Abstract
Objective
The purpose of this study is to evaluate the additional effect of exercise to intermittent fasting (IF) on body composition and cardiometabolic health in adults with overweight/obesity.
Method
Relevant studies were identified through a systematic search across five databases. A random-effects meta-analysis was conducted on outcomes including body composition and cardiometabolic health markers, to compare the effect of combining IF with exercise against IF alone. The certainty of the evidence was evaluated using the GRADE approach, while the quality of the included studies was assessed using the revised Cochrane risk-of-bias tool and the TESTEX scale.
Result
In total, twelve studies including 616 participants (Age: 40 ± 9 years; BMI: 33.6 ± 4.8 kg/m2; 87.3% female) were included in this systematic review and meta-analysis. The combined intervention was more effective, leading to greater reductions in fat mass (-0.93 kg [95% CI: -1.69, -0.18]) and waist circumference (-2.51 cm [95% CI: -3.70, -1.32]) when compared to IF alone. Cardiometabolic health parameters also showed greater improvements, with decreased insulin (-3.1uIU/ml [95%CI: -4.25; -1.95]), HOMA-IR (-0.57 [95%CI: -0.83; -0.31]), LDL (-10.67 mg/dl [95%CI: -20; -1.35]), resting heart rate (-2.68 bpm [95%CI: -4.71; -0.64]), along with enhanced cardiorespiratory fitness (VO2 max:1.92 ml/kg/min [95%CI: 0.32; 3.52]). For the remaining outcome variables, no statistically meaningful differences emerged between the groups.
Conclusion
The potential benefits of incorporating exercise into IF for adults with overweight/obesity, particularly in terms of body composition, glycemic control, and cardiorespiratory fitness, appear promising. Nevertheless, given the limited amount of data, future investigations are essential to strengthen the evidence base and investigate the influence of specific exercise and IF types in enhancing treatment outcomes.
Registry and registry number for systematic reviews or meta-analyses: CRD42024550753.
Supplementary Information
The online version contains supplementary material available at 10.1007/s13679-025-00645-9.
Keywords: Intermittent fasting, Exercise, Overweight/Obesity, Body composition, Cardiometabolic health, Meta-analysis
Introduction
Overweight and obesity are major public health concerns worldwide. The global prevalence of excess body weight has increased substantially over the past few decades and is expected to continue to rise [1, 2]. According to data from the World Health Organization, in 2022, more than 2.5 billion adults were living with excess weight, and of these, 890 million were living with obesity. This trend is particularly alarming, as living with obesity is linked to cardiometabolic risk factors, increasing the risk of dyslipidemia, hypertension, and type 2 diabetes [3, 4]. Given the obesity epidemic, it is crucial to prevent and manage excess body weight from early life through adulthood using primary care such as diet modification, physical activity, and behavioral changes [5, 6].
Intermittent fasting (IF) has emerged as a promising dietary strategy for weight management and improving metabolic health in individuals with overweight and obesity [7, 8]. Apart from Ramadan intermittent fasting, which follows a religious fasting pattern, various IF protocols are employed outside religious contexts. These include diverse eating patterns such as time-restricted eating (TRE), intermittent dry fasting, specific fasting days per week, and alternate day (modified) fasting (ADF) [9]. Characterized by alternating cycles of eating and fasting, IF has been associated with numerous health benefits, including weight loss [10, 11], improved insulin sensitivity [12–14], and reduced inflammation [15–17]. While dietary strategy focuses on energy intake, exercise, which increases energy expenditure, plays an essential role, and offers numerous health benefits in adults with overweight/obesity [18]. Exercise is globally recognized for its popularity, accessibility, and established health benefits across diverse populations, including individuals with various health conditions although through different modalities [19–21]. It plays a significant role in promoting overall health and addressing metabolic disorders [22], improved glycolipid profiles [23, 24], reduced blood pressure [25], and enhanced cardiorespiratory fitness (CRF) [26]. CRF is a key indicator of cardiovascular health [27], reflects the body’s efficiency in oxygen usage during physical activity, and is associated with lower risks of chronic diseases and better metabolic functioning [28]. Given these marked benefits, exercise appears to be a valuable addition to dietary interventions, such as IF, for managing excess body weight and its associated complications. There has been growing interest in exploring the synergistic effects of combining IF with exercise. This combination has the potential to improve body composition and enhance training adaptations, though its impact on lean mass and cardiometabolic markers remains unclear [29]. Exercise plays a crucial role in supporting endocrine health by regulating metabolic hormones like insulin and cortisol, which may amplify the benefits of IF by improving insulin sensitivity and reducing stress-related hormonal responses [30]. Understanding whether exercise provides significant additional benefits when combined with IF is crucial, as it would allow clinicians and health professionals to tailor interventions more effectively for individuals with overweight or obesity.
Existing literature indicates that adding exercise to hypocaloric diets enhances cardiovascular fitness but no effects in body composition or glycemic control in adults with overweight/obesity and type 2 diabetes [31]. While previous studies have explored the combined effects of IF and exercise, one was a narrative review reporting equivocal evidence [29], another was a network meta-analysis focusing on weight loss outcomes [32], and others were meta-analyses that quantitatively analyzed the data but primarily compared IF combined with exercise to non-fasting diets with exercise [33, 34]. However, there remains limited synthesized evidence on the additional benefits of combining exercise with IF for body composition and cardiometabolic health in adults with overweight/obesity. This meta-analysis aims to evaluate randomized controlled trials (RCTs) that assessed the additional effect of incorporating exercise into IF protocols on body composition and cardiometabolic health in adults with overweight/obesity. By synthesizing data from multiple studies, we seek to determine whether this combined approach offers greater health benefits compared to IF alone, thereby providing evidence-based insights and practical guidelines for tailoring interventions to optimize clinical outcomes in this population.
Methods
Design
This systematic review and meta-analysis were registered at PROSPERO (registration number CRD42024550753) and conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement guidelines and the Cochrane Handbook of Systematic Reviews of Interventions [35].
Search Strategy
A systematic literature search was conducted to identify studies evaluating how IF combined with exercise impacts cardiometabolic outcomes and body composition. Searches were performed within electronic databases such as PubMed, Embase, SPORTDiscus, Web of Science, and Cochrane Central Register of Controlled Trials (CENTRAL), covering all available records up to July 2024. The search strategy included various combinations of the keywords and MeSH terms: (“Intermittent fasting” OR “alternate-day fasting” OR “intermittent energy restriction” OR “intermittent calorie restriction” OR “intermittent restrictive diet” OR “periodic fasting” OR “sporadic fasting” OR “time-restricted feeding” OR “time-restricted eating” OR “5:2 diet” OR “5:2 fasting” OR “Ramadan” OR “Ramadhan” OR “time-restricted fasting” OR “periodic diet” OR “reduced meal frequency” OR “alternate day modified fasting” OR “modified alternate-day fasting” OR “whole day fasting”) AND (Exercise* OR aerobic* OR running OR jogging OR walk* OR hiking OR swim* OR aquatic* OR cycling OR bicycle* OR strength* OR physical activity* OR fitness OR train* OR resistance) AND (Obesity OR Obese or Overweight). Table S1 provides a detailed description of the search methods. Further relevant articles were discovered by screening the reference lists of the studies obtained via the systematic search.
