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. 2024 Dec 26;7(12):e2452185. doi: 10.1001/jamanetworkopen.2024.52185

Aerobic Exercise and Weight Loss in Adults

A Systematic Review and Dose-Response Meta-Analysis

Ahmad Jayedi 1,2,, Sepideh Soltani 3, Alireza Emadi 4, Mahdieh-Sadat Zargar 5, Ali Najafi 6
PMCID: PMC11672165  PMID: 39724371

Key Points

Question

What is the dose-response association between aerobic exercise and measurements of body weight, waist circumference, and body fat?

Findings

This meta-analyses of 116 randomized clinical trials involving 6880 adults with overweight or obesity found that levels of body weight, waist circumference, and body fat decreased linearly or monotonically with increasing duration of aerobic exercise at moderate to vigorous intensities to 300 minutes per week. Aerobic exercise at least 150 minutes per week was associated with clinically important reductions in waist circumference and measures of body fat.

Meaning

These results suggest that aerobic exercise training at least 150 minutes per week at moderate intensity or higher may be needed to achieve clinically important reductions in waist circumference and measures of body fat.

Abstract

Importance

Current guidance on the duration of aerobic exercise recommended in existing guidelines comes primarily from individual trials. Meta-analyses are lacking to examine the dose-response association of aerobic exercise with adiposity measures.

Objective

To clarify the dose-response association of aerobic exercise with adiposity measures.

Data Sources

PubMed, Scopus, the Cochrane Central Register of Controlled Trials, and gray literature sources (ProQuest and ClinicalTrials.gov) from inception to April 30, 2024.

Study Selection

Randomized clinical trials with intervention durations of at least 8 weeks evaluating the effects of supervised aerobic training on adults with overweight or obesity.

Data Extraction and Synthesis

The PRISMA guidelines were followed to report the results of the meta-analysis. Data extraction was conducted by 2 teams of 2 reviewers each, working independently and in duplicate. Random-effects meta-analyses were performed to estimate mean differences and 95% CIs for each 30-minute per week aerobic exercise and to clarify the shape of the curvilinear associations.

Main Outcomes and Measures

Measures of body weight, waist circumference, body fat, adverse events, medication use reduction, and health-related quality of life score. The certainty of evidence was assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) tool, with a range from very low to high certainty.

Results

In total, 116 randomized clinical trials involving 6880 participants (4199 [61%] female; mean [SD] age, 46 [13] years) with overweight or obesity were included. Each 30 minutes per week of aerobic exercise was associated with reduced body weight by 0.52 kg (95% CI, −0.61 to −0.44 kg; n = 109 trials, GRADE = moderate), waist circumference by 0.56 cm (95% CI, −0.67 to −0.45 cm; n = 62 trials, GRADE = high), body fat percentage by 0.37% (95% CI, −0.43% to −0.31%; n = 65 trials, GRADE = moderate), as well as the areas of visceral (mean difference, −1.60 cm2 [95% CI, −2.12 to −1.07 cm2]; n = 26 trials, GRADE = high) and subcutaneous (mean difference, −1.37 cm2 [95% CI, −1.82 to −0.92 cm2]; n = 27 trials, GRADE = moderate) adipose tissues. Aerobic exercise was associated with modestly increased physical (standardized mean difference, 1.69 SD [95% CI, 1.18-2.20 SD]) and mental (standardized mean difference, 0.74 SD [95% CI, 0.29-1.19 SD]) aspects of quality of life (1 trial with 80 participants, GRADE = low). It was associated with modestly increased mild to moderate adverse events, which were mostly musculoskeletal symptoms (risk difference, 2 more events per 100 participants [95% CI, 1 to 2 more]; GRADE = low). Dose-response meta-analyses indicated that body weight, waist circumference, and body fat measures decreased linearly or monotonically in association with increasing duration of aerobic exercise to 300 minutes per week, with aerobic exercise lasting 150 minutes per week at moderate to vigorous intensities resulting in clinically important reductions in waist circumference and body fat.

Conclusions and Relevance

In this meta-analysis of randomized clinical trials, engaging in 30 minutes of aerobic exercise per week was associated with modest reductions in body weight, waist circumference, and body fat measures among adults with overweight or obesity. However, aerobic training exceeding 150 minutes per week at moderate intensity or greater may be needed to achieve clinically important reductions.


This dose-response meta-analysis of randomized clinical trials assesses the association of aerobic exercise duration and intensity with measures of adiposity among adults with overweight or obesity.

Introduction

Overweight and obesity are among the most important health problems worldwide.1 During the past 45 years, the prevalence of overweight and obesity has tripled globally, resulting in approximately 50% of adults having excess body weight.2 Current guidelines recommend that exercise programs, mainly in the form of aerobic exercise or aerobic and resistance exercises combined, should be one of the key elements of lifestyle modification programs designed to manage obesity.3,4,5,6,7

It is generally recommended in the guidelines that at least 150 minutes per week of aerobic exercise at moderate intensity is required to achieve clinically important weight loss.3,4,5,6,7 The American College of Sport Medicine suggested that exercise programs shorter than 150 minutes per week promote minimal weight loss, and that exercise programs at least 150 minutes per week are required for modest weight loss of 2 to 3 kg.3 The guideline also recommended that an exercise program of 225 to 420 minutes per week at moderate intensity is required for weight loss of 5.0 to 7.5 kg.3 However, current guidance on the duration of aerobic exercise programs recommended in existing guidelines comes primarily from individual trials and is predominantly from older data.

Although previous meta-analyses of randomized clinical trials have provided a wealth of evidence that aerobic exercise is an effective intervention for weight loss in adults with overweight or obesity, the results of these meta-analyses are mainly based on pairwise comparisons between intervention and control groups.8,9,10 In fact, systematic reviews and meta-analyses are lacking to examine the possible dose-response association of aerobic exercise with body weight, waist size, and fat. Evaluating the potential dose-response association is of clinical and public health importance11 because it can determine how body weight, waist size, and fat change with increasing aerobic training dose, thereby contributing to providing useful information needed for decision-making. Therefore, our aim was to perform a systematic review and meta-analysis of randomized clinical trials to investigate the possible dose-response association of aerobic exercise of varying intensity with measures of body weight, waist size, and fat in adults with overweight or obesity.

Methods

We reported the meta-analysis according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 statement for systematic reviews of interventions. The protocol of the present systematic review was registered with PROSPERO (CRD42023460474).12 Given that this is a review study, we were not required to secure approval for the study protocol from an ethics committee or institutional review board, nor was informed consent from study participants necessary.

Systematic Search

PubMed, Scopus, the Cochrane Central Register of Controlled Trials, and gray literature sources (ProQuest and ClinicalTrials.gov) were selected for the systematic search from inception until April 30, 2024. See eMethods 1 in Supplement 1 for additional information and eTable 1 in Supplement 1 for the search strategy.

Study Selection

Using our a priori protocol,12 we searched for randomized clinical trials that (1) had an intervention duration of at least 8 weeks13; (2) included adults older than 18 years with either overweight or obesity (defined as body mass index [BMI, calculated as weight in kilograms divided by height in meters squared] >25 in Western countries6 and >23 in Asian countries14) or central obesity; (3) conducted a supervised continuous aerobic training program (eg, walking, running) as an intervention; (4) reported the efficacy of aerobic exercise on 1 of the study outcomes (mean [SD] of change for continuous outcomes, number of events for binary outcomes); and (5) reported frequency (sessions per week), duration (minutes per session), and intensity (moderate, vigorous, or combined) of aerobic exercise in the intervention arm. Detailed information on criteria applied for excluding studies is provided in eMethods 1 in Supplement 1.

Outcomes

We considered body weight change (in kg) and adverse events as our primary outcomes. Secondary outcomes included changes in waist circumference (in cm), body fat percentage, fat mass (in kg), area of visceral adipose tissue (in cm2), area of subcutaneous adipose tissue (in cm2), health-related quality of life score, and medication reduction (eg, antidiabetic or antihypertensive medications).

Data Extraction and Risk of Bias Assessment

Data extraction was conducted by 2 teams of 2 reviewers (A.J. and S.S.; A.E. and M.-S.Z.) working independently and in duplicate. Detailed information on data extraction and risk of bias assessment is provided in eMethods 2 in Supplement 1. We assessed risk of bias of the trials using version 2 of the Cochrane risk of bias tool.15

Intensity of Aerobic Exercise Programs

The intensity of aerobic exercise programs in the included trials was classified as follows16: (1) light (1.6 to <3.0 metabolic equivalents [METs], or 40% to <55% maximum heart rate, or 20% to <40% maximum oxygen consumption [V̇o2max]); (2) moderate (3.0 to <6.0 METs, or 55% to <70% maximum heart rate, or 40% to <60% V̇o2max); and (3) vigorous (6.0 to <9.0 METs, or 70% to <90% maximum heart rate, or 60% to <85% V̇o2max). Programs of moderate to vigorous intensity were those that included both moderate and vigorous categories.

Statistical Analysis

We used a random-effects model (DerSimonian and Laird method)17 to calculate summary effect estimates for primary and secondary outcomes. We considered the mean difference and its 95% CI as the effect size for continuous outcomes. The exception was health-related quality of life, for which we calculated standardized mean differences in scores. For binary outcomes (adverse events and medication reduction), we reported measures of relative (risk ratio) and absolute (risk difference) risks. Two-sided P < .05 was deemed to be statistically significant.

For continuous outcomes, we first calculated changes (mean and SD of change) from baseline values in each study arm. We computed the mean and SD of changes for the trials that did not report this information by using information from preintervention and postintervention measures.18 Second, we followed the method introduced by Crippa and Orsini19 to assess mean differences and their corresponding 95% CIs for each 30-minute per week increment in aerobic exercise.20 Trial-specific effect estimates were combined using a random-effects model.17 The number of participants, the mean (SD) of the change in continuous outcomes, and the dose (minutes per week) of aerobic exercise across study arms were required for this method.

We performed predefined subgroup analyses based on the intensity of aerobic exercise, health status of the participants, and study risk of bias. We used meta-regression analysis to calculate the P value for the subgroup difference. The Instrument to Assess the Credibility of Effect Modification Analyses (ICEMAN)21 recently introduced 8 criteria that we used to determine whether or not subgroup differences were credible. We applied the ICEMAN tool to assess the credibility of subgroup differences when the P value for the group difference was lower than .10.21 eTable 2 in Supplement 1 presents the domains of the ICEMAN tool and each domain was evaluated.

We also performed post hoc subgroup analyses based on geographical location, intervention duration, sex, baseline weight status, type of aerobic exercise, exercise frequency, exercise modality, degree of adherence to the intervention program, dropout, and the existence of calorie restriction as a co-intervention.

