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It is increasingly recognized that the location of excess adiposity, particularly increased deposition of visceral adipose tissue (VAT), is important when determining the adverse health effects of overweight and obesity. Exercise therapy is an integral component of obesity management, but the most potent exercise prescription for VAT benefit is unclear. We aimed to evaluate the independent and synergistic effects of aerobic exercise (AEx) and progressive resistance training (PRT) and to directly compare the efficacy of AEx and PRT for beneficial VAT modulation. A systematic review and meta-analysis was performed to assess the efficacy of exercise interventions on VAT content/volume in overweight and obese adults. Relevant databases were searched to November 2010. Included studies were randomized controlled designs in which AEx or PRT in isolation or combination were employed for 4 weeks or more in adult humans, where computed tomography (CT) or magnetic resonance imaging (MRI) was used for quantification of VAT pre- and post-intervention. Of the 12196 studies from the initial search, 35 were included. After removal of outliers, there was a significant pooled effect size (ES) for the comparison between AEx therapy and control (-0.33, 95% CI: -0.52 to -0.14; P < 0.01) but not for the comparison between PRT therapy and control (0.09, 95% CI: -0.17 to -0.36; P = 0.49). Of the available nine studies which directly compared AEx with PRT, the pooled ES did not reach statistical significance (ES = 0.23, 95% CI: -0.02 to 0.50; P = 0.07 favouring AEx). The pooled ES did not reach statistical significance for interventions that combined AEx and PRT therapy vs. control (-0.28, 95% CI: -0.69 to 0.14; P = 0.19), for which only seven studies were available. These data suggest that aerobic exercise is central for exercise programmes aimed at reducing VAT, and that aerobic exercise below current recommendations for overweight/obesity management may be sufficient for beneficial VAT modification. Further investigation is needed regarding the efficacy and feasibility of multi-modal training as a means of reducing VAT.
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Obesity Treatment/Management
A systematic review and meta-analysis of the effect of
aerobic vs. resistance exercise training on visceral fatobr_
931 68..9168..91
I. Ismail1, S. E. Keating1, M. K. Baker2,3 and N. A. Johnson1,3
1Discipline of Exercise and Sport Science,
University of Sydney, Sydney, New South
Wales, Australia; 2School of Exercise and
Health Sciences, Edith Cowan University,
Joondalup, Western Australia, Australia;
3Boden Institute of Obesity, Nutrition and
Exercise, University of Sydney, Sydney,
New South Wales, Australia
Received 19 June 2011; revised 25 July 2011;
accepted 26 July 2011
Address for correspondence: Dr N Johnson,
Discipline of Exercise and Sport Science,
Faculty of Health Sciences, The University of
Sydney, C42 Cumberland Campus,
Lidcombe, NSW 2141, Australia. E-mail:
nathan.johnson@sydney.edu.au
Summary
It is increasingly recognized that the location of excess adiposity, particularly
increased deposition of visceral adipose tissue (VAT), is important when deter-
mining the adverse health effects of overweight and obesity. Exercise therapy is an
integral component of obesity management, but the most potent exercise prescrip-
tion for VAT benefit is unclear. We aimed to evaluate the independent and
synergistic effects of aerobic exercise (AEx) and progressive resistance training
(PRT) and to directly compare the efficacy of AEx and PRT for beneficial VAT
modulation. A systematic review and meta-analysis was performed to assess the
efficacy of exercise interventions on VAT content/volume in overweight and obese
adults. Relevant databases were searched to November 2010. Included studies
were randomized controlled designs in which AEx or PRT in isolation or combi-
nation were employed for 4 weeks or more in adult humans, where computed
tomography (CT) or magnetic resonance imaging (MRI) was used for quantifi-
cation of VAT pre- and post-intervention. Of the 12196 studies from the initial
search, 35 were included. After removal of outliers, there was a significant pooled
effect size (ES) for the comparison between AEx therapy and control (-0.33, 95%
CI: -0.52 to -0.14; P<0.01) but not for the comparison between PRT therapy
and control (0.09, 95% CI: -0.17 to -0.36; P=0.49). Of the available nine
studies which directly compared AEx with PRT, the pooled ES did not reach
statistical significance (ES =0.23, 95% CI: -0.02 to 0.50; P=0.07 favouring
AEx). The pooled ES did not reach statistical significance for interventions that
combined AEx and PRT therapy vs. control (-0.28, 95% CI: -0.69 to 0.14;
P=0.19), for which only seven studies were available. These data suggest that
aerobic exercise is central for exercise programmes aimed at reducing VAT, and
that aerobic exercise below current recommendations for overweight/obesity
management may be sufficient for beneficial VAT modification. Further investi-
gation is needed regarding the efficacy and feasibility of multi-modal training as a
means of reducing VAT.
Keywords: Aerobic training,obesity,physical activity,strength training.
obesity reviews (2012) 13, 68–91
Financial support: none.
obesity reviews doi: 10.1111/j.1467-789X.2011.00931.x
68 © 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Introduction
The increased risk of cardiovascular and metabolic mor-
bidity and mortality as result of obesity has been well
described. However, it is increasingly recognized that
the location of excess adiposity, particularly increased
deposition of visceral adipose tissue (VAT), is of greater
importance in determining the adverse health effects of
overweight and obesity. VAT volume is an independent
predictor of elevated blood pressure (1), myocardial infarc-
tion (2) and insulin resistance (2–4). Lifestyle interventions
incorporating restriction of caloric intake and/or increased
energy expenditure via exercise reduce VAT content,
thereby ameliorating this risk. Serial quantification of VAT
content/volume by computed tomography (CT) and mag-
netic resonance imaging (MRI) has shown that the synergy
of aerobic exercise training and calorie restriction posi-
tively affects VAT content when weight loss approximating
4–9% of body weight is achieved (5), and larger reductions
in VAT have also been shown following a mean 10%
reduction in body weight (6).
Current physical activity recommendations suggest that
~250 min of weekly aerobic-type exercise is required for
body weight management (7) (8). The actual reduction of
weight (and body fat) with this dose of regular exercise in
overweight and obese individuals is often small (~2–3 kg)
but increases (~5–7.5 kg) with exercise levels up to
420 min/week (9–11). However, there is an emerging
acceptance that even with intensive programmes, weight
loss in excess of 3–4 kg is difficult to sustain (12–14),
highlighting the need for alternative strategies and further
rationale for promotion of VAT reduction as opposed to
weight loss per se. A systematic review of the available
randomized control trials to 2006 suggested that interven-
tions involving increased aerobic exercise can beneficially
alter VAT in overweight and obese individuals, and that
this may occur independent of weight loss (5). Recent
evidence has shown that aerobic exercise training (AEx)
programmes of lower energy expenditure than current
guidelines can induce a clinically significant reduction in
VAT, even in the absence of weight loss (15). Although
there are currently no guidelines for progressive resistance
exercise training (PRT) in the management of obesity, PRT
is known to positively affect insulin sensitivity and other
processes associated with VAT accumulation (16), and
there is evidence that despite incurring a significantly lower
energy expenditure than aerobic exercise therapy, PRT may
directly reduce VAT (5).
The aim of this study was to conduct a systematic review
with meta-analysis of randomized controlled trials to assess
the efficacy of exercise interventions on visceral adiposity in
adults. Specifically, we aimed to evaluate the effect of (i)
aerobic exercise therapy vs. control; (ii) PRT therapy vs.
control; (iii) aerobic exercise vs. PRT therapy; and (iv)
combined aerobic and PRT therapy vs. control on VAT
change. We hypothesized that, when compared with a
control condition, both aerobic and PRT therapies would
significantly reduce VAT. Secondly, we hypothesized that
aerobic exercise would have a greater effect than PRT
therapy on VAT. We further hypothesized that combined
aerobic exercise and PRT therapy would have a greater
effect on VAT than either therapy in isolation.
Methods
Design
Electronic database searches were performed in AMED,
MEDLINE, MEDLINE Daily Update, PREMEDLINE (via
OvidSP), SPORTDiscus, CINAHL (via EBSCO), EMBASE
and Web of Science from earliest record to November
2010. The search strategy combined terms covering the
areas of strength training, aerobic exercise training and
visceral fat (Fig. 1).
The database searches were performed using the key-
words: (strength training, weight training, resistance train-
ing, progressive training, progressive resistance, weight
lifting) or (aerobic exercise, endurance exercise, aerobic
training, endurance training, cardio training, exercise,
physical endurance, physical exertion) and (visceral,
abdominal fat, abdominal adiposity, abdominal lipid,
regional adiposity, intra-abdominal, adipose tissue distribu-
tion). Reference lists of all retrieved papers were manually
searched for potentially eligible papers. Randomized con-
trolled trials (RCTs) were reviewed while non-RCTs, uncon-
trolled trials and cross-sectional studies were excluded
from analysis. Manuscripts published in all languages were
included. Theses were not included in this systematic review.
Interventions
Studies were included if the exercise intervention was of 4
weeks or more. This cut-off was established to differentiate
studies examining the acute effects of exercise from those
examining training adaptations. Trials where participants
were randomized to an intervention involving either AEx
or PRT, or both, were included. Studies involving dietary
control/intervention were included only if the diet was the
same between the exercise and control groups.
Participants
Studies with adult participants greater than or equal to 18
years were considered. Studies of individuals with type 2
diabetes were included but those of HIV-infected popula-
tions were excluded because of specific medications affect-
ing abdominal fat (5).
obesity reviews Exercise for visceral fat I. Ismail et al.69
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Outcome measures
Studies were selected if the effect of exercise alone on visceral
fat was presented, and if computed tomography (CT) or
magnetic resonance imaging (MRI) was used for quantifi-
cation of visceral fat area/volume. Studies providing
outcome measures of visceral fatness/trunk adiposity using
any other method such as ultrasound or dual energy X-ray
absorptiometry (DXA) were excluded.
Selection of studies
After eliminating duplications, the search results were
screened by one investigator (II) against the eligibility cri-
teria, and those references which could not be eliminated
by title or abstract were retrieved and independently
reviewed by two reviewers (II, NJ) in an unblinded manner.
Disagreements were resolved by discussion or by a third
researcher (MB). In cases where journal articles contained
Figure 1 Flowchart of outcomes of search
strategy.
70 Exercise for visceral fat I. Ismail et al.obesity reviews
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
insufficient information, attempts were made to contact
authors to obtain missing details.
Data extraction and calculations
Data relating to participant characteristics (age, sex, body
mass index {BMI]} ), exercise details (mode of exercise,
nutritional intervention, exercise frequency, intensity, dura-
tion and intervention duration) and visceral fat quantifica-
tion (measurement technique and region) were extracted
independently by two researchers (II, SK), with disagree-
ments resolved by discussion or by a third researcher (NJ).
For one study which presented data graphically, mean and
standard deviation were estimated in duplicate manually.
One author was contacted and provided standard deviation
data that were missing from the study.
Assessment of methodological quality
Included studies met a minimum quality threshold, defined
as having met all inclusion criteria. Study quality was
further assessed by two researchers (II, SK) in a blinded
manner using a modified assessment scale created by
Downs & Black (17). The scale was modified to include
criteria for adequate description of control and whether
CT/MRI reliability for VAT quantification was reported.
Analyses
The between-trial standardized mean difference, or effect
size (ES) and 95% confidence intervals (CIs) were calcu-
lated. Between-study variability was examined using the I2
measure of inconsistency. This statistic, expressed as a per-
centage between 0–100, provides a measure of how much
of the variability between studies is due to heterogeneity
rather than chance. Publication bias was assessed by exam-
ining asymmetry of funnel plots (precision vs. ES) using
Egger’s test. Relationships were analyzed using simple
linear regression.
Meta-analyses
Pooled estimates of the effect of exercise on VAT, using ES,
were obtained using fixed- and random-effects models. We
presumed a correlation of 0.5 between outcomes measured
within each comparison group. If we identified studies
where there were two interventions of different exercise
intensity, the intervention of higher intensity was selected.