Criteria for Eligibility and Selection of Studies
After identifying studies through databases, registries, and additional sources, all records were imported into Endnote 20 software. All titles and abstracts underwent independent screening by two authors (ZD and KW), followed by full-text assessment for final study inclusion. Any differences identified by the two reviewers were resolved by consulting a third reviewer (PW) and engaging in discussion until agreement was achieved. Studies meeting the following criteria were included: 1) adults with overweight and/or obesity, BMI ≥ 23 kg/m2 (Asians study [36] BMI ≥ 23 kg/m2); 2) Randomized controlled trials with a matched comparison between IF combined with exercise (IF + EX) and IF alone; 3) Evaluation of body composition and/or cardiometabolic outcomes, with body mass, fat mass, fat-free mass, body mass index (BMI), visceral fat mass, waist circumference (WC), fasting glucose, insulin, homeostatic model assessment for insulin resistance (HOMA-IR), low-density lipoprotein cholesterol (LDL), high-density lipoprotein cholesterol (HDL), total cholesterol (TC), triglycerides (TG), systolic blood pressure (SBP), diastolic blood pressure (DBP), resting heart rate, and maximal oxygen uptake (VO2 max), leptin and adiponectin. The searches were restricted to studies involving humans, with the availability of full-text articles published exclusively in English; however, no limitations were imposed regarding the date of publication.
Data Extraction
Data extraction from the selected studies was conducted by a single author (ZD) using an electronic spreadsheet (Excel, 2023) based on the specified study characteristics, including study details (first author, publication year, country, participant characteristics, study design), intervention specifics encompassing types of IF and exercise, comparator details, intervention duration, and outcomes. The dataset included the number of participants, mean differences, and standard deviations (SD) of the outcomes from baseline to endpoint for both the intervention and control groups. These final data were prepared for analysis in the R statistical software (version 4.4.1). When obtaining complete data was not feasible, we employed a correlation coefficient (Corr) to calculate the SD of the pre-post change (SDchange). The Corr was derived based on the calculated coefficients [37]. The following formula was applied to compute the standard deviations of the SDchange. . All outcome measures were converted into consistent units, such as fasting glucose (mg/dl), TC (mg/dl), TG (mg/dl). In cases where change values were not reported, we reached out to the corresponding authors of the articles to obtain the necessary data. When sufficient data was unavailable, values were retrieved from graphs utilizing the WebPlotDigitizer software. All extracted information was independently verified for correctness by another author (KW).
Study Risk of Bias Assessment
Two reviewers (ZD and PW) independently assessed the risk of bias using the revised Cochrane Risk of Bias tool (RoB 2) [38]. Discrepancies in their assessments were resolved through discussions with an additional author (KW) until a consensus was achieved. Five domains were assessed to evaluate the quality of the included RCTs, including bias from the randomization process, deviations from intended interventions, missing outcome data, outcome measurement, and the selection of reported results. Each study was subsequently assigned an overall risk of bias classification as either “low risk”, “some concerns,” or “high risk,” based on these assessments.
Certainty of Evidence
The overall certainty of evidence was evaluated using the Grading of Recommendation Assessment, Development, and Evaluation (GRADE) approach. This method evaluated the certainty of evidence across five key domains: risk of bias, inconsistency, indirectness, imprecision, and publication bias [39]. The GRADE approach was applied to evaluate all outcomes in this meta-analysis, and any author disagreements were addressed through discussion until consensus was achieved.
Assessment of Study Quality and Reporting in Exercise
The quality of the included studies was also evaluated using the Tool for the assessment of study quality and reporting in exercise (TESTEX) scale, a tool specifically designed for assessing the quality and reporting of exercise-based studies. This evaluation covered 12 domains, encompassing both study quality and reporting components. Based on their total TESTEX scores, the studies were categorized as high quality, good quality, or low quality [40].
Data Synthesis and Analysis
One author (ZD) performed data synthesis and analysis, and meta-analyses were completed utilizing R statistical software (version 4.4.1) with the metafor package (version 7.0–0) when data were available from a minimum of two reports. These analyses involved calculating mean differences (MD) and standardized mean differences (SMD) along with 95% confidence intervals (CI), to assess and compare the effects of IF + EX with IF alone on the outcomes. Random-effect models were utilized for calculations, considering potential heterogeneity stemming from clinical or methodological variations that might have impacted the results. Heterogeneity was assessed using the I-squared (I2) statistic, with heterogeneity considered high when I2 exceeded 50%. Prediction intervals (PI) were reported to illustrate the degree of heterogeneity in forest plots of random-effects meta-analyses [41]. For analyses with I2 > 50%, sensitivity analyses were performed by systematically excluding one study at a time to determine whether any specific study contributed significantly to the heterogeneity. To delve deeper into the effects of the intervention on body composition and cardiometabolic outcomes, subgroup analyses were conducted based on the participant’s age, sex, intervention duration, IF type, and EX type. Furthermore, potential publication bias was assessed using funnel plots and Egger’s regression analysis, provided the meta-analysis included at least ten studies. A P-value of < 0.05 was considered indicative of publication bias.
Results
Study Selection
A total of 2,634 articles were initially retrieved through the database searches. Detailed records from each of the five databases are provided in Table S1. After deduplicating and screening titles and abstracts, 56 full-text papers were evaluated for eligibility. Ultimately, 12 articles derived from 10 studies met the criteria for inclusion in the systematic review and meta-analysis [42–53]. The detailed selection procedure is illustrated clearly in the PRISMA flowchart shown in Fig. 1.
Fig. 1.
Flowchart of study selection
Study Characteristics
Table 1 provides an overview of the main characteristics of the twelve RCTs selected for inclusion in the meta-analysis [42–53]. Together, these studies involved a total of 616 participants, with an overall mean age of 40 ± 9 years, a mean BMI of 33.6 ± 4.8 kg/m2, and a sample that was 87.3% female. Among the 12 studies, three studies were conducted in the USA [45, 46, 49], two in Tunisia [42, 52], two in Brazil [43, 44], two in Korea [47, 53], one in Thailand [51], one in Norway [50], and one in Australia [48] with a total of 616 participants (sample size ranging from 20 to 131). Notably, Bhutani et al. [45, 46] and Batitucci et al. [43, 44] contributed two articles each, reporting on different outcomes. Intervention durations varied from 4 to 16 weeks; specifically, one study lasted 4 weeks [52], one study spanned 7 weeks [50], three studies lasted 8 weeks [43, 44, 53], six studies lasted 12 weeks [42, 45–47, 49, 51], and one study lasted 16 weeks [48]. In addition, one study exclusively enrolled male participants [52], five studies recruited only female participants [42–44, 50, 51], while the remaining six studies included participants of both sexes [45–49, 53]. Exercise interventions included continuous training [45, 46, 49], concurrent training [47, 51–53], and high-intensity interval [43, 44, 48, 50]/functional training [42]. As for IF type, two studies used TRE [42, 50], five studies used ADF [45–47, 49, 53], four studies performed 5:2 diet [43, 44, 48, 51] and one study used Ramadan IF [52].
Table 1.
