Abstract
Purpose
Magnesium is a profuse intracellular cation with a key role in muscle function and cellular senescence. The aim was to examine the prospective association between 5 year changes in dietary intake of magnesium and changes in physical performance among older men and women.
Methods
Prospective study conducted over 863 community-dwellers aged ≥ 65 years from the Seniors-ENRICA cohort (Spain). In 2012 and 2017, a validated computerized face-to-face diet history was used to record the consumption of up to 880 foods. From these data, we estimated changes in dietary magnesium intake. The Short Physical Performance Battery (SPPB) was also conducted in both time points and we obtained changes in the score during follow-up, with positive values indicating physical performance improvement.
Results
Over 5 years of follow-up, an increase in magnesium intake was associated with an increment in the SPPB score among older women [multivariate β (95% confidence interval): 1.01 (0.49; 1.52), p-trend: 0.001]. In addition, changes from non-adherence to adherence to both estimated average requirement and recommended dietary allowance during follow-up period were associated with an increment in SPPB score among older women [1.14 (0.36; 1.92) and 0.84 (0.22; 1.47), respectively]. No significant associations between changes in magnesium intake and changes in SPPB score were observed in men.
Conclusions
Both increase of magnesium intake and change from non-adherence to adherence to dietary reference magnesium intake was prospectively associated with better physical performance among older women, but not among men.
Supplementary Information
The online version contains supplementary material available at 10.1007/s00394-022-02808-z.
Keywords: Diet, Magnesium, Physical functional performance, Older adults
Introduction
Magnesium (Mg) is a very abundant intracellular cation which sustains several basic cellular processes. Among older adults, Mg deficiency is frequent because of the age-related decline in dietary intake combined with alterations in the Mg absorption/excretion balance [1]. There is evidence linking the Mg deficiency to cellular senescence and to an accelerated aging phenotype [2]. Specifically, given that Mg exerts a key role in muscle function, an inadequate dietary intake could have a negative impact on physical performance in the old age [3, 4].
Slowing the progressive decline in physical performance is one of the keys strategies to achieve healthy aging. To the date, in addition to the fact that studies addressing the association between Mg and physical performance among older adults are scarce and conflicting, it is unclear which method is the most ideal to assess the association. A cross-sectional analysis using baseline data from the InCHIANTI study (aging in the Chianti area, Italy) showed, for the first time, that serum Mg concentration was an independent determinant of muscle performance in older adults [5]. But, given there is controversy about whether serum Mg is an appropriate proxy of Mg stores or not, other studies used dietary Mg intake to address the association, which can also lead to more practical conclusions for clinical counselling and public health interventions [6]. Using a dietetic approach, Veronese et al. found that a daily Mg supplementation improved the physical performance of healthy older women who participated in a parallel randomized controlled trial [7]. Nevertheless, a recent study found no effect of Mg intake on changes in physical performance [8]. Moreover, none of these studies accounted for sex differences, although women could be more susceptible to Mg deficiencies than men, because of their higher frequency of musculoskeletal disorders, including osteoporosis, which is known to limit Mg exchange between bone and blood [7, 9].
Therefore, our study aimed to assess the prospective association between 5 year changes in dietary intake of Mg and changes in physical performance among older men and women.
Methods
Study design and participants
This was a prospective study using data from the Seniors-ENRICA cohort (Spain), whose methods have been reported elsewhere [10, 11]. This cohort included community-dwelling adults aged 60 years and older, who were recruited in 2008–10. At baseline, information about lifestyle, health status, morbidity and use of health services was collected with a standardized phone interview. Then, two home visits were conducted to perform a physical examination and to obtain data on habitual diet. In 2012 and 2017, two subsequent waves of data collection were performed, using the same procedures, to update baseline information. Given that physical performance, as measured by the Short Physical Performance Battery (SPPB) [12], was first assessed in 2012, analyses for this work were conducted with the 2519 participants in 2012 who were followed-up to 2017.
Written informed consent was given by all study participants. The Seniors-ENRICA cohort was approved by the Clinical Research Ethics Committee of the La Paz University Hospital in Madrid (registration number: 2144).
Study variables
Diet history and mineral intake
In 2012 and 2017, a validated computerized face-to-face diet history was used to assess habitual food consumption during the previous year [13]. This instrument included 880 foods and beverages as well as sets of photographs to help participants estimate serving sizes. Daily Mg intakes were estimated using standard Spanish food composition tables [14]. Mineral intake through supplements was not considered due to its low use (< 1%) and the lack of data on the specific type consumed. The validity of the diet assessment was evaluated by comparing information obtained using the diet history with seven 24-h recalls over a period of 1 year among a subsample of participants; the Pearson correlation coefficient was moderately good for Mg intake (r = 0.46) [13]. Intake of Mg was adjusted for total energy using the residuals method [15].
Physical performance
The SPPB was used, according to protocol of the National Institute on Aging [12], to assess physical function in 2012 and 2017. The SPPB comprises three standardized timed components: standing balance, gait speed and chair stand. To assess the balance, participants were asked to stand in three progressively difficult positions for 10 s each: feet side by side, semi-tandem, and full-tandem position. Then, gait speed was measured as the shortest time (seconds) of two consecutive walks at a normal pace along a corridor of 2.44 m long (8-foot walk), using their assistive device if needed. Finally, the chair-stand test was performed by asking participants to stand up from a chair and sit down five times with no help from their arms. Each of these three tests was scored from 0 (inability to perform the task) to 4 (highest level of performance). Therefore, a global SPPB score was created by adding each component test score, ranging from 0 to 12 (best performance).