If we identified studies where there were two interventions
of identical exercise intensity, the intervention of highest
volume (exercise duration x weekly frequency) was
selected. We performed four analyses to compare the effect
of i) AEx vs. Control; ii) PRT vs. control; iii) AEx vs. PRT;
iv) combined AEx and PRT vs. control on VAT change. All
analyses were conducted using Comprehensive Meta-
analysis, version 2 (Biostat Inc, Englewood, NJ).
Results
Identification and selection of studies
The original search netted 12 196 studies. Three more
studies were found from the reference lists of the manu-
scripts retrieved. After removal of duplicates and elimina-
tion of papers based on the eligibility criteria, 35 studies
remained (Fig. 1).
Cohort characteristics
When combined, 2145 individuals (702 male; 1422 female;
21 not reported) participated in the trials (Table 1). Seven-
teen studies exclusively recruited female participants
(17–33), five studies exclusively recruited male participants
(34–38), with 11 studies recruiting both men and women
(9,39–48). Sex was not reported in one study (49). The mean
age of participants ranged from 28–83 years, and 11 studies
did not report mean age. On the basis of body mass index
(BMI) classification criteria (50), 18 studies had participants
who were classified on average as obese, 15 as overweight
and two within normal range. Fourteen studies specifically
recruited obese participants, nine studies recruited partici-
pants with type 2 diabetes, three studies with metabolic
syndrome and two studies recruited Asian-only cohorts.
Exercise characteristics
Cycle ergometry was the most common mode of AEx while
resistance training on a weight machine was most com-
monly used for PRT (Table 2). Within the 27 studies that
conducted AEx training, the frequency of AEx was most
commonly 3 d per week (10 of 27 studies) followed by 5 d
per week (7 of 27 studies). The frequency for PRT was
most commonly 3 d per week (9 of 13 studies), with three
studies training with PRT 2 d per week (20,21,33). Six
studies combined AEx and PRT training, three of which
conducted training on 3 d per week (18,46,48) and one
study conducted on 4 d (25), 5 d (23) and 6 d per week
(30), respectively.
Aerobic exercise intensities, expressed as a percentage
of maximal heart rate, percentage of heart rate reserve or
peak rate of oxygen consumption (VO2peak) ranged from
40–55% in initial weeks progressing to 60–90% in the final
weeks of the programmes. The most commonly prescribed
intensity was 60–75% of maximal heart which is classified
as ‘moderate intensity’. Rating of Perceived Exertion (RPE)
and metabolic equivalents (METs) were also used to
express intensity. The intensity of PRT, quantified as a
percentage of one-repetition maximum (1-RM) in most
obesity reviews Exercise for visceral fat I. Ismail et al.71
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Table 1 Participant characteristics
Reference Subjects % Male % Female Age BMI
Binder et al. 2005 (39) 91; Older sedentary with physical frailty C: 45% C: 55 C: 83.0(4.0) C: 26.0(4.0)
PRT: 47 PRT: 53 PRT: 83.0(3.0) PRT: 27.0(5.0)
Boudou et al. 2003 (34) 16; Men with type 2 diabetes 100.0 0.0 45.4(7.2) 29.6(4.6)
Brochu et al. 2009 (17) 107; Postmenopausal women 0 100 C: 58.0(4.7) C: 32.2(4.6)
Carr et al. 2005 (40) 62; Japanese-Americans with impaired
glucose tolerance
C: 53.1 C: 46.9 56.5(10.2) C: 26.6(2.5)
A: 40 A: 60 A: 25.7(4.5)
Coker et al. 2009 (41) 18; Overweight elderly 50 50 71.0(4.2) 30(4.2)
Cuff et al. 2003 (18) 28; Postmenopausal with type-2
diabetes
0 100 C: 60.0(8.7) C: 36.7(6.0)
A+PRT: 63.4 (7.0) A +PRT: 33.3(4.7)
A: 59.4 (5.7) A: 32.5(4.2)
DiPietro et al. 1998 (42) 16; Healthy older 18.8 81.3 73.0(4.0) C: 73.0(5.3)
A: 27.7(7.1)
Donnelly et al. 2003 (7) 74; Sedentary overweight and
moderately obese
41.9 58.1 C: Men: 24.0(4.0), Women: 21.0(4.0) C: Men: 29.0(3.0), Women: 29.3(2.3)
A: Men: 22.0(4.0), A: Men29.7(2.9),
Women: 24.0(5.0) Women: 28.7(3.2)
Giannopoulou et al. 2005
(19)
22; Obese post menopausal women
with type 2 diabetes
0 100 50–70 34.6(3.3)
Hunter et al. 2010 (20) 69; Healthy premenopausal women 0 100 C: 34.8(5.6) C: 23.9(1.1)
A: 34.7(8.4) A: 23.5(1.0)
PRT: 34.1(7.2) PRT: 23.9(1.0)
Ibanez et al. 2010 (21) 25; Obese women 0 100 C:54.4(5.5) C: 34.6(3.4)
PRT: 48.6(6.4) PRT: 35.0(3.1)
Irving et al. 2008 (22) 16; Obese women with metabolic
syndrome
0 100 51.0(9.0) 34.0(6.0)
Irwin et al. 2003 (23) 173; Overweight postmenopausal
women
0 100 C: 60.6(7.1) C: 30.6(3.8)
A+PRT: 61.0(6.9) A: +PRT 30.5(4.3)
Janssen et al. 1999 (43) 60; Upper body obese 50 50 Male: C: 45.6 (6.6); A: 47.4 (6.6); PRT:
37.9 (13.3)
Male: C: 31.6(2.8); A: 33.0(3.5); PRT:
33.6(4.4)
Female: C: 39.6(7.6); A: 39.0(6.3); PRT:
37.3(4.4)
Female: C: 34.5(4.4); A: 35.5 (6.6);
PRT: 32.5 (4.7)
Janssen et al. 2002 (24) 38; Premenopausal obese women 0 100 C: 40.1(6.7) C: 33.7(4.1)
A: 37.5(6.0) A: 36.0(7.1)
PRT: 34.8(5.8) PRT: 31.6(4.3)
Johnson et al. 2009 (14) 19; Obese sedentary 68.0 32.0 C: 47.3(9.5) 31.1(2.9)
Kim et al. 2008 (25) 20; Women of advanced age with
metabolic syndrome
0 100 >75 C: 25.7(2.8)
A+PRT: 26.0(2.4)
Ku et al. 2010 (26) 44; Overweight Korean women with
type 2 diabetes
0 100 C: 57.8 (8.1) C: 27.4(2.8)
A: 55.7(7.0) A:27.1(2.4)
PRT:55.7(6.2) PRT: 27.1(2.3)
Kwon et al. 2010 (27) 28; Overweight type 2 diabetics 0 100 56.4 (7.1) 27.4(2.5)
Kwon et al. 2010 (28) 27;Obese type 2 diabetics 0 100 56.6(8) 27.3(2.7)
McTiernan et al. 2007 (44) 202; Sedentary 50.5 49.5 C: Men: 56.6(7.6), Women: 53.7(5.6) C: Men: 30.1(4.8), Women: 28.5(4.8)
A: Men: 56.2(6.7), Women: 54(7.1) A: Men: 29.7(3.7), Women: 28.9(5.5)
Mourier et al. 1997 (49) 21; NIIDM NR 45.0(9.8) 30.2(4.4)
Nicklas et al. 2009 (29) 72; Overweight and obese
postmenopausal women
0 100 C: 58.4(6.0) C: 33.9(4.0)
A: 59.0(5.0) A: 32.9(3.7)
Park et al. 2003 (30) 30; Middle-aged obese women 0 100 C: 43.1(1.7) C: 25.5(0.9)
A: 42.2(1.9) A: 25.3(1.7)
A+PRT: 43.4(1.0) A +PRT: 25.8(1.4)
Poehlman et al. 2000 (31) 51; Non-obese younger women 0 100 C:28.0(4.0) C: 22.0(2.0)
A:29.0(5.0) A: 22.0(2.0)
PRT: 28.0(3.0) PRT: 22.0(2.0)
Rice et al. 1999 (35) 29; Obese men 100 0 C: 44.4(6.1) C: 31.9(2.8)
A: 47.4(6.1) A: 32.2(3.7)
PRT: 39.8(13.2) PRT: 33.8(4.2)
72 Exercise for visceral fat I. Ismail et al.obesity reviews
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
studies (17,20,21,25,27,30,31,39,48) ranged between
30–100% 1 RM. Two studies (24,43) prescribed one set of
8–12 repetitions until volitional fatigue.
Ten studies stated that diet was not controlled, nine
studies required participants to recall/record diet and
analysis was reported, and eight studies required the par-
ticipants to follow a prescribed diet. Eight studies did not
report on dietary intervention or control.
Methodological quality
Assessment of the study quality is presented in Table 3. All
included studies specified their hypotheses, main outcomes,
participant characteristics, interventions, main findings,
variability estimates, statistical tests, accuracy of measures
and randomization procedure. Eight studies did not report
adverse events while five studies did not provide an
adequate description of the control group. Eighteen studies
reported the reliability of the VAT measure. Only two
studies made an attempt to blind study participants to the
intervention they received (15,49), and only two studies
made an attempt to blind those measuring the main
outcome of the intervention (15,46).
Study outcomes
All studies provided sufficient data to enable calculation
of mean differences, ES and 95% CIs (Table 4). For AEx,
26 of the 29 studies showed an ES favouring aerobic
exercise therapy, ranging from – 0.07 to -6.09. Five of
these studies showed a statistically significant effect
for aerobic exercise. None of the four studies with an
ES favouring the control intervention (ES range: 0.10–
0.61) reached statistical significance. For PRT, seven
of the 14 studies showed an ES favouring resistance
exercise training, ranging from -0.04 to -0.58, with only
one of these studies showing a statistically significant
effect for resistance exercise. Five studies favoured the
control intervention vs. resistance exercise (ES range:
0.13–1.67), with two of these reaching statistical signifi-
cance. Of the nine studies comparing AEx with PRT,
seven favoured aerobic exercise vs. resistance training,
ranging from 0.02 to 1.02, two of which were statistically
significant. None of the two studies which reported an
ES favouring resistance training vs. aerobic exercise
reached statistical significance. Six of the seven studies
which combined AEx with PRT, reported an ES favouring
the intervention group, half of these reached statistical
significance (range: -0.13 to -4.62). One study showed a
statistically significant ES for control vs. combined AEx
plus PRT.
A linear regression analysis was performed to assess the
relationship between VAT reduction and change in weight
in all of the exercise groups (AEx, PRT and AEx +PRT). A
significant relationship between VAT reduction and weight
loss was found (r =0.42, P=0.014).
Table 1 Continued
Reference Subjects % Male % Female Age BMI
Ross et al. 2000 (36) 24; Obese men 100 0 C: 46.0 (10.9) C: 30.7(1.9)
A: 45.0 (7.5) A:32.3(1.9)
Ross et al. 2004 (32) 27; Premenopausal women with
abdominal obesity
0 100 C: 43.7(6.4) C: 32.4(2.8)
A:43.2(5.1) A: 32.8(3.9)
Ross et al. 1996 (37) 33; Obese men 100 0 C: 46.8(7.6) C: 31.6(2.7)
A: 47.6(6.4) A: 32.6(3.6)
PRT: 39.0(12.9) PRT: 33.5(4.1)
Schmitz et al. 2007 (33) 133; Overweight or obese 0 100 C: 36.0(6.0) C: 29.4 (0.4)
PRT: 37.0(5.0) PRT: 29.4 (0.4)
Short et al. 2003 (45) 102; Healthy sedentary men and
women
52 48 21–87 C: 25.7(2.4)
A:26.6 (1.8)
Sigal et al. 2007 (46) 251; Type 2 diabetes 63.7 36.3 C: 54.8(7.2) C: 35.0(9.5)
A: 53.9(6.6) A: 35.6(10.1)
PRT:54.7(7.5) PRT: 34.1(9.6)
A+PRT: 53.5(7.3) A +PRT: 35.0 (9.6)
Slentz et al. 2005 (47) 89; Sedentary overweight with mild to
moderate dyslipidemia
52 48 C: 52.7(6.5) C: 29.6(3.0)
A: 51.5(5.3) A: 29.1(2.4)
Stewart et al. 2005 (48) 104; 49 51 63.6(5.7) C: Male: 29.7(3.8), Female: 29.6(6.1)
A+PRT: Male: 29.7(3.0),
Thong et al. 2000 (38) 24; Obese men 100 0 C: 46.0(10.7) C: 30.7(1.7)
A: 45.0(7.6) A: 32.3(2.0)
All data reported as means SD. Studies reporting age and BMI as range only are reported in that format.