The main characteristics of the included studies
| Author (year) | Country | Age, years Mean ± SD |
Sex (F/M) |
BMI, kg/m2 Mean ± SD |
Participants number |
Duration | IG IF + EX |
CG IF |
Outcome examined |
|---|---|---|---|---|---|---|---|---|---|
| Ameur et al., 2024 | Tunisia | 32.1 ± 10.0 |
Female 64/0 |
35.0 ± 3.8 | 64 | 12 weeks | TRE + HIFT | TRE | Body mass, BMI, DBP, FFM, FG, FM, HDL, HOMA-IR, insulin, LDL, SBP, TC, TG, WC, |
| Batitucci et al., 2022 | Brazil | 32.2 ± 4.4 |
Female 36/0 |
34.0 ± 3.2 | 36 | 8 weeks | 5:2 + HIIT | 5:2 | Body mass, BMI, WC |
| Batitucci et al., 2024 | Brazil | 32.2 ± 4.4 |
Female 36/0 |
34.0 ± 3.2 | 36 | 8 weeks | 5:2 + HIIT | 5:2 | FFM, FM |
| Bhutani et al., 2013a | US | 44.0 ± 13.0 |
Both 80/3 |
35.0 ± 4.6 | 83 | 12 weeks | ADF + CT | ADF | Body mass, BMI, DBP, FFM, FG, FM, HDL, HOMA-IR, RHR, insulin, LDL, SBP, TC, TG, WC |
| Bhutani et al., 2013b | US | 44.0 ± 13.0 |
Both 80/3 |
35.0 ± 4.6 | 83 | 12 weeks | ADF + CT | ADF | Adiponectin, leptin |
| Cho et al., 2019 | Korea | 36.7 ± 7.3 |
Both 16/15 |
27.3 ± 3.4 | 31 | 12 weeks | ADF + CON | ADF | Body mass, BMI, FG, FM, HDL, HOMA-IR, insulin, LDL, TC, TG, VFM, VO2 max |
| Cooke et al., 2022 | Australia | 35.4 ± 8.4 |
Both 28/6 |
31.3 ± 3.5 | 34 | 16 weeks | 5:2 + HIIT | 5:2 | Body mass, DBP, FFM, FG, FM, HDL, HOMA-IR, LDL, SBP, TC, TG, VFM, VO2 max, WC |
| Ezpeleta et al., 2023 | US | 44.0 ± 13.0 |
Both 65/15 |
36.0 ± 6.0 | 80 | 12 weeks | ADF + CT | ADF | Body mass, BMI, DBP, FFM, FG, FM, HDL, HOMA-IR, RHR, insulin, LDL, SBP, TC, TG, VFM, WC |
| Haganes et al., 2022 | Norway | 36.2 ± 6.2 |
Female 131/0 |
36.2 ± 6.2 | 131 | 7 weeks | TRE + HIIT | TRE | Adiponectin, Body mass, DBP, FFM, FG, FM, HDL, HOMA-IR, leptin, RHR, insulin, LDL, SBP, TC, TG, VFM, VO2 max |
| Keawtep et al., 2024 | Thailand | 52.9 ± 3.4 |
Female 92/0 |
29.1 ± 3.4 | 92 | 12 weeks | 5:2 + CON | 5:2 | Adiponectin, Body mass, BMI, FFM, FG, FM, HOMA-IR, insulin, TC, TG, VO2 max |
| Maaloul et al., 2023 | Tunisia | 31.8 ± 7.1 |
Male 0/20 |
33.1 ± 4.2 | 20 | 4 weeks | RIF + CON | RIF | Body mass, FFM, FG, FM, HDL, LDL, TC, TG, WC |
| Oh et al., 2018 | Korea | 36.4 ± 8.1 |
Both 26/19 |
27.4 ± 3.1 | 45 | 8 weeks | ADF + CON | ADF | Body mass, BMI, DBP, FFM, FG, FM, HDL, HOMA-IR, insulin, SBP, TC, TG, WC |
5:2, 5:2 diet; ADF, alternate day fasting; BMI, body mass index; CG, control group; CON, concurrent training; DBP, diastolic blood pressure; EE, endurance exercise; FFM, fat-free mass; FG, fasting glucose; FM, fat mass; HDL, high density lipoprotein cholesterol; HIFT, high intensity function training; HIIT, high intensity interval training; HOMA-IR, homeostatic model assessment for insulin resistance; IG, intervention group; LDL, low density lipoprotein cholesterol; RIF, Ramadan intermittent fasting; RHR, resting heart rate; SBP, systolic blood pressure; TC, total cholesterol; TG, triglycerides; TRE, time restricted eating; VFM, visceral fat mass; VO2 max, maximal oxygen uptake; WC, waist circumference
The Effects of IF + EX Versus IF Alone on Anthropometric and Body Composition Outcomes
In Figure S1, ten studies [42, 43, 45, 47–53] including 319 participants, examined body mass as an outcome. The analysis showed no significant difference between the combined intervention and IF alone (MD −0.15 kg; 95%CI [−0.84, 0.54]; P = 0.67; I2 = 0%, 95%PI [−1.20, 0.90]), and the certainty of this evidence was rated as very low. Seven studies [42, 43, 45, 47, 49, 51, 53] involving 224 participants, investigated the impact on BMI as an outcome (Figure S2). The analysis showed no significant difference between the combined intervention and IF alone (MD −0.26 kg/m2; 95%CI [−0.67, 0.15]; P = 0.21; I2 = 0%, 95%PI [−0.78, 0.25]), and the certainty of this evidence was rated as low. In terms of fat mass, the combined strategy showed a lower level (MD −0.93 kg; 95%CI [−1.69, −0.18]; P = 0.01; I2 = 27%, 95%PI [−2.39, 0.52]) compared to IF alone, supported by moderate certainty of evidence from a comprehensive analysis involving 10 studies [42, 43, 45, 47–53] encompassing 319 participants (Fig. 2). For fat-free mass, the analysis of nine studies [42, 43, 45, 48–53] involving a total of 302 participants revealed no significant difference between the combined strategy and the IF alone (MD 0.75 kg; 95%CI [−0.41, 1.90]; P = 0.20; I2 = 86%, 95%PI [−3.04, 4.53]) (Figure S3). The certainty of this evidence was assessed as very low. Sensitivity analyses indicated that eliminating heterogeneity, notably by excluding the study by Ameur et al. [42], did not alter the statistical significance. In the analysis of WC, seven studies [42, 43, 45, 48, 49, 52, 53] involving 200 participants, with low certainty of evidence (Fig. 3), indicated that the combined strategy led to a lower reduction in WC (MD −2.51 cm; 95%CI [−3.70, −1.32]; P < 0.001; I2 = 0%, 95%PI [−4.00, −1.03]). Regarding the assessment of visceral fat from four studies [47–50] encompassing 131 participants (Figure S4), it was found that there was no significant difference between the combined strategy and the control group (SMD −0.20; 95%CI [−0.55, 0.15]; P = 0.26; I2 = 6%, 95%PI [−0.76, 0.36]), supported by evidence of low certainty.
Fig. 2.
Meta-analysis of IF + EX vs. IF alone on fat mass. Values are reported as mean difference (MD)
Fig. 3.
Meta-analysis of IF + EX vs. IF alone on waist circumference. (MD)
The Effects of IF + EX Versus IF Alone on Glycemic Outcomes
In the analysis of fasting glucose levels across nine studies [42, 45, 47–53] involving 293 participants (Figure S5), no significant difference was observed between the combined strategy and the control group (MD −1.92 mg/dl; 95%CI [−4.47, 0.62]; P = 0.14; I2 = 51%, 95%PI [−8.73, 4.89]), supported by evidence of very low certainty. Sensitivity analysis indicated that removing the study conducted by Maaloul et al. [52] decreased heterogeneity to 10%, although it had no impact on the statistical significance of the results. Insulin levels were assessed as an outcome in seven studies [42, 45, 47, 49–51, 53], encompassing a total of 250 participants (Fig. 4). It was observed that the combined strategy showed lower insulin (MD −3.10 uIU/ml; 95%CI [−4.25, −1.95]; P < 0.001; I2 = 0%, 95%PI [−4.82, −1.37]) with low certainty of evidence compared with the IF alone. HOMA-IR was evaluated as an outcome measure in eight studies [42, 45, 47–51, 53], involving a total of 269 individuals. (Fig. 5). It was observed that the combined strategy showed lower HOMA-IR (SMD −0.57; 95%CI [−0.83, −0.31]; P < 0.001; I2 = 6%, 95%PI [−1.01, −0.13]) with low certainty of evidence compared with the IF alone.