Finally, to investigate the dose-response association of aerobic exercise duration (minutes per week) with our continuous outcomes, we conducted a nonlinear dose-response meta-analysis.19 Publication bias was tested using the Egger test (P value <.10)22 and inspection of the funnel plot. We assessed heterogeneity using the I2 statistic and performed a χ2 test for homogeneity.23 Statistical analyses were conducted using STATA software, version 17.0 (StataCorp LLC).

Grading the Evidence

Two authors (A.J. and M.-S.Z.) judged the certainty of evidence according to the Grading of Recommendations Assessment, Development and Evaluation (GRADE) tool, with a range from very low to high certainty.24 Detailed information on the domains of the GRADE tool is provided in eMethods 3 in Supplement 1.

Results

Literature Search and Study Selection Process

The flowchart of the systematic search is given in eFigure 1 in Supplement 1. We removed 8975 duplicates, leaving 21 518 records for screening of the title and abstract. At this step, we excluded 21 163 records. We read the full text of 351 records and, finally, 116 trials with 6880 participants (4199 [61%] female and 2681 [39%] male; mean [SD] age, 46 [13] years) with overweight or obesity were eligible for inclusion. We excluded 235 full texts for reasons presented in eTable 3 in Supplement 1.

Characteristics of Trials Included in the Meta-Analysis

eTable 4 in Supplement 1 gives the characteristics of the trials included in the meta-analysis.25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140 All trials implemented a supervised aerobic exercise program. The control groups received no intervention or continued a sedentary lifestyle or maintained their usual activity. In brief, 48 trials were conducted in North America, 39 in Asia, 18 in Europe, 5 in Australia, 4 in South America, and 2 in Africa. Forty-seven trials were conducted with female participants, 30 with male participants, and 39 with both sexes. Among the trials, 42 involved participants with obesity, 2 involved participants with overweight, and the remaining 72 trials involved mixed populations. There were 41 trials that involved patients with overweight or obesity and a comorbidity (eg, type 2 diabetes, hypertension, or fatty liver disease) and 75 trials that involved otherwise healthy people. The mean age of the participants in the included trials ranged from 19 to 74 years, and the mean BMI ranged from 25 to 44 (mean [SD], 31 [3]). Among the trials, 78 implemented a progressive aerobic training program, and 38 implemented a nonprogressive training program. The duration of the intervention (minutes of aerobic exercise per week) ranged from 55 to 300 minutes per week (mean [SD], 167 [54] minutes per week). The degree of adherence to the intervention program was excellent, good, or high, or at least 80% in 48 trials and less than 80% in 6 trials. In 60 trials, no information was provided on the level of adherence. The dropout rate was lower than 20% in 80 trials and 20% or higher in 27 trials (eTable 5 in Supplement 1). Adverse events were mostly mild to moderate musculoskeletal symptoms, including knee and ankle injury, pain in the knee or back, and arthritis, as well as an increase in blood pressure in 1 trial (eTable 5 in Supplement 1). Fourteen trials were at low risk of bias, 48 trials had some level of concern, and 54 trials were at serious risk of bias (eTable 6 in Supplement 1).

Primary Outcomes

There were 109 trials with 6298 participants that reported on body weight.26,27,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,51,52,53,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,110,112,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140 Each 30 minutes per week of aerobic exercise was associated with body weight reduced by 0.52 kg (95% CI, −0.61 to −0.44; I2 = 88%; GRADE = moderate) (Table). A forest plot was not provided because there were too many trials. Aerobic exercise was associated with increased mild to moderate adverse events by 2 more events per 100 patients (95% CI, 1 to 2 more; 9 trials; GRADE = low) (eFigures 2 and 3 in Supplement 1; Table).34,38,44,45,55,71,119,130,140 Aerobic exercise was not associated with an increase in hypoglycemic reactions (risk difference, 1 more per 100 patients [95% CI, 1 fewer to 3 more]; 3 trials; GRADE = very low]) (eFigures 4 and 5 in Supplement 1; Table).38,71,119

Table. Association of Supervised Aerobic Exercise With Body Weight, Waist Circumference, and Body Fat Among Participants With Overweight or Obesity.

Outcome Anticipated absolute effect (95% CI) Relative effect, RR (95% CI) No. of participants/No. of studies Certainty of the evidence (GRADE)
Risk with control group Risk with intervention, No. of events per 1000 participants
Body weight 0.52 (0.61-0.44) kg Lower than control NA NA 6298/109 Moderate
Waist circumference 0.56 (0.67-0.45) cm Lower than control NA NA 4281/62 High
Body fat percentage 0.37% (0.43%-0.31%) Lower than control NA NA 3466/65 Moderate
Body fat massa 0.20 (0.32-0.08) kg Lower than control NA NA 410/7 High
Visceral adipose tissue area 1.60 (2.12-1.07) cm2 Lower than control NA NA 1501/26 High
Subcutaneous adipose tissue area 1.37 (1.82-0.92) cm2 Lower than control NA NA 1634/27 Moderate
Adverse events 27 Events per 1000 participants 46 (27-79) 1.74 (1.02-2.97) 1170/9 Low
Hypoglycemia 6 Events per 1000 participants 15 (3-77) 2.51 (0.49-12.78) 335/3 Very low
Medication use reduction 36 Events per 1000 participants 52 (21-131) 1.43 (0.57-3.60) 587/2 Low
Health-related quality of life mental score 1.69 (SD, 1.18-2.20) Points higher than control NA NA 80/1 Low
Health-related quality of life physical score 0.74 (SD, 0.29-1.19) Points higher than control NA NA 80/1 Low

Abbreviations: GRADE, Grading of Recommendations Assessment, Development and Evaluation (range is very low, low, moderate, and high); NA, not applicable; RR relative risk.

a

There was significant and credible difference based on study risk of bias, where trials with a low risk of bias reported a smaller effect; results of trials with a low risk of bias are presented.

Secondary Outcomes

A summary of the association of aerobic exercise with body waist circumference and measures of fat is given in the Table. Each 30 minutes per week of aerobic exercise was associated with lower waist circumference (mean difference, −0.56 cm [95% CI, −0.67 to −0.45 cm]; I2 = 88%; GRADE = high; for 62 trials with 4281 participants) (eFigure 6 in Supplement 1),25,26,32,34,37,39,40,41,45,46,47,49,54,55,59,61,62,64,65,66,69,71,73,76,77,78,79,80,81,82,83,91,92,93,94,95,97,102,104,105,106,108,109,110,111,112,113,114,116,117,118,119,122,123,125,128,132,136,137,139 lower body fat percentage (mean difference: −0.37% [95% CI, −0.43% to −0.31%]; I2 = 83%; GRADE = moderate; for 65 trials with 3466 participants) (eFigure 7 in Supplement 1),26,27,28,30,31,33,34,35,36,38,40,41,42,44,45,46,48,51,56,58,59,62,63,65,73,74,75,76,77,78,79,80,84,86,90,93,96,98,99,100,101,104,105,108,109,114,116,117,119,121,123,126,127,128,129,131,132,134,135,136,137,138,139,140 and lower body fat mass (mean difference, −0.20 kg [95% CI, −0.32 to −0.08 kg]; I2 = 26%; GRADE = high; for 7 trials with a low risk of bias and 410 participants) (eFigure 8 in Supplement 1).55,61,65,69,79,112,138 There was also moderate to high certainty that aerobic exercise was associated with lower visceral (mean difference, −1.60 cm2 [95% CI, −2.12 to −1.07 cm2]; n = 26 trials, GRADE = high)47,50,51,53,56,66,69,75,76,78,79,81,82,83,89,91,99,110,117,119,120,135,136,137,138,140 and subcutaneous (mean difference, −1.37 cm2 [95% CI, −1.82 to −0.92 cm2]; n = 27 trials, GRADE = moderate)47,51,53,56,63,66,69,75,79,81,82,83,89,91,93,98,99,110,114,117,119,120,135,136,137,138,140 adipose tissues (eFigures 9 and 10 in Supplement 1; Table). Aerobic exercise was not associated with lower antidiabetic34,119 and antihypertensive34 medication use (risk difference, 1 more per 100 patients [95% CI, 2 fewer to 5 more; 2 trials; GRADE = low) (eFigures 11 and 12 in Supplement 1) but was associated with modestly increased physical (standardized mean difference, 1.69 SD [95% CI, 1.18-2.20 SD] and mental (standardized mean difference, 0.74 SD [95% CI, 0.29-1.19 SD] aspects of quality of life (1 trial with 80 participants, GRADE = low) (eFigures 13 and 14 in Supplement 1; Table).130

Subgroup Analyses

We considered 3 plausible effect modifiers, including risk of bias, intensity of aerobic exercise, and presence of comorbidity in the study participants, and applied the ICEMAN criteria to identify credible subgroup differences with P < .10 for the group difference21 (eTables 7-18 in Supplement 1). There was no significant or credible difference across subgroups defined based on study risk of bias, except for body fat mass, for which trials with a low risk of bias reported smaller effects than those with some concerns or high risk of bias (P = .007 for subgroup difference; ICEMAN credibility = moderate). Therefore, we reported the results of the trials with a low risk of bias. In addition, we conducted a series of post hoc subgroup analyses to identify potential sources of heterogeneity and potential effect modifiers. Although there were some significant differences between some subgroups, further detailed evaluation based on the 8 criteria introduced by ICEMAN suggested that there was no credible difference across post hoc subgroup analyses (eTables 7-18 in Supplement 1). For example, we found that trials that implemented a progressive aerobic training indicated greater association with weight reduction (mean difference, −0.58 kg [95% CI, −0.69 to −0.46 kg]; 73 trials) compared with trials that implemented a nonprogressive exercise (mean difference, −0.39 kg [−0.50 to −0.28]; 36 trials); however, the credibility of this subgroup difference was rated low as this subgroup was not based on an a priori hypothesis and change may be a likely explanation (P = .02 for subgroup difference). Interestingly, there were no significant differences among subgroups categorized by the duration of the intervention (8 to ≤12, 12-24, and >24 weeks) for most outcomes, except for visceral and subcutaneous adipose tissue areas, where short-term trials (8 to ≤12 weeks) indicated greater associations with reduction in visceral (P = .004 for subgroup difference) and subcutaneous (P = .02 for subgroup difference) adipose tissue areas than trials with longer duration (12-24 and >24 weeks).