BMI, body mass index; A, aerobic exercise training; PRT, progressive resistance training; C, controls; NR, not reported.
obesity reviews Exercise for visceral fat I. Ismail et al.73
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Table 2 Exercise details
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Binder et al.
2005 (39)
C: n=38; 9 of 22 exercises in
phase 1, primary focus on
flexibility.
Supplemental calcium and
vitamin D
0.0(0.0) 2–3/7 6 months
PRT: n=53; Phase 1: flexibility,
balance coordination, speed of
reaction. Phase 2: PRT, knee
extension, flexion, seated bench
press, seated row, leg press,
biceps curl on weightlifting
machine. +shortened version of
phase 1.
0.0(0.0) 3/7 for 36
sessions/each phase.
Phase 2: PRT, 1–2 sets of 6–8 reps
at 65% of 1 RM to progress to 3
sets of 8–12 at 85–100% of initial
1RM
Phase 2: 60–90 min 6 months: 3
months/phase
Boudou et al.
2003 (34)
C: n=8; bicycle ergometer at
60 rpm
Maintain usual diet (~50%
CHO, 30% lipids, 20%
proteins).
-1.7(16.1) 1/7 Low intensity (30 W) 20 min 8 weeks
A: n=8; bicycle ergometer -1.9(19.2) 3/7 Continuous 75% VO2peak 2/7 and
intermittent exercise at 85%:50%
for 2 min:3 min, respectively, 1/7
Continuous: 45 min;
Intermittent: NR
Brochu et al.
2009 (17)
C: n=71 55% CHO; 30% fat; 15%
protein
-5.1(4.7) 3/7 NR NR 6 months
PRT: n=36; leg press, chest
press, lat pull down, shoulder
press, arm curls, triceps
extensions
-5.8(4.9) Four progressive phases:
1 (3 weeks): 15 reps/65% 1 RM,
2–3 sets per exercise, 90–120 s
rest b/w sets
2 (5 weeks): 12 reps/70% 1 RM,
2–3 sets per exercise, 90 s rest
b/w sets3 (9 weeks):
10 reps/75–80% 1 RM, 2–4 sets
per exercise, 120–180 s rest b/w
sets
4 (8 weeks): 10–12 reps/70–75%
1 RM, 2–4 sets per exercise
60–90 s rest b/w sets.
Carr et al. 2005
(40)
C: n=32: Stretching exercises Isocaloric with 30% fat (<7%
saturated), 50% CHO, 20%
protein with <300 mg
cholesterol/d
0.6 (2.8) 3/7 NR 60 min 24 months
A: n=32; walking or jogging on a
treadmill
Isocaloric with 30% fat (10%
saturated), 55% CHO, 15%
protein with <200 mg
cholesterol/d
-1.8(2.7) 3/7 70% HRR
74 Exercise for visceral fat I. Ismail et al.obesity reviews
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Coker et al. 2009
(41)
C: n=6 Mixed diet (35% fat, 20%
protein, 45% CHO) during 4 d
controlled feeding prior to
baseline and post intervention
testing period
NR Maintain habitual
physical activity
12 weeks
A: n=6; cycle ergometer NR 4–5/7 75% of VO2peak
Caloric expenditure matched at
1,000 kcal/7
NR
Cuff et al. 2003
(18)
C: n=9
A+PRT n=10 Aerobic exercise
on treadmills, stationary bicycles,
recumbent steppers, ellipitical
trainers and rowing machines.
Resistance training on leg press,
leg curl, hip extension, chest
press, latissimus pulldown
A: n=9 as above exercise with
low impact low intensity dynamic
movement
Continue with current diet
patterns
2.0(3.6)
-2.9(4.1)
-1.2(2.1)
Continue with current
physical activity
patterns
3/7
3/7
A: 60–75% HRR;
PRT: 2 sets of 12 reps.
A: 60–75% HRR
75 min
75 min
16 weeks
DiPietro et al.
1998 (42)
C: n=7; stretching, yoga, stretch
bands
NR 0.0(15.0) 4/7 HR did not exceed 90 bpm 60 min 4 months
A: n=9; mini trampoline -1.0(19.2) 4/7 55–60% HR max for 1 month; 75%
HR max for 3 months
20–40 min 1st month
progressing to 60 min for
3 months
Donnelly et al.
2003 (7)
C: n=33; Maintain usual dietary intake M: -0.5(16.3)
F: 2.9(12.3)
NR Maintain usual physical activity 16 months
A: n=41; Treadmill, stationary
bike or elliptical trainer
M: -5.2(15.8)
F: 0.6(17.1)
60% HRR at baseline to 75% at 6
months
20 min at baseline to
45 min at 6 months
Giannopoulou
et al. 2005 (19)
C: n=11; Hypocaloric
monounsaturated fat diet (40%
fat (30% monounsaturated, 5%
polyunsaturated, 5% saturated),
40% CHO (15% simple, 25%
complex) and 20% protein with
600 kcal/d deficit.
A: n=11 walking
40% fat, 40% CHO, 20%
protein
3.6(27.2)
-5.5(27.2)
Refrain from any type
of regular physical
activity during study
3/7 65–70% VO2peak 50 min
14 weeks
obesity reviews Exercise for visceral fat I. Ismail et al.75
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Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Hunter et al.
2010 (20)
C: n=30 800 k/cal per day (20–22% fat,
18–22% protein, 58–62%
CHO)
6.4(9.4) NR 1 year
A: n=18; walking or jogging on a
treadmill
PRT: n=21; squats, leg
extension, leg curl, elbow flexion,
triceps extension, lateral pull
down, bench press, military
press, lower back extension, bent
leg sit ups
3.1(8.8)
3.9(11.5)
2–3/7 Week 1: 67% HR max progressing
to 80% HR max in week 8.
Week 1–4: 1 set of 10 reps then 2
sets of 10 reps. 2 min rest
between sets; 80% of 1 RM
20–40 min
NR
Ibáñez et al.
2010 (21)
C: Diet only
PRT: n=13; Diet +bilateral leg
press, bilateral knee extension,
bench press, and 4–5 exercises
for main muscle groups of body;
all on resistance machines
55% CHO, 15% protein, 30%
fat, 500 kcal/d
-5.7(20.7) NR 16 weeks
-7.1(16.7) 2/7 Week 1–8: 50–70% 1 RM; Week
9–16: 70–80% 1 RM +20% of leg
extensor and bench press sets
with 30–50% 1 RM.
45–60 min
Irving et al. 2008
(22)
C: n=7; NR -0.9(15.4) Maintain current level of physical activity 16 weeks
A: n=9; Walk/run on indoor or
outdoor track
-3.5(24.0) Weeks 1–2: 3/7
Weeks 3–4: 4/7
Weeks 5–16: 5/7
RPE 15–17 on 3/7 and 10–12 on
2/7
Time to expend 300 kcal
in weeks 1–2, 350 kcal in
weeks 3–4, and 400 kcal
in weeks 5–16
Irwin et al. 2003
(23)
C: n=86; stretching sessions Maintain usual diet 0.1 (NR) 1/7 NR 45 min 12 months
A+PRT: n=87; A: treadmill
walking, stationary bike. PRT: leg
extensions, leg curls, leg press,
chest press, seated dumbbell
row.
-1.3 (NR) 5/7 A: 40% HR max progressing to
60–75% HR max by week 8
PRT: 2 sets of 10 reps
45 min
Janssen et al.
1999 (43)
C: n=20; Diet only Weight maintenance energy
intake reduces by
1,000 kcal/d. Limit dietary fat
intake to <30%.
M: -11.7(3.5)
F: -10.7(3.8)
NR 16 weeks
A: n=20; brisk walking on a
treadmill, stationary cycling or
stair stepping
PRT: n=20; Leg extension, leg
flexion, super pullover (latissimus
dorsi), bench press, shoulder
press, triceps extension, bicep
curl and sit ups
M: -11.4(3.8)
F: -11.5(3.2)
M: -12.7(3.8)
F: -10.0(2.8)
5/7
3/7
50–85% MHR
1 set of 8–12 reps to volitional
fatigue
15 min progressing to
maximum of 60 min.
30 min
76 Exercise for visceral fat I. Ismail et al.obesity reviews
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Janssen et al.
2002 (24)
C: n=13; dietary intervention Reduce weight maintenance
energy intake by 1,000 kcal/d,
limit dietary fat intake to <30%
-10.0(3.9) Maintain pre-study physical activity levels. 16 weeks
A: n=11; dietary
intervention +treadmill, cycle
ergometer or stair stepping.
PRT: n=14; dietary
intervention +leg extension, leg
flexion, super pullover, bench
press, shoulder press, triceps
extension, biceps curl, sit ups.
-11.1(4.4)
-10.0(3.0)
5/7
3/7
50% progressing to 85% of HR
max
1 set of 8–12 reps until volitional
fatigue
15 min progressing to
60 min.
Approx. 30 min
Johnson et al.
2009 (15)
C: n=7; stretching Consume habitual diet
for 3 d before and after
intervention provided with diet
(60% CHO, 20% protein, 20%
fat)
-0.2(16.2) 3/7 30 min 4 weeks
A: n=12; cycle ergometer -0.3(19.2) 3/7 Week 1: 50% VO2peak
Week 2: 60% VO2peak
Week 3&4: 70% VO2peak
30–45 min (15 min bouts
with intervening 5 min
rests)
Kim et al. 2008
(25)
C: n=10 NR 0.57(8.8) NR 12 weeks
A+PRT: n=10; A: speedy
walking, V step, Cha cha step,
Mambo step, step aerobics, Gait
training with dance. PRT: Push
up, sit up, sit down and up, leg
raise, leg extension, leg curl, leg
press on free weights. Asana
Yoga
-0.3(8.8) 4/7 Week 1: -4: 40–55% HRR, week
5–8: 55–65%, week 9–12: 65–75%
PRT 75% 1 RM
60 min; 30 min aerobics,
15 min Resistance, 15 min
Yoga
Ku et al. 2010
(26)
C: n=16; diabetes education Maintain standard calorific
intake (ideal body weight
(kg) ¥30 kcal/kg/d)
-0.6(1.7) Maintain sedentary
lifestyle
A: n=15; walking -1.9(1.2) 5/7 3.6–5.2 METs 60 min 12 weeks
PRT: n=13; elastic band
exercises including bicep curl,
triceps extension, upright row,
shoulder chest press, trunk side
bending, seated row, leg press,
hip flexion, leg flexion, leg
extension
-1.1(1.3) 40–50% max 3 sets, 15–20 reps
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Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Kwon et al. 2010
(27)
C: n=15
PRT: n=13; Bicep curls, triceps
extensions, upright rows,
shoulder press, chest press,
seated rows, leg press, hip
flexion, leg flexion, leg extension,
side bends with resistance bands
NR 0.7(10.5)
1.1(6.4)
No exercise
3/7 40–50% 1 RM
3 sets 10-15 reps for
40 min plus 10 min warm
up and cool down
12 weeks
Kwon et al. 2010
(28)
C: n=14 NR NR Maintain routine activity 12 weeks
A: n=13; Walking NR 5/7 Anaerobic threshold 60 min
McTiernan et al.
2007 (44)
C: n=102 Asked not to change dietary
habits
M: -0.1(25.2)
F: 0.7(18.6)
Asked not to change
exercise habits
12 months
A: n=100; Treadmills, stationary
bikes, elliptical machines and
rowers
M: -1.8(21.0)
F: -1.4(24.9)
6/7 60–85% HR max 60 min
Mourier et al.