Fig. 4.
Meta-analysis of IF + EX vs. IF alone on insulin. (MD)
Fig. 5.
Meta-analysis of IF + EX vs. IF alone on HOMA-IR. Values are reported as standardized mean differences (SMD)
The Effects of IF + EX Versus IF Alone on Lipid Profiles
Nine studies [42, 45, 47–53] were included in the TC analysis, with 290 participants evaluated (Figure S6). The analysis found no significant difference between the groups regarding TC levels (MD −7.39 mg/dl; 95%CI [−16.53, 1.74]; P = 0.11; I2 = 65%, 95%PI [−35.25, 20.46]), with evidence rated as having very low certainty. Sensitivity analyses demonstrated that removing the study by Ameur et al. [42] resolved heterogeneity, although it did not alter the statistical significance of the results. Eight studies [42, 45, 47–50, 52, 53], comprising 244 participants, evaluated HDL cholesterol as an outcome measure (Figure S7). The analysis showed no significant difference in HDL cholesterol levels between groups (MD 3.32 mg/dl; 95%CI [−1.56, 8.21]; P = 0.18; I2 = 81%, 95%PI [−12.72, 19.36]), with the certainty of evidence assessed as very low. After sensitivity analysis, we found that removing any study did not reduce heterogeneity. LDL cholesterol was analyzed in seven studies [42, 45, 47–50, 52], involving a total of 219 participants (Fig. 6). The results indicated the combined strategy showed a lower LDL level when compared to IF alone (MD −10.67 mg/dl; 95%CI [−20.00, −1.35]; P = 0.02; I2 = 67%, 95%PI [−37.87, 16.53]) with very low certainty of evidence. Sensitivity analysis demonstrated that excluding the study by Maaloul et al. [52] had no impact on statistical significance but lowered heterogeneity to 22%. Nine studies [42, 45, 47–53], including a total of 290 participants, evaluated TG levels as an outcome measure (Figure S8). The results showed no notable difference in TG levels between the groups (MD −12.86 mg/dl; 95%CI [−34.11, 8.40]; P = 0.24; I2 = 82%, 95%PI [−83.20, 57.48]), with the evidence quality assessed as very low. After sensitivity analysis, we found that removing any study did not reduce heterogeneity.
Fig. 6.
Meta-analysis of IF + EX vs. IF alone on low-density lipoprotein cholesterol. (MD)
The Effects of IF + EX Versus IF Alone on Blood Pressure and CRF
In the assessment of SBP and DBP across six studies [42, 45, 48–50, 53] involving 209 participants (Figure S9 and Figure S10), no significant differences were noted in SBP and DBP between the groups, supported by evidence of very low certainty. The mean differences were 0.16 mmHG (95%CI [−2.66, 2.99]; P = 0.91; I2 = 64%, 95%PI [−7.64, 7.97]) for SBP and −0.05 mmHg (95%CI [−1.98, 1.88]; P = 0.96; I2 = 53%, 95%PI [−5.10, 5.00]) for DBP. Sensitivity analyses indicated that removing the study by Ameur et al. [42] eliminated heterogeneity without altering the statistical significance of the results. In the analysis of resting heart rate from 3 studies [45, 49, 50] involving 125 participants (Fig. 7). It was observed that the combined strategy may result in a lower resting heart rate (MD −2.68 bpm; 95%CI [−4.71, −0.64]; P = 0.01; I2 = 0%, 95%PI [−7.14, 1.79]) with low certainty of evidence. VO2 max was analyzed from 4 studies [47, 48, 50, 51], including a total of 136 participants (Fig. 8). It was observed that the combined strategy showed higher VO2 max (MD 1.80 ml/kg/min; 95%CI [0.12, 3.48]; P = 0.036; I2 = 65%, 95%PI [−2.56, 6.15]) with very low certainty of evidence when compared to the IF alone. Upon performing sensitivity analysis, the exclusion of the trial conducted by Keawtep et al. [51] had no impact on the significance of the findings; however, it eliminated heterogeneity, reducing the I2 value to 0%.
Fig. 7.
Meta-analysis of IF + EX vs. IF alone on resting heart rate. (MD)
Fig. 8.
Meta-analysis of IF + EX vs. IF alone on VO2 max. (MD)
The Effects of IF + EX Versus IF Alone on Leptin, Adiponectin
In terms of leptin, the combined strategy showed a lower concentration (MD −13.76 ng/ml; 95%CI [−25.76, −1.76]; P = 0.02; I2 = 47%, 95%PI [−129.39, 101.87]) when compared to the IF alone with low certainty of evidence in 2 studies [46, 50] involving 82 participants (Figure S11). In the analysis of adiponectin levels from three studies [46, 50, 51] comprising 126 participants (Figure S12), the evidence indicated low certainty and showed no significant difference between the combined intervention and IF alone (SMD 0.35; 95%CI [0.00, 0.70]; P = 0.05; I2 = 0%, 95%PI [−0.42, 1.13]).
Subgroup Analysis
Detailed results of the subgroup analysis are provided in Supplementary Table S2, which presents SMD/MD with corresponding 95% CIs for each subgroup separately. Significant group differences were observed in fasting glucose (based on the participant age and sex), LDL (based on the participant sex and IF type), TG (based on the participant age and sex, IF type and EX type) and VO2 max (based on the participant age, intervention duration, and EX type), while the other outcomes did not observe any subgroup difference.
Risk of Bias
The ROB 2 tool was used to assess the risk of bias in each study included. A summary of the overall assessments for all five domains of bias is presented in Table 2. Risk of bias assessment revealed that three studies [45, 46, 52] were categorized as high risk, whereas nine studies [42–44, 47–51, 53] presented some concerns. Among studies classified as having some concerns, all were missing details regarding deviations from intended interventions. Additionally, six studies [42–44, 47, 48, 51] did not adequately describe allocation concealment within the randomization process domain. Furthermore, one study [48] did not report the measurement of outcomes, and another study [42] lacked sufficient information concerning the selection of reported results. Among the studies with a high risk of bias, two [45, 46] had significant baseline differences between the intervention and control groups, together with randomization issues, and the third [52] lacked baseline information and a randomization process. The three studies identified as having a high risk of bias [45, 46, 52] also raised some concerns regarding the domains of deviations from the intended intervention, missing outcome data, and selection of the reported results. More specific assessment justification can be found in Table S3.
Table 2.