Nonlinear Dose-Response Meta-Analyses

In the main analysis, our dose-response meta-analysis suggested a linear reduction in body weight associated with increasing duration of aerobic exercise to 300 minutes per week (P = .17 for nonlinearity; P < .001 for dose response; n = 109 trials) (Figure 1). The degree of weight loss was −2.79 kg (95% CI, −3.29 to −2.29 kg) at 150 minutes per week and −4.19 kg (95% CI, −5.98 to −2.41 kg) at 300 minutes per week (eTable 19 in Supplement 1). A similar linear reduction in body weight was also observed in the dose-response analyses of trials with moderate, moderate to vigorous, and vigorous exercise intensities (Figure 1; eTable 19 in Supplement 1). For waist circumference, there was a nonlinear reduction associated with dose of aerobic exercise in the main analysis (P = .04 for nonlinearity; P < .001 for dose response; n = 62 trials) (Figure 2); however, the analysis of trials with moderate to vigorous intensity showed a linear reduction in waist circumference associated with the dose of aerobic exercise. The degree of reduction in waist circumference was −4.21 cm (95% CI, −6.85 to −1.58 cm) at 300 minutes per week of aerobic exercise at moderate intensity and −5.34 cm (95% CI, −9.05 to −1.63 cm) at 300 minutes per week of aerobic exercise at moderate to vigorous intensity (eTable 19 in Supplement 1). The results suggested that the association of aerobic exercise with waist circumference surpassed the threshold set as the minimum clinically important difference for waist circumference (2 cm), with higher duration indicating greater reduction in waist circumference.

Figure 1. Dose-Response Association of Aerobic Exercise With Body Weight Among Adults With Overweight or Obesity.

Figure 1.

Solid lines represent the dose-response lines, and lines above and below are 95% CIs. Circles represent relative risk point estimates for aerobic exercise from each study, with circle size proportional to the inverse of standard error. The vertical orange lines represent the baseline aerobic exercise dose across studies.

Figure 2. Dose-Response Association of Aerobic Exercise With Waist Circumference Among Adults With Overweight or Obesity.

Figure 2.

Solid lines represent the dose-response lines, and lines above and below are 95% CIs. Circles represent relative risk point estimates for aerobic exercise from each study, with circle size proportional to the inverse of the standard error. The vertical orange lines represent the baseline aerobic exercise dose across studies.

For body fat percentage associated with dose of aerobic exercise, the greatest reduction was observed at 150 minutes per week (mean difference, −2.08% [95% CI, −2.47% to −1.69%]) (Figure 3; eTable 19 in Supplement 1), surpassing the threshold (2%) as the minimum clinically important difference for body fat percentage. Similar findings were observed for body fat mass associated with dose of aerobic exercise, in which the size of the effect was larger than the minimum clinically important difference threshold (2 kg) at 100 minutes per week in the main analysis (mean difference, −2.03 kg [95% CI, −2.77 to −1.29 kg]) and in the analysis of trials with moderate to vigorous exercise intensity (mean difference, −2.23 kg [95% CI, −3.36 to −1.10 kg]) (Figure 4; eTable 19 in Supplement 1). The dose-dependent associations of aerobic exercise with areas of visceral and subcutaneous adipose tissues are indicated in eFigures 15 and 16 and eTable 19 in Supplement 1.

Figure 3. Dose-Response Association of Aerobic Exercise With Body Fat Percentage Among Adults With Overweight or Obesity.

Figure 3.

Solid lines represent the dose-response lines, and lines above and below are 95% CIs. Circles represent relative risk point estimates for aerobic exercise from each study, with circle size proportional to the inverse of the standard error. Small vertical orange lines represent the baseline aerobic exercise dose across studies.

Figure 4. Dose-Response Association of Aerobic Exercise With Fat Mass Among Adults With Overweight or Obesity.

Figure 4.

Solid lines represent the dose-response lines, and lines above and below are 95% CIs. Circles represent relative risk point estimates for aerobic exercise from each study, with circle size proportional to the inverse of the standard error. The vertical orange lines represent the baseline aerobic exercise dose across studies.

Publication Bias

It is possible that the associations were overestimated due to the asymmetry observed in the funnel plots for body fat percentage (Egger test = 0.003) and subcutaneous adipose tissue area (Egger test, <0.001). For the other outcomes, the funnel plots showed no signs of asymmetry (eFigures 17-22 in Supplement 1). For body fat precentage, trim-and-fill analysis found 1 potentially missing study, and the main effect size did not change after imputing this study (mean differemce, −0.37% [95% CI, −0.43% to −0.30%]; 66 trials). For subcutaneous adipose tissue, trim-and-fill analysis found 11 potentially missing studies, and the main effect size attenuated but remained significant after imputing these studies (mean difference, −1.03 cm2 [95% CI, −1.46 to −0.60 cm2]; 38 trials).

Grading the Evidence

The certainty of evidence was rated moderate for body weight due to downgrades for imprecision (effect size smaller than the minimum clinically important difference) and study risk of bias and an upgrade for the dose-response gradient. The certainty of evidence was also downgraded for publication bias and serious risk of bias for body fat percentage (eTable 20 in Supplement 1).

Discussion

To answer an important question that is relevant to patients and practice, this meta-analysis of randomized clinical trials gathered the available data assessing the associations of aerobic exercise with body weight, waist circumference, and body fat. Our findings suggested that each 30 minutes of aerobic exercise per week may help adults who have overweight or obesity slightly reduce body weight, waist circumference, and measures of fat. Our nonlinear dose-response meta-analyses indicated that body weight decreased linearly in association with increasing duration of aerobic exercise up to 300 minutes per week at a variety of intensities. Relatively similar findings were found for waist circumference, with waist circumference decreasing linearly or monotonically in association with increasing duration of aerobic exercise. The analyses of body fat percentage suggested a nonlinear association, with greatest improvement associated with 150 minutes per week. There was low certainty of evidence that aerobic exercise was associated with increased health-related quality of life score.

A recent network meta-analysis compared different types of long-term (≥6 months) exercise and concluded that aerobic exercise is the most effective exercise associated with weight loss in adults with obesity.13 Their findings indicated that, when compared with no intervention, aerobic exercise was associated with reduced body weight by 2.18 kg and waist circumference by 2.33 cm.13 According to pairwise meta-analyses, aerobic exercise was associated with reduced waist circumference by 2.12 to 3.20 cm8,10 and body weight by 1.60 to 2.00 kg.9,10 The greatest number of trials included in the earlier reviews were 45 trials for body weight141 and 25 trials for waist circumference.8 We included 109 trials assessing body weight and 62 trials assessing waist circumference, enabling us to provide the most comprehensive review in this area. Additionally, our nonlinear dose-response meta-analyses enabled us to show the dose and intensity of exercise associated with the greatest improvements in body weight, waist circumference, and fat percentage, which were not reported in previous reviews. For instance, the range of weight loss in a previous review was between 1.60 and 2.39 kg, and the range of waist circumference loss was from 2.12 to 3.70 cm.9 By comparison, we found a 4.19 kg decrease in body weight associated with 300 minutes of aerobic exercise per week, and decreases in waist circumference associated with 300 minutes of aerobic exercise per week of 4.21 cm for moderate intensity and 5.34 cm for moderate to vigorous intensity.

Our findings indicated that body weight and waist circumference decreased linearly or monotonically in association with increasing duration of aerobic exercise at different intensities. Such a linear reduction was also found associated with body fat mass and subcutaneous adipose tissue area. The results suggest that longer durations of aerobic exercise are associated with greater reductions in body weight, waist circumference, and fat tissue. The nonlinear dose-response analyses indicated that aerobic exercise at least 150 minutes per week was associated with clinically important reductions in waist circumference and measures of body fat; thus, aerobic training at least 150 minutes per week may be needed to achieve important reductions in waist circumference and body fat. Point-specific estimates for different aerobic exercise duration and intensity can help patients and health care professionals select the optimal aerobic exercise duration and intensity according to their weight loss goals.

A series of analyses was conducted to assess the associations across various subgroups. In terms of modality, progressive exercise demonstrated greater association with weight reduction compared with nonprogressive exercise; however, the credibility of this subgroup difference was rated low and the analyses of other outcomes did not reveal any significant subgroup difference. The analyses of body fat percentage, waist circumference, and visceral adipose tissue area indicated that the size of the effect surpassing the minimum clinically important difference threshold was larger with vigorous exercise compared with light or moderate exercise intensities, suggesting better outcomes with more vigorous exercise. The findings were largely consistent among subgroups categorized by the duration of the intervention (8-12, 12-24, and >24 weeks). However, only 2 trials reported on intervention durations longer than 48 weeks,88,140 both of which showed small mean differences. This raises concerns about the association of aerobic exercise with weight loss beyond 1 year.

Our findings did not indicate any significant reduction in medication use associated with aerobic exercise. This finding could be because only 2 trials were included in the analysis34,119 and the follow-up period was relatively short (12 to 16 weeks). A recent meta-analysis found that aerobic exercise was associated with a modest reduction in medication use among patients with type 2 diabetes.20

Limitations

There were several shortcomings of this study that need further evaluation in future research and should be considered when interpreting the results. First, there was high heterogeneity in the data, which may limit the generalizability of the findings. However, there were many trials included in almost all analyses. In these situations, even a slight variation in the effect estimates can lead to substantial data heterogeneity.142 Additionally, trials assessing continuous outcomes typically report narrower CIs, which in turn may result in less overlap between CIs and higher I2 values.142,143 Considering these limitations and based on the GRADE approach,144 we focused on the similarity of the point estimates and the degree of overlap of the CIs. In fact, there was high consistency in effect estimates between trials included in the analyses. For example, of 109 trials included in the analysis of body weight, 104 trials reported a reduction in body weight associated with aerobic exercise. We did not downgrade the certainty of the evidence for inconsistencies given the high consistency in the direction of the effect estimates. Second, due to the low number of studies, we could not perform nonlinear dose-response meta-analyses based on the health status of the participants (eg, in patients with type 2 diabetes). Third, a low number of trials were available for some outcomes, such as health-related quality of life and medication use reduction. Fourth, we used study level data for dose-response meta-analyses; thus, our results are subject to an aggregation bias. Fifth, there was substantial evidence of publication bias for subcutaneous adipose tissue, and trim-and-fill analysis indicated a weaker association. Thus, the magnitude of the findings between aerobic exercise and subcutaneous adipose tissue may have been overestimated. Finally, the trials included in the meta-analysis provided insufficient data regarding the dietary habits and smoking status of the participants. Consequently, we could not account for the influence of these important effect modifiers in our estimates of effects.

