The DOI matches its Crossref record; 97 of the 97 references it cites were found in a registry or an index; 39 of the 61 sources its claims cite were checked for support.
Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition?
Open accessAbstract
This narrative review highlights the degree to which new antiobesity medications based on gut-derived nutrient-stimulated hormones (incretins) cause loss of lean mass, and the importance of resistance exercise to preserve muscle. Glucagon-like peptide 1 receptor agonists (GLP-1RA) induce substantial weight loss in randomized trials, effects that may be enhanced in combination with glucose-dependent insulinotropic polypeptide (GIP) receptor agonists. Liraglutide and semaglutide (GLP-1RA), tirzepatide (GLP-1 and GIP receptor dual agonist), and retatrutide (GLP-1, GIP, and glucagon receptor triple agonist) are peptides with incretin agonist activity that induce ∼15-24% weight loss in adults with overweight and obesity, alongside beneficial impacts on blood pressure, cholesterol, blood glucose, and insulin. However, these agents also cause rapid and significant loss of lean mass (∼10% or ∼6 kg), comparable to a decade or more of aging. Maintaining muscle mass and function as humans age is crucial to avoiding sarcopenia and frailty, which are strongly linked to morbidity and mortality. Studies indicate that supervised resistance exercise training interventions with a duration >10 weeks can elicit large increases in lean mass (∼3 kg) and strength (∼25%) in men and women. After a low-calorie diet, combining aerobic exercise with liraglutide improved weight loss maintenance compared with either alone. Retaining lean mass during incretin therapy could blunt body weight (and fat) regain on cessation of weight loss pharmacotherapy. We propose that tailored resistance exercise training be recommended as an adjunct to incretin therapy to optimize changes in body composition by preserving lean mass while achieving fat loss.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
This narrative review argues that incretin-based obesity therapies produce substantial fat loss but also meaningful lean mass loss, and proposes tailored resistance training as an adjunct to preserve muscle. It synthesizes trial and exercise literature and hypothesizes that preserving lean mass may reduce weight and fat regain after pharmacotherapy cessation, though this remains untested.
Key findings
- Incretin therapies produce roughly 15–24% weight loss: semaglutide 14.9% (−15.3 kg) over 68 weeks, tirzepatide 20.9% (−22.1 kg) over 72 weeks, and retatrutide 24.2% (−26.4 kg) at 48 weeks.
- Body composition analyses show lean mass loss alongside fat loss: semaglutide was associated with 13.9% (−6.9 kg) lean mass loss, and tirzepatide with an absolute lean mass decrease of 6 kg (10.9%), despite a rise in lean mass percentage. Liraglutide trials reported smaller lean mass losses, such as 0.5–1.5 kg depending on dose.
- Resistance training is more effective than endurance training for improving or preserving lean mass: in one crossover study, resistance training increased lean mass by 1.2 kg versus 0.4 kg for endurance training; in dieting older adults, resistance training resulted in less lean mass loss (−1 kg, −2%) than combined training (−1.7 kg, −3%) or endurance training (−2.7 kg, −5%).
- After stopping incretins, weight regain is common: semaglutide withdrawal led to regaining 67% (12.2 kg) or 55% (6.1 kg) of lost weight, and tirzepatide withdrawal led to regaining 54.5% (12 kg). The authors hypothesize that resistance-training preservation of lean mass could reduce rebound weight and fat gain, but this is proposed rather than demonstrated.
Methods
- Narrative review, not a systematic review or meta-analysis, synthesizing randomized trials, observational studies, and prior meta-analyses on incretin pharmacotherapy, body composition, exercise training, and weight regain.
- Includes a table summarizing body composition changes from incretin studies and figures illustrating trial results and hypothesized effects; dual-energy X-ray absorptiometry is discussed as a common lean mass measure, while MRI and computed tomography are noted as gold standards but impractical for widespread use.
- No new primary data collection or formal quantitative synthesis; the final model of resistance training effects on weight, fat, and lean mass after incretin cessation is explicitly hypothetical.
Limitations
- The paper states that large randomized controlled trials have generally not reported body composition or lean mass outcomes, that few studies have addressed body composition, and that no studies have used individually tailored resistance training combined with incretins. It also notes that the key exercise-plus-liraglutide trial used endurance rather than resistance training, was not designed to test exercise plus incretin as primary weight-loss therapy, and that semaglutide and tirzepatide have larger weight and lean mass effects than liraglutide.