Risk of bias assessment
| Study | Randomization process | Deviations from the intended interventions | Missing outcome data | Measurement of the outcome | Selection of the reported result | Overall Bias |
|---|---|---|---|---|---|---|
| Ameur et al., 2024 | Some concerns | Some concerns | Low | Low | Some concerns | Some concerns |
| Batitucci et al., 2022 | Some concerns | Some concerns | Low | Low | Low | Some concerns |
| Batitucci et al., 2024 | Some concerns | Some concerns | Low | Low | Low | Some concerns |
| Bhutani et al., 2013a | High | Some concerns | Low | Low | Some concerns | High |
| Bhutani et al., 2013b | High | Some concerns | Some concerns | Low | Some concerns | High |
| Cho et al., 2019 | Some concerns | Some concerns | Low | Low | Low | Some concerns |
| Cooke et al., 2022 | Some concerns | Some concerns | Low | Some concerns | Low | Some concerns |
| Ezpeleta et al., 2023 | Low | Some concerns | Low | Low | Low | Some concerns |
| Haganes et al., 2022 | Low | Some concerns | Low | Low | Low | Some concerns |
| Keawtep et al., 2024 | Some concerns | Some concerns | Low | Low | Low | Some concerns |
| Maaloul et al., 2022 | High | Some concerns | Low | Low | Some concerns | High |
| Oh et al., 2018 | Low | Some concerns | Low | Low | Low | Some concerns |
Certainty of Evidence
The GRADE approach was utilized to evaluate the overall certainty of evidence, and the detailed assessment is summarized in Table S4. Among the 19 outcomes analyzed, the certainty of evidence was downgraded to moderate for fat mass. The certainty for BMI, WC, visceral fat, insulin, HOMA-IR, resting heart rate, leptin, and adiponectin were downgraded to low. Body mass, fat-free mass, fasting glucose, SBP, DBP, TC, TG, HDL, LDL, and VO2 max were downgraded to very low certainty of evidence.
Assessment of Study Quality and Reporting in Exercise
The quality of the included studies was evaluated using the TESTEX scale. A summary of the assessments across the twelve domains is provided in Table S5. Of the 12 included studies, nine were rated as good quality [42–47, 50, 52, 53], two as high quality [49, 51], and one as low quality [48].
Publication Bias
We conducted a publication bias assessment to determine the potential impact of selective reporting on the findings of our meta-analysis. This assessment was specifically performed for body mass and fat mass outcomes, as these variables fulfilled the minimum criterion of having at least ten studies included (Table S6). Egger’s linear regression test was used to assess funnel plot asymmetry as an indicator of the risk of publication bias. The results indicated no significant risk of publication bias for fat mass (P = 0.06), but suggested a risk of publication bias for body mass (P = 0.0023).
Discussion
This systematic review and meta-analysis investigated whether combining IF with exercise provides additional benefits on cardiometabolic health and body composition in adults with overweight/obesity. Our findings demonstrate significant improvements in CRF, body composition, and specific metabolic parameters when exercise is added to IF.
Previous systematic reviews and meta-analyses have consistently demonstrated weight loss following IF in adults with overweight/obesity [54]. However, this current study represents the first known investigation quantitatively assessing the additional effects of exercise on body composition in this population. The findings of this study indicate that incorporating exercise alongside IF resulted in significantly favorable effects on body composition rather than solely promoting weight loss. Specifically, significant reductions were observed in fat mass (P = 0.01), and WC (P < 0.001), while no significant changes were noted in body mass (P = 0.67), BMI (P = 0.21), and fat-free mass (P = 0.20). In our study, while total body mass reduction was comparable between the IF-only and combined intervention groups, the combined group exhibited significantly greater fat mass reduction. A recent network meta-analysis showed that combining ADF with moderate-intensity continuous training achieved the greatest weight and fat mass reductions, followed by ADF with exercise and the 5:2 diet with exercise among all IF and/or exercise interventions [32]. These findings indicate that while IF primarily drives overall weight loss, exercise plays a distinct role in optimizing body composition through targeted fat mass reduction. Prior research has highlighted the influences of training modalities during energy intake restriction on fat-mass loss [55], indicating that endurance exercise serves as a key predictor of fat-mass reduction in interventional studies. While resistance training during dietary restriction may not independently enhance fat-mass loss, it contributes to improved body composition through increases in fat-free mass. In our current meta-analysis, we examined various exercise modalities, including continuous training [45, 46, 49], concurrent training [47, 51–53], and high-intensity interval [43, 44, 48, 50]/functional [42] training. Despite conducting subgroup analyses, we observed no significant differences in weight management outcomes among exercise types when combined with IF, possibly due to the heterogeneity of existing protocols and limited available data. Therefore, well-designed RCTs are needed to elucidate the optimal combination of IF and specific exercise modalities. Further research is needed to establish optimal combinations of IF and exercise modalities for enhancing body composition and maintaining long-term weight management in individuals with overweight/obesity.
Various IF regimens have shown promise in reducing fasting insulin, insulin resistance, and HbA1c levels in healthy individuals with obesity and prediabetes [56]. IF diets also have certain therapeutic effects on blood glucose in patients with metabolic syndrome and significantly improve insulin resistance [14]. In adults with overweight/obesity, substantial evidence supports that exercise enhances glycemic control by boosting insulin sensitivity and glucose uptake in muscles [57]. Physical activity induces muscle contractions that prompt glucose transporters (GLUT4) to translocate to the cell surface, facilitating insulin-independent glucose entry [58]. Furthermore, exercise activates AMP-activated protein kinase (AMPK), a key enzyme that enhances insulin signaling and mitochondrial function, collectively improving the body's capacity to regulate blood sugar levels and reduce insulin resistance [59]. The findings of the meta-analysis indicate that incorporating exercise alongside IF could lead to reductions in HOMA-IR (−0.57 [95% CI: −0.83; −0.31], P = P < 0.001) and insulin levels (−3.1 uIU/ml [95% CI: −4.25; −1.95], P < 0.001). Although our meta-analysis showed no statistically significant differences in fasting glucose between the combined group versus IF alone, subgroup analyses revealed differential responses based on age and sex, highlighting the importance of considering these demographic factors when tailoring combined IF and exercise interventions. The combined intervention showed a larger reduction in LDL levels, consistent with evidence showing that exercise improves lipid profiles through LDL reduction and HDL increase [24]. Although our meta-analysis did not demonstrate statistically significant improvements in HDL, several individual studies reported greater HDL increases in the combined group [42, 45, 52, 53], the synergistic effect of combining IF with exercise appears to enhance lipid metabolism more effectively than IF alone, possibly through increased lipolysis and fat oxidation during fasting periods coupled with exercise-induced metabolic adaptations [60]. These findings suggest the need for larger-scale, well-designed RCTs to better elucidate the mechanisms underlying these potential beneficial effects on lipid metabolism in individuals with overweight/obesity.
CRF improvements were evident through increased VO2 max and reduced resting heart rate in the combined group. Our qualitative synthesis indicated that the addition of exercise to IF leads to a lower resting heart rate (−2.68 bpm [95%CI: −4.71; −0.64], P = 0.01) and an elevation VO2 max (1.80 ml/kg/min [95%CI: 0.12; 3.48], P = 0.036). While IF alone may maintain CRF in healthy adults [61], however, its impact on individuals with overweight/obesity remains ambiguous. Our findings indicate that exercise is necessary for enhancing this parameter during weight loss [62]. Exercise remains a key intervention for improving CRF, as supported by numerous meta-analyses across different populations and exercise types [63–65]. Low CRF levels are strongly associated with increased risk of cardiovascular disease, and all-cause mortality [28, 66]. Notably, higher CRF levels can help protect against obesity-related cardiovascular complications [62], highlighting the clinical significance of incorporating exercise into weight management programs.