Conclusions

This dose-response meta-analysis of 116 randomized clinical trials presented evidence of moderate to high certainty that aerobic exercise may be associated with clinically important reductions in waist circumference and measures of body fat, including body fat percentage, fat mass, and visceral and subcutaneous adipose tissue areas. The results indicated that levels of body weight, waist circumference, and fat decreased linearly or monotonically in association with increasing duration of aerobic exercise, suggesting that longer durations of aerobic exercise may be associated with more beneficial weight or waist circumference outcomes. By contrast, we did not find any credible subgroup differences based on the intensity of aerobic exercise. Specifically, our results suggest that aerobic training exceeding 150 minutes per week at moderate intensity or greater may be needed to achieve associations with clinically important reductions.

Supplement 1.

eMethods 1. Detailed information on criteria applied for excluding studies

eMethods 2. Detailed information on systematic search, data extraction and risk of bias assessment

eMethods 3. Detailed information to evaluate the overall quality of the evidence using GRADE tool

eTable 1. Search strategy to find potential eligible trials for inclusion in the meta-analysis of supervised aerobic exercise and measures of body weight, waist and fat (April 2024)

eTable 2. Description of the ICEMAN domains and how to judge each domain

eTable 3. List of studies that were excluded via full text assessment

eTable 4. Characteristics of the trials included in the meta-analysis of aerobic exercise and measures of body weight, waist, and fat

eTable 5. Dropout, degree of adherence to the intervention program, and adverse events in the trials included in the meta-analysis of aerobic exercise and measures of body weight, waist, and fat

eTable 6. Risk of bias of the trials included in the meta-analysis of aerobic exercise and measures of body weight, waist and fat

eTable 7. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with body weight (kg)

eTable 8. Assessment of credibility of subgroup difference based on ICEMAN for body weight

eTable 9. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with waist circumference (cm)

eTable 10. Assessment of credibility of subgroup difference based on ICEMAN for waist circumference

eTable 11. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with body fat percentage (%)

eTable 12. Assessment of credibility of subgroup difference based on ICEMAN for body fat percentage

eTable 13. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with body fat mass (kg)

eTable 14. Assessment of credibility of subgroup difference based on ICEMAN for body fat mass

eTable 15. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with visceral adipose tissue (cm2)

eTable 16. Assessment of credibility of subgroup difference based on ICEMAN for visceral adipose tissue

eTable 17. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with subcutaneous adipose tissue (cm2)

eTable 18. Assessment of credibility of subgroup difference based on ICEMAN for visceral adipose tissue

eTable 19. The association of different doses of aerobic exercise with measures of body weight, waist and fat in adults with overweight or obesity (mean difference and 95%CI)

eTable 20. GRADE evidence for the association of aerobic exercise with measures of body weight, waist and fat

eFigure 1. Literature search and study selection process

eFigure 2. Absolute effect of aerobic exercise on adverse events in the study participants

eFigure 3. Relative effect of aerobic exercise on adverse events in the study participants

eFigure 4. Absolute effect of aerobic exercise on hypoglycemic reactions in the study participants

eFigure 5. Relative effect of aerobic exercise on hypoglycemic reactions in the study participants

eFigure 6. Association of aerobic exercise (30 min/week) with waist circumference (cm)

eFigure 7. Association of aerobic exercise (30 min/week) with body fat percentage (%)

eFigure 8. Association of aerobic exercise (30 min/week) with body fat mass (km)

eFigure 9. Association of aerobic exercise (30 min/week) with visceral adipose tissue (cm2)

eFigure 10. Association of aerobic exercise (30 min/week) with subcutaneous adipose tissue (cm2)

eFigure 11. Absolute effect of aerobic exercise on medication reduction

eFigure 12. Relative effect of aerobic exercise on medication reduction

eFigure 13. Effect of aerobic exercise on health-related quality of life (mental score)

eFigure 14. Effect of aerobic exercise on health-related quality of life (physical score)

eFigure 15. Dose-dependent association of aerobic exercise with visceral adipose tissue (cm2)

eFigure 16. Dose-dependent association of aerobic exercise with subcutaneous adipose tissue (cm2)

eFigure 17. Funnel plot of the association of aerobic exercise with body weight (Egger’s test = 0.42)

eFigure 18. Funnel plot of the association of aerobic exercise with waist circumference (Egger’s test = 0.21)

eFigure 19. Funnel plot of the association of aerobic exercise with body fat percentage (Egger’s test = 0.003)

eFigure 20. Funnel plot of the association of aerobic exercise with body fat mass (Egger’s test = 0.55)

eFigure 21. Funnel plot of the association of aerobic exercise with visceral adipose tissue (Egger’s test = 0.15)

eFigure 22. Funnel plot of the association of aerobic exercise with subcutaneous adipose tissue (Egger’s test <0.001)

Supplement 2.