- The paper states uncertainty about whether slower dose titration would reduce lean mass loss, whether lean mass loss has long-term detrimental cardiovascular effects, whether resistance training prevents strength deficits, and whether the proposed prevention of rebound weight gain will be confirmed in future studies.
- Evident from the text: as a narrative review, it lacks a systematic search and formal quality appraisal; body composition findings come from varied samples and methods, including DXA, bioimpedance, and air displacement plethysmography; and the central claims about resistance training preserving lean mass and reducing fat regain during or after incretin therapy are extrapolated from other settings rather than directly tested.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
39 of 61 cited sources checked · 16 supported · 1 flagged · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Recent evidence indicates that individuals in the lowest muscle mass tertile had an 81% higher risk of cardiovascular events compared with those in the highest muscle mass tertile (45)”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Disputedcites [45] Tyrovolas, 2020, Skeletal muscle mass in relation to 10 year cardiovascular disease incidence among middle aged and older adults: the ATTICA study, J Epidemiol Community Health sourceExperimental — accuracy not yet measured
The Results and Table 3 report a hazard ratio of 0.19 for the highest muscle-mass tertile relative to the lowest, which is the reference group. That means an 81% lower hazard in the highest tertile relative to the lowest—not an 81% higher hazard in the lowest relative to the highest. (LLM, conf=0.90)
Checked by a reasoning model — may be wrong.
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Disputed
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Elderly individuals classified as having low strength have a 50% higher likelihood of death from all-cause mortality compared with those with normal strength at the same age (44).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Partly supportedcites [44] Ruiz, 2008, Association between muscular strength and mortality in men: prospective cohort study, BMJ sourceExperimental — accuracy not yet measured
The Results report that men in the lowest strength third had an all-cause mortality rate 1.50 times that of men in the middle third, but that figure is for the cohort overall, not specifically older men. In the age-stratified Results, the lowest-to-highest strength comparison ranges from 1.4-fold to 2.2-fold across age groups. The study included only men, so it does not establish the stated figure for elderly individuals generally. Page numbers are unavailable in our copy. (LLM, conf=0.87)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“evidence indicates that excess adipose tissue impairs muscle recruitment and activation, even in young individuals (38).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Could not verifycites [38] Tomlinson, 2014, The impact of obesity on skeletal muscle architecture in untrained young vs. old women, J Anat sourceExperimental — accuracy not yet measured
The Methods and Discussion report muscle size, architecture and contraction torque in young and older women, but do not assess muscle recruitment or activation. Searches for recruitment and voluntary or neural activation found no passage establishing the claimed impairment in young individuals. (LLM, conf=0.74)
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Could not verify
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“while greater incretin-induced body weight reduction induces larger improvements in HbA 1c , triglycerides, ALT, waist circumference, and blood pressure (48)”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Partly supportedcites [48] Małecki, 2023, Predictors of ≥15% weight reduction and associated changes in cardiometabolic risk factors with tirzepatide in adults with type 2 diabetes in SURPASS 1-4, Diabetes Care sourceExperimental — accuracy not yet measured
The Results (Characterization of Achieving Different Categorical Measures of BW Reduction With Tirzepatide) associate greater weight reduction with larger improvements in all five listed measures. The paper studied tirzepatide-treated adults with type 2 diabetes and reports associations; it does not establish that weight reduction caused those improvements or that the finding applies to incretin treatments generally. (LLM, conf=0.88)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“individuals with obesity possess lower levels of muscular strength than normal-weight counterparts when strength is adjusted for body mass (35).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Supportedcites [35] Tomlinson, 2016, The impact of obesity on skeletal muscle strength and structure through adolescence to old age, Biogerontology source
The Abstract states that people with obesity appear weaker when maximum muscular strength is normalized to body mass. The Introduction likewise reports lower body-mass-normalized strength in loaded muscles compared with non-obese individuals. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“They found fat mass losses of 13.9% (À6 kg), 13% (À5.9 kg), 16.5% (À7 kg), and 15.4% (À6.8 kg), respectively.Lira also induced LM losses of 0.9% (À0.5 kg), 2.9% (À1.5 kg), 2.6% (À1.3 kg), and 2% (À1.1 kg).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > IMPACT OF INCRETIN THERAPY ON FAT AND LEAN MASS
What the sources say
- Partly supportedcites [31] Astrup, 2012, Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide, Int J Obes sourceExperimental — accuracy not yet measured