1997 (49)
C: n=11 Maintain usual diet
50% of C and A group
supplemented with BCAA
(46% leucine, 24% isoleucine,
30% valine; protein intake
0.6 g/kg/d)
0.2(21.4) 1/7 Low intensity 20 min–45 min 2 weeks
pre-training
8 weeks
A: n=10; Ergocycle -1.5(17.3) Pre-training 3/7
Trial: 2/7 continuous
exercise
1/7
intermittent
Pre-training
75%
Continuous: 75%V02peak
Intermittent
85% V02peak
for 2 min 50% V02peak
for 3 min x five exercises
NR
Continuous: 45 min
NR
Nicklas et al.
2009 (53)
C: n=34; Calorie restriction Total calorie deficit of
400 kcal/d, 25–30% fat,
15–20% protein, 50–60% CHO
-11.8(4.1) Not to alter sedentary lifestyle 20 weeks
A: n=38; Calorie
restriction +treadmill walking
-12.3(4.9) 3/7 70–75% HRR 10–15 min progressing to
30 min by end of 6th
week
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Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Park et al. 2003
(30)
C: n=10 NR 0.6(2.3) NR 24 weeks
A: n=10; Aerobics: week 1–12:
side by side, step touch, lunge
side, v-step, grape vine, pivot
turn, Cha cha, Mambo rock,
diamond step, single hamstring
walking, heel touch, sit up, push
up. Week 13–24: fast walking,
turn round, heel side, knee up,
scissor double, hop and jump,
jumping jack, side kick, full turn,
double kick
-4.7(4.7) 6/7 60–70% HR max 60 min
A+PRT: n=10; Aerobic
programme +bench press, side
raise, tricep push down, barbell
curl, leg curl, leg extension, leg
press, leg raise, abdominal
crunch, latissimus pull down
-6.4(6.6) 6/7 A (3/7) 60–70% HR max
PRT (3/7) Week 1–12 60% 1 RM,
Week 13–24 70% 1 RM
Poehlman et al.
2000 (31)
C: n=20 NR 1.0(10.6) NR 6 months
A: n=14; jogging 0.0(7.1) 3/7 Weeks 1–16: 5% increase in HR
max each week progressing to
90% HR max
Weeks 17–28:
Mon: 80% HR max
Wed: 95% HR max
Fri: 75–80% HR max.
By last session at 85% HRmax
Weeks 1–16: 25 min
progressing to 40 min
Weeks 17–28:
Mon: 45 min
Wed: 4 ¥5 min bouts with
3 min rests
Fri: 45 min.
By last session: 60 min
PRT: n=17; leg press, bench
press, leg extension, shoulder
press, sit up, seated row, tricep
extension, arm curls, leg curls
2.0(8.5) 3 sets 10 reps, 1–1.5 min between
sets
80% 1 RM
Rice et al. 1999 C: n=9; diet intervention only Energy intake reduced by
1,000 kcal/d, limit dietary fat
intake to <30%
-12.1(3.4) NR 16 weeks
A: n=10; diet
intervention +treadmill walking,
stationary cycle or stair stepping
-11.5(3.9) 5/7 19 min progressing to 60 min 50% progressing to
85%HR max
PRT: n=10; diet
intervention +leg extension, leg
flexion, super pullover, bench
press, shoulder press, triceps
extension, biceps curl, sit ups
-13.6(4.1) 3/7 1 set of 8–12 reps ~30 min
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Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Ross et al. 2000
(36)
C: n=8; Maintain body weight Weight maintenance diet
(55–60% CHO, 15–20%
protein, 20–25% fat) for 4- to
5-week baseline period
0.1(NR) NR 12 weeks
A: n=16; Brisk walking or light
jogging on motorized treadmill.
maintain isocaloric diet and
perform exercise that expended
700 kcal/d
-7.5(NR) 7/7 <70% VO2peak (80% MHR) Time taken to expend
700 kcal
Ross et al. 2004
(32)
C: n=10; Maintain body weight
A: n=17; Brisk walking or light
jogging on motorized treadmill;
maintain isocaloric diet and
expend 500 kcal/d with exercise
Weight maintenance diet
(50–60% CHO, 15–20%
protein, 20–30% fat) for 4- to
5-week baseline period
0.5(11. 0)
-5.9(15.3)
NR
7/7
80% of HRmax Time required to expend
500 kcal.
14 weeks
Ross et al. 1996
(37)
C: n=11; Diet intervention only Energy intake reduced by
1,000 kcal/d and limit dietary
fat intake to <30% of total
energy intake
-11.4(3.5) NR 16 weeks
A: n=11; Diet
intervention +stationary cycle,
treadmill or stair stepping
PRT: n=11; Diet
intervention +leg extension, leg
flexion, superpullover, chest
press and cross, shoulder press,
triceps extension and biceps curl
on Nautilus weight training
stations and Sit ups
-11.6(3.7)
-13.2(4.1)
5/7
3/7
NR
1 set of 12 reps
15 min progressing to
60 min.
NR
Schmitz et al.
2007 (33)
C: n=63; Walking programme as
per AHA guidelines
PRT: n=70; isotonic variable
resistance machines and free-
weight exercises for quadriceps,
hamstrings, gluteal, pectoral,
erector spinae, latissimus dorsi,
rhomboid, deltoid, bicpes, triceps
No changes to diet 2.0(0.7)
1.4(0.6)
Most days of the
week
2/7
Moderate intensity
Year 1: 3 sets, 8–10 reps
Year 2: 2 sets and maintain the
highest weight lifted each exercise
30 min
Year 1: 1 h
Year 2: 45 min
2 years
80 Exercise for visceral fat I. Ismail et al.obesity reviews
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Table 2 Continued
Reference Mode Nutritional intervention Weight
change
(kg)
Frequency Intensity Session duration Intervention
duration
Short et al. 2003
(45)
C: n=37 Weight maintaining diet
(55%CHO, 30%fat and 15%
protein)
0.3(17.3) Flexibility exercises to perform at home; maintain regular lifestyle 16 weeks
A: n=65; stationary bicycle -1.5(18.2) 3/7 progressing to 4/7 70% HR max progressing to 80%
HR max
20 min progressing to
40 min
Sigal et al. 2007
(46)
C: n=63 Recommended diet that would
not cause weight loss.
Prescribed energy
intake 90% estimated
weight maintenance
requirement
-0.3(39.9) Revert to pre-study
activity levels
26 weeks
A: n=60; treadmills or bicycle
ergometers
-2.6(43.3) 3/7 60–75% HR max 15–45 min
PRT: n=64; 7 different machine
weight exercises
-0.8(43.0) 2–3 sets of 7–9 reps NR
A+PRT: n=64 -2.6(43.0) Combined aerobic and resistance training programmes
Slentz et al. 2005
(47)
C: n=47 Not to diet/change their diet 0.87(NR) NR 6 months
A: n=42; treadmills, elliptical
trainers, cycle ergometers
-2.3(NR) Equivalent to jogging
20 miles/week
65–80% VO2peak Expend 23 kcal/kg/week 8 months
Stewart et al.
2005 (48)
C: n=53
A+PRT: n=51; aerobic:
treadmill, stationary cycle, stair
stepper; PRT: bench press,
shoulder press, seated
mid-rowing, lat-pulldown, leg
extension, leg curl, leg press
AHA Step 1 diet; Maintain
normal caloric intake
M: -0.63
F: -0.5(2.3)
National Institute of Aging Guidelines for Exercise 6 months
M: -2.2(2.7)
F: -2.3(3.4)
3/7 A: 60–90% HR max
PRT: 2 sets, 10–15 reps of 50%
1RM
A: 45 min
PRT: NR
Thong et al. 2000
(38)
C: n=8 Weight maintenance diet for
4–5-week baseline period
consisting of 55–60% CHO,
15–20% protein, 20–25% fat
0.1(0.8) NR 12 weeks
A: n=14; Perform exercise that
expended 700 kcal/d; brisk
walking or light jogging on a
motorized treadmill
Matched exercise expenditure
with additional 700 kcal/d
-7.6(0.4) 7/7 80% HR max Time required to expend
700 kcal
n, number of subjects; mg, milligram, kcal, kilocalorie, BMI, body mass index; A, aerobic training; PRT, progressive resistance training; C, controls; NR, not reported; HRR, heart rate reserve; HR, heart rate; RM, maximal repetition; CHO,
carbohydrates; PRO, proteins; FAT, fats; VO2peak, peak oxygen consumption.
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Table 3 Quality ratings of study
Study 1. Hypothesis
stated
2. Main
outcomes
3. Participants
characteristics
4. Interventions
described
6. Main
findings
described
7. Variability
estimates
8. Adverse
events reported
9. Patients
lost to
follow up
10. Actual
Pvalue
reported
Binder et al. 2005 (39) Y Y Y Y Y Y Y Y Y
Boudou et al. 2003 (34) Y Y Y Y Y Y N N Y
Brochu et al. 2009 (17) Y Y Y Y Y Y N Y Y
Carr et al. 2005 (40) Y Y Y Y Y Y N Y Y
Coker et al. 2009 (41) Y Y Y Y Y Y N Y N
Cuff et al. 2003 (18) Y Y Y Y Y Y N Y N
DiPietro et al. 1998 (42) Y Y Y Y Y Y N Y N
Donnelly et al. 2003 (7) Y Y Y Y Y Y Y Y Y
Giannopoulou et al. 2005 (19) Y Y Y Y Y Y N Y N
Hunter et al. 2010 (20) Y Y Y Y Y Y N Y N
Ibáñez et al. 2010 (21) Y Y Y Y Y Y N Y N
Irving et al. 2008 (22) Y Y Y Y Y Y N Y Y
Irwin et al. 2003 (23) Y Y Y Y Y Y N Y Y
Janssen et al. 1999 (43) Y Y Y Y Y Y N Y N
Janssen et al. 2002 (24) Y Y Y Y Y Y N Y N
Johnson et al. 2009 (15) Y Y Y Y Y Y N Y Y
Kim et al. 2008 (25) Y Y Y Y Y Y N Y Y
Ku et al. 2010 (26) Y Y Y Y Y Y N Y Y
Kwon et al. 2010 (27) Y Y Y Y Y Y N Y Y
Kwon et al. 2010 (28) Y Y Y Y Y Y N Y Y
McTiernan et al. 2007 (44) Y Y Y Y Y Y Y Y Y
Mourier et al. 1997 (49) Y Y Y Y Y Y N Y N
Nicklas et al. 2009 (29) Y Y Y Y Y Y Y Y Y
Park et al. 2003 (30) Y Y Y Y Y Y N Y N
Poehlman et al. 2000 (31) Y Y Y Y Y Y Y Y N
Rice et al. 1999 (35) Y Y Y Y Y Y N Y N
Ross et al. 2000 (36) Y Y Y Y Y Y Y Y N
Ross et al. 2004 (32) Y Y Y Y Y Y N Y N
Ross et al. 1996 (37) Y Y Y Y Y Y N Y N
Schmitz et al. 2007 (33) Y Y Y Y Y Y N Y N
Short et al. 2003 (45) Y Y Y Y Y Y N Y N
Sigal et al. 2007 (46) Y Y Y Y Y Y Y Y Y
Slentz et al. 2005 (47) Y Y Y Y Y Y N Y Y
Stewart et al. 2005 (48) Y Y Y Y Y Y Y Y N
Thong et al. 2000 (38) Y Y Y Y Y Y N Y N
82 Exercise for visceral fat I. Ismail et al.obesity reviews
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Table 3 Continued
Study 11. Representative
participants
14. Participants
blinded
18. Statistical
tests
20. Accurate
measures
21. Same
population
recruited
22. Same time
recruitment
24. Randomized
to groups
25. Adequate
description of
control
26. Reliability
of VAT measure
reported
Binder et al. 2005 (39) Y N Y Y Y U Y Y Y
Boudou et al. 2003 (34) Y N Y Y Y Y Y Y Y
Brochu et al. 2009 (17) Y N Y Y Y Y Y Y Y
Carr et al. 2005 (40) Y N Y Y Y Y Y Y N
Coker et al. 2009 (41) Y N Y Y Y Y Y Y Y
Cuff et al. 2003 (18) Y N Y Y Y Y Y N N
DiPietro et al. 1998 (42) Y N Y Y Y Y Y Y N
Donnelly et al. 2003 (7) Y N Y Y Y Y Y Y N
Giannopoulou et al. 2005 (19) Y N Y Y Y Y Y Y Y
Hunter et al. 2010 (20) Y N Y Y Y Y Y N Y
Ibáñez et al. 2010 (21) Y N Y Y Y Y Y Y Y
Irving et al. 2008 (22) Y N Y Y Y Y Y Y Y
Irwin et al. 2003 (23) Y N Y Y Y U Y Y N
Janssen et al. 1999 (43) Y N Y Y Y Y Y Y N
Janssen et al. 2002 (24) N Y Y Y Y Y Y Y Y
Johnson et al. 2009 (15) Y Y Y Y Y Y Y Y Y
Kim et al. 2008 (25) N N Y Y Y Y Y N N
Ku et al. 2010 (26) N N Y Y Y Y Y Y N
Kwon et al. 2010 (27) N N Y Y Y Y Y Y N
Kwon et al. 2010 (28) N N Y Y Y Y Y Y N
McTiernan et al. 2007 (44) N N Y Y Y Y Y Y Y
Mourier et al. 1997 (49) Y Y Y Y Y Y Y Y Y
Nicklas et al. 2009 (29) N Y Y Y Y Y Y Y Y
Park et al. 2003 (30) N Y Y Y U U Y N N
Poehlman et al. 2000 (31) N Y Y Y Y Y Y N Y
Rice et al. 1999 (35) N Y Y Y Y Y Y Y N
Ross et al. 2000 (36) N Y Y Y Y Y Y Y N
Ross et al. 2004 (32) N Y Y Y Y Y Y Y N
Ross et al. 1996 (37) N Y Y Y Y Y Y Y Y
Schmitz et al. 2007 (33) N Y Y Y Y Y Y Y N
Short et al. 2003 (45) N Y Y Y Y Y Y Y N
Sigal et al. 2007 (46) N Y Y Y Y Y Y Y N
Slentz et al. 2005 (47) N Y Y Y Y Y Y Y Y
Stewart et al. 2005 (48) N Y Y Y Y Y Y Y Y
Thong et al. 2000 (38) N Y Y Y Y Y Y Y N
Y, Yes; N, No; U, Undeterminable; VAT, visceral adipose tissue.