Data Sharing Statement

References

  • 1.World Health Organization. Overweight and obesity. WHO Fact Sheet No. 311. 2020. Accessed November 15, 2024. https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight
  • 2.Abarca-Gómez L, Abdeen ZA, Hamid ZA, et al. ; NCD Risk Factor Collaboration (NCD-RisC) . Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults. Lancet. 2017;390(10113):2627-2642. doi: 10.1016/S0140-6736(17)32129-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Donnelly JE, Blair SN, Jakicic JM, Manore MM, Rankin JW, Smith BK; American College of Sports Medicine . American College of Sports Medicine position stand. appropriate physical activity intervention strategies for weight loss and prevention of weight regain for adults. Med Sci Sports Exerc. 2009;41(2):459-471. doi: 10.1249/MSS.0b013e3181949333 [DOI] [PubMed] [Google Scholar]
  • 4.Garvey WT, Mechanick JI, Brett EM, et al. ; Reviewers of the AACE/ACE Obesity Clinical Practice Guidelines . American Association of Clinical Endocrinologists and American College of Endocrinology comprehensive clinical practice guidelines for medical care of patients with obesity. Endocr Pract. 2016;22(suppl 3):1-203. doi: 10.4158/EP161365.GL [DOI] [PubMed] [Google Scholar]
  • 5.Department of Health and Human Services. 2018 Physical activity Guidelines Advisory Committee scientific report. Accessed November 15, 2024. https://odphp.health.gov/sites/default/files/2019-09/PAG_Advisory_Committee_Report.pdf
  • 6.Jensen MD, Ryan DH, Apovian CM, et al. ; American College of Cardiology/American Heart Association Task Force on Practice Guidelines; Obesity Society . 2013 AHA/ACC/TOS guideline for the management of overweight and obesity in adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Obesity Society. J Am Coll Cardiol. 2014;63(25, pt B):2985-3023. doi: 10.1016/j.jacc.2013.11.004 [DOI] [PubMed] [Google Scholar]
  • 7.Yumuk V, Tsigos C, Fried M, et al. ; Obesity Management Task Force of the European Association for the Study of Obesity . European guidelines for obesity management in adults. Obes Facts. 2015;8(6):402-424. doi: 10.1159/000442721 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Armstrong A, Jungbluth Rodriguez K, Sabag A, et al. Effect of aerobic exercise on waist circumference in adults with overweight or obesity: a systematic review and meta-analysis. Obes Rev. 2022;23(8):e13446. doi: 10.1111/obr.13446 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Bellicha A, van Baak MA, Battista F, et al. Effect of exercise training on weight loss, body composition changes, and weight maintenance in adults with overweight or obesity: an overview of 12 systematic reviews and 149 studies. Obes Rev. 2021;22(suppl 4):e13256. doi: 10.1111/obr.13256 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Thorogood A, Mottillo S, Shimony A, et al. Isolated aerobic exercise and weight loss: a systematic review and meta-analysis of randomized controlled trials. Am J Med. 2011;124(8):747-755. doi: 10.1016/j.amjmed.2011.02.037 [DOI] [PubMed] [Google Scholar]
  • 11.Bretz F, Hsu J, Pinheiro J, Liu Y. Dose finding—a challenge in statistics. Biom J. 2008;50(4):480-504. doi: 10.1002/bimj.200810438 [DOI] [PubMed] [Google Scholar]
  • 12.Effects of supervised aerobic exercise on measures of body weight, waist, and fat in adults with overweight or obesity: a protocol for a systematic review and dose-response meta-analysis of randomised trials. PROSPERO identifier: CRD42023460474. Accessed September 15, 2023. https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023460474
  • 13.Morze J, Rücker G, Danielewicz A, et al. Impact of different training modalities on anthropometric outcomes in patients with obesity: a systematic review and network meta-analysis. Obes Rev. 2021;22(7):e13218. doi: 10.1111/obr.13218 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.World Health Organization. The Asia-Pacific perspective: redefining obesity and its treatment. Sydney: Health Communications Australia. February 2000. Accessed May 24, 2023. https://iris.who.int/bitstream/handle/10665/206936/0957708211_eng.pdf?sequence=1&isAllowed=y
  • 15.Sterne JA, Savović J, Page MJ, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366:14898. doi: 10.1136/bmj.l4898 [DOI] [PubMed] [Google Scholar]
  • 16.Norton K, Norton L, Sadgrove D. Position statement on physical activity and exercise intensity terminology. J Sci Med Sport. 2010;13(5):496-502. doi: 10.1016/j.jsams.2009.09.008 [DOI] [PubMed] [Google Scholar]
  • 17.DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177-188. doi: 10.1016/0197-2456(86)90046-2 [DOI] [PubMed] [Google Scholar]
  • 18.Higgins JPT, Thomas J, Chandler J, et al, eds. Cochrane Handbook for Systematic Reviews of Interventions. 2nd ed. Chichester (UK): John Wiley & Sons, 2019. [Google Scholar]
  • 19.Crippa A, Orsini N. Dose-response meta-analysis of differences in means. BMC Med Res Methodol. 2016;16(1):91. doi: 10.1186/s12874-016-0189-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Jayedi A, Emadi A, Shab-Bidar S. Dose-dependent effect of supervised aerobic exercise on HbA1c in patients with type 2 diabetes: a meta-analysis of randomized controlled trials. Sports Med. 2022;52(8):1919-1938. doi: 10.1007/s40279-022-01673-4 [DOI] [PubMed] [Google Scholar]
  • 21.Schandelmaier S, Briel M, Varadhan R, et al. Development of the Instrument to Assess the Credibility of Effect Modification Analyses (ICEMAN) in randomized controlled trials and meta-analyses. CMAJ. 2020;192(32):E901-E906. doi: 10.1503/cmaj.200077 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629-634. doi: 10.1136/bmj.315.7109.629 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Higgins JP, Savović J, Page MJ, Elbers RG, Sterne JA. Assessing risk of bias in a randomized trial. In: Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA, eds. Cochrane Handbook for Systematic Reviews of Interventions. Version 6.5. Cochrane Collaboration; 2024:205-228. [Google Scholar]
  • 24.Guyatt GH, Oxman AD, Vist GE, et al. ; GRADE Working Group . GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336(7650):924-926. doi: 10.1136/bmj.39489.470347.AD [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Abdelaal AAM, Mohamad MA. Obesity indices and haemodynamic response to exercise in obese diabetic hypertensive patients: randomized controlled trial. Obes Res Clin Pract. 2015;9(5):475-486. doi: 10.1016/j.orcp.2014.11.001 [DOI] [PubMed] [Google Scholar]
  • 26.Ahmadi H, Ghanbarzadeh M, Nikbakht M, Ranjbar R. Effects of eight-weeks aerobic exercise on leptin to adiponectin ratio and glycemic control indices in men with type 2 diabetes. Sport Physiology. 2021;13(51):93-116. doi: 10.22089/spj.2021.10260.2122 [DOI] [Google Scholar]
  • 27.Ahmadizad S, Haghighi AH, Hamedinia MR. Effects of resistance versus endurance training on serum adiponectin and insulin resistance index. Eur J Endocrinol. 2007;157(5):625-631. doi: 10.1530/EJE-07-0223 [DOI] [PubMed] [Google Scholar]
  • 28.Akbarpour M. The effect of aerobic training on serum adiponectin and leptin levels and inflammatory markers of coronary heart disease in obese men. Biol Sport. 2013;30(1):21-27. doi: 10.5604/20831862.1029817 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Alves JG, Gale CR, Mutrie N, Correia JB, Batty GD. A 6-month exercise intervention among inactive and overweight favela-residing women in Brazil: the Caranguejo Exercise Trial. Am J Public Health. 2009;99(1):76-80. doi: 10.2105/AJPH.2007.124495 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Amanat S, Sinaei E, Panji M, et al. A randomized controlled trial on the effects of 12 weeks of aerobic, resistance, and combined exercises training on the serum levels of nesfatin-1, irisin-1 and HOMA-IR. Front Physiol. 2020;11:562895. doi: 10.3389/fphys.2020.562895 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.AminiLari Z, Fararouei M, Amanat S, et al. The effect of 12 weeks aerobic, resistance, and combined exercises on omentin-1 levels and insulin resistance among type 2 diabetic middle-aged women. Diabetes Metab J. 2017;41(3):205-212. doi: 10.4093/dmj.2017.41.3.205 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Anderssen SA, Carroll S, Urdal P, Holme I. Combined diet and exercise intervention reverses the metabolic syndrome in middle-aged males: results from the Oslo Diet and Exercise Study. Scand J Med Sci Sports. 2007;17(6):687-695. doi: 10.1111/j.1600-0838.2006.00631.x [DOI] [PubMed] [Google Scholar]
  • 33.Armannia F, Ghazalian F, Shadnoush M, Keyvani H, Gholami M. Effects of high-intensity interval vs. moderate-intensity continuous training on body composition and gene expression of ACE2, NLRP3, and FNDC5 in obese adults: a randomized controlled trial. Med J Islam Repub Iran. 2022;36:161. doi: 10.47176/mjiri.36.161 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Arsenault BJ, Côté M, Cartier A, et al. Effect of exercise training on cardiometabolic risk markers among sedentary, but metabolically healthy overweight or obese post-menopausal women with elevated blood pressure. Atherosclerosis. 2009;207(2):530-533. doi: 10.1016/j.atherosclerosis.2009.05.009 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Arslan E, Can S, Demirkan E. Effect of short-term aerobic and combined training program on body composition, lipids profile and psychological health in premenopausal women. Sci Sports. 2017;32(2):106-113. doi: 10.1016/j.scispo.2016.11.004 [DOI] [Google Scholar]
  • 36.Auerbach P, Nordby P, Bendtsen LQ, et al. Differential effects of endurance training and weight loss on plasma adiponectin multimers and adipose tissue macrophages in younger, moderately overweight men. Am J Physiol Regul Integr Comp Physiol. 2013;305(5):R490-R498. doi: 10.1152/ajpregu.00575.2012 [DOI] [PubMed] [Google Scholar]
  • 37.Baria F, Kamimura MA, Aoike DT, et al. Randomized controlled trial to evaluate the impact of aerobic exercise on visceral fat in overweight chronic kidney disease patients. Nephrol Dial Transplant. 2014;29(4):857-864. doi: 10.1093/ndt/gft529 [DOI] [PubMed] [Google Scholar]
  • 38.Beavers KM, Ambrosius WT, Rejeski WJ, et al. Effect of exercise type during intentional weight loss on body composition in older adults with obesity. Obesity (Silver Spring). 2017;25(11):1823-1829. doi: 10.1002/oby.21977 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Bell GJ, Harber V, Murray T, Courneya KS, Rodgers W. A comparison of fitness training to a pedometer-based walking program matched for total energy cost. J Phys Act Health. 2010;7(2):203-213. doi: 10.1123/jpah.7.2.203 [DOI] [PubMed] [Google Scholar]
  • 40.Belli T, Ribeiro LFP, Ackermann MA, Baldissera V, Gobatto CA, Galdino da Silva R. Effects of 12-week overground walking training at ventilatory threshold velocity in type 2 diabetic women. Diabetes Res Clin Pract. 2011;93(3):337-343. doi: 10.1016/j.diabres.2011.05.007 [DOI] [PubMed] [Google Scholar]
  • 41.Benito PJ, Bermejo LM, Peinado AB, et al. ; PRONAF Study Group . Change in weight and body composition in obese subjects following a hypocaloric diet plus different training programs or physical activity recommendations. J Appl Physiol (1985). 2015;118(8):1006-1013. doi: 10.1152/japplphysiol.00928.2014 [DOI] [PubMed] [Google Scholar]
  • 42.Bertram SR, Venter I, Stewart RI. Weight loss in obese women–exercise v. dietary education. S Afr Med J. 1990;78(1):15-18. [PubMed] [Google Scholar]
  • 43.Blond MB, Rosenkilde M, Gram AS, et al. How does 6 months of active bike commuting or leisure-time exercise affect insulin sensitivity, cardiorespiratory fitness and intra-abdominal fat? a randomised controlled trial in individuals with overweight and obesity. Br J Sports Med. 2019;53(18):1183-1192. doi: 10.1136/bjsports-2018-100036 [DOI] [PubMed] [Google Scholar]
  • 44.Blumenthal JA, Sherwood A, Gullette ECD, et al. Exercise and weight loss reduce blood pressure in men and women with mild hypertension: effects on cardiovascular, metabolic, and hemodynamic functioning. Arch Intern Med. 2000;160(13):1947-1958. doi: 10.1001/archinte.160.13.1947 [DOI] [PubMed] [Google Scholar]
  • 45.Chin EC, Yu AP, Lai CW, et al. Low-frequency HIIT improves body composition and aerobic capacity in overweight men. Med Sci Sports Exerc. 2020;52(1):56-66. doi: 10.1249/MSS.0000000000002097 [DOI] [PubMed] [Google Scholar]
  • 46.Chiu CH, Ko MC, Wu LS, et al. Benefits of different intensity of aerobic exercise in modulating body composition among obese young adults: a pilot randomized controlled trial. Health Qual Life Outcomes. 2017;15(1):168. doi: 10.1186/s12955-017-0743-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Cho JK, Lee SH, Lee JY, Kang HS. Randomized controlled trial of training intensity in adiposity. Int J Sports Med. 2011;32(6):468-475. doi: 10.1055/s-0031-1271789 [DOI] [PubMed] [Google Scholar]
  • 48.Chow BC, Li S, Zhu X, et al. Effects of descending or ascending stair exercise on body composition, insulin sensitivity, and inflammatory markers in young Chinese women with obesity: a randomized controlled trial. J Sports Sci. 2021;39(5):496-502. doi: 10.1080/02640414.2020.1829362 [DOI] [PubMed] [Google Scholar]
  • 49.Christiansen T, Paulsen SK, Bruun JM, et al. Comparable reduction of the visceral adipose tissue depot after a diet-induced weight loss with or without aerobic exercise in obese subjects: a 12-week randomized intervention study. Eur J Endocrinol. 2009;160(5):759-767. doi: 10.1530/EJE-08-1009 [DOI] [PubMed] [Google Scholar]