The Abstract Results (page not provided) report that, at 20 weeks, liraglutide 3.0 mg reduced body fat by 15.4% and lean tissue by 2.0%. The Clinical outcomes section confirms that body composition was measured in a subgroup, but the retrieved passages do not substantiate the other dose-specific percentages or the subgroup size of 72. (LLM, conf=0.84)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“A subsequent 68-week intervention in middle-aged adults with overweight or obesity using semaglutide (Sema) (2.4 mg) reduced body weight by 14.9% (À15.3 kg) versus 2.4% (À2.6 kg) in the placebo group (17).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > IMPACT OF INCRETIN THERAPY ON BODY WEIGHT
What the sources say
- Supportedcites [17] Wilding, 2021, Once-weekly semaglutide in adults with overweight or obesity, N Engl J Med source
The Abstract reports a 68-week trial of semaglutide 2.4 mg versus placebo, with mean weight changes of −14.9% versus −2.4%. The Change in Body Weight section reports the corresponding changes of −15.3 kg versus −2.6 kg, and Study Participants reports a mean age of 46 years. Both groups also received lifestyle intervention. (LLM, conf=0.94)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“In a 68-week comparison of Sema 2.4 mg weekly versus once-daily Lira 3.0 mg in adults with obesity, all of whom received counseling to achieve a 500 kcal/day energy deficit and meet physical activity recommendations ($150 min/week), the mean weight change from baseline was -15.8% with Sema versus -6.4% with Lira (19).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > IMPACT OF INCRETIN THERAPY ON BODY WEIGHT
What the sources say
- Supportedcites [19] Rubino, 2022, Effect of weekly subcutaneous semaglutide vs daily liraglutide on body weight in adults with overweight or obesity without diabetes: the STEP 8 randomized clinical trial, JAMA source
The Procedures section describes a 68-week comparison of weekly semaglutide 2.4 mg and daily liraglutide 3.0 mg, with all participants counseled toward a 500-kcal/day deficit and at least 150 minutes of physical activity per week. The Primary Outcome section reports mean weight changes at week 68 of −15.8% and −6.4%, respectively, with significantly greater loss on semaglutide. Page numbers were not available in our copy. (LLM, conf=0.95)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Moreover, loss of muscle is associated with increased risk of cardiovascular disease and death (43).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Partly supportedcites [43] McLeod, 2016, Live strong and prosper: the importance of skeletal muscle strength for healthy ageing, Biogerontology sourceExperimental — accuracy not yet measured
The Introduction (page unavailable) describes sarcopenia as loss of muscle mass and strength associated with adverse outcomes including death. The section ‘The importance of skeletal muscle strength for healthy ageing’ reports higher all-cause mortality among people with low muscle strength, but the cited passages do not link muscle loss specifically to increased cardiovascular disease risk. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“an analysis of the impacts of bariatric surgery (47), which indicated that the $8-kg loss in LM (reflecting 21% of the total weight lost) may have long-term implications for functional capacity, resting energy expenditure, bone strength, metabolic health, the drive to eat, and weight regain.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > WHY MUSCLE MASS MATTERS
What the sources say
- Partly supportedcites [47] Nuijten, 2022, The magnitude and progress of lean body mass, fat-free mass, and skeletal muscle mass loss following bariatric surgery: a systematic review and meta-analysis, Obes Rev sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
- It may state two separate claims as one. 33
- The quote only partly states this claim. 1
- Probably not a substantial claim. 2
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In the context of a body weight reduction of 14.9% (À15.3 kg) and fat reduction of 24.7% (À10.4 kg), individuals also lost an average of 13.9% of their total LM (À6.9 kg) (17).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > IMPACT OF INCRETIN THERAPY ON FAT AND LEAN MASS
What the sources say
- Partly supportedcites [17] Wilding, 2021, Once-weekly semaglutide in adults with overweight or obesity, N Engl J Med sourceExperimental — accuracy not yet measured
The Abstract reports 14.9% (15.3 kg) mean weight loss at week 68 with semaglutide. “Change in Body Composition” reports reduced fat and lean mass in a 140-participant DXA subpopulation, but our copy does not give the claimed 24.7% (10.4 kg) or 13.9% (6.9 kg) reductions. The full trial enrolled 1,961 participants, not 140. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“A study of 23 older individuals (71 years) observed that, after 18 weeks, RT increased knee extensor maximal torque by 41.7% in men and 15.8% in women.Differences in muscle quality were also reported, whereby muscle quality increased by 33.7% in males compared with 8.8% in females (63).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact of Sex
What the sources say
- Supportedcites [63] Da Boit, 2016, Sex differences in the response to resistance exercise training in older people, Physiol Rep source
Methods > Participants reports 23 volunteers with a mean age of 71.3 years. Results > Muscle strength and functional abilities gives the 18-week maximal-torque increases of 41.7% in men and 15.8% in women; Results > Muscle cross-sectional area, fat/water ratio, and quality gives the muscle-quality increases of 33.7% and 8.8%, respectively. No page numbers are available in our copy. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Both cognitive restraint and moderate to vigorous physical activity were associated with less weight regain.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