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Table 4 Outcomes of intervention studies for change in visceral fat
Reference Mode Measure Region Pre, mean (SD) Post, mean (SD) Change Score
Binder et al.
2005 (39)
C(n=38) MRI
(20 C,
34 PRT)
Serial images above and below the
L4-L5 interspace
179.0 (85.0) cm2NR -3.8(29.0)
PRT (n=53) 195.0 (104.0) cm2NR -7.0(43.0)
Boudou et al.
2003 (34)
C: n=8 MRI Umbilicus (L4-L5) 156.85 (23.4) cm2150.35(23.25) cm2NR
A: n=8 153.25 (38.55) cm284.20(21.30) cm2
Brochu et al.
2009
C: n=71 CT L4-L5 vertebral disc using a scout
image of the body
186.0 (56.0) cm2NR -23.0(30.0) cm2
PRT: n=36 183.0 (52.0) cm2NR -23.0(34.0) cm2
Carr et al. 2005
(40)
C: n=32 CT At level of umbilicus 112.3(56.0) cm2112.7(58.8) cm2-1.6(39.0) cm2
A: n=30 87.2(40.0) cm275.0(43.3) cm2-10.6(19.2) cm2
Coker et al. 2009
(41)
C: n=6 CT L4-L5 vertebral disc space NR NR C: 5(14.7)
A: n=6 A: -39.0(26.9)cm2
Cuff et al. 2003
(18)
C: n=9 CT L4/L5 vertebral disc space 259.1 (103.2) cm2NR -0.4(36.0) cm2
A+PRT: n=10 251.1 (72.4) cm2-26.3 (23.4) cm2
A: n=9 215.7 (77.4) cm2-8.8 (16.2) cm2
DiPietro et al.
1998 (42)
C: n=7 CT 4th to 5th lumbar body 136.0(74.1)cm2118.0(71.4)cm2NR
A: n=9 116.0(93.0)cm2106.0(72.0)cm2
Donnelly et al.
2003 (7)
C: n=33
A: n=41
CT L4-5 ver tebral space Men: 91.7(29.7) cm2
Women: 62.9(21.8) cm2
Men: 97.9(22.5) cm2
Women: 60.6(25.5) cm2
85.4(39.7) cm2
66.0(13.9) cm2
75.5(18.3) cm2
57.4(28.4) cm2
NR
Giannopoulou
et al. 2005 (19)
C: n=11 MRI From superior portion of head of
femur to most superior part of
kidneys
4785.0(1,592.0) cm34425.0(1,442.7) cm3NR
A: n=11 5912.0(1,605.2) cm35152.0(1,456.0) cm3-12.8%
Hunter et al.
2010 (20)
C: n=30 CT Supine position with arms
stretched above head; at levels of
L4 and L5
50.0(20.8) cm262.4(28.2) cm212.4 cm2,
A: n=18 48.0(17.7) cm248.8(20.1) cm20.8 cm2,
PRT: n=21 43.7(14.4) cm243.3(15.5) cm20.8 cm2,-0.4 cm2
Ibáñez et al.
2010 (21)
C: n=12 MRI Abdominal and thigh; Supine
position with both arms parallel
along sides of the body
3340.0(977.0) cm22724.0(1,052.0) cm2NR
PRT n=13 3290.0 (1,141.0) cm22633.0 (1,000.0) cm2
Irving et al. 2008
(22)
C: n=7 CT L4-L5 intervertebral disc space at
midpoint between inguinal crease
and top of patella
157.0(71.0) cm2155.0(71.0) cm2-2.0 cm2
A: n=9 173.0(73.0) cm2148.0(59.0) cm2-24.0 cm2
Irwin et al. 2003
(23)
C: n=86 CT L4-L5 intervertebral space 147.6(57.7) g/cm2NR 0.1(31.5) g/cm2
A+PRT: n=87 147.6(63.5) g/cm2-8.5(40.7) g/cm2
Janssen et al.
1999 (43)
C: n=20
A: n=20
PRT: n=20
MRI Intervertebral space between L4
and L5 as point of origin
Male: 188.0(69.6)
Female: 142.0(53.8)
Male: 159.0(37.9)
Female: 128.0(31.6)
Male: 149.0(123.3)
Female: 89.0(28.5)
NR -58.0(31.6) cm2
-51.0(22.1) cm2
-67.0(37.9) cm2
-37.0(22.1) cm2
-50.0(47.4) cm2
-15.0(19.0) cm2
Janssen et al.
2002 (24)
C: n=13
A: n=11
PRT: n=14
MRI 5 cm below to 15 cm above L4-L5 2.3(1.1)kg,
131.0(50.0)cm2
1.9(0.9)kg,
120.0(42.0)cm2
1.50(0.59)kg,
84.0(27.0)cm2
NR -0.65(0.37) kg,
-51(21) cm2
-0.6(0.4) kg
-39.0(24.0) cm2
-0.4(0.2) kg
-19.0(16.0) cm2
Johnson et al.
2009 (15)
C: n=7 MRI L4-L5 intervertebral space 154.3(56.1) cm2158.6(63.2) cm2NR
A: n=12 164.3(63.4) cm2143.6(64.8) cm2
Kim et al. 2008
(25)
C: n=10 CT L4 vertebrae close to umbilicus 391.9(206.7) 408.4(189.7) 16.5
A+PRT: n=10 387.7(111.3) 356.9(93.0) -30.80
Ku et al. 2010
(26)
C: n=16 CT Abdominal 17 530.0(4,747.0)g 17 362.0(4,728.0)g -168.0(1,801.0)g
A: n=15 15 890.0(4,593.0)g 15 038.0(3,369.0)g -852.0(2,839.0)g
PRT: n=13 15 658.0(4,754.0)g 14 678.0(3,456.0)g -980.0(2,353.0)g
Kwon et al. 2010
(27)
C: n=15 CT 10 mm line from lumbar vertebrae
4 and 5 to bellybutton
17 268.7(5,060.9)mm217 745.1(4,715.0)mm24.4%
PRT: n=13 15 657.8(4,753.6)mm214 677.8(3,455.9)mm2NR
Kwon et al. 2010
(28)
C: n=14 CT Cross-sectional area of L4-L5
vertebrae
17 204.5(4,674.4)mm217 216.3(4,560.8)mm20.9%
A: n=13 16 291.5(4,808.5)mm214 682.7(3,494.7)mm28.4%
84 Exercise for visceral fat I. Ismail et al.obesity reviews
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Effect of exercise therapy on visceral adiposity
(Meta-analyses)
The effect of exercise therapy on visceral adiposity is sum-
marized in Table 4 and Figs 2–5.
Aerobic exercise
There was a significant pooled ES for the comparison
between aerobic exercise therapy and control (ES =-0.23,
95% CI: -0.35 to -0.12; P<0.001). Significant heteroge-
neity among studies was observed (I2=71.0%, P<0.001).
Table 4 Continued
Reference Mode Measure Region Pre, mean (SD) Post, mean (SD) Change Score
McTiernan et al.
2007 (44)
C: n=102
A: n=100
CT L4-L5 space Men: 176.7(79.1) cm2
Women: 102.6(55.8)
cm2
Men: 161.8(66.3) cm2
Women: 105.9(60.8)
cm2
170.5(72.2) cm2
104.2(59.6) cm2
149.6(76.6) cm2
100.1(58.8) cm2
-6.2(-3.5)%
1.6(1.6)%
-12.2(7.5)%
-5.8(-5.5)%
Mourier et al.
1997 (49)
C: n=11 MRI Level of the umbilicus 139.4(36.8) cm2134.9(33.8) cm2NR
A: n=10 156.1(47.4) cm280.4(22.1) cm2
Nicklas et el.
2009 (29)
C: n=34 CT Within 15 mm centres at L4-L5
level
2369.0(870.0) cm3NR -612.0(338.0)
cm3
A: n=38 2509.0(737.0) cm3-630.0(298.0)
cm3
Park et al. 2003
(30)
C: n=10 CT L4 close to umbilicus 182.9(16.8) cm3190.4(15.7) cm37.5 cm3
A: n=10 195.0(12.6) cm3112.4(10.5) cm3-82.6 cm3
A+PRT: n=10 201.6(28.0) cm3108.6(17.9) cm3-93.0 cm3
Poehlman et al.
2000 (31)
C: n=20 CT L4-L5 vertebral level 36.0(13.0) cm241.0(15.0) cm2NR
A: n=14 40.0(11.0) cm241.0(13.0) cm2
PRT: n=17 36.0(17.0) cm236.0(13.0) cm2
Rice et al. 1999
(35)
C: n=9 MRI 1 image below and 4 images
above the L4-L5 intervertebral
space
4.6(1.6)L NR -1.5(0.9)L
A: n=10 4.6(1.5)L -1.8(1.0)L
PRT: n=10 4.1(2.4)L -1.5(0.7)L
Ross et al. 2000
(36)
C: n=8 MRI Whole body 198.0(71.0) cm2198.0 cm2NR
A: n=16 186.0(59.0) cm2134.0 cm2
Ross et al. 2004
(32)
C: n=10 MRI Whole body 2.3(0.9)kg 2.2(0.9)kg NR
A: n=17 2.3(0.8)kg 1.6(0.7)kg -0.7(0.5)
Ross et al. 1996
(37)
C: n=11 MRI Two sets from L4-L5 to upper
thorax and one extended from
L4-L4 to approximate level of
femoral head
4.7(1.6)L NR -1.5(0.8)L
A: n=11 4.6(1.4)L -1.8(1.0)L
PRT: n=11 3.9(2.3)L -1.4(0.7)
Schmitz et al.
