio J, Kreider RB. Effectiveness of creatine supplementation on aging muscle and bone: focus on falls prevention and inflammation. J Clin Med. 2019;8(4). 10.3390/jcm8040488. [DOI] [PMC free article] [PubMed]
- 95.Hall M, Trojian TH. Creatine supplementation. Curr Sports Med Rep. 2013;12(4):240–4. 10.1249/JSR.0b013e31829cdff2. [DOI] [PubMed] [Google Scholar]
- 96.Harris RC, Söderlund K, Hultman E. Elevation of creatine in resting and exercised muscle of normal subjects by creatine supplementation. Clin Sci (London Engl 1979). 1992;83(3):367–74. 10.1042/cs0830367. [DOI] [PubMed] [Google Scholar]
- 97.Persky AM, Brazeau GA. Clinical Pharmacology of the dietary supplement creatine monohydrate. Pharmacol Rev. 2001;53(2):161–76. [PubMed] [Google Scholar]
- 98.Kreider RB, Kalman DS, Antonio J, Ziegenfuss TN, Wildman R, Collins R, Candow DG, Kleiner SM, Almada AL, Lopez HL. International society of sports nutrition position stand: safety and efficacy of creatine supplementation in exercise, sport, and medicine. J Int Soc Sports Nutr. 2017;14:18. 10.1186/s12970-017-0173-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Branch JD. Effect of creatine supplementation on body composition and performance: a meta-analysis. Int J Sport Nutr Exerc Metab. 2003;13(2):198–226. 10.1123/ijsnem.13.2.198. [DOI] [PubMed] [Google Scholar]
- 100.Maughan RJ, Burke LM, Dvorak J, Larson-Meyer DE, Peeling P, Phillips SM, Rawson ES, Walsh NP, Garthe I, Geyer H, Meeusen R, van Loon LJC, Shirreffs SM, Spriet LL, Stuart M, Vernec A, Currell K, Ali VM, Budgett RG, Ljungqvist A, Mountjoy M, Pitsiladis YP, Soligard T, Erdener U, Engebretsen L. IOC consensus statement: dietary supplements and the high-performance athlete. Br J Sports Med. 2018;52(7):439–55. 10.1136/bjsports-2018-099027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 101.Candow DG, Chilibeck PD, Forbes SC, Fairman CM, Gualano B, Roschel H. Creatine supplementation for older adults: focus on sarcopenia, osteoporosis, frailty and cachexia. Bone. 2022;162:116467. 10.1016/j.bone.2022.116467. [DOI] [PubMed] [Google Scholar]
- 102.Brose A, Parise G, Tarnopolsky MA. Creatine supplementation enhances isometric strength and body composition improvements following strength exercise training in older adults. J Gerontol A. 2003;58(1):11–9. 10.1093/gerona/58.1.b11. [DOI] [PubMed] [Google Scholar]
- 103.Candow DG, Ostojic SM, Chilibeck PD, Longobardi I, Gualano B, Tarnopolsky MA, Wallimann T, Moriarty T, Kreider RB, Forbes SC, Schlattner U, Antonio J. Creatine monohydrate supplementation for older adults and clinical populations. J Int Soc Sports Nutr. 2025;22(sup1):2534130. 10.1080/15502783.2025.2534130. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 104.Smith-Ryan AE, Cabre HE, Eckerson JM, Candow DG. Creatine Supplementation in Women’s Health: A Lifespan Perspective. Nutrients. 2021;13(3). 10.3390/nu13030877. [DOI] [PMC free article] [PubMed]
- 105.Dos Santos EEP, de Araújo RC, Candow DG, Forbes SC, Guijo JA, de Almeida Santana CC, WLd P, Botero JP. Efficacy of creatine supplementation combined with resistance training on muscle strength and muscle mass in older females: A systematic review and Meta-Analysis. Nutrients. 2021;13(11). 10.3390/nu13113757. [DOI] [PMC free article] [PubMed]
- 106.Saei-Dehkordi SS, Tajik H, Moradi M, Khalighi-Sigaroodi F. Chemical composition of essential oils in Zataria multiflora Boiss. From different parts of Iran and their radical scavenging and antimicrobial activity. Food Chem Toxicol Int J Published Br Industrial Biol Res Association. 2010;48(6):1562–7. 10.1016/j.fct.2010.03.025. [DOI] [PubMed] [Google Scholar]