What the sources say
- Supportedcites [78] Jensen, 2022, Exploratory analysis of eating- and physical activity-related outcomes from a randomized controlled trial for weight loss maintenance with exercise and liraglutide single or combination treatment, Nat Commun source
The Results section, under “Increased cognitive restraint and moderate-to-vigorous intensity physical activity are associated with maintained weight loss,” explicitly reports that increases in both were associated with less weight regain during weight maintenance. Table 5 reports the corresponding negative associations with percentage change in body weight. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“As discussed above, Sema administration is associated with an LM loss of 13.9% ($6.9 kg) over a period of 68 weeks (17), while Tz induced a 10.9% (6 kg) loss over 72 weeks of therapy (20).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > IMPACT OF INCRETIN THERAPIES COMPARED WITH OTHER FORMS OF MUSCLE LOSS
What the sources say
- Partly supportedcites [17] Wilding, 2021, Once-weekly semaglutide in adults with overweight or obesity, N Engl J Med sourceExperimental — accuracy not yet measured
The Change in Body Composition section (page unavailable) reports that lean body mass decreased in absolute terms in the semaglutide DXA subpopulation. Our copy does not give the claimed 13.9% or 6.9 kg lean-mass loss, although it confirms the trial’s 68-week duration. The tirzepatide result is attached to a different citation and is not assessed here. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [20] Jastreboff, 2022, Tirzepatide once weekly for the treatment of obesity, N Engl J Med source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The exercise group increased LM by 3.4% (12.1 kg) compared with the Lira group (0.0 kg; 95% CI À1.0 to 1.1), while the combination group also exhibited an increase of 0.8% (10.5 kg).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
What the sources say
- Partly supportedcites [77] Lundgren, 2021, Healthy weight loss maintenance with exercise, liraglutide, or both combined, N Engl J Med sourceExperimental — accuracy not yet measured
The Metabolic Health-Related End Points section (page not supplied) reports increased lean mass with exercise, and the Discussion (page not supplied) says the combination preserved lean mass. Our copy does not give the claimed 3.4%, 2.1 kg, 0.8%, or 0.5 kg changes, or the liraglutide group's 0.0 kg estimate and confidence interval; preservation alone does not establish an increase in the combination group. (LLM, conf=0.82)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes? Based: unclearIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Studies indicate that, from the third to fourth decade onwards, aging is accompanied by loss of strength of around 2.5-4.0%per year (73), with leg strength declining despite habitual endurance exercise in active older adults (74).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Relationship to Strength
What the sources say
- Partly supportedcites [73] Mitchell, 2012, Sarcopenia, dynapenia, and the impact of advancing age on human skeletal muscle size and strength; a quantitative review, Front Physiol sourceExperimental — accuracy not yet measured
The Function section reports that strength declines with advancing age at an average rate of 2–4% per year, supporting the approximate rate. It does not establish that this rate begins in the third or fourth decade; the early-onset ages discussed in the Size section concern muscle mass, not strength. The endurance-exercise clause has a separate citation and is not assessed here. No page numbers were supplied for these passages. (LLM, conf=0.86)
- Not checked — no full text of the sourcecites [74] Marcell, 2014, Leg strength declines with advancing age despite habitual endurance exercise in active older adults, J Strength Cond Res source
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“A study comparing the independent and combined effects of caloric restriction and exercise in 107 elderly (70 years) individuals with obesity reported that, after 12 months, the exercise group increased LM by 2.3% (11.3 kg), while the dietplus-exercise and diet-only groups experienced decreases in LM of 3.1% (À1.8 kg) and 5.2% (À3.2 kg).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact on Diet-Related Weight Loss
What the sources say
- Partly supportedcites [70] Villareal, 2011, Weight loss, exercise, or both and physical function in obese older adults, N Engl J Med sourceExperimental — accuracy not yet measured
The Results section (Body Weight and Composition; page unavailable) reports the stated directions and kilogram changes in lean mass for all three groups, and the Methods describe a one-year trial of 107 older adults with obesity. However, the citing sentence as printed says the exercise group gained 11.3 kg, whereas the source reports 1.3 kg. The supplied paraphrase corrects that figure. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“After a 36-week lead-in involving Tz treatment (10 mg or 15 mg), which induced weight reduction of 20.9% (À22.1 kg), individuals were randomized to continued Tz treatment for another 52 weeks (additional weight reduction of 5.5% or À4.7 kg, totaling À25.8%, or À26.8 kg, over the 88-week treatment period) or placebo injections (regaining 54.5%, or 12 kg, of the total body weight loss during the 36-”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN MAINTENANCE OF LM PREVENT REBOUND WEIGHT GAIN AFTER INCRETIN THERAPY?