No prior systematic review and meta-analysis have specifically evaluated the additional effect of incorporating exercise to IF on body composition and cardiometabolic health in adults with overweight/obesity. Our work highlights the relevance of combining exercise into IF intervention as an effective strategy to enhance body composition and cardiometabolic health in individuals with overweight/obesity. However, several limitations should be considered. The included studies used different exercise types and IF protocols, potentially affecting result interpretation. Furthermore, limiting our meta-analysis to English-language publications may have introduced bias by excluding relevant studies published in other languages. Also, it should be noted that the included studies are from around the globe, encompassing six continents and various ethnicities. The studies'relatively narrow age range limits applicability to middle-aged and older adults. Additionally, the limited number of available studies and the wide prediction intervals for some outcomes (fat mass, LDL, and cardiorespiratory fitness) necessitates further research to strengthen these findings. Future research should examine the effectiveness of different exercise modalities and fasting protocols across diverse populations. Large-scale RCTs are needed to identify optimal combinations of exercise modality and dietary approach for improving weight management and cardiometabolic health in individuals with overweight/obesity.
Conclusion
In conclusion, integrating exercise into IF regimens may provide holistic health benefits beyond weight management alone, including improved glycemic control, and cardiovascular fitness. While these results are promising, more research is needed to confirm these findings and establish optimal intervention protocols. This meta-analysis provides valuable insights for healthcare practitioners in designing lifestyle interventions that combine both dietary and exercise strategies to optimize health outcomes in individuals with overweight/obesity.
Key references
- Gabel K, Hamm A, Czyzewski O, Perez JS, Fought-Boudaia A, Motl RW, et al. A narrative review of intermittent fasting with exercise. Journal of the Academy of Nutrition and Dietetics. 2024.
- This narrative review examines the combined effects of intermittent fasting (IF) and exercise, providing evidence that these interventions can synergistically reduce body weight and fat mass.
- Cheng X, Sun S, Chen M, Zhou X, Rao M, Guo D, et al. Evaluating the efficacy of intermittent fasting and exercise combinations for weight loss: A network meta‐analysis. Obesity Reviews.e13834.
- This study is the first to apply network meta-analysis to compare various IF and exercise combinations, synthesizing data from relevant randomized controlled trials (RCTs). It identifies the most effective intervention strategies for weight loss, providing valuable evidence for optimizing IF and exercise regimens.
- Varady KA, Cienfuegos S, Ezpeleta M, Gabel K. Clinical application of intermittent fasting for weight loss: progress and future directions. Nature Reviews Endocrinology. 2022;18(5):309–21.
- This review highlights the effects of intermittent fasting (IF) on body weight and cardiometabolic health, evaluates the safety of IF regimens, and offers practical guidance for incorporating IF into daily life.
- Lang JJ, Prince SA, Merucci K, Cadenas-Sanchez C, Chaput J-P, Fraser BJ, et al. Cardiorespiratory fitness is a strong and consistent predictor of morbidity and mortality among adults: an overview of meta-analyses representing over 20.9 million observations from 199 unique cohort studies. British journal of sports medicine. 2024;58(10):556–66.
- This study highlights the strong predictive value of cardiorespiratory fitness for health outcomes and mortality, emphasizing its importance as a clinical risk stratification tool.
- Kazeminasab F, Baharlooie M, Karimi B, Mokhtari K, Rosenkranz SK, Santos HO. Effects of intermittent fasting combined with physical exercise on cardiometabolic outcomes: systematic review and meta-analysis of clinical studies. Nutrition Reviews. 2023:nuad155.
- This meta-analysis finds that combining intermittent fasting with exercise leads to better improvements in weight loss, blood pressure, and lipid profiles compared to control diets with exercise.
- Ashcroft SP, Stocks B, Egan B, Zierath JR. Exercise induces tissue-specific adaptations to enhance cardiometabolic health. Cell metabolism. 2024.
- This review explains how exercise-induced tissue-specific adaptations improve cardiometabolic health and highlights its benefits for preventing and treating non-communicable diseases.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
None.
Author Contributions
Z.D. assumed the lead role in this study, overseeing data access, systematic search for eligible studies, data ex-traction, result interpretation, manuscript drafting, and serving as the guarantor. K.W., P.W., W.H., A.Y., and S.W. actively participated in the study's conception, design, systematic search for eligible studies, data extraction, and manuscript composition. S.W. played a key role in drafting the manuscript and providing critical revisions. The final manuscript was comprehensively reviewed and approved by all authors before submission.
Funding
This study did not receive funding from any external sources.
Data Availability
The datasets utilized and/or analyzed in this study can be ontained from the corresponding author upon reasonable request.
Declarations
Ethics Approval
Not applicable.
Conflict of interest
The authors declare no competing interests.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Ng M, Dai X, Cogen RM, Abdelmasseh M, Abdollahi A, Abdullahi A, et al. National-level and state-level prevalence of overweight and obesity among children, adolescents, and adults in the USA, 1990–2021, and forecasts up to 2050. The Lancet. 2024;404(10469):2278–98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Valenzuela PL, Carrera-Bastos P, Castillo-García A, Lieberman DE, Santos-Lozano A, Lucia A. Obesity and the risk of cardiometabolic diseases. Nat Rev Cardiol. 2023;20(7):475–94. [DOI] [PubMed] [Google Scholar]
- 3.Kahn SE, Hull RL, Utzschneider KM. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature. 2006;444(7121):840–6. [DOI] [PubMed] [Google Scholar]
- 4.Powell-Wiley TM, Poirier P, Burke LE, Després J-P, Gordon-Larsen P, Lavie CJ, et al. Obesity and cardiovascular disease: a scientific statement from the American Heart Association. Circulation. 2021;143(21):e984–1010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Kushner RF. Weight loss strategies for treatment of obesity: lifestyle management and pharmacotherapy. Prog Cardiovasc Dis. 2018;61(2):246–52. [DOI] [PubMed] [Google Scholar]
- 6.Semlitsch T, Stigler FL, Jeitler K, Horvath K, Siebenhofer A. Management of overweight and obesity in primary care—A systematic overview of international evidence-based guidelines. Obes Rev. 2019;20(9):1218–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Patikorn C, Roubal K, Veettil SK, Chandran V, Pham T, Lee YY, et al. Intermittent fasting and obesity-related health outcomes: an umbrella review of meta-analyses of randomized clinical trials. JAMA network open. 2021;4(12):e2139558-e. [DOI] [PMC free article] [PubMed]