2007 (33)
C: n=63 CT L2-L3 interspace 67.4 (36.5) cm281.8 cm221.36 (5.3) %
PRT: n=70 71.8(36.8) cm276.9 cm27.05 (5.1) %
Short et al. 2003
(45)
C: n=37 CT L4-L5 intevertebral space 122.0(79.1) cm2121.0(73.0) cm2NR
A: n=65 133.0(88.7) cm2124.0(88.7) cm2
Sigal et al. 2007
(46)
C: n=63 CT Transverse cut at L4-L5 252.0 (147.0) cm2250.0(147.0) cm2NR
A: n=60 257.0(161.0) cm2244.0(161.0) cm2
PRT: n=64 228.0(156.0) cm2218.0(156.0) cm2
A+PRT: n=64 246.0(159.0) cm2224.0 (159.0) cm2
Slentz et al. 2005
(47)
C: n=47 CT L4 pedicle 165.0(68.0) 179.2 8.6(17.2)%
A: n=42 168.0(64.0) 156.4 -6.9(20.8)%
Stewart et al.
2005 (48)
C: n=53
A+PRT: n=51
MRI One slice below, at and above
umbilicus
Male: 162.7(70.3) cm2
Female: 123.4(62.6)
cm2
Male: 186.5(63.4) cm2
Female: 109.6(47.7)
cm2
NR -7.4 (27.88) cm2
-0.3(23.1) cm2
-40.6(33.0) cm2
-14.5(23.2) cm2
Thong et al. 2000
(38)
C: n=8 MRI Whole body 4.1(1.7)kg NR -0.003(0.3)
A: n=16 3.9(0.8)kg -1.1(0.4)
All data reported as means SD.
BMI, body mass index; A, aerobic training; PRT, progressive resistance training; C, controls; NR, not reported.
obesity reviews Exercise for visceral fat I. Ismail et al.85
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obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Figure 2 Forest plot for AEx studies (n=29). Graph depicts ES and 95% CI for individual studies and the pooled estimate.
86 Exercise for visceral fat I. Ismail et al.obesity reviews
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Further examination of these showed that one study was an
outlier with much larger effect size. This study employed
high volume (6 d per week, ~60 min per session). After
re-analysis via random effects model with this outlier
removed, there remained a significant pooled ES (-0.33,
95% CI: -0.52 to -0.14; P<0.01) (Fig. 2).
Progressive resistance therapies
The pooled ES for the comparison between resistance
exercise therapy and control did not reach significance
(ES =0.05, 95% CI: -0.10 to 0.20; P=0.52). Significant
heterogeneity among studies was observed (I2=61.7%,
P<0.01). After re-analysis via random effects model, the
pooled ES was 0.09 (95% CI: -0.17 to 0.36; P=0.49)
(Fig. 3).
Aerobic exercise vs. progressive resistance therapies
The pooled ES for the comparison between aerobic exercise
and resistance exercise therapies showed a non-significant
effect which tended to favour aerobic training (ES =0.20,
95% CI: -0.02 to 0.42; P=0.08). Low heterogeneity
among studies was observed (I2=20.1%, P=0.26). Analy-
sis via random effects model showed that the pooled ES did
not reach statistical significance (ES =0.23, 95% CI: -0.02
to 0.50; P=0.07) (Fig. 4).
Combined aerobic exercise and progressive
resistance therapies
There was a significant pooled ES for interventions
that combined aerobic and resistance exercise therapy
vs. control (ES =-0.27, 95% CI: -0.46 to -0.08;
P<0.01). Significant heterogeneity among studies was
observed (I2=87.1%, P<0.01). Further examination of
these showed that one study was an outlier with much
larger effect size and low precision. It is noteworthy that
this study had a low sample size (10 subjects per
group). After re-analysis with this outlier removed using
random effects the pooled ES did not reach statistical sig-
nificance (-0.28, 95% CI: -0.69 to 0.14; P=0.19)
(Fig. 5).
Figure 3 Forest plot for PRT studies (n=14). Graph depicts ES and 95% CI for individual studies and the pooled estimate.
obesity reviews Exercise for visceral fat I. Ismail et al.87
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Figure 4 Forest plot for PRT vs. AEx studies (n=9). Graph depicts ES and 95% CI for individual studies and the pooled estimate.
Figure 5 Forest plot for combined AEx and PRT studies (n=6). Graph depicts ES and 95% CI for individual studies and the pooled estimate.
88 Exercise for visceral fat I. Ismail et al.obesity reviews
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
Discussion
This is the first systematic review with meta-analyses to
investigate the independent and combined effects of aerobic
and resistance training modalities on visceral adiposity in
adults. The data show that when compared with a control
intervention, AEx therapy is effective in lowering VAT.
Resistance training itself failed to induce significant reduc-
tion in VAT when compared with the control group. In
studies where AEx and PRT were directly compared, the
effect size favoured AEx training but did not reach statis-
tical significance. From available studies in which com-
bined interventions using both AEx and PRT were
employed, the pooled effect size was not significantly dif-
ferent from a control group.
This systematic review and meta-analyses combined 35
studies involving a total of 2145 adult participants. Of the
studies examined, the majority were conducted in over-
weight or obese populations, predominantly with female
cohorts. Twelve of the studies specifically included partici-
pants with type 2 diabetes or metabolic syndrome. Aerobic
training interventions ranged from four to 52 weeks in
duration and prescribed exercise on one to 7 d per week at
intensities between 49% and 85% of peak aerobic capacity.
Such interventions are consistent with current public health
recommendations for improving cardiorespiratory fitness
(51), but the majority of studies fell below the recom-
mended exercise guidelines for the prevention and manage-
ment of overweight and obesity (52). Progressive resistance
training interventions ranged from 12 to 104 weeks in
duration and employed resistance exercise on two to 5 d
per week at intensities between 30% and 100% of one
repetition maximum (27,39). Most studies employed PRT
interventions, which were consistent with the minimum
frequency and volume of currently recommended for
improving muscular fitness in adults (51).
Excess visceral adipose tissue is a well-established risk
factor for cardiovascular disease (53), and small differ-
ences in VAT area/volume can significantly alter risk
profile (54). The present data demonstrate that AEx itself
is effective in favourably modifying VAT, but that inter-
ventions involving PRT do not significantly influence VAT.
It has been suggested that a doseresponse relationship
exists between exercise volume and VAT reduction, which
has been attributed to a greater amount of energy expen-
diture leading to greater weight loss. However, on the
basis of the present data, although there was a significant
relationship between mean weight loss and VAT reduction
(r2=0.17, P<0.05) as expected, we found no evidence to
suggest a relationship between total weekly AEx volume
or mean intensity and VAT reduction (r2<0.15 for both),
and there are a number of examples of RCTs in which
VAT reduction occurred in the absence of significant
weight loss (15,32,47). Other studies have found that,
when caloric expenditure of exercise is matched, higher
intensity exercise is more effective for reduction in VAT22
which has been attributed to the augmented secretion of
lipolytic hormones such as growth hormone (GH) (55).
GH acts to stimulate adipose tissue directly via hormone
sensitive lipase and also indirectly by enhancing insulin
sensitivity (56,57). Although resistance training induces
acute increases in GH secretion, chronic aerobic training
(particularly at higher intensities) can lead to chronic
increases in 24-h GH release (58). This is consistent with
our observation of a significant reduction in VAT follow-
ing aerobic but not resistance exercise training. However,
our failure to observe a relationship between exercise
intensity and VAT reduction is likely to be due to hetero-
geneity in study duration, training frequency, modality
and cohort characteristics.
Several limitations exist which should be considered when
interpreting the results of this review. Although the majority
of the cohorts examined were overweight or obese, there
were two studies which included lean participants and others
with known metabolic disease. Furthermore, differences in
exercise prescription (intensity, duration, modality, fre-
quency and intervention length) contributed to heterogeneity.
Only one study in this review (15) attempted to blind the
control group using a sham-exercise design. Blinding of the
researcher/s conducting the baseline and post-intervention
assessment of the main outcome measures occurred in just
two studies (15,46). Other potential confounders included
differences in dietary intake and activity performed outside
of the interventions. Four of the 29 studies examined
reported non-significant or near significant effects of AEx
intervention on VAT and were likely limited by low subject
numbers. Our finding of a strong statistically significant
effect for AEx on VAT highlights the relevance of a pooled
analysis approach for providing clarity on this effect.
Despite these limitations, this systematic review with
meta-analyses provides useful information for the clinical
application of exercise in the management of obesity. There
is strong evidence for the effectiveness of AEx therapy but
not for resistance exercise. However, the goal of reducing
visceral adiposity in isolation is unlikely in most obese
individuals in whom multiple cardiometabolic risk factors
are likely to be present, and PRT has been shown to be
effective for improving risk factors including insulin resis-
tance and dyslipidaemia (59). Although direct comparison
between AEx and PRT is problematic due to differences in
metabolic strain and appropriate dosage/volume, it is clear
from the present results that the aerobic component of
exercise therapy is central to exercise-induced VAT modi-
fication. The present study highlights the need for more
research examining the efficacy of combined AEx and PRT
modalities but suggests that combined interventions should
not sacrifice an adequate volume of aerobic training for the
inclusion of PRT. Given that the studies reviewed in this
obesity reviews Exercise for visceral fat I. Ismail et al.89
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
investigation comply with current recommendations for
improvement in cardiorespiratory fitness (150 min/week
of moderate intensity aerobic activity) (51), these recom-
mendations appear sufficient for favourably modifying
VAT despite being lower than specific overweight/obesity
management guidelines.
Conflict of Interest Statement
No conflict of interest was declared.
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obesity reviews Exercise for visceral fat I. Ismail et al.91
© 2011 The Authors
obesity reviews © 2011 International Association for the Study of Obesity 13, 68–91
... Combination training is considered the best exercise because it has the most anti-inflammatory effect compared to aerobic exercise and resistance training [48,49]. Combination exercise reduces serum IL-6 and TNF-α levels more effectively than aerobic or resistance training [50]. Our study results reported that combined training is better at reducing pro-inflammatory cytokines than aerobic and resistance training independently. ...
... A metaanalysis of patients with obesity who participated in an exercise intervention for at least 4 weeks discovered that aerobic exercise burns visceral fat more effectively than resistance training or combination therapy. Resistance training and post-exercise combinations did not significantly change visceral fat levels [50]. However, this might be influenced by the participant's diet, which cannot be controlled in the study; therefore, it is possible that participants from certain groups consumed foods with high fat content. ...
Article
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A sedentary lifestyle and an unhealthy diet increase the risk of obesity. People with obesity experience adipocyte hypertrophy and hyperplasia, which increases the production of pro-inflammatory cytokines, thereby increasing the risk of morbidity and mortality. Lifestyle modification using non-pharmacological approaches such as physical exercise prevents increased morbidity through its anti-inflammatory effects. The purpose of this study was to examine the effects of different types of exercise on decreased proinflammatory cytokines in young adult females with obesity. A total of 36 female students from Malang City aged 21.86 ± 1.39 years with body mass index (BMI) of 30.93 ± 3.51 kg/m 2 were recruited and followed three different types of exercise interventions: moderate-intensity endurance training (MIET), moderate-intensity resistance training (MIRT), and moderate-intensity combined training (MICT). The exercise was performed at a frequency of 3x/week for 4 weeks. Statistical analysis was performed using the Statistical Package for Social Science (SPSS) version 21.0, using the paired sample t-test. The results revealed that serum IL-6 and TNF-α levels were significantly decreased between pre-training and post-training in the three types of exercise (MIET, MIRT, and MICT) (p ≤ 0.001). The percentage change in IL-6 levels from pre-training in CTRL was (0.76 ± 13.58%), in MIET was (−82.79 ± 8.73%), in MIRT was (−58.30 ± 18.05%), in MICT was (−96.91 ± 2.39%), and (p ≤ 0.001). There was a percentage change in TNF-α levels from pre-training in CTRL (6.46 ± 12.13%), MIET (−53.11 ± 20.02%), MIRT (−42.59 ± 21.64%), and MICT (−73.41 ± 14.50%), and (p ≤ 0.001). All three types of exercise consistently reduced pro-inflammatory cytokines such as serum levels of IL-6 and TNF-α.