What the sources say
- Partly supportedcites [83] Aronne, 2024, Continued treatment with tirzepatide for maintenance of weight reduction in adults with obesity: the SURMOUNT-4 randomized clinical trial, JAMA sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“After 12 months, greater weight loss was observed in the combination group (Lira 1 exercise, 3.5% or À3.4 kg) than the Lira-only group (0.7% or À0.7 kg).The exercise-only group increased body weight by 2% (12.0 kg).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
What the sources say
- Supportedcites [77] Lundgren, 2021, Healthy weight loss maintenance with exercise, liraglutide, or both combined, N Engl J Med source
The Body Weight and Body-Fat Percentage section reports a further 3.4-kg loss in the combination group. Its reported placebo gain of 6.1 kg and treatment differences imply a 0.7-kg loss with liraglutide alone and a 2.0-kg gain with exercise alone, consistent with the claim’s rounded percentages. The combination–liraglutide difference was not statistically significant (P=0.13), but the claim describes observed losses rather than claiming significance. (LLM, conf=0.87)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one. The quote only partly states this claim.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“After an initial 8-week period of caloric restriction during which participants with obesity lost an average of 12% ($13 kg) of their initial body weight, 5.1 kg LM, and 7.3 kg fat mass, this study randomized 195 participants (42 ± 12 years) to four groups: placebo, exercise (combined training), Lira alone, or Lira 1 exercise (Fig. 5).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
What the sources say
- Partly supportedcites [77] Lundgren, 2021, Healthy weight loss maintenance with exercise, liraglutide, or both combined, N Engl J Med sourceExperimental — accuracy not yet measured
The Low-Calorie Diet section reports a mean weight loss of 13.1 kg (12%) over eight weeks. Table 1 shows lower fat and lean mass after the diet, but its before-and-after groups differ in size (215 versus 195), and it does not report mean losses of 7.3 kg fat mass or 5.1 kg lean mass. Those exact figures are not verified by our copy. (LLM, conf=0.88)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Better results in the combined group were also found in terms of fat loss, with a reduction of 3.5% (À4.7 kg), approximately twice the decrease in the exercise group (À1.8% or À1.4 kg) and the Lira group (À1.6% or À2.0 kg) (77).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
What the sources say
- Partly supportedcites [77] Lundgren, 2021, Healthy weight loss maintenance with exercise, liraglutide, or both combined, N Engl J Med sourceExperimental — accuracy not yet measured
The Body Weight and Body-Fat Percentage section reports a greater reduction in body-fat percentage with the combination than with either treatment alone, and the Discussion says fat-mass loss was approximately twice that of the single treatments. Our copy does not report the cited group-specific figures of 3.5%, 1.8%, and 1.6%, or the corresponding kilogram losses; its reported percentage-point figures are treatment comparisons, not those values. (LLM, conf=0.86)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“an initial 20-week Sema (2.4 mg) administration reduced body weight by 10.6% (À11.1 kg) (82).Thereafter, an additional body weight reduction of 7.9% (À7.1 kg) was reported for those maintained on Sema treatment until 68 weeks, whereas the group that discontinued treatment at 20 weeks demonstrated body weight regain of 6.9% (6.1 kg) (82).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN MAINTENANCE OF LM PREVENT REBOUND WEIGHT GAIN AFTER INCRETIN THERAPY?