Other variables
Data on potential confounders of the study association were also collected in 2012 and 2017. We assessed sociodemographic characteristics (sex, age, education level) and health behaviours, including smoking, alcohol consumption, and time spent watching TV as a proxy of sedentariness [11]. Recreational physical activity, measured in metabolic equivalents hours per week (MET-h/w), was assessed with the validated questionnaire used in the EPIC-Spain cohort study [16].
Data on morbidity were also collected. Body Mass Index (BMI) was calculated as measured weight (kg) divided by square height (m), and obesity was defined as BMI ≥ 30 kg/m2. Diabetes was defined as fasting plasma glucose ≥ 126 mg/dl or taking antidiabetic therapy [17]. Blood pressure was measured under standardized conditions [18], and hypertension was defined as systolic/diastolic blood pressure ≥ 140/ ≥ 90 mmHg or being under hypertensive drug treatment. Finally, hypercholesterolemia was defined as cholesterol ≥ 200 mg/dl or undergoing lipid-lowering treatment. Participants also reported the following physician-diagnosed diseases: cardiovascular disease (heart failure, heart attack or stroke), musculoskeletal disease (arthritis, osteoarthritis or hip fracture) and cancer.
Statistical analysis
Of the 2519 participants in the Seniors-ENRICA in 2012, 1185 were lost to follow-up and 196 died up to 2017. Also, we excluded individuals lacking data on Mg intake (n = 263), implausible low or high energy intake values (n = 2) or without information on any of the rest of study variables (n = 10). Therefore, the analyses were conducted with 863 individuals (424 men and 439 women).
We used multivariable linear regression to study the associations between changes in Mg intake and changes in the SPPB score from 2012 to 2017. The dependent variable was the continuous change in SPPB score, resulting from the subtraction of 2017 minus 2012 values. The main independent variables were sex-specific tertiles of Mg intake change between 2012 and 2017: the first tertile reflected an intake decrease, the second tertile a small intake change, and the third tertile an intake increase. First, residual plots were used to check the assumption of linearity and homoscedasticity. Then, two regression models were fitted with the second tertile as reference: (1) the first model was adjusted for baseline SPPB score, age, educational level, baseline physical activity, smoker status, BMI, TV-watching and alcohol intake; (2) the second model was additionally adjusted for baseline morbidity, including diabetes, hypertension, hypercholesterolemia, cardiovascular disease, cancer and musculoskeletal disease. The linear dose–response association (p value for trend) was tested by modelling Mg intake as a continuous variable. We also repeated the analyses using a 1 SD-increment of Mg intake change during the 5-year period as the independent variable. To assess the consistency of results, the analyses were stratified by physical activity, musculoskeletal disease, obesity, cardiometabolic disease (diabetes and cardiovascular disease) and alcohol intake; likelihood-ratio tests comparing models with and without interactions terms were used to assess whether results varied across strata.
In addition, we classified participants according to their level of compliance with the current US dietary reference intake for Mg [19], using both the estimated average requirement (EAR) (≥ 350 mg/d for men and ≥ 265 mg/d for women) and the recommended dietary allowance (RDA) (≥ 420 mg/d for men and ≥ 320 mg/d for women). According to these cut-off points, we defined four categories of participants: non-compliers both in 2012 and 2017; those who moved from non-compliance in 2012 to compliance in 2017; those who moved from compliance in 2012 to non-compliance in 2017; and compliers both in 2012 and 2017. Then, we fitted the same regression models described above, using non-compliers in both time points as the reference group. Moreover, to aim for consistency and generalization, we repeated the analyses using the cut-off points from the European Food Safety Authority (EFSA). Given that the EFSA considers that EAR or RDA for Mg cannot be derived for adults, we used its defined adequate intake (AI) (≥ 350 mg/d for men and ≥ 300 mg/d for women) [20].
Sex differences in the association between changes in Mg intake and SPPB scores were tested with likelihood-ratio tests, which compared models with and without cross-product interaction terms. Given that we found a sex interaction (p for interaction = 0.02 in the fully-adjusted model) in main analyses, all results are presented for men and women separately.
Analyses were performed with the STATA software, 15.0 version (Stata Corp, College Station, TX). This manuscript follows the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) recommendations.
Results
Table 1 shows the main characteristics of participants according to sex and year of data collection. Throughout the follow-up period, there was a decrease in tobacco consumption, daily energy intake and BMI for both sexes. Likewise, the daily intake of Mg was reduced, leading to a lower percentage of compliance for EAR and RDA recommendations in 2017 compared to 2012. Lastly, the prevalence of chronic diseases was higher in 2017 than in 2012 for both men and women. Over the 5-year follow-up period, we identified 453 (52.5%) participants with minimal or no changes in the SPPB score, 202 (23.4%) with a decrease and 208 (24.1%) with an increase in the score. As a result, there was only a slight decrease in the mean SPPB score between 2012 and 2017 in both men and women.
Table 1.