  • 50.Coker RH, Williams RH, Kortebein PM, Sullivan DH, Evans WJ. Influence of exercise intensity on abdominal fat and adiponectin in elderly adults. Metab Syndr Relat Disord. 2009;7(4):363-368. doi: 10.1089/met.2008.0060 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Cooper JH, Collins BE, Adams DR, Robergs RA, Donges CE. Limited effects of endurance or interval training on visceral adipose tissue and systemic inflammation in sedentary middle-aged men. J Obes. 2016;2016:2479597. doi: 10.1155/2016/2479597 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Cornish S, Peeler J. The effect of a lower body positive pressure supported treadmill exercise regime on systemic biomarkers of inflammation and cartilage degradation in individuals with knee osteoarthritis: a pilot study. International Journal of Kinesiology and Sports Science. 2021;9(3):18-27. doi: 10.7575/aiac.ijkss.v.9n.3p18 [DOI] [Google Scholar]
  • 53.Cuff DJ, Meneilly GS, Martin A, Ignaszewski A, Tildesley HD, Frohlich JJ. Effective exercise modality to reduce insulin resistance in women with type 2 diabetes. Diabetes Care. 2003;26(11):2977-2982. doi: 10.2337/diacare.26.11.2977 [DOI] [PubMed] [Google Scholar]
  • 54.Dash C, Taylor TR, Makambi KH, Hicks J, Hagberg JM, Adams-Campbell LL. Effect of exercise on metabolic syndrome in black women by family history and predicted risk of breast cancer: the FIERCE study. Cancer. 2018;124(16):3355-3363. doi: 10.1002/cncr.31569 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Davidson LE, Hudson R, Kilpatrick K, et al. Effects of exercise modality on insulin resistance and functional limitation in older adults: a randomized controlled trial. Arch Intern Med. 2009;169(2):122-131. doi: 10.1001/archinternmed.2008.558 [DOI] [PubMed] [Google Scholar]
  • 56.Dengel DR, Pratley RE, Hagberg JM, Rogus EM, Goldberg AP. Distinct effects of aerobic exercise training and weight loss on glucose homeostasis in obese sedentary men. J Appl Physiol (1985). 1996;81(1):318-325. doi: 10.1152/jappl.1996.81.1.318 [DOI] [PubMed] [Google Scholar]
  • 57.Donges CE, Duffield R, Guelfi KJ, Smith GC, Adams DR, Edge JA. Comparative effects of single-mode vs. duration-matched concurrent exercise training on body composition, low-grade inflammation, and glucose regulation in sedentary, overweight, middle-aged men. Appl Physiol Nutr Metab. 2013;38(7):779-788. doi: 10.1139/apnm-2012-0443 [DOI] [PubMed] [Google Scholar]
  • 58.Donnelly JE, Honas JJ, Smith BK, et al. Aerobic exercise alone results in clinically significant weight loss for men and women: midwest exercise trial 2. Obesity (Silver Spring). 2013;21(3):E219-E228. doi: 10.1002/oby.20145 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Eizadi M, Bagheri G, Kasparast J, Zahedmanesh F, Afsharmand Z. Effects of training on body composition, blood lipids, and glucose homeostasis assessed by the homeostasis model assessment. Sci Sports. 2013;28(2):75-80. doi: 10.1016/j.scispo.2012.01.001 [DOI] [Google Scholar]
  • 60.Elsayed MM, Rabiee A, El Refaye GE, Elsisi HF. Aerobic exercise with Mediterranean-DASH Intervention for Neurodegenerative Delay diet promotes brain cells’ longevity despite sex hormone deficiency in postmenopausal women: a randomized controlled trial. Oxid Med Cell Longev. 2022;2022:4146742. doi: 10.1155/2022/4146742 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Ezpeleta M, Gabel K, Cienfuegos S, et al. Effect of alternate day fasting combined with aerobic exercise on non-alcoholic fatty liver disease: a randomized controlled trial. Cell Metab. 2023;35(1):56-70.e3. doi: 10.1016/j.cmet.2022.12.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Fenkci S, Sarsan A, Rota S, Ardic F. Effects of resistance or aerobic exercises on metabolic parameters in obese women who are not on a diet. Adv Ther. 2006;23(3):404-413. doi: 10.1007/BF02850161 [DOI] [PubMed] [Google Scholar]
  • 63.Fisher G, Hyatt TC, Hunter GR, Oster RA, Desmond RA, Gower BA. Effect of diet with and without exercise training on markers of inflammation and fat distribution in overweight women. Obesity (Silver Spring). 2011;19(6):1131-1136. doi: 10.1038/oby.2010.310 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Fogelholm M, Kukkonen-Harjula K, Nenonen A, Pasanen M. Effects of walking training on weight maintenance after a very-low-energy diet in premenopausal obese women: a randomized controlled trial. Arch Intern Med. 2000;160(14):2177-2184. doi: 10.1001/archinte.160.14.2177 [DOI] [PubMed] [Google Scholar]
  • 65.Foster-Schubert KE, Alfano CM, Duggan CR, et al. Effect of diet and exercise, alone or combined, on weight and body composition in overweight-to-obese postmenopausal women. Obesity (Silver Spring). 2012;20(8):1628-1638. doi: 10.1038/oby.2011.76 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Fu CP, Oczypok EE, Ali H, et al. Effect of physical activity in a weight loss program on circulating total ANGPTL8 concentrations in northern Americans with obesity: a prospective randomized controlled trial. Nutr Metab Cardiovasc Dis. 2022;32(7):1725-1733. doi: 10.1016/j.numecd.2022.04.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Geliebter A, Maher MM, Gerace L, Gutin B, Heymsfield SB, Hashim SA. Effects of strength or aerobic training on body composition, resting metabolic rate, and peak oxygen consumption in obese dieting subjects. Am J Clin Nutr. 1997;66(3):557-563. doi: 10.1093/ajcn/66.3.557 [DOI] [PubMed] [Google Scholar]
  • 68.Giannopoulou I, Fernhall B, Carhart R, et al. Effects of diet and/or exercise on the adipocytokine and inflammatory cytokine levels of postmenopausal women with type 2 diabetes. Metabolism. 2005;54(7):866-875. doi: 10.1016/j.metabol.2005.01.033 [DOI] [PubMed] [Google Scholar]
  • 69.Goodpaster BH, Delany JP, Otto AD, et al. Effects of diet and physical activity interventions on weight loss and cardiometabolic risk factors in severely obese adults: a randomized trial. JAMA. 2010;304(16):1795-1802. doi: 10.1001/jama.2010.1505 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Gram AS, Bladbjerg EM, Quist JS, Petersen MB, Rosenkilde M, Stallknecht B. Anti-inflammatory effects of active commuting and leisure time exercise in overweight and obese women and men: a randomized controlled trial. Atherosclerosis. 2017;265:318-324. doi: 10.1016/j.atherosclerosis.2017.06.923 [DOI] [PubMed] [Google Scholar]
  • 71.Gram B, Christensen R, Christiansen C, Gram J. Effects of Nordic walking and exercise in type 2 diabetes mellitus: a randomized controlled trial. Clin J Sport Med. 2010;20(5):355-361. doi: 10.1227/NEU.0b013e3181e56e0a [DOI] [PubMed] [Google Scholar]
  • 72.Gulsin GS, Swarbrick DJ, Athithan L, et al. Effects of low-energy diet or exercise on cardiovascular function in working-age adults with type 2 diabetes: a prospective, randomized, open-label, blinded end point trial. Diabetes Care. 2020;43(6):1300-1310. doi: 10.2337/dc20-0129 [DOI] [PubMed] [Google Scholar]
  • 73.Guzel Y, Atakan MM, Areta JL, Turnagol HH, Kosar SN. Ten weeks of low-volume walking training improve cardiometabolic health and body composition in sedentary postmenopausal women with obesity without affecting markers of bone metabolism. Res Sports Med. 2024;32(2):331-343. doi: 10.1080/15438627.2022.2113877 [DOI] [PubMed] [Google Scholar]
  • 74.Hara T, Fujiwara H, Nakao H, Mimura T, Yoshikawa T, Fujimoto S. Body composition is related to increase in plasma adiponectin levels rather than training in young obese men. Eur J Appl Physiol. 2005;94(5-6):520-526. doi: 10.1007/s00421-005-1374-8 [DOI] [PubMed] [Google Scholar]
  • 75.Hays NP, Starling RD, Sullivan DH, et al. Effects of an ad libitum, high carbohydrate diet and aerobic exercise training on insulin action and muscle metabolism in older men and women. J Gerontol A Biol Sci Med Sci. 2006;61(3):299-304. doi: 10.1093/gerona/61.3.299 [DOI] [PubMed] [Google Scholar]
  • 76.Herzig KH, Ahola R, Leppäluoto J, Jokelainen J, Jämsä T, Keinänen-Kiukaanniemi S. Light physical activity determined by a motion sensor decreases insulin resistance, improves lipid homeostasis and reduces visceral fat in high-risk subjects: PreDiabEx study RCT. Int J Obes (Lond). 2014;38(8):1089-1096. doi: 10.1038/ijo.2013.224 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Ho SS, Dhaliwal SS, Hills AP, Pal S. The effect of 12 weeks of aerobic, resistance or combination exercise training on cardiovascular risk factors in the overweight and obese in a randomized trial. BMC Public Health. 2012;12(1):704. doi: 10.1186/1471-2458-12-704 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Hong HR, Jeong JO, Kong JY, et al. Effect of walking exercise on abdominal fat, insulin resistance and serum cytokines in obese women. J Exerc Nutrition Biochem. 2014;18(3):277-285. doi: 10.5717/jenb.2014.18.3.277 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Irwin ML, Yasui Y, Ulrich CM, et al. Effect of exercise on total and intra-abdominal body fat in postmenopausal women: a randomized controlled trial. JAMA. 2003;289(3):323-330. doi: 10.1001/jama.289.3.323 [DOI] [PubMed] [Google Scholar]
  • 80.Jang SH, Paik IY, Ryu JH, Lee TH, Kim DE. Effects of aerobic and resistance exercises on circulating apelin-12 and apelin-36 concentrations in obese middle-aged women: a randomized controlled trial. BMC Womens Health. 2019;19(1):23. doi: 10.1186/s12905-019-0722-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Janssen I, Ross R. Effects of sex on the change in visceral, subcutaneous adipose tissue and skeletal muscle in response to weight loss. Int J Obes Relat Metab Disord. 1999;23(10):1035-1046. doi: 10.1038/sj.ijo.0801038 [DOI] [PubMed] [Google Scholar]
  • 82.Jung JY, Han KA, Ahn HJ, et al. Effects of aerobic exercise intensity on abdominal and thigh adipose tissue and skeletal muscle attenuation in overweight women with type 2 diabetes mellitus. Diabetes Metab J. 2012;36(3):211-221. doi: 10.4093/dmj.2012.36.3.211 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Jung JY, Min KW, Ahn HJ, et al. Arterial stiffness by aerobic exercise is related with aerobic capacity, physical activity energy expenditure and total fat but not with insulin sensitivity in obese female patients with type 2 diabetes. Diabetes Metab J. 2014;38(6):439-448. doi: 10.4093/dmj.2014.38.6.439 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Kadoglou NP, Iliadis F, Sailer N, et al. Exercise training ameliorates the effects of rosiglitazone on traditional and novel cardiovascular risk factors in patients with type 2 diabetes mellitus. Metabolism. 2010;59(4):599-607. doi: 10.1016/j.metabol.2009.09.002 [DOI] [PubMed] [Google Scholar]
  • 85.Kadoglou NP, Perrea D, Iliadis F, Angelopoulou N, Liapis C, Alevizos M. Exercise reduces resistin and inflammatory cytokines in patients with type 2 diabetes. Diabetes Care. 2007;30(3):719-721. doi: 10.2337/dc06-1149 [DOI] [PubMed] [Google Scholar]
  • 86.Kang SJ. Trekking exercise promotes cardiovascular health and fitness benefits in older obese women. J Exerc Rehabil. 2014;10(4):225-229. doi: 10.12965/jer.140136 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Kempen KP, Saris WH, Westerterp KR. Energy balance during an 8-wk energy-restricted diet with and without exercise in obese women. Am J Clin Nutr. 1995;62(4):722-729. doi: 10.1093/ajcn/62.4.722 [DOI] [PubMed] [Google Scholar]
  • 88.Kirk EP, Jacobsen DJ, Gibson C, Hill JO, Donnelly JE. Time course for changes in aerobic capacity and body composition in overweight men and women in response to long-term exercise: the Midwest Exercise Trial (MET). Int J Obes Relat Metab Disord. 2003;27(8):912-919. doi: 10.1038/sj.ijo.0802317 [DOI] [PubMed] [Google Scholar]
  • 89.Koo BK, Han KA, Ahn HJ, Jung JY, Kim HC, Min KW. The effects of total energy expenditure from all levels of physical activity vs. physical activity energy expenditure from moderate-to-vigorous activity on visceral fat and insulin sensitivity in obese type 2 diabetic women. Diabet Med. 2010;27(9):1088-1092. doi: 10.1111/j.1464-5491.2010.03045.x [DOI] [PubMed] [Google Scholar]
  • 90.Kraemer WJ, Volek JS, Clark KL, et al. Influence of exercise training on physiological and performance changes with weight loss in men. Med Sci Sports Exerc. 1999;31(9):1320-1329. doi: 10.1097/00005768-199909000-00014 [DOI] [PubMed] [Google Scholar]
  • 91.Ku YH, Han KA, Ahn H, et al. Resistance exercise did not alter intramuscular adipose tissue but reduced retinol-binding protein-4 concentration in individuals with type 2 diabetes mellitus. J Int Med Res. 2010;38(3):782-791. doi: 10.1177/147323001003800305 [DOI] [PubMed] [Google Scholar]
  • 92.Lanting S, Way K, Sabag A, et al. the efficacy of exercise training for cutaneous microvascular reactivity in the foot in people with diabetes and obesity: secondary analyses from a randomized controlled trial. J Clin Med. 2022;11(17):5018. doi: 10.3390/jcm11175018 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Lesser IA, Singer J, Hoogbruin A, et al. Effectiveness of exercise on visceral adipose tissue in older South Asian women. Med Sci Sports Exerc. 2016;48(7):1371-1378. doi: 10.1249/MSS.0000000000000906 [DOI] [PubMed] [Google Scholar]
  • 94.Mager U, Kolehmainen M, de Mello VD, et al. Expression of ghrelin gene in peripheral blood mononuclear cells and plasma ghrelin concentrations in patients with metabolic syndrome. Eur J Endocrinol. 2008;158(4):499-510. doi: 10.1530/EJE-07-0862 [DOI] [PubMed] [Google Scholar]