- 8.Sun M-L, Yao W, Wang X-Y, Gao S, Varady KA, Forslund SK, et al. Intermittent fasting and health outcomes: an umbrella review of systematic reviews and meta-analyses of randomised controlled trials. EClinicalMedicine. 2024;70. [DOI] [PMC free article] [PubMed]
- 9.Koppold DA, Breinlinger C, Hanslian E, Kessler C, Cramer H, Khokhar AR, et al. International consensus on fasting terminology. Cell Metabolism. 2024. [DOI] [PMC free article] [PubMed]
- 10.Varady KA, Cienfuegos S, Ezpeleta M, Gabel K. Clinical application of intermittent fasting for weight loss: progress and future directions. Nat Rev Endocrinol. 2022;18(5):309–21. [DOI] [PubMed] [Google Scholar]
- 11.Ezpeleta M, Cienfuegos S, Lin S, Pavlou V, Gabel K, Tussing-Humphreys L, et al. Time-restricted eating: Watching the clock to treat obesity. Cell Metab. 2024;36(2):301–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Patterson RE, Sears DD. Metabolic effects of intermittent fasting. Annu Rev Nutr. 2017;37(1):371–93. [DOI] [PubMed] [Google Scholar]
- 13.Sutton EF, Beyl R, Early KS, Cefalu WT, Ravussin E, Peterson CM. Early time-restricted feeding improves insulin sensitivity, blood pressure, and oxidative stress even without weight loss in men with prediabetes. Cell metabolism. 2018;27(6):1212–21. e3. [DOI] [PMC free article] [PubMed]
- 14.Yuan X, Wang J, Yang S, Gao M, Cao L, Li X, et al. Effect of intermittent fasting diet on glucose and lipid metabolism and insulin resistance in patients with impaired glucose and lipid metabolism: a systematic review and meta-analysis. International journal of endocrinology. 2022;2022(1):6999907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Mulas A, Cienfuegos S, Ezpeleta M, Lin S, Pavlou V, Varady KA. Effect of intermittent fasting on circulating inflammatory markers in obesity: A review of human trials. Front Nutr. 2023;10:1146924. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Wang X, Yang Q, Liao Q, Li M, Zhang P, Santos HO, et al. Effects of intermittent fasting diets on plasma concentrations of inflammatory biomarkers: a systematic review and meta-analysis of randomized controlled trials. Nutrition. 2020;79:110974. [DOI] [PubMed] [Google Scholar]
- 17.Aamir AB, Kumari R, Latif R, Ahmad S, Rafique N, Salem AM, et al. Effects of intermittent fasting and caloric restriction on inflammatory biomarkers in individuals with obesity/overweight: A systematic review and meta-analysis of randomized controlled trials. Obes Rev. 2025;26(1):e13838. [DOI] [PubMed] [Google Scholar]
- 18.Batrakoulis A, Jamurtas AZ, Metsios GS, Perivoliotis K, Liguori G, Feito Y, et al. Comparative efficacy of 5 exercise types on cardiometabolic health in overweight and obese adults: a systematic review and network meta-analysis of 81 randomized controlled trials. Circulation: Cardiovascular Quality and Outcomes. 2022;15(6):e008243. [DOI] [PubMed]
- 19.Al-Mhanna SB, Rocha-Rodriguesc S, Mohamed M, Batrakoulis A, Aldhahi MI, Afolabi HA, et al. Effects of combined aerobic exercise and diet on cardiometabolic health in patients with obesity and type 2 diabetes: a systematic review and meta-analysis. BMC Sports Sci Med Rehabil. 2023;15(1):165. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Al-Mhanna SB, Franklin BA, Jakicic JM, Stamatakis E, Pescatello LS, Riebe D, et al. Impact of resistance training on cardiometabolic health-related indices in patients with type 2 diabetes and overweight/obesity: a systematic review and meta-analysis of randomised controlled trials. British J Sports Med. 2025. [DOI] [PubMed]
- 21.Poon ET-C, Wongpipit W, Li H-Y, Wong SH-S, Siu PM, Kong AP-S, et al. High-intensity interval training for cardiometabolic health in adults with metabolic syndrome: a systematic review and meta-analysis of randomised controlled trials. British Journal of Sports Medicine. 2024;58(21):1267–84. [DOI] [PubMed]
- 22.Esteves JV, Stanford KI. Exercise as a tool to mitigate metabolic disease. American Journal of Physiology-Cell Physiology. 2024. [DOI] [PMC free article] [PubMed]
- 23.Bird SR, Hawley JA. Update on the effects of physical activity on insulin sensitivity in humans. BMJ Open Sport Exerc Med. 2017;2(1):e000143. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Mann S, Beedie C, Jimenez A. Differential effects of aerobic exercise, resistance training and combined exercise modalities on cholesterol and the lipid profile: review, synthesis and recommendations. Sports Med. 2014;44:211–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Pescatello LS, MacDonald HV, Lamberti L, Johnson BT. Exercise for hypertension: a prescription update integrating existing recommendations with emerging research. Curr Hypertens Rep. 2015;17:1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee I-M, et al. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc. 2011;43(7):1334–59. [DOI] [PubMed] [Google Scholar]
- 27.Lang JJ, Prince SA, Merucci K, Cadenas-Sanchez C, Chaput J-P, Fraser BJ, et al. Cardiorespiratory fitness is a strong and consistent predictor of morbidity and mortality among adults: an overview of meta-analyses representing over 20.9 million observations from 199 unique cohort studies. British J Sports Med. 2024;58(10):556–66. [DOI] [PMC free article] [PubMed]
- 28.Ross R, Blair SN, Arena R, Church TS, Després J-P, Franklin BA, et al. Importance of assessing cardiorespiratory fitness in clinical practice: a case for fitness as a clinical vital sign: a scientific statement from the American Heart Association. Circulation. 2016;134(24):e653–99. [DOI] [PubMed] [Google Scholar]
- 29.Gabel K, Hamm A, Czyzewski O, Perez JS, Fought-Boudaia A, Motl RW, et al. A narrative review of intermittent fasting with exercise. Journal of the Academy of Nutrition and Dietetics. 2024. [DOI] [PMC free article] [PubMed]
- 30.Athanasiou N, Bogdanis GC, Mastorakos G. Endocrine responses of the stress system to different types of exercise. Rev Endocr Metab Disord. 2023;24(2):251–66. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Memelink RG, Hummel M, Hijlkema A, Streppel MT, Bautmans I, Weijs PJ, et al. Additional effects of exercise to hypocaloric diet on body weight, body composition, glycaemic control and cardio-respiratory fitness in adults with overweight or obesity and type 2 diabetes: a systematic review and meta-analysis. Diabet Med. 2023;40(7):e15096. [DOI] [PubMed] [Google Scholar]
- 32.Cheng X, Sun S, Chen M, Zhou X, Rao M, Guo D, et al. Evaluating the efficacy of intermittent fasting and exercise combinations for weight loss: A network meta‐analysis. Obesity Reviews.e13834. [DOI] [PubMed]
- 33.Dai Z, Wan K, Miyashita M, Ho RS-t, Zheng C, Poon ET-c, et al. The effect of time-restricted eating combined with exercise on body composition and metabolic health: a systematic review and meta-analysis. Adv Nutri. 2024:100262. [DOI] [PMC free article] [PubMed]
- 34.Kazeminasab F, Baharlooie M, Karimi B, Mokhtari K, Rosenkranz SK, Santos HO. Effects of intermittent fasting combined with physical exercise on cardiometabolic outcomes: systematic review and meta-analysis of clinical studies. Nutri Rev. 2023:nuad155. [DOI] [PubMed]
- 35.Moher D, Shamseer L, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev. 2015;4:1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Tan K. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. The lancet. 2004. [DOI] [PubMed]
- 37.Higgins JP, Li T, Deeks JJ. Choosing effect measures and computing estimates of effect. Cochrane handbook for systematic reviews of interventions. 2019:143–76.