Women (n = 439) | Men (n = 424) | ||||||
---|---|---|---|---|---|---|---|
2012 | 2017 | p valuea | 2012 | 2017 | p valuea | ||
Age, year | 70.9 (5.36) | 75.6 (5.24) | N/A | 70.0 (5.38) | 74.8 (5.33) | N/A | |
Primary education or less, n (%) | 254 (57.9) | – | N/A | 162 (38.2) | – | N/A | |
Physical activity, METs-h/w | 18.8 (12.1) | – | N/A | 25.8 (17.0) | – | N/A | |
TV-watching, h/d | 19.6 (10.9) | 20.4 (11.9) | 0.160 | 17.1 (9.66) | 19.3 (11.6) | < 0.001 | |
Current smokers, n (%) | 17 (3.87) | 16 (3.64) | 0.01 | 59 (13.9) | 43 (10.1) | < 0.001 | |
Alcohol intake, g/d | 4.36 (8.34) | 3.66 (8.49) | 0.05 | 15.6 (16.6) | 14.1 (15.9) | 0.04 | |
Energy intake, kcal/d | 1868 (387) | 1,692 (290) | < 0.001 | 2238 (460) | 2029 (363) | < 0.001 | |
BMI, kg/m2 | 28.4 (4.89) | 27.4 (4.82) | < 0.001 | 28.5 (3.65) | 27.9 (3.63) | < 0.001 | |
Mg intake, mg/d | 332 (114) | 300 (76.3) | < 0.001 | 360 (95.8) | 339 (77.8) | < 0.001 | |
Mg intake compliance | |||||||
EAR, n (%) | 310 (70.6) | 271 (64.7) | < 0.001 | 187 (44.1) | 156 (36.8) | < 0.001 | |
RDA, n (%) | 187 (42.6) | 153 (34.9) | < 0.001 | 81 (19.1) | 61 (14.4) | < 0.001 | |
Morbidity | |||||||
Diabetes, n (%) | 56 (12.8) | 71 (16.2) | < 0.001 | 94 (22.2) | 109 (25.7) | < 0.001 | |
Hypertension, n (%) | 245 (55.8) | 275 (62.6) | < 0.001 | 240 (56.6) | 273 (64.4) | < 0.001 | |
Hypercholesterolemia, n (%) | 231 (52.6) | 263 (59.9) | < 0.001 | 200 (47.1) | 223 (52.6) | < 0.001 | |
Cardiovascularb, n (%) | 16 (3.64) | 32 (7.29) | < 0.001 | 25 (5.90) | 39 (9.20) | < 0.001 | |
Cancer, n (%) | 7 (1.59) | 13 (2.96) | < 0.001 | 8 (1.89) | 27 (6.37) | < 0.001 | |
Musculoskeletalc, n (%) | 256 (58.3) | 327 (74.5) | < 0.001 | 146 (34.4) | 207 (48.8) | < 0.001 | |
SPPB, score | 8.46 (2.15) | 8.32 (2.72) | 0.23 | 9.31 (2.03) | 9.27 (2.45) | 0.72 |
Note for continuous variables, mean value (standard deviation) is reported
SPPB Short Physical Performance Battery test, MET metabolic equivalent, TV Television, EAR estimated average requirement, RDA recommended dietary allowance
aPaired t-test for continuous variables and McNemar’s test for categorical variables were used for statistical comparison
bCardiovascular diseases include heart failure, heart attack and stroke
cMusculoskeletal diseases include arthritis, osteoarthritis and hip fracture
Table 2 shows the associations between changes in daily Mg intake and changes in the SPPB score between 2012 and 2017, overall and by sex. Compared to women with small changes in Mg intake (tertile 2), those who increased their intake over follow-up (tertile 3) showed beneficial changes in the SPPB score. Specifically, a mean increase in Mg intake of 44.2 mg/d from 2012 to 2017 was associated with an increment of 1.01 points (95% confidence interval: 0.49; 1.52) in the SPPB score; the corresponding value for a 1-SD increase in Mg intake was 0.28 (0.01; 0.47) points. However, no association was observed for men. The study associations did not significantly vary across predefined strata (all p for interaction > 0.05), though the association tended to be stronger in women with low physical activity, with musculoskeletal disease, without obesity or cardiometabolic disease and abstainers (Supplementary Table 1).
Table 2.