  • 95.Makiel K, Suder A, Targosz A, Maciejczyk M, Kozioł-Kozakowska A, Haim A. Impact of two types of exercise interventions on leptin and omentin concentrations and indicators of lipid and carbohydrate metabolism in males with metabolic syndrome. J Clin Med. 2023;12(8):2822. doi: 10.3390/jcm12082822 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Marks BL, Ward A, Morris DH, Castellani J, Rippe JM. Fat-free mass is maintained in women following a moderate diet and exercise program. Med Sci Sports Exerc. 1995;27(9):1243-1251. doi: 10.1249/00005768-199509000-00003 [DOI] [PubMed] [Google Scholar]
  • 97.Middlebrooke AR, Elston LM, Macleod KM, et al. Six months of aerobic exercise does not improve microvascular function in type 2 diabetes mellitus. Diabetologia. 2006;49(10):2263-2271. doi: 10.1007/s00125-006-0361-x [DOI] [PubMed] [Google Scholar]
  • 98.Moghadasi M, Mohebbi H, Rahmani-Nia F, Hassan-Nia S, Noroozi H, Pirooznia N. High-intensity endurance training improves adiponectin mRNA and plasma concentrations. Eur J Appl Physiol. 2012;112(4):1207-1214. doi: 10.1007/s00421-011-2073-2 [DOI] [PubMed] [Google Scholar]
  • 99.Mohanka M, Irwin M, Heckbert SR, et al. Serum lipoproteins in overweight/obese postmenopausal women: a one-year exercise trial. Med Sci Sports Exerc. 2006;38(2):231-239. doi: 10.1249/01.mss.0000184584.95000.e4 [DOI] [PubMed] [Google Scholar]
  • 100.Romero Moraleda B, Morencos E, Peinado AB, Bermejo L, Gómez Candela C, Benito PJ; PRONAF Study group . Can the exercise mode determine lipid profile improvements in obese patients? Nutr Hosp. 2013;28(3):607-617. [DOI] [PubMed] [Google Scholar]
  • 101.Nie J, Zhang H, Kong Z, et al. Impact of high-intensity interval training and moderate-intensity continuous training on resting and postexercise cardiac troponin T concentration. Exp Physiol. 2018;103(3):370-380. doi: 10.1113/EP086767 [DOI] [PubMed] [Google Scholar]
  • 102.Nishijima H, Satake K, Igarashi K, Morita N, Kanazawa N, Okita K. Effects of exercise in overweight Japanese with multiple cardiovascular risk factors. Med Sci Sports Exerc. 2007;39(6):926-933. doi: 10.1249/mss.0b013e3180383d84 [DOI] [PubMed] [Google Scholar]
  • 103.Pavlou KN, Steffee WP, Lerman RH, Burrows BA. Effects of dieting and exercise on lean body mass, oxygen uptake, and strength. Med Sci Sports Exerc. 1985;17(4):466-471. doi: 10.1249/00005768-198508000-00011 [DOI] [PubMed] [Google Scholar]
  • 104.Poon ETC, Siu PMF, Wongpipit W, Gibala M, Wong SHS. Alternating high-intensity interval training and continuous training is efficacious in improving cardiometabolic health in obese middle-aged men. J Exerc Sci Fit. 2022;20(1):40-47. doi: 10.1016/j.jesf.2021.11.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Potteiger JA, Jacobsen DJ, Donnelly JE, Hill JO; Midwest Exercise Trial . Glucose and insulin responses following 16 months of exercise training in overweight adults: the Midwest Exercise Trial. Metabolism. 2003;52(9):1175-1181. doi: 10.1016/S0026-0495(03)00146-X [DOI] [PubMed] [Google Scholar]
  • 106.Pugh CJ, Spring VS, Kemp GJ, et al. Exercise training reverses endothelial dysfunction in nonalcoholic fatty liver disease. Am J Physiol Heart Circ Physiol. 2014;307(9):H1298-H1306. doi: 10.1152/ajpheart.00306.2014 [DOI] [PubMed] [Google Scholar]
  • 107.Racette SB, Schoeller DA, Kushner RF, Neil KM. Exercise enhances dietary compliance during moderate energy restriction in obese women. Am J Clin Nutr. 1995;62(2):345-349. doi: 10.1093/ajcn/62.2.345 [DOI] [PubMed] [Google Scholar]
  • 108.Rezaeeshirazi R. Aerobic versus resistance training: Leptin and metabolic parameters improvement in type 2 diabetes obese men. Res Q Exerc Sport. 2022;93(3):537-547. doi: 10.1080/02701367.2021.1875111 [DOI] [PubMed] [Google Scholar]
  • 109.Rezende RE, Duarte SM, Stefano JT, et al. Randomized clinical trial: benefits of aerobic physical activity for 24 weeks in postmenopausal women with nonalcoholic fatty liver disease. Menopause. 2016;23(8):876-883. doi: 10.1097/GME.0000000000000647 [DOI] [PubMed] [Google Scholar]
  • 110.Rice B, Janssen I, Hudson R, Ross R. Effects of aerobic or resistance exercise and/or diet on glucose tolerance and plasma insulin levels in obese men. Diabetes Care. 1999;22(5):684-691. doi: 10.2337/diacare.22.5.684 [DOI] [PubMed] [Google Scholar]
  • 111.Roberson KB, Potiaumpai M, Widdowson K, et al. Effects of high-velocity circuit resistance and treadmill training on cardiometabolic risk, blood markers, and quality of life in older adults. Appl Physiol Nutr Metab. 2018;43(8):822-832. doi: 10.1139/apnm-2017-0807 [DOI] [PubMed] [Google Scholar]
  • 112.Ross R, Dagnone D, Jones PJ, et al. Reduction in obesity and related comorbid conditions after diet-induced weight loss or exercise-induced weight loss in men. a randomized, controlled trial. Ann Intern Med. 2000;133(2):92-103. doi: 10.7326/0003-4819-133-2-200007180-00008 [DOI] [PubMed] [Google Scholar]
  • 113.Ross R, Hudson R, Stotz PJ, Lam M. Effects of exercise amount and intensity on abdominal obesity and glucose tolerance in obese adults: a randomized trial. Ann Intern Med. 2015;162(5):325-334. doi: 10.7326/M14-1189 [DOI] [PubMed] [Google Scholar]
  • 114.Ryan AS, Ortmeyer HK, Sorkin JD. Exercise with calorie restriction improves insulin sensitivity and glycogen synthase activity in obese postmenopausal women with impaired glucose tolerance. Am J Physiol Endocrinol Metab. 2012;302(1):E145-E152. doi: 10.1152/ajpendo.00618.2010 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Saeidi A, Shishvan SR, Soltani M, et al. Differential effects of exercise programs on neuregulin 4, body composition and cardiometabolic risk factors in men with obesity. Front Physiol. 2022;12:797574. doi: 10.3389/fphys.2021.797574 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Said MA, Abdelmoneim MA, Alibrahim MS, Kotb AAH. Aerobic training, resistance training, or their combination as a means to fight against excess weight and metabolic syndrome in obese students—which is the most effective modality? a randomized controlled trial. Appl Physiol Nutr Metab. 2021;46(8):952-963. doi: 10.1139/apnm-2020-0972 [DOI] [PubMed] [Google Scholar]
  • 117.Saremi A, Shavandi N, Parastesh M, Daneshmand H. Twelve-week aerobic training decreases chemerin level and improves cardiometabolic risk factors in overweight and obese men. Asian J Sports Med. 2010;1(3):151-158. doi: 10.5812/asjsm.34860 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118.Sarsan A, Ardiç F, Özgen M, Topuz O, Sermez Y. The effects of aerobic and resistance exercises in obese women. Clin Rehabil. 2006;20(9):773-782. doi: 10.1177/0269215506070795 [DOI] [PubMed] [Google Scholar]
  • 119.Sigal RJ, Kenny GP, Boulé NG, et al. Effects of aerobic training, resistance training, or both on glycemic control in type 2 diabetes: a randomized trial. Ann Intern Med. 2007;147(6):357-369. doi: 10.7326/0003-4819-147-6-200709180-00005 [DOI] [PubMed] [Google Scholar]
  • 120.Slentz CA, Aiken LB, Houmard JA, et al. Inactivity, exercise, and visceral fat: STRRIDE: a randomized, controlled study of exercise intensity and amount. J Appl Physiol (1985). 2005;99(4):1613-1618. doi: 10.1152/japplphysiol.00124.2005 [DOI] [PubMed] [Google Scholar]
  • 121.Soori R, Rezaeian N, Khosravi N, et al. Effects of water-based endurance training, resistance training, and combined water and resistance training programs on visfatin and ICAM-1 levels in sedentary obese women. Sci Sports. 2017;32(3):144-151. doi: 10.1016/j.scispo.2016.12.004 [DOI] [Google Scholar]
  • 122.Swift DL, Nevels TR, Solar CA, et al. the effect of aerobic training and increasing nonexercise physical activity on cardiometabolic risk factors. Med Sci Sports Exerc. 2021;53(10):2152-2163. doi: 10.1249/MSS.0000000000002675 [DOI] [PubMed] [Google Scholar]
  • 123.Tok Ö, Kişioğlu SV, Ersöz HÖ, Kahveci B, Göktaş Z. Effects of increased physical activity and/or weight loss diet on serum myokine and adipokine levels in overweight adults with impaired glucose metabolism. J Diabetes Complications. 2021;35(5):107892. doi: 10.1016/j.jdiacomp.2021.107892 [DOI] [PubMed] [Google Scholar]
  • 124.Tokarenko O, Andreieva I, Tokarenko O, Surmilo M.. Effect of diet and exercise-induce weight loss on level of resistin in patient with obesity. Modern Medical Technology. 2021;(4):11-15. doi: 10.34287/MMT.4(51).2021.2 [DOI] [Google Scholar]
  • 125.Tseng ML, Ho CC, Chen SC, Huang YC, Lai CH, Liaw YP. A simple method for increasing levels of high-density lipoprotein cholesterol: a pilot study of combination aerobic- and resistance-exercise training. Int J Sport Nutr Exerc Metab. 2013;23(3):271-281. doi: 10.1123/ijsnem.23.3.271 [DOI] [PubMed] [Google Scholar]
  • 126.Utter AC, Nieman DC, Shannonhouse EM, Butterworth DE, Nieman CN. Influence of diet and/or exercise on body composition and cardiorespiratory fitness in obese women. Int J Sport Nutr. 1998;8(3):213-222. doi: 10.1123/ijsn.8.3.213 [DOI] [PubMed] [Google Scholar]
  • 127.van Aggel-Leijssen DP, Saris WH, Homan M, van Baak MA. The effect of exercise training on β-adrenergic stimulation of fat metabolism in obese men. Int J Obes Relat Metab Disord. 2001;25(1):16-23. doi: 10.1038/sj.ijo.0801470 [DOI] [PubMed] [Google Scholar]
  • 128.Venojärvi M, Wasenius N, Manderoos S, et al. Nordic walking decreased circulating chemerin and leptin concentrations in middle-aged men with impaired glucose regulation. Ann Med. 2013;45(2):162-170. doi: 10.3109/07853890.2012.727020 [DOI] [PubMed] [Google Scholar]
  • 129.Verity LS, Ismail AH. Effects of exercise on cardiovascular disease risk in women with NIDDM. Diabetes Res Clin Pract. 1989;6(1):27-35. doi: 10.1016/0168-8227(89)90054-5 [DOI] [PubMed] [Google Scholar]
  • 130.Villareal DT, Aguirre L, Gurney AB, et al. Aerobic or resistance exercise, or both, in dieting obese older adults. N Engl J Med. 2017;376(20):1943-1955. doi: 10.1056/NEJMoa1616338 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Wang J. Impacts of combining aerobic exercises with resistance training on chemerin level in obese undergraduates. Biomedical Research. 2017:654-658. [Google Scholar]
  • 132.Womack CJ, Harris DL, Katzel LI, Hagberg JM, Bleecker ER, Goldberg AP. Weight loss, not aerobic exercise, improves pulmonary function in older obese men. J Gerontol A Biol Sci Med Sci. 2000;55(8):M453-M457. doi: 10.1093/gerona/55.8.M453 [DOI] [PubMed] [Google Scholar]
  • 133.Wood PD, Stefanick ML, Williams PT, Haskell WL. The effects on plasma lipoproteins of a prudent weight-reducing diet, with or without exercise, in overweight men and women. N Engl J Med. 1991;325(7):461-466. doi: 10.1056/NEJM199108153250703 [DOI] [PubMed] [Google Scholar]
  • 134.Wu S, Park KS, McCormick JB. Effects of exercise training on fat loss and lean mass gain in Mexican-American and Korean premenopausal women. Int J Endocrinol. 2017;2017:5465869. doi: 10.1155/2017/5465869 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.You T, Berman DM, Ryan AS, Nicklas BJ. Effects of hypocaloric diet and exercise training on inflammation and adipocyte lipolysis in obese postmenopausal women. J Clin Endocrinol Metab. 2004;89(4):1739-1746. doi: 10.1210/jc.2003-031310 [DOI] [PubMed] [Google Scholar]
  • 136.Zhang H, KTong T, Qiu W, Wang J, Nie J, He Y. Effect of high-intensity interval training protocol on abdominal fat reduction in overweight Chinese women: a randomized controlled trial. Kinesiology. 2015;47(1):57-66. [Google Scholar]
  • 137.Zhang H, Tong TK, Qiu W, et al. Comparable effects of high-intensity interval training and prolonged continuous exercise training on abdominal visceral fat reduction in obese young women. J Diabetes Res. 2017;2017:5071740. doi: 10.1155/2017/5071740 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 138.Zhang HJ, He J, Pan LL, et al. Effects of moderate and vigorous exercise on nonalcoholic fatty liver disease: a randomized clinical trial. JAMA Intern Med. 2016;176(8):1074-1082. doi: 10.1001/jamainternmed.2016.3202 [DOI] [PubMed] [Google Scholar]
  • 139.Zhao XG, Huang HM, Du CY. Effect of a combination of aerobic exercise and dietary modification on liver function in overweight and obese men. J Mens Health. 2021;17(4):176-182. [Google Scholar]
  • 140.Donnelly JE, Hill JO, Jacobsen DJ, et al. Effects of a 16-month randomized controlled exercise trial on body weight and composition in young, overweight men and women: the Midwest Exercise Trial. Arch Intern Med. 2003;163(11):1343-1350. doi: 10.1001/archinte.163.11.1343 [DOI] [PubMed] [Google Scholar]
  • 141.Batrakoulis A, Jamurtas AZ, Metsios GS, 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. Circ Cardiovasc Qual Outcomes. 2022;15(6):e008243. doi: 10.1161/CIRCOUTCOMES.121.008243 [DOI] [PubMed] [Google Scholar]
  • 142.Rücker G, Schwarzer G, Carpenter JR, Schumacher M. Undue reliance on I(2) in assessing heterogeneity may mislead. BMC Med Res Methodol. 2008;8(1):79. doi: 10.1186/1471-2288-8-79 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 143.Iorio A, Spencer FA, Falavigna M, et al. Use of GRADE for assessment of evidence about prognosis: rating confidence in estimates of event rates in broad categories of patients. BMJ. 2015;350:h870. doi: 10.1136/bmj.h870 [DOI] [PubMed] [Google Scholar]
  • 144.Guyatt G, Zhao Y, Mayer M, et al. GRADE guidance 36: updates to GRADE’s approach to addressing inconsistency. J Clin Epidemiol. 2023;158:70-83. doi: 10.1016/j.jclinepi.2023.03.003 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplement 1.