What the sources say
- Supportedcites [82] Rubino, 2021, Effect of continued weekly subcutaneous semaglutide vs placebo on weight loss maintenance in adults with overweight or obesity: the STEP 4 randomized clinical trial, JAMA source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“An overview of 12 systematic reviews and meta-analyses summarizing the impact of exercise training (with or without diet) on body composition during weight loss reported significant weight (À1.5 to 3.5 kg) and fat mass (À1.3 to 2.6 kg) losses in response to exercise training (68) but no net increase in LM.However, RT reduced the loss in LM by 0.8 kg in comparison with diet only.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact on Diet-Related Weight Loss
What the sources say
- Supportedcites [68] Bellicha, 2021, Effect of exercise training on weight loss, body composition changes, and weight maintenance in adults with overweight or obesity: an overview of 12 systematic reviews and 149 studies, Obes Rev source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“muscle mass is highly metabolically active, with muscle loss linked to decreased metabolic rate (84).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN MAINTENANCE OF LM PREVENT REBOUND WEIGHT GAIN AFTER INCRETIN THERAPY?
What the sources say
- Supportedcites [84] Christoffersen, 2022, Beyond appetite regulation: targeting energy expenditure, fat oxidation, and lean mass preservation for sustainable weight loss, Obesity (Silver Spring) source
The “Lean mass preservation” section describes lean mass as metabolically active and reports that resting energy expenditure falls by approximately 13 kcal/day for each kilogram of muscle lost. The “Targeting energy expenditure” section also attributes approximately 20% of resting energy expenditure to skeletal muscle. (LLM, conf=0.92)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“It was not designed to evaluate the effects of combining exercise and incretin treatment as the primary weight loss therapy.It is also relevant that the exercise intervention involved ET rather than RT and that Sema and Tz have much”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
What the sources say
- Supportedcites [77] Lundgren, 2021, Healthy weight loss maintenance with exercise, liraglutide, or both combined, N Engl J Med source
The Methods state that participants first completed an 8-week low-calorie diet and were then assigned to exercise, liraglutide, both, or placebo for a year; the Discussion describes the trial as studying weight-loss maintenance, not the combination as primary weight-loss therapy. The Interventions section describes a predominantly aerobic program of cycling, running, and brisk walking. It also included brief circuit training in supervised sessions, so “rather than resistance training” describes the program’s emphasis, not an absolute exclusion. (LLM, conf=0.92)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Another systematic review and meta-analysis, which summarized six articles regarding the impact of RT on diet-induced loss in LM mass, concluded that adding RT to diet attenuated the loss of LM by 93.5%, with an absolute difference in LM of approximately 1 kg.Similar reductions in fat mass and body weight were reported between RT-with-diet and diet-alone groups (69) (Fig. 4).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact on Diet-Related Weight Loss
What the sources say
- Supportedcites [69] Sardeli, 2018, Resistance training prevents muscle loss induced by caloric restriction in obese elderly individuals: a systematic review and meta-analysis, Nutrients source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“a recent report indicated that, in middle-aged (49 ± 12 years) individuals with obesity (BMI $30 kg/m 2 ) (81), 68 weeks of Sema therapy induced mean weight loss of 17.3% (À18.3 kg) vs. 2% (À2.1 kg) for placebo, but 52 weeks after therapy, participants had regained 67% (112.2 kg) of their lost weight.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN MAINTENANCE OF LM PREVENT REBOUND WEIGHT GAIN AFTER INCRETIN THERAPY?