Tertile 1 (intake decrease) |
Tertile 2 (intermediate change) |
Tertile 3 (intake increase) |
p-trend | Per 1-SD increase during 5 year periodb | |
---|---|---|---|---|---|
Overall | |||||
Participants, n (%) | 289 (33.5) | 287 (33.3) | 287 (33.2) | ||
Change in Mg intake, mg/d | − 109.6 (66.7) | − 22.8 (49.1) | 54.5 (49.2) | ||
Multivariable model 1c | 0.03 (− 0.32;0.39) | Ref | 0.40 (0.05;0.76) | 0.042 | 0.13 (− 0.02; 0.27) |
Multivariable model 2d | 0.04 (− 0.31; 0.39) | Ref | 0.43 (0.07; 0.78) | 0.034 | 0.13 (− 0.02; 0.28) |
Women | |||||
Participants, n (%) | 147 (33.5) | 146 (33.3) | 146 (33.3) | ||
Change in Mg intake, mg/d | − 130.4 (76.6) | − 30.1 (15.4) | 44.2 (48.5) | ||
Multivariable model 1c | 0.11 (− 0.40; 0.62) | Ref | 1.00 (0.48; 1.51) | 0.001 | 0.34 (0.13; 0.56) |
Multivariable model 2d | 0.09 (− 0.41; 0.61) | Ref | 1.01 (0.49; 1.52) | 0.001 | 0.35 (0.14; 0.57) |
Men | |||||
Participants, n (%) | 142 (33.5) | 141 (33.3) | 141 (33.3) | ||
Change in Mg intake, mg/d | − 88.05 (45.8) | − 15.2 (15.3) | 65.2 (47.7) | ||
Multivariable model 1c | 0.02 (− 0.17; 0.50) | Ref | − 0.16 (− 0.65; 0.34) | 0.494 | − 0.11 (− 0.32; 0.09) |
Multivariable model 2d | 0.05 (− 0.44; 0.54) | Ref | − 0.09 (− 0.59; 0.41) | 0.592 | − 0.10 (− 0.30; 0.11) |
SPPBShort Physical Performance Battery test
aSex-specific tertile cut-points were − 59.8 and − 5.99 mg/d in women and − 42.6 and 11.6 mg/d in men for magnesium
b1-SD increase = 89.2 mg/d in women and 73.9 mg/d in men
cAdjusted for baseline SPPB score (tertiles of score), age (< 70, 70–79, ≥ 80 y), educational level (primary, secondary, university) and physical activity (tertiles of METs-h/w), smoking status (current, former, never), BMI (tertiles of kg/m2), TV-watching (tertiles of h/wk) and alcohol intake (tertiles of g/d)
dAdditionally adjusted for baseline morbidity, including diabetes, hypertension, hypercholesterolemia, cardiovascular disease, cancer, and musculoskeletal disease
Table 3 shows the associations between changes in adherence to the Mg reference intake and changes in SPPB score from 2012 to 2017 stratified by sex. In general, women who became compliant with the EAR between 2012 and 2017 had an increased SPPB score, in comparison with those who were no-compliant in both time points. Specifically, an improvement in EAR adherence (from non-compliance to compliance) was associated with a 1.14 (95% CI 0.36; 1.92) point increase in SPPB. Also, an improvement in the adherence to RDA (from non-compliance to compliance) was associated with an increase of 0.84 (0.22; 1.47) points on the score in women. Again, no associations were observed in men. Similar results were observed when we used the AI from EFSA to define cut-off points for Mg intake recommendations (Supplementary Table 2).
Table 3.
Consistent non-compliancea | From non-compliance to compliancea | From compliance to non-compliancea | Consistent compliancea | |
---|---|---|---|---|
Estimated average requirement | ||||
Overall | ||||
Participants, n (%) | 235 (27.2) | 131 (15.2) | 201 (23.3) | 296 (34.3) |
Mean change, g/d | − 21.4 (42.5) | 50.1 (65.4) | − 68.7 (67.4) | − 34.8 (99.2) |
Multivariable modelb | Ref | 0.46 (− 0.01;0.92) | − 0.42 (− 0.83; − 0.01) | 0.08 (− 0.30; 0.46) |
Women | ||||
Participants, n (%) | 67 (15.3) | 62 (14.1) | 101 (23.0) | 209 (47.6) |
Mean change, g/d | − 34.1 (38.0) | 36.6 (58.7) | − 76.4 (70.0) | − 44.9 (102.4) |
Multivariable modelb | Ref | 1.14 (0.36; 1.92) | − 0.12 (− 0.82; 0.58) | 0.55 (− 0.07; 1.18) |
Men | ||||
Participants, n (%) | 168 (39.6) | 69 (16.3) | 100 (23.6) | 87 (20.5) |
Mean change, g/d | − 16.4 (43.2) | 62.2 (69.0) | − 60.9 (64.1) | − 10.5 (86.7) |
Multivariable modelc | Ref | 0.06 (− 0.54; 0.67) | − 0.33 (− 0.86; 0.21) | 0.04 (− 0.51;0.61) |
Recommended dietary allowance | ||||
Overall | ||||
Participants, n (%) | 494 (57.2) | 101 (11.7) | 155 (18.0) | 113 (13.1) |
Mean change, g/d | − 17.3 (51.1) | 66.1 (67.4) | − 104.3 (93.5) | − 40.3 (93.7) |
Multivariable modelb | Ref | 0.45 (− 0.02; 0.91) | 0.07 (− 0.33; 0.47) | − 0.07 (− 0.51; 0.38) |
Women | ||||
Participants, n (%) | 184 (41.9) | 68 (15.5) | 102 (23.2) | 85 (19.4) |
Mean change, g/d | − 29.3 (42.2) | 52.8 (62.0) | − 112 (100.5) | − 46.0 (94.1) |
Multivariable modelb | Ref | 0.84 (0.22; 1.47) | 0.19 (− 0.37; 0.74) | 0.34 (− 0.25; 0.93) |
Men | ||||
Participants, n (%) | 310 (73.3) | 33 (7.80) | 53 (12.5) | 28 (6.60) |
Mean change, g/d | − 10.2 (54.5) | 93.7 (71.1) | − 89.6 (77.1) | − 23.0 (92.2) |
Multivariable modelb | Ref | 0.02 (− 0.75; 0.79) | 0.13 (− 0.49; 0.76) | − 0.28 (− 1.10; 0.55) |
SPPB Short Physical Performance Battery test
aCut-off points for recommendations compliance were ≥ 350 mg/d (women) and ≥ 265 mg/d (men) for Estimated Average Requirement, and ≥ 420 mg/d (women) and ≥ 320 mg/d (men) for Recommended Dietary Allowance
bAdjusted for baseline SPPB score (tertiles of score), age (< 70, 70–79, ≥ 80 y), educational level (primary, secondary, university) and physical activity (tertiles of METs-h/w), smoking status (current, former, never), BMI (tertiles of kg/m2), TV-watching (tertiles of h/wk) and alcohol intake (tertiles of g/d)
Discussion
In this prospective study of community-dwelling older adults followed over a 5-year period, an increase of dietary Mg intake was associated with an improvement of physical performance, assessed by the SPPB, in women but not in men. Consistently, a change from non-compliance to compliance with the reference intake resulted in a better SPPB score among women.