eMethods 1. Detailed information on criteria applied for excluding studies

eMethods 2. Detailed information on systematic search, data extraction and risk of bias assessment

eMethods 3. Detailed information to evaluate the overall quality of the evidence using GRADE tool

eTable 1. Search strategy to find potential eligible trials for inclusion in the meta-analysis of supervised aerobic exercise and measures of body weight, waist and fat (April 2024)

eTable 2. Description of the ICEMAN domains and how to judge each domain

eTable 3. List of studies that were excluded via full text assessment

eTable 4. Characteristics of the trials included in the meta-analysis of aerobic exercise and measures of body weight, waist, and fat

eTable 5. Dropout, degree of adherence to the intervention program, and adverse events in the trials included in the meta-analysis of aerobic exercise and measures of body weight, waist, and fat

eTable 6. Risk of bias of the trials included in the meta-analysis of aerobic exercise and measures of body weight, waist and fat

eTable 7. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with body weight (kg)

eTable 8. Assessment of credibility of subgroup difference based on ICEMAN for body weight

eTable 9. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with waist circumference (cm)

eTable 10. Assessment of credibility of subgroup difference based on ICEMAN for waist circumference

eTable 11. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with body fat percentage (%)

eTable 12. Assessment of credibility of subgroup difference based on ICEMAN for body fat percentage

eTable 13. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with body fat mass (kg)

eTable 14. Assessment of credibility of subgroup difference based on ICEMAN for body fat mass

eTable 15. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with visceral adipose tissue (cm2)

eTable 16. Assessment of credibility of subgroup difference based on ICEMAN for visceral adipose tissue

eTable 17. Subgroup analyses of the association of supervised aerobic exercise (each 30 min/week) with subcutaneous adipose tissue (cm2)

eTable 18. Assessment of credibility of subgroup difference based on ICEMAN for visceral adipose tissue

eTable 19. The association of different doses of aerobic exercise with measures of body weight, waist and fat in adults with overweight or obesity (mean difference and 95%CI)

eTable 20. GRADE evidence for the association of aerobic exercise with measures of body weight, waist and fat

eFigure 1. Literature search and study selection process

eFigure 2. Absolute effect of aerobic exercise on adverse events in the study participants

eFigure 3. Relative effect of aerobic exercise on adverse events in the study participants

eFigure 4. Absolute effect of aerobic exercise on hypoglycemic reactions in the study participants

eFigure 5. Relative effect of aerobic exercise on hypoglycemic reactions in the study participants

eFigure 6. Association of aerobic exercise (30 min/week) with waist circumference (cm)

eFigure 7. Association of aerobic exercise (30 min/week) with body fat percentage (%)

eFigure 8. Association of aerobic exercise (30 min/week) with body fat mass (km)

eFigure 9. Association of aerobic exercise (30 min/week) with visceral adipose tissue (cm2)

eFigure 10. Association of aerobic exercise (30 min/week) with subcutaneous adipose tissue (cm2)

eFigure 11. Absolute effect of aerobic exercise on medication reduction

eFigure 12. Relative effect of aerobic exercise on medication reduction

eFigure 13. Effect of aerobic exercise on health-related quality of life (mental score)

eFigure 14. Effect of aerobic exercise on health-related quality of life (physical score)

eFigure 15. Dose-dependent association of aerobic exercise with visceral adipose tissue (cm2)

eFigure 16. Dose-dependent association of aerobic exercise with subcutaneous adipose tissue (cm2)

eFigure 17. Funnel plot of the association of aerobic exercise with body weight (Egger’s test = 0.42)

eFigure 18. Funnel plot of the association of aerobic exercise with waist circumference (Egger’s test = 0.21)

eFigure 19. Funnel plot of the association of aerobic exercise with body fat percentage (Egger’s test = 0.003)

eFigure 20. Funnel plot of the association of aerobic exercise with body fat mass (Egger’s test = 0.55)

eFigure 21. Funnel plot of the association of aerobic exercise with visceral adipose tissue (Egger’s test = 0.15)

eFigure 22. Funnel plot of the association of aerobic exercise with subcutaneous adipose tissue (Egger’s test <0.001)

Supplement 2.

Data Sharing Statement


Articles from JAMA Network Open are provided here courtesy of American Medical Association

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