... Interestingly, the recent investigation also showed significant improvements in body composition and aerobic capacity in the overweight men when following HIIT once a week, which was much less than the usual levels (the usual protocol for HIIT consists of running three times a week) (29) . Energetic restriction is the most effective way for weight loss, while exercise is more influential on the visceral fat reduction (30) . In addition, a greater weight loss was observed during energy restriction, which was partly related to a marked reduction in LBM and muscle wasting. ...
Article
The beneficial effects of high-intensity interval training (HIIT) and chlorella vulgaris (CV) on body composition and mitochondrial biogenesis have been shown in some mechanistic studies. This study aimed to determine the effects of CV and/or HIIT on mitochondrial biogenesis, performance and body composition among overweight/obese women. There was a significant reduction in the fat mass (FM) of the CV þ HIIT group, as compared with the placebo group (P = 0·005). A marginal significant increase in body water (P = 0·050) and PPAR-γ coactivator-1α (P = 0·050) was also found only in the CV þ HIIT group, as compared with the placebo. Relative (P < 0·001) and absolute (P < 0·001) VO 2max , as well as Bruce MET (P < 0·001), were significantly increased in the HIIT and HIIT þ CV groups. Besides, the synergistic effect of CV and HIIT on the Bruce MET increment was found (interaction P-value = 0·029). No significant changes were observed in BMI, fat-free mass, visceral fat, silent information regulator 1 and fibroblast growth factor-21. In this randomised clinical trial, forty-six overweight/obese women were assigned to four groups including CV þ HIIT and HIIT þ placebo groups that received three capsules of CV (300 mg capsules, three times a day) or corn starch, in combination with three sessions/week of HIIT. CV and placebo groups only received 900 mg of CV or corn starch, daily, for 8 weeks. Biochemical assessments, performance assessment and body composition were obtained at the beginning and end of the intervention. HIIT may be, therefore, effective in improving mitochondrial biogenesis, performance and body composition in overweight/obese women. Total body fat is associated with impaired mitochondrial function , thus indicating a strong relationship between body composition and mitochondrial energy metabolism (1). Mitochondria, as an important cell organelle, is involved in many crucial cell functions such as metabolism, regulating the maximal oxygen consumption (VO 2max), which is important for endurance performance (2). VO 2max is the maximum (max) amount of oxygen (O 2) a person utilises during his/her exercise; it is considered as a common measurement of aerobic power. Some characteristics including sex, age, body composition, exercise history and diet can affect VO 2max (3). Endurance exercise-induced adaptations in mitochondrial activity can improve the metabolic health and decrease the risk of obesity and other metabolic disturbances (4). Higher mitochondrial biogenesis is associated with aerobic performance as well as muscle oxidative capacity and regulated by transcriptional cofactors such as PPAR-γ coactivator-1α (PGC-1α) (5). Deacetylation of PGC-1α by silent information regulator 1 (SIRT1) which is an NAD-dependent deacetylase increases PGC-1α activity, resulting in the activation of mitochondrial bio-genesis (6,7). Besides, the gene expression of PGC-1α is up-regulated via fibroblast growth factor-21 (FGF-21) (8) .
... Krafttraining zeigt grundsätzlich einen leicht-moderat positiven Effekt auf intraabdominales oder viszerales Körperfett(Strasser et al. 2012). Allerdings wird für Kraft-im Vergleich zu Ausdauertraining ein geringerer Effekt berichtet(Ismail et al. 2012). Dieses Ergebnis ist allerdings auch dem Umstand geschuldet, dass die Studiendauer der vorliegenden Untersuchungen nur selten 16 Wochen überschreiten. ...
Chapter
Sportmotorische Basisfertigkeiten wie Laufen, Springen, Werfen als auch Alltagsbewegungen wie Sitzen, Stehen, Gehen setzen ein bestimmtes Maß an Kraft bzw. Kraftfähigkeit voraus. Daher kommt der energetisch determinierten Kraftfähigkeit, der Strukturierung der jeweiligen trainingsmethodischen Differenzierung als auch der zielorientierten Umsetzung eine zentrale Rolle zu. Die Kraftfähigkeit spielt einerseits eine immer wichtigere Rolle im Hinblick auf allgemeine Fitness, Gesundheit und Rehabilitation, andererseits ist das Krafttraining seit Jahren in nahezu allen Sportarten und Disziplinen ein elementarer Bestandteil eines zielorientierten Trainings. Dieser Beitrag ist Teil der Sektion Sportmotorische Fähigkeiten und sportliches Training, herausgegeben vom Teilherausgeber Michael Fröhlich, innerhalb des Handbuchs Sport und Sportwissenschaft, herausgegeben von Arne Güllich und Michael Krüger.
... Meta-analyses showed that aerobic endurance training with moderate or high intensity had a greater effect on VAT than resistance training. 26,27 However, there is a great heterogeneity among strength training studies in terms of training protocols, cohort characteristics and study designs. 26 Furthermore, Vissers et al included fewer strength training than aerobic exercise studies in their metaanalysis. ...
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Purpose: To evaluate the effect of a high-intensity resistance training (HIT-RT) on visceral adipose tissue (VAT) and abdominal aortic calcifications (AAC). Patients and methods: We conducted a post hoc analysis of the Franconian Osteopenia and Sarcopenia Trial (FrOST). 43 community-dwelling men with osteosarcopenia aged 72 years and older were randomly allocated to a supervised high-intensity resistance training (HIT-RT) twice weekly for 18 months (EG; n=21) and a non-training control group (CG; n=22). Non-contrast enhanced 2-point Dixon MRI scans covering mid L2 to mid L3 were acquired to measure VAT volume inside the abdominal cavity. Volume of AAC and hard plaques in renal arteries, truncus celiacus and superior mesenteric artery was measured by computed tomography (CT) scans covering mid T12 to mid L3. Intention-to-treat analysis with imputation for missing data was used to determine longitudinal changes in VAT and AAC volume. Correlations were used to determine associations between VAT and AAC. Results: Significant reduction of VAT volume in the EG (-7.7%; p<0.001) combined with no change in the CG (-1.3%; p=0.46) resulted in a significant 6.4% between group effect (p=0.022). We observed a significant increase of AAC volume in EG (+10.3%; p<0.001) and CG (12.0%; p<0.001). AAC differences between groups were not significant (p=0.57). In vascular outlets increases in volume of the hard plaques were observed in both groups, however, not all of them were significant. There was no significant correlation between changes in VAT and AAC volumes. Conclusion: The study confirmed a positive impact of HIT-RT on the metabolic and cardiovascular risk profile with respect to reduction of VAT volume. No positive exercise effect on AAC was observed. However, there was a further progression of AAC volume independent of group affiliation. Whether different exercise regimen may show a positive effect on AAC remains subject to further studies.
... However, findings are further supported by the only other meta-analysis conducted in post-menopausal women, showing significant reductions in WC with aerobic exercise training of !12 weeks [84]. These findings share similarities with other previous meta-analyses conducted in adults, where they found aerobic exercise of at least moderate intensity [31,85,86] was effective in reducing VAT and WC [87], specifically three times per week for 12e16 weeks [86]. It is understood that WC is surrogate marker for VAT and cannot depict true representation of VAT reductions within this study, which warrants further research required to ascertain the effects of exercise training on VAT in post-menopausal women. ...
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Background & Aims Alterations in the hormonal profiles as women transition to the menopause predisposes individuals to the metabolic syndrome (MetS). In post-menopausal women, this can be exacerbated by sedentary behaviour and physical inactivity. Physical activity can convey many health benefits including improvement in MetS risk factors. However, it remains to be elucidated how differing exercise intensities and its mode of delivery can ameliorate MetS risk factors and resultant progression amongst post-menopausal women. The purpose of this systematic review and meta-analysis was to investigate the effects and efficacy of exercise training on MetS risk factors in post-menopausal women. Methods Database searches using PubMed, Scopus, Web of Science and the Cochrane Central Register of Controlled Trials were conducted from inception to December 2021 for randomised controlled studies (RCTs) investigating exercise training (>8 weeks) in at least one of the MetS risk factors in post-menopausal women. Utilising the random-effects model, appropriate standardised mean differences (SMD) or mean differences (MD) with 95% confidence interval (CI) for each MetS risk factor were used to calculate the overall effect size between the exercise and control groups. Sub-group analyses were performed for exercise intensity, modality, and duration for each risk factor. Meta-regression was performed for categorical (health status) and continuous (body mass index) covariates. Results 39 RCTs (40 studies) involving 2,132 participants were identified as eligible. Overall, the meta-analysis shows that exercise training significantly improved all MetS risk factors: waist circumference (WC) [MD: -2.61 cm; 95% CI: -3.39 to -1.86 cm; p < 0.001; 21 studies]; triglycerides (TG) [SMD: -0.40 mmol/L; 95% CI: -0.71 to -0.09 mmol/L; p = 0.01; 25 studies]; high-density lipoprotein (HDL) [SMD: 0.84 mmol/L; (95% CI: 0.41 to 1.27 mmol/L; p < 0.001; 26 studies]; fasting glucose (BG) [SMD: -0.38 mmol/L (95% CI: -0.60 to -0.16 mmol/L; p < 0.001; 20 studies]; systolic blood pressure (SBP) [MD: -5.95 mmHg (95% CI: -7.98 to -3.92 mmHg; p < 0.001; 23 studies]; and diastolic blood pressure (DBP) [MD: -4.14 mmHg (95% CI: -6.19 to -2.08 mmHg; p < 0.001; 23 studies]. Furthermore, sub-group analyses identified that moderate intensity and combined exercise training significantly improved MetS risk factors (p < 0.05) except for HDL, with combined exercise being the most effective. Long duration (≥12 weeks) training also significantly improved MetS risk factors except for TG. Meta-regression revealed no moderating effects on any MetS risk variables. Conclusion This study reinforces the importance of regular physical activity as a non-pharmacological tool in the reduction of MetS risk in post-menopausal women, with significant metabolic improvements seen in interventions spanning 8 – 10 weeks. Moderate intensity and combined training significantly benefitted abdominal obesity, dyslipidaemia, dysglycaemia and hypertension in post-menopausal women. Improvements in at least one MetS risk were also seen with other exercise modalities and intensities.
... Moreover, the type of work itself could cause damage to workers' health and targeted physical activity (PA) protocols may be able to prevent it [13][14][15]. Indeed, structured and supervised physical exercise interventions carried out in the workplace, with a minimum duration of four months and with at least two weekly sessions, allow a significant decrease in BMI, an increase in muscle mass [16,17], and an improvement in systolic blood pressure [18]. Consequently, promoting and developing a PA protocol in the workplace can represent a focal point in the prevention, treatment and management of several diseases, including osteoporosis in postmenopausal women. ...
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The goal of the following work was to identify the effects, positive or negative, of performing group-based physical activity (GBPA) in the workplace. In addition, the scope of the present research was to investigate some social and relational aspects of medical origin associated with the Happy Bones project. The sample consisted of 28 women between 47 and 67 years old, employees of the University of Rome “Foro Italico”, in menopause, and inactive. The explorative nature of the investigation and the multidimensional aspect of the variables suggested the adoption of a qualitative method. Even though the survey did not fulfil the minimum standards of representativeness, interview analysis showed a positive trend in joining physical activity in the workplace, as shown by the good compliance of the participants with the proposed workplace training protocol. Personal motivation linked to the project itself or to the corresponding activity existed albeit to a secondary extent; the unifying element of the group existed regardless of the project and was due to the home institution, hence to the workplace.
... For instance, it has been shown that CRF exercise of 10 metabolic equivalents often resulted in a visceral fat decrease and that exercise intensity affected the speed of the visceral fat decrease 48 . In this context, CRF training has been considered a cornerstone of programs aiming to decrease visceral fat 49 . In elite youth soccer during the pre-season period, the improvement in CRF was positively related to the exercise intensity of CRF training 50 . ...