Magnesium intake and physical performance
Our results are in line with those from the single randomized controlled trial conducted to the date that investigated if Mg supplementation improves physical performance. Veronese et al. [7] recruited 124 healthy women > 65 years attending to a mild fitness program, and then compared with a group than received supplementation with 300 mg/d of bioavailable Mg with a placebo group. After 12 weeks, women from the treatment group experienced a significant increment of 0.41 points in the SPPB score, compared to women under placebo. In our study, women in tertile 3 of change in Mg intake achieved even larger positive changes in the SPPB score over 5 years (0.98 points). Previously, Lukaski et al. [21] had examined the effects of Mg depletion induced by dietary restriction on physiologic responses during submaximal exercise in ten postmenopausal middle-aged women (45–71 years old). They found that women fed with 180 versus 320 mg/d had worse cardiovascular function during submaximal work, supporting the current RDA for Mg. Moreover, findings from previous observational research are in the same direction. Two large studies with the EPIC-Norfolk and the UK-Biobank cohorts, found a clear cross-sectional positive dose–response between Mg intake and muscle mass [22, 23], which is a strong determinant of physical performance. Other studies have also shown that sarcopenic older adults consumed less Mg than non-sarcopenic ones [24, 25].
Nevertheless, serum Mg does not seem to correlate well with Mg intakes [6]. Indeed, supplementation with dietary Mg increases serum Mg only among subjects with low basal circulating Mg [26]. This is consistent with our study findings. On one hand, the positive effects of dietary Mg were particularly observed in women moving from baseline low levels of intake to an appropriate Mg intake at the end of follow-up (i.e. above EAR or RDA). On the other hand, we found that participants reducing Mg intake during follow-up preserved physical performance if they continued to meet with dietary reference intake, suggesting that supplementation with Mg or dietary modifications to increase serum Mg are only necessary when older adults consume Mg bellow EAR or RDA.
The mechanisms of the effect of Mg on muscle mass or function are only partially known. Dietary Mg regulates some key mechanisms of muscle function, including protein and ATP synthesis, glycogenolysis, fatty acid oxidation, oxygen consumption and electrolyte balance [4]. It has also been postulated that oxidative stress and alterations in calcium homeostasis triggered by Mg reductions can lead to muscle cells damage [27–29]. Furthermore, Mg may exert certain protection against inflammation, which has been associated with an acceleration of age-related loss of skeletal muscle [4, 28, 29]. Moreover, Mg stimulates the process of bone development and mineralization through several mechanisms [28], and there is strong evidence of the positive role of Mg on fracture risk reduction and on bone mineral density [29], which is essential for physical performance [30]. Lastly, results from a recent analysis of US National Health and Nutrition Examination Survey (NHANES) suggested that high Mg intake may have a positive role in cognitive function [31]; thereby, physical performance improvement could be parallel to cognitive impairment prevention.
Sex differences
The reasons why in our study women but not men benefited from an increase in Mg intake are unknown but could be related to biological differences between sexes. First, there is some evidence of the beneficial effect of Mg on several highly prevalent chronic morbid conditions, such as cardiovascular disease or type 2 diabetes [32–34], which are also associated to physical performance [35, 36]. Given that the positive effects of Mg on cardiometabolic health seem to be greater among women [32, 33], our results could partially be due to beneficial effect of Mg preventing the development of cardiovascular diseases and type 2 diabetes. Indeed, in our sample, the prevalence of these diseases in women were lower than in men. Second, postmenopausal women are affected more often than men from musculoskeletal disorders and sarcopenia [37, 38]. These health conditions, specially osteoporosis, lead to an imbalance in bone deposition and resorption, altering the serum Mg level and making subjects more sensitive to dietary supplements [38, 39]. This is consistent with our findings from stratified analyses, as the observed effect of Mg intake on physical performance tended to be stronger among women with musculoskeletal diseases. Third, Mg is potentially important for the metabolism of anabolic–androgenic steroids and other sex hormones during aging, such as testosterone, progesterone and insulin‐like growth factor 1 [40]. Some studies conducted only with men have found that Mg acts on the muscle via the endocrine system [41]. Given that the levels of these hormones are sex-dependent, it can be expected that the effects of Mg intake on muscle differ between sexes. Nevertheless, given that hormonal decline is steep during ageing, the endocrine pathway would be more plausible among younger subjects. More research is clearly needed to understand why dietary Mg intake improves physical performance only in women and, from a broader perspective, to understand the suggested sex-dependent effects of Mg intake on healthy ageing [39, 42].
Practical implications
In our longitudinal study, an overall reduction in Mg intake was observed, even among those who were consistently compliant with dietary recommendations. It seems clear that the risk of Mg deficiency is hanging over most of the people during aging process. Therefore, it could be advised a periodically assessment of available Mg to early detect older adults moving to levels below the recommended Mg thresholds. However, there are still no valid and simple methods to determine the available Mg. For instance, serum Mg only represents 1% of total body magnesium, which is mainly intracellular [6, 43]. Thereby, clinical assessment of patients at risk for Mg deficiency could be actually recommended, which may include the routine evaluation of Mg intake. Given that it is unrealistic to ask clinicians to perform a complete diet history to estimate Mg intake, they could be requested to inquire and counsel about the consumption of main food sources Mg. These sources include foods who are usually part of most healthy diet patterns, such as whole grain cereals, vegetables, nuts, and legumes [43]. For instance, in our cohort of Spanish older adults, main sources of Mg were cereals, dairy products and nuts. Conversely, ultra-processed foods, which are predominant in the Western diet, are normally poor in Mg [43].