- 107.Hosseinimehr SJ, Mahmoudzadeh A, Ahmadi A, Ashrafi SA, Shafaghati N, Hedayati N. The radioprotective effect of Zataria multiflora against genotoxicity induced by γ irradiation in human blood lymphocytes. Cancer Biother Radiopharm. 2011;26(3):325–9. 10.1089/cbr.2010.0896. [DOI] [PubMed] [Google Scholar]
- 108.Lalia AZ, Dasari S, Robinson MM, Abid H, Morse DM, Klaus KA, Lanza IR. Influence of omega-3 fatty acids on skeletal muscle protein metabolism and mitochondrial bioenergetics in older adults. Aging. 2017;9(4):1096–129. 10.18632/aging.101210. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 109.Strandberg E, Ponsot E, Piehl-Aulin K, Falk G, Kadi F. Resistance training alone or combined with N-3 PUFA-Rich diet in older women: effects on muscle fiber hypertrophy. J Gerontol A. 2019;74(4):489–94. 10.1093/gerona/gly130. [DOI] [PubMed] [Google Scholar]
- 110.Da Boit M, Sibson R, Sivasubramaniam S, Meakin JR, Greig CA, Aspden RM, Thies F, Jeromson S, Hamilton DL, Speakman JR, Hambly C, Mangoni AA, Preston T, Gray SR. Sex differences in the effect of fish-oil supplementation on the adaptive response to resistance exercise training in older people: a randomized controlled trial. Am J Clin Nutr. 2017;105(1):151–8. 10.3945/ajcn.116.140780. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 111.Strandberg E, Edholm P, Ponsot E, Wåhlin-Larsson B, Hellmén E, Nilsson A, Engfeldt P, Cederholm T, Risérus U, Kadi F. Influence of combined resistance training and healthy diet on muscle mass in healthy elderly women: a randomized controlled trial. Journal of applied physiology (Bethesda, Md. 1985) 2015; 119(8):918–25. 10.1152/japplphysiol.00066.2015 [DOI] [PubMed]
- 112.Rodacki CLN, Rodacki ALF, Pereira G, Naliwaiko K, Coelho I, Pequito D, Fernandes LC. Fish-oil supplementation enhances the effects of strength training in elderly women. Am J Clin Nutr. 2012;95(2):428–36. 10.3945/ajcn.111.021915. [DOI] [PubMed] [Google Scholar]
- 113.Nadeem M, Khan MA, Ahmad FJ, Parvez S, Akhtar M, Najmi AK. Exploring the neuroprotective role of asparagus racemosus (Shatavari) in alzheimer’s disease: mechanisms, evidence, and future directions. 3 Biotech. 2025;15(7):197. 10.1007/s13205-025-04355-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 114.Bopana N, Saxena S. Asparagus racemosus–ethnopharmacological evaluation and conservation needs. J Ethnopharmacol. 2007;110(1):1–15. 10.1016/j.jep.2007.01.001. [DOI] [PubMed] [Google Scholar]
- 115.Dalvi K, Vaykos R, Sanap G, Nikam S. Plant Profile, phytochemistry and Pharmacology of asparagus racemosus (Shatavari): A review. IJRASET. 2022;10(3):1418–22. 10.22214/ijraset.2022.40892. [Google Scholar]
- 116.Anders JPV, Keller JL, Smith CM, Hill EC, Housh TJ, Schmidt RJ, Johnson GO. The effects of asparagus racemosus supplementation plus 8 weeks of resistance training on muscular strength and endurance. J Funct Morphology Kinesiol. 2020;5(1). 10.3390/jfmk5010004. [DOI] [PMC free article] [PubMed]
- 117.O’Leary MF, Jackman SR, Sabou VR, Campbell MI, Tang JCY, Dutton J, Bowtell JL. Shatavari supplementation in postmenopausal women improves handgrip strength and increases Vastus lateralis myosin regulatory light chain phosphorylation but does not alter markers of bone turnover. Nutrients. 2021;13(12). 10.3390/nu13124282. [DOI] [PMC free article] [PubMed]
- 118.O’Leary MF, Jackman SR, Bowtell JL. Shatavari supplementation in postmenopausal women alters the skeletal muscle proteome and pathways involved in training adaptation. Eur J Nutr. 2024;63(3):869–79. 10.1007/s00394-023-03310-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 119.Organization WH. Global action plan on physical activity 2018–2030: more active people for a healthier world. Geneva: World Health Organization; 2019. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Data described in the manuscript, code book, and analytic code will be made available upon request pending.