- 38.Sterne JA, Savović J, Page MJ, Elbers RG, Blencowe NS, Boutron I, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. bmj. 2019;366. [DOI] [PubMed]
- 39.Zhang Y, Alonso-Coello P, Guyatt GH, Yepes-Nuñez JJ, Akl EA, Hazlewood G, et al. GRADE Guidelines: 19. Assessing the certainty of evidence in the importance of outcomes or values and preferences—Risk of bias and indirectness. Clin Epidemiol. 2019;111:94–104. [DOI] [PubMed]
- 40.Smart NA, Waldron M, Ismail H, Giallauria F, Vigorito C, Cornelissen V, et al. Validation of a new tool for the assessment of study quality and reporting in exercise training studies: TESTEX. JBI Evidence Implementation. 2015;13(1):9–18. [DOI] [PubMed] [Google Scholar]
- 41.Borg DN, Impellizzeri FM, Borg SJ, Hutchins KP, Stewart IB, Jones T, et al. Meta-analysis prediction intervals are under reported in sport and exercise medicine. Scand J Med Sci Sports. 2024;34(3):e14603. [DOI] [PubMed] [Google Scholar]
- 42.Ameur R, Maaloul R, Tagougui S, Neffati F, Hadj Kacem F, Najjar MF, et al. Unlocking the power of synergy: High-intensity functional training and early time-restricted eating for transformative changes in body composition and cardiometabolic health in inactive women with obesity. PLoS ONE. 2024;19(5):e0301369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Batitucci G, Faria Junior EV, Nogueira JE, Brandão CF, Abud GF, Ortiz GU, et al. Impact of intermittent fasting combined with high-intensity interval training on body composition, metabolic biomarkers, and physical fitness in women with obesity. Front Nutr. 2022;9:884305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Batitucci G, Almeida OG, De Martinis EC, Solar I, Cintra Sr DE, de Freitas EC. Intermittent fasting and high-intensity interval training do not alter gut microbiota composition in adult women with obesity. Am J Physiol-Endocrinol Metabolism. 2024. [DOI] [PubMed]
- 45.Bhutani S, Klempel MC, Kroeger CM, Trepanowski JF, Varady KA. Alternate day fasting and endurance exercise combine to reduce body weight and favorably alter plasma lipids in obese humans. Obesity. 2013;21(7):1370–9. [DOI] [PubMed] [Google Scholar]
- 46.Bhutani S, Klempel MC, Kroeger CM, Trepanowski J, Phillips SA, Norkeviciute E, et al. Alternate day fasting with or without exercise: effects on endothelial function and adipokines in obese humans. e-SPEN Journal. 2013;8(5):e205-e9.
- 47.Cho A-R, Moon J-Y, Kim S, An K-Y, Oh M, Jeon JY, et al. Effects of alternate day fasting and exercise on cholesterol metabolism in overweight or obese adults: a pilot randomized controlled trial. Metabolism. 2019;93:52–60. [DOI] [PubMed] [Google Scholar]
- 48.Cooke MB, Deasy W, Ritenis EJ, Wilson RA, Stathis CG. Effects of intermittent energy restriction alone and in combination with sprint interval training on body composition and cardiometabolic biomarkers in individuals with overweight and obesity. Int J Environ Res Public Health. 2022;19(13):7969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Ezpeleta M, Gabel K, Cienfuegos S, Kalam F, Lin S, Pavlou V, et al. Effect of alternate day fasting combined with aerobic exercise on non-alcoholic fatty liver disease: A randomized controlled trial. Cell metabolism. 2023;35(1):56–70. e3. [DOI] [PMC free article] [PubMed]
- 50.Haganes KL, Silva CP, Eyjolfsdottir SK, Steen S, Grindberg M, Lydersen S, et al. Time-restricted eating and exercise training improve HbA1c and body composition in women with overweight/obesity: A randomized controlled trial. Cell Metabolism. 2022;34(10):1457–71. e4. [DOI] [PubMed]
- 51.Keawtep P, Sungkarat S, Boripuntakul S, Sa-Nguanmoo P, Wichayanrat W, Chattipakorn SC, et al. Effects of combined dietary intervention and physical-cognitive exercise on cognitive function and cardiometabolic health of postmenopausal women with obesity: a randomized controlled trial. Int J Behav Nutr Phys Act. 2024;21(1):28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Maaloul R, Marzougui H, Dhia IB, Ghroubi S, Tagougui S, Kallel C, et al. Effectiveness of Ramadan diurnal intermittent fasting and concurrent training in the management of obesity: is the combination worth the weight? Nutr Metab Cardiovasc Dis. 2023;33(3):659–66. [DOI] [PubMed] [Google Scholar]
- 53.Oh M, Kim S, An K-Y, Min J, Yang HI, Lee J, et al. Effects of alternate day calorie restriction and exercise on cardio-metabolic risk factors in overweight and obese adults: an exploratory randomized controlled study. BMC Public Health. 2018;18:1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Ma Y, Sun L, Mu Z. Network meta-analysis of three different forms of intermittent energy restrictions for overweight or obese adults. Int J Obes. 2024;48(1):55–64. [DOI] [PubMed] [Google Scholar]
- 55.Hansen D, Dendale P, Berger J, Van Loon LJ, Meeusen R. The effects of exercise training on fat-mass loss in obese patients during energy intake restriction. Sports Med. 2007;37:31–46. [DOI] [PubMed] [Google Scholar]
- 56.Varady KA, Cienfuegos S, Ezpeleta M, Gabel K. Cardiometabolic benefits of intermittent fasting. Annu Rev Nutr. 2021;41(1):333–61. [DOI] [PubMed] [Google Scholar]
- 57.Smith JA, Murach KA, Dyar KA, Zierath JR. Exercise metabolism and adaptation in skeletal muscle. Nat Rev Mol Cell Biol. 2023;24(9):607–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Sylow L, Kleinert M, Richter EA, Jensen TE. Exercise-stimulated glucose uptake—regulation and implications for glycaemic control. Nat Rev Endocrinol. 2017;13(3):133–48. [DOI] [PubMed] [Google Scholar]
- 59.Kjøbsted R, Munk-Hansen N, Birk JB, Foretz M, Viollet B, Björnholm M, et al. Enhanced muscle insulin sensitivity after contraction/exercise is mediated by AMPK. Diabetes. 2017;66(3):598–612. [DOI] [PubMed] [Google Scholar]
- 60.Ashcroft SP, Stocks B, Egan B, Zierath JR. Exercise induces tissue-specific adaptations to enhance cardiometabolic health. Cell metabolism. 2024. [DOI] [PubMed]
- 61.Wan K-w, Dai Z-h, Ho RS-t, Yajun HW, Wong SH-S. Comparative effects of time-restricted feeding versus normal diet on physical performance and body composition in healthy adults with regular exercise habits: a systematic review and meta-analysis. BMJ Open Sport & Exercise Medicine. 2024;10(3):e001831. [DOI] [PMC free article] [PubMed]
- 62.Elagizi A, Kachur S, Carbone S, Lavie CJ, Blair SN. A review of obesity, physical activity, and cardiovascular disease. Curr Obes Rep. 2020;9:571–81. [DOI] [PubMed] [Google Scholar]
- 63.Poon ETC, Li HY, Gibala MJ, Wong SHS, Ho RST. High-intensity interval training and cardiorespiratory fitness in adults: An umbrella review of systematic reviews and meta-analyses. Scand J Med Sci Sports. 2024;34(5):e14652. [DOI] [PubMed] [Google Scholar]
- 64.O’Donoghue G, Blake C, Cunningham C, Lennon O, Perrotta C. What exercise prescription is optimal to improve body composition and cardiorespiratory fitness in adults living with obesity? A network meta-analysis. Obes Rev. 2021;22(2):e13137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Boulé NG, Kenny GP, Haddad E, Wells GA, Sigal RJ. Meta-analysis of the effect of structured exercise training on cardiorespiratory fitness in Type 2 diabetes mellitus. Diabetologia. 2003;46:1071–81. [DOI] [PubMed] [Google Scholar]
- 66.Blair SN, Kohl HW, Paffenbarger RS, Clark DG, Cooper KH, Gibbons LW. Physical fitness and all-cause mortality: a prospective study of healthy men and women. JAMA. 1989;262(17):2395–401. [DOI] [PubMed] [Google Scholar]
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Supplementary Materials
Data Availability Statement
The datasets utilized and/or analyzed in this study can be ontained from the corresponding author upon reasonable request.