Strengths and limitations
Among the strengths of our study is a rather large sample size, a long follow-up that allows to detect substantial changes in physical performance, and a separate data analyses in men and women. Also, we used a validated diet history to ascertain changes in Mg dietary intake across the follow-up period. Lastly, statistical analyses were adjusted for a good number of potential confounders and included several sensitivity analyses to provide robustness. Nevertheless, this study also has some limitations. First, as in any nutritional epidemiological study, there could be some recall bias; however, this type of bias usually tends to underestimate study associations. Second, although having information on serum Mg levels would have been desirable, studies have shown a lack of correlation between Mg intake and its serum levels suggesting that the latter should not be used to predict disease risk [44]. Third, although we used musculoskeletal disorders as a proxy of bone health, we lacked data about osteoporosis, which is closely related to minerals and physical performance. Finally, despite the prospective nature of the study reverse causality cannot completely be ruled out, since participants might have first experimented a deterioration in physically performance and later, a decrease in their capacity to buy and cook a healthy diet with the appropriate amount of magnesium. Nevertheless, if this was the actual direction of causality, we would have expected the same results for women and men.
Conclusions
An increase of dietary Mg intake was prospectively associated with better physical performance in older women. Adhering to reference Mg intake in the old age could help women to maintain physical functioning and delay the disability process. Further studies are needed to confirm and understand why this association might occur exclusively in women.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
This work was supported by grants from the Instituto de Salud Carlos III, State Secretary of R+D+I of Spain and FEDER/FSE (FIS 20/140), the European Union (FP7-HEALTH-2012-Proposal No: 305483-2, FRAILOMIC Initiative), the ATHLOS project (EU H2020—Project ID: 635316).
Abbreviations
- Mg
Magnesium
- SPPB
Short Physical Performance Battery
- BMI
Body mass index
- EAR
Estimated Average Requirement
- RDA
Recommended Dietary Allowance
- EFSA
European Food Safety Authority
- AI
Adequate intake
- NHANES
National Health and Nutrition Examination Survey
Author contributions
All authors contributed to the study conception and design. LA-F: data curation; formal analysis; writing—original draft; validation. EAS: data curation; software; writing—review and editing. FFC: data curation; software; writing—review and editing. RO: data curation; software; writing—review and editing. EG-E: data curation; software; writing—review and editing. FR-A: funding acquisition; project administration; resources; writing—review and editing. EL-G; funding acquisition; supervision; investigation; methodology; validation; writing—review and editing. AL: supervision; investigation; methodology; validation; formal analysis; writing—original draft.
Funding
Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This work was supported by grants from the Instituto de Salud Carlos III, State Secretary of R + D + I of Spain and FEDER/FSE (FIS 13/0288, 16/609 and 16/1512), the European Union (FP7-HEALTH-2012-Proposal No: 305483-2, FRAILOMIC Initiative), the ATHLOS project (EU H2020—Project ID: 635316).
Availability of data and materials
Lucía Arias-Fernández, Ellen A Struijk, Francisco Félix Caballero, Rosario Ortolá, Esther García-Esquinas, Fernando Rodríguez-Artalejo, Esther Lopez-Garcia, and Alberto Lana comply with the Ethical guidelines for authorship and publishing in the European Journal of Nutrition.
Code availability
Not applicable.
Declarations
Conflict of interest
Lucía Arias-Fernández, Ellen A Struijk, Francisco Félix Caballero, Rosario Ortolá, Esther García-Esquinas, Fernando Rodríguez-Artalejo, Esther Lopez-Garcia, and Alberto Lana declare no conflict of interest.
Ethics approval
The Seniors-ENRICA cohort was approved by the Clinical Research Ethics Committee of the La Paz University Hospital in Madrid and has been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.
Consent to participate
Written informed consent was given by all study participants prior to their inclusion in the study.