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OBJECTIVE: The aim of the present study was to examine skinfold thickness (SKF) distribution in youth and adult male soccer players regarding cardiorespiratory fitness (CRF) and the role of age. MATERIALS AND METHODS: Participants were youth (n=83, age 16.2 (1.0) years, mean (standard deviation)) and adult male soccer players (n=121, 23.2 (4.3) years), who were tested for SKF on 10 anatomical sites and Conconi test to assess vVO2max. RESULTS: A between-within subjects analysis of variance revealed a small interaction between the anatomical site and age group on SKF (p=0.006, η2=0.022), where adolescents had larger cheek (+0.7 mm; p=0.022; 95% confidence intervals – CI – 0.1, 1.3), triceps (+0.9 mm; p=0.017; 95% CI 0.2, 1.6) and calf (+0.9 mm; p=0.014; 95% CI 0.2, 1.5) SKF, while adults had larger chin (+0.5 mm; p=0.007; 95% CI 0.1, 0.8) SKF, and no difference was observed for the rest of the anatomical sites. No difference between adolescent and adult age groups was observed in average SKF (SKFavg) (9.0 (2.7) versus 9.1 (2.5) mm; difference -0.1 mm; 95% CI, -0.8, 0.6; p=0.738). Compared to adults, adolescents had a lower SKF coefficient of variation (SKFcv) (0.34 (0.10) versus 0.37 (0.09); difference-0.03; 95% CI, -0.06, -0.01; p=0.020) and subscapular-to-triceps ration (STR) (1.08 (0.28) versus 1.29 (0.37); difference-0.21; 95% CI, -0.31, -0.12; p<0.001). The largest Pearson moment correlation coefficient between vVO2max and SKF was shown in subscapular (r=-0.411; 95% CI, -0.537, -0.284; p<0.001) and the smallest in the patellar anatomical site (r=-0.221; 95% CI, -0.356, -0.085; p=0.002). In addition, vVO2max correlated moderately with SKFavg (r=-0.390; 95% CI, -0.517, -0.262; p<0.001) and SKFcv (r=-0.334; 95% CI, -0.464, -0.203; p<0.001). CONCLUSIONS: In summary, CRF was related to the thickness of specific SKF and the magnitude of thickness variation by the anatomical site (i.e., the smaller the variation, the better the CRF). Considering the relevance of specific SKF for CRF, their further use would be recommended for monitoring physical fitness in soccer players. Keywords: adiposity; age groups; anthropometry; exercise test, football; men
Chapter
Not all women who have a normal weight are healthy. There are three main types of unhealthy lean including metabolically unhealthy normal weight (MUNW), normal weight with central obesity (NWCO), and normal weight obesity (NWO). These unhealthy lean individuals have an increased risk for cardiometabolic disease and mortality compared to healthy lean, but often, they are undiagnosed, since their body weight is considered “normal”. Some associations between age, sex, ethnicity, genetics, and lifestyle factors with unhealthy lean have been described. Lifestyle interventions including diet and exercise may help to improve the health of these individuals. However, there are many gaps in the past literature regarding etiology, pathophysiology, and interventions, because this is an understudied area. Furthermore, there is a lack of consensus regarding the definition of different types of unhealthy lean.
Article
Background Regular physical activity (PA) plays a key role in the management and prevention of numerous chronic diseases. However, recent studies have suggested that occupational physical activity (OPA) may not always have health benefits. The aim of the present study was to examine the respective contributions of OPA vs. leisure-time physical activity (LTPA) to the variation in the cardiometabolic profile, including cardiorespiratory fitness (CRF) of employees involved in a workplace lifestyle modification program. Our study hypothesis was that LTPA would show a stronger association with indices of cardiometabolic health than OPA. Methods A mobile health assessment unit was used to assess 5145 workers (3397 men and 1748 women) on site at their workplace. Assessments included lifestyle questionnaires (overall diet quality, type of OPA and level of LTPA), blood pressure measurements, blood tests, anthropometric measurements, and a submaximal treadmill exercise test to assess CRF. Results were adjusted for education, household income and age. Results When workers were classified on the basis of their OPA (sedentary work, standing work, physical work, and heavy manual work), only a few significant differences in the cardiometabolic profile were observed in men, with those in the physical work category having more favorable values than sedentary workers. However, substantial and significant differences were observed among employees classified on the basis of their LTPA, these differences being observed in both men and women. For instance, waist circumference, the cholesterol/HDL cholesterol ratio, triglyceride concentrations and resting heart rate were lower in active individuals compared to inactive and moderately inactive individuals (p < 0.01). Furthermore, irrespective of whether or not employees were sedentary at work, a high level of LTPA was associated with a greater CRF (p < 0.001). Finally, we found that the lowest prevalence of hypertriglyceridemic waist (p < 0.01) and the highest score of overall diet quality (p < 0.001) were observed in active individuals, irrespective of their OPA category. Conclusion Levels of LTPA were more strongly associated with cardiometabolic health than OPA in a cohort of blue- and white-collar employees. Furthermore, high levels of LTPA were found to counteract the potentially deleterious effects of a sedentary work on cardiometabolic health.
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In 1995 the American College of Sports Medicine and the Centers for Disease Control and Prevention published national guidelines on Physical Activity and Public Health. The Committee on Exercise and Cardiac Rehabilitation of the American Heart Association endorsed and supported these recommendations. The purpose of the present report is to update and clarify the 1995 recommendations on the types and amounts of physical activity needed by healthy adults to improve and maintain health. Development of this document was by an expert panel of scientists, including physicians, epidemiologists, exercise scientists, and public health specialists. This panel reviewed advances in pertinent physiologic, epidemiologic, and clinical scientific data, including primary research articles and reviews published since the original recommendation was issued in 1995. Issues considered by the panel included new scientific evidence relating physical activity to health, physical activity recommendations by various organizations in the interim, and communications issues. Key points related to updating the physical activity recommendation were outlined and writing groups were formed. A draft manuscript was prepared and circulated for review to the expert panel as well as to outside experts. Comments were integrated into the final recommendation. Primary recommendation: To promote and maintain health, all healthy adults aged 18 to 65 yr need moderate-intensity aerobic (endurance) physical activity for a minimum of 30 min on five days each week or vigorous-intensity aerobic physical activity for a minimum of 20 min on three days each week. [I (A)] Combinations of moderate- and vigorous-intensity activity can be performed to meet this recommendation. [IIa (B)] For example, a person can meet the recommendation by walking briskly for 30 min twice during the week and then jogging for 20 min on two other days. Moderate-intensity aerobic activity, which is generally equivalent to a brisk walk and noticeably accelerates the heart rate, can be accumulated toward the 30-min minimum by performing bouts each lasting 10 or more minutes. [I (B)] Vigorous-intensity activity is exemplified by jogging, and causes rapid breathing and a substantial increase in heart rate. In addition, every adult should perform activities that maintain or increase muscular strength and endurance a minimum of two days each week. [IIa (A)] Because of the dose-response relation between physical activity and health, persons who wish to further improve their personal fitness, reduce their risk for chronic diseases and disabilities or prevent unhealthy weight gain may benefit by exceeding the minimum recommended amounts of physical activity. [I (A)]
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Physical activity, including appropriate endurance and resistance training, is a major therapeutic modality for type 2 diabetes. Unfortunately, too often physical activity is an underutilized therapy. Favorable changes in glucose tolerance and insulin sensitivity usually deteriorate within 72 h of the last exercise session; consequently, regular physical activity is imperative to sustain glucose-lowering effects and improved insulin sensitivity. Individuals with type 2 diabetes should strive to achieve a minimum cumulative total of 1000 kcal · wk-1 from physical activities. Those with type 2 diabetes generally have a lower level of fitness (VO(2max)) than nondiabetic individuals, and therefore exercise intensity should be at a comfortable level (RPE 10-12) in the initial periods of training and should progress cautiously as tolerance for activity improves. Resistance training has the potential to improve muscle strength and endurance, enhance flexibility and body composition, decrease risk factors for cardiovascular disease, and result in improved glucose tolerance and insulin sensitivity. Modifications to exercise type and/or intensity may be necessary for those who have complications of diabetes. Individuals with type 2 diabetes may develop autonomic neuropathy, which affects the heart rate response to exercise, and as a result, ratings of perceived exertion rather than heart rate may need to be used for moderating intensity of physical activity. Although walking may be the most convenient low-impact mode, some persons, because of peripheral neuropathy and/or foot problems, may need to do non- weight-bearing activities. Outcome expectations may contribute significantly to motivation to begin and maintain an exercise program. Interventions designed to encourage adoption of an exercise regimen must be responsive to the individual's current stage of readiness and focus efforts on moving the individual through the various 'stages of change'.
Article
Background: American women aged 25-44 y gain 0.5-1 kg yearly, most of which is fat. Because few midlife women participate in strength training, this mode of activity may be a novel intervention for preventing age-associated fat increases in this population. Objectives: The primary aim was to assess the efficacy of twice-weekly strength training to avoid increases in percentage body fat and intraabdominal fat. Design: A randomized controlled trial was conducted in an ethnically diverse sample of 164 overweight and obese [body mass index (in kg/m(2)): 25-35] women aged 25-44 y. The treatment group did twice-weekly strength training for 2 y. The standard care comparison group was given brochures recommending aerobic exercise. Assessments at baseline, 1, and 2 y included intraabdominal fat by computed tomography scan and body fat and fat-free mass by dual-energy X-ray absorptiometry. Results: During 2 y, percentage body fat changes were -3.68 +/- 0.99% for the treatment group and -0.14 +/- 1.04% for the control group, P = 0.01. Two-year intraabdominal fat changes were 7.05 +/- 5.07% for the treatment group and 21.36 +/- 5.34% for the control group, P = 0.05. Conclusion: This study suggests that strength training is an efficacious intervention for preventing percentage body fat increases and attenuating intraabdominal fat increases in overweight and obese premenopausal women. This is relevant to public health efforts for obesity prevention because most weight gain can be assumed to be fat, including abdominal fat.
Article
The purpose of this study was to investigate the changes in functional fitness and risk factors for metabolic syndrome after 12 weeks of combined exercise in women of advanced age. Subjects consisted of twenty women of advanced age with metabolic syndrome (Control, 10 ; Combined, 10) whose age was over 75. The combined exercise program included stretching for 20 minutes, aerobic exercise for 30 minutes, resistance training for 15 minutes, and Asana yoga for 15 minutes. Subjects exercised 4 times a week for 12 weeks. We found that LBM (lean body mass) was significantly increased and visceral fat was significantly decreased after 12 weeks. Also, self-reliance fitness and the risk factors for metabolic syndrome were significantly improved after 12 weeks in the combined exercise group. Therefore, it appears that combined exercise plays a positive role in body composition and fitness and reduces the risk factors for metabolic syndrome in women of advanced age.
Article
Background: The independent effects of diet- or exercise-induced weight loss on the reduction of obesity and related comorbid conditions are not known. The effects of exercise without weight loss on fat distribution and other risk factors are also unclear. Objective: To determine the effects of equivalent diet- or exercise-induced weight loss and exercise without weight loss on subcutaneous fat, visceral fat, skeletal muscle mass, and insulin sensitivity in obese men. Design Randomized, controlled trial. Setting: University research center. Participants: 52 obese men (mean body mass index [±SD], 31.3 ± 2.0 kg/m 2 ) with a mean waist circumference of 110.1 ± 5.8 cm. Intervention: Participants were randomly assigned to one of four study groups (diet-induced weight loss, exercise-induced weight loss, exercise without weight loss, and control) and were observed for 3 months. Measurements: Change in total, subcutaneous, and visceral fat; skeletal muscle mass; cardiovascular fitness; glucose tolerance and insulin sensitivity. Results: Body weight decreased by 7.5 kg (8%) in both weight loss groups and did not change in the exercise without weight loss and control groups. Compared with controls, cardiovascular fitness (peak oxygen uptake) in the exercise groups improved by approximately 16% (P 0.2). However, these values were significantly greater than those in the control and exercise without weight loss groups (P < 0.001). Conclusions: Weight loss induced by increased daily physical activity without caloric restriction substantially reduces obesity (particularly abdominal obesity) and insulin resistance in men. Exercise without weight loss reduces abdominal fat and prevents further weight gain.