Consent for publication
All authors agree the content to be submitted and to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
References
- 1.Barbagallo M, Veronese N, Dominguez LJ. Magnesium in aging, health and diseases. Nutrients. 2021;13:463. doi: 10.3390/nu13020463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Killilea DW, Maier JA. A connection between magnesium deficiency and aging: new insights from cellular studies. Magnes Res. 2008;21:77–82. [PMC free article] [PubMed] [Google Scholar]
- 3.Wang R, Chen C, Liu W, et al. The effect of magnesium supplementation on muscle fitness: a meta-analysis and systematic review. Magnes Res. 2017;30:120–132. doi: 10.1684/mrh.2018.0430. [DOI] [PubMed] [Google Scholar]
- 4.Perna S, Alalwan TA, Al-Thawadi S, et al. Evidence-based role of nutrients and antioxidants for chronic pain management in musculoskeletal frailty and sarcopenia in aging. Geriatrics (Basel) 2020;5:16. doi: 10.3390/geriatrics5010016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Dominguez LJ, Barbagallo M, Lauretani F, et al. Magnesium and muscle performance in older persons: the InCHIANTI study. Am J Clin Nutr. 2006;84:419–426. doi: 10.1093/ajcn/84.1.419. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.van Dam RM. Serum magnesium and risk of coronary artery disease: are there implications for dietary interventions? Am J Clin Nutr. 2020;111:6–7. doi: 10.1093/ajcn/nqz289. [DOI] [PubMed] [Google Scholar]
- 7.Veronese N, Berton L, Carraro S, et al. Effect of oral magnesium supplementation on physical performance in healthy elderly women involved in a weekly exercise program: a randomized controlled trial. Am J Clin Nutr. 2014;100:974–981. doi: 10.3945/ajcn.113.080168. [DOI] [PubMed] [Google Scholar]
- 8.Asamane EA, Greig CA, Thompson JL. The association between nutrient intake, nutritional status and physical function of community-dwelling ethnically diverse older adults. BMC Nutr. 2020;6:36. doi: 10.1186/s40795-020-00363-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Rude RK, Singer FR, Gruber HE. Skeletal and hormonal effects of magnesium deficiency. J Am Coll Nutr. 2009;28:131–141. doi: 10.1080/07315724.2009.10719764. [DOI] [PubMed] [Google Scholar]
- 10.Rodríguez-Artalejo F, Graciani A, Guallar-Castilón P, et al. Rationale and methods of the study on nutrition and cardiovascular risk in Spain (ENRICA) Rev Esp Cardiol. 2011;64:876–682. doi: 10.1016/j.recesp.2011.05.019. [DOI] [PubMed] [Google Scholar]
- 11.Lana A, Struijk EA, Ortolá R, Rodríguez-Artalejo F, Lopez-Garcia E. Longitudinal association between sodium and potassium intake and physical performance in older adults. J Gerontol A Biol Sci Med Sci. 2020;75:2379–2386. doi: 10.1093/gerona/glaa031. [DOI] [PubMed] [Google Scholar]
- 12.Guralnik JM, Ferrucci L, Pieper CF, et al. Lower extremity function and subsequent disability: consistency across studies, predictive models, and value of gait speed alone compared with the short physical performance battery. J Gerontol A Biol Sci Med Sci. 2000;55:M221–231. doi: 10.1093/gerona/55.4.m221. [DOI] [PubMed] [Google Scholar]
- 13.Guallar-Castillón P, Sagardui-Villamor J, Balboa-Castillo T, et al. Validity and reproducibility of a Spanish dietary history. PLoS ONE. 2014;9:e86074. doi: 10.1371/journal.pone.0086074. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Moreiras O, Carvajal A, Cabrera L, Cuadrado C. Tablas de composición de alimentos. 11. Madrid: Ediciones Pirámide; 2007. [Google Scholar]
- 15.Van Dam RM. Biochemical indicators of dietary intake. In: Willet WC, editor. Nutritional epidemiology. 3. Oxford: Oxford University Press; 2012. [Google Scholar]
- 16.Pols MA, Peeters PH, Ocké MC, Slimani B-d-M, Collette HJ. Estimation of reproducibility and relative validity of the questions included in the EPIC physical activity questionnaire. Int J Epidemiol. 1997;26:S181–189. doi: 10.1093/ije/26.suppl_1.s181. [DOI] [PubMed] [Google Scholar]
- 17.American Diabetes Association Diagnosis and classification of diabetes mellitus. Diabetes Care. 2014;37(Suppl 1):S81–90. doi: 10.2337/dc14-S081. [DOI] [PubMed] [Google Scholar]
- 18.Banegas JR, Graciani A, de la Cruz-Troca JJ, et al. Achievement of cardiometabolic goals in aware hypertensive patients in Spain: a nationwide population-based study. Hypertension. 2012;60:898–905. doi: 10.1161/HYPERTENSIONAHA.112.193078. [DOI] [PubMed] [Google Scholar]
- 19.Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes . Dietary reference intakes for calcium, phosphorus, magnesium, vitamin D, and fluoride. Washington (DC): National Academies Press; 1997. [PubMed] [Google Scholar]
- 20.Panel on Dietetic Products Nutrition and Allergies Scientific opinion on dietary reference values for magnesium. EFSA J. 2015;13:4186. doi: 10.2903/j.efsa.2015.4186. [DOI] [Google Scholar]
- 21.Lukaski HC, Nielsen FH. Dietary magnesium depletion affects metabolic responses during submaximal exercise in postmenopausal women. J Nutr. 2002;132:930–935. doi: 10.1093/jn/132.5.930. [DOI] [PubMed] [Google Scholar]
- 22.Hayhoe RPG, Lentjes MAH, Mulligan AA, Luben RN, Khaw KT, Welch AA. Cross-sectional associations of dietary and circulating magnesium with skeletal muscle mass in the EPIC-Norfolk cohort. Clin Nutr. 2019;38:317–323. doi: 10.1016/j.clnu.2018.01.014. [DOI] [PubMed] [Google Scholar]
- 23.Welch AA, Skinner J, Hickson M. Dietary magnesium may be protective for aging of bone and skeletal muscle in middle and younger older age men and women: cross-sectional findings from the UK biobank cohort. Nutrients. 2017;9:E1189. doi: 10.3390/nu9111189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Ter Borg S, de Groot LC, Mijnarends DM, et al. Differences in nutrient intake and biochemical nutrient status between sarcopenic and nonsarcopenic older adults-results from the maastricht sarcopenia study. J Am Med Dir Assoc. 2016;17:393–401. doi: 10.1016/j.jamda.2015.12.015. [DOI] [PubMed] [Google Scholar]
- 25.Verlaan S, Aspray TJ, Bauer JM, et al. Nutritional status, body composition, and quality of life in community-dwelling sarcopenic and non-sarcopenic older adults: a case-control study. Clin Nutr. 2017;36:267–274. doi: 10.1016/j.clnu.2015.11.013. [DOI] [PubMed] [Google Scholar]
- 26.Zhang X, Del Gobbo LC, Hruby A, et al. The circulating concentration and 24-h urine excretion of magnesium dose- and time-dependently respond to oral magnesium supplementation in a meta-analysis of randomized controlled trials. J Nutr. 2016;146:595–602. doi: 10.3945/jn.115.223453. [DOI] [PubMed] [Google Scholar]
- 27.Furutani Y, Funaba M, Matsui T. Magnesium deficiency up-regulates Myod expression in rat skeletal muscle and C2C12 myogenic cells. Cell Biochem Funct. 2011;29:577–581. doi: 10.1002/cbf.1790. [DOI] [PubMed] [Google Scholar]
- 28.Ciosek Ż, Kot K, Kosik-Bogacka D, Łanocha-Arendarczyk N, Rotter I. The effects of calcium, magnesium, phosphorus, fluoride, and lead on bone tissue. Biomolecules. 2021;11:506. doi: 10.3390/biom11040506. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Rondanelli M, Faliva MA, Tartara A, et al. An update on magnesium and bone health. Biometals. 2021;34:715–736. doi: 10.1007/s10534-021-00305-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Unocc CP, Valdez LI, Segura ER. A critical appraisal on the association and effects of magnesium and bone density on physical performance in elderly women. Am J Clin Nutr. 2015;101:889. doi: 10.3945/ajcn.114.100677. [DOI] [PubMed] [Google Scholar]
- 31.Peeri NC, Egan KM, Chai W, Tao MH. Association of magnesium intake and vitamin D status with cognitive function in older adults: an analysis of US National Health and Nutrition Examination Survey (NHANES) 2011 to 2014. Eur J Nutr. 2021;60:465–474. doi: 10.1007/s00394-020-02267-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Rooney MR, Alonso A, Folsom AR, et al. Serum magnesium and the incidence of coronary artery disease over a median 27 years of follow-up in the atherosclerosis risk in communities (ARIC) study and a meta-analysis. Am J Clin Nutr. 2020;111:52–60. doi: 10.1093/ajcn/nqz256. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Fang X, Han H, Li M, et al. Dose-response relationship between dietary magnesium intake and risk of type 2 diabetes mellitus: a systematic review and meta-regression analysis of prospective cohort studies. Nutrients. 2016;8:739. doi: 10.3390/nu8110739. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Veronese N, Demurtas J, Pesolillo G, et al. Magnesium and health outcomes: an umbrella review of systematic reviews and meta-analyses of observational and intervention studies. Eur J Nutr. 2020;59:263–272. doi: 10.1007/s00394-019-01905-w. [DOI] [PubMed] [Google Scholar]
- 35.Bellettiere J, Lamonte MJ, Unkart J, et al. Short physical performance battery and incident cardiovascular events among older women. J Am Heart Assoc. 2020;9:e016845. doi: 10.1161/JAHA.120.016845. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Kang S, Oh TJ, Cho BL, et al. Sex differences in sarcopenia and frailty among community-dwelling Korean older adults with diabetes: the Korean frailty and aging cohort study. J Diabetes Investig. 2021;12:155–164. doi: 10.1111/jdi.13348. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Lin YJ, Anzaghe M, Schülke S. Update on the pathomechanism, diagnosis, and treatment options for rheumatoid arthritis. Cells. 2020;9:880. doi: 10.3390/cells9040880. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Greco EA, Pietschmann P, Migliaccio S. Osteoporosis and sarcopenia increase frailty syndrome in the elderly. Front Endocrinol (Lausanne) 2019;10:255. doi: 10.3389/fendo.2019.00255. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Veronese N, Stubbs B, Solmi M, et al. Dietary magnesium intake and fracture risk: data from a large prospective study. Br J Nutr. 2017;117:1570–1576. doi: 10.1017/S0007114517001350. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Janjuha R, Bunn D, Hayhoe R, et al. Effects of dietary or supplementary micronutrients on sex hormones and IGF-1 in middle and older age: a systematic review and meta-analysis. Nutrients. 2020;12:1457. doi: 10.3390/nu12051457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Maggio M, Ceda GP, Lauretani F, et al. Magnesium and anabolic hormones in older men. Int J Androl. 2011;34:e594–600. doi: 10.1111/j.1365-2605.2011.01193.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Veronese N, Stubbs B, Maggi S, et al. Dietary magnesium and incident frailty in older people at risk for knee osteoarthritis: an eight-year longitudinal study. Nutrients. 2017;9:1253. doi: 10.3390/nu9111253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Dominguez L, Veronese N, Barbagallo M. Magnesium and hypertension in old age. Nutrients. 2020;13:139. doi: 10.3390/nu13010139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Razzaque MS. Magnesium: are we consuming enough? Nutrients. 2018;10:1863. doi: 10.3390/nu10121863. [DOI] [PMC free article] [PubMed] [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
Lucía Arias-Fernández, Ellen A Struijk, Francisco Félix Caballero, Rosario Ortolá, Esther García-Esquinas, Fernando Rodríguez-Artalejo, Esther Lopez-Garcia, and Alberto Lana comply with the Ethical guidelines for authorship and publishing in the European Journal of Nutrition.
Not applicable.