What the sources say
- Supportedcites [81] Wilding, 2022, Weight regain and cardiometabolic effects after withdrawal of semaglutide: the STEP 1 trial extension, Diabetes Obes Metab source
The Results (section 3.2) report mean weight loss of 17.3% with semaglutide versus 2.0% with placebo over 68 weeks, followed by regain of 11.6 percentage points in the semaglutide arm. The Discussion (section 4) describes this as regaining a mean of two-thirds of prior weight loss during the one-year extension. The kilogram figures are approximate conversions consistent with the reported mean baseline weight of 105.5 kg; the treatment also included lifestyle intervention. (LLM, conf=0.87)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, it is germane that while the weight loss is primarily fat, a considerable amount is lean or muscle mass.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CONCLUSIONS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Liraglutide and semaglutide (GLP-1RA), tirzepatide (GLP-1 and GIP receptor dual agonist), and retatrutide (GLP-1, GIP, and glucagon receptor triple agonist) are peptides with incretin agonist activity that induce $ $ $ $15-24% weight loss in adults with overweight and obesity, alongside beneficial impacts on blood pressure, cholesterol, blood glucose, and insulin.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Studies indicate that supervised resistance exercise training interventions with a duration >10 weeks can elicit large increases in lean mass ($ $ $ $3 kg) and strength ($ $ $ $25%) in men and women.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes? Based: unclearIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Maintaining muscle mass and function as humans age is crucial to avoiding sarcopenia and frailty, which are strongly linked to morbidity and mortality.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, these agents also cause rapid and significant loss of lean mass ($ $ $ $10% or $ $ $ $6 kg), comparable to a decade or more of aging.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Glucagon-like peptide 1 receptor agonists (GLP-1RA) induce substantial weight loss in randomized trials, effects that may be enhanced in combination with glucose-dependent insulinotropic polypeptide (GIP) receptor agonists.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Incretin therapies induce significant weight loss, part of which is lean mass ($10% or $6 kg), comparable to a decade or more of aging.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This suggests that compensation for LM loss is effective using RT, but overcompensation (i.e., increase in mass rather than prevention of loss) does not typically occur.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Summary
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Based on well-established effects on LM in obesity, sarcopenia, and type 2 diabetes, it is plausible that RT would mitigate LM loss, and perhaps promote greater fat mass loss, in participants administered incretin therapy.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: The mechanisms by which resistance exercise preserves lean mass in obesity, sarcopenia, and type 2 diabetes are similar enough to those in patients receiving incretin therapy for the effects to translate.
In the paper
“In 94 premenopausal women (35 ± 6.2 years) who were overweight (BMI 27-30 kg/m 2 ), after 1 year of dietary intervention, RT improved fat-free mass (10.3 kg, or 0.6%), whereas ET (À1.0 kg or À2.2%) and no exercise training (À1.5 kg or À3.1%) reduced fat-free mass (61).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact of Exercise Modality
What the sources say
- Not checked — no full text of the sourcecites [61] Hunter, 2008, Resistance training conserves fat-free mass and resting energy expenditure following weight loss, Obesity (Silver Spring) source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The absolute magnitude of RT impact in terms of LM mitigation depends upon factors such as whether the exercise is combined with protein supplementation or whether the LM loss is induced by diet ($1-kg effect) or disease (>1-kg effect).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Summary
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“In healthy untrained men (n = 38, age 37 ± 7 years), the cross-sectional area of the quadriceps femoris increased by 6% after 21 weeks of RT, while endurance training (ET) (e.g., cycling) induced a modest increase of 2% (56).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact of Exercise Modality
What the sources say
- Not checked — no full text of the sourcecites [56] Mikkola, 2012, Neuromuscular and cardiovascular adaptations during concurrent strength and endurance training in untrained men, Int J Sports Med source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“an RT study of individuals ($70 years) with presarcopenia (based on appendicular LM index) observed no significant differences between males and females in LM but that only males significantly improved their strength (64).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact of Sex
What the sources say
- Not checked — no full text of the sourcecites [64] Vikberg, 2019, Effects of resistance training on functional strength and muscle mass in 70-year-old individuals with pre-sarcopenia: a randomized controlled trial, J Am Med Dir Assoc source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“we propose that RT may be a key intervention that, when performed in conjunction with incretin treatment, could improve body composition and provide additional health benefits.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN EXERCISE TRAINING PRESERVE LM AND FUNCTION IN INDIVIDUALS TAKING INCRETIN THERAPY?
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
- Rests on an assumption: The mechanisms by which resistance exercise preserves lean mass in obesity, sarcopenia, and type 2 diabetes are similar enough to those in patients receiving incretin therapy for the effects to translate.
- Rests on an assumption: Resistance exercise training can be feasibly and safely adopted by patients receiving incretin therapy.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Collectively, this evidence supports RT as an effective approach to increase or maintain LM or at least mitigate the decrease of LM associated with diet interventions.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact of Exercise Modality
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Larger improvements in LM have been reported after RT in younger (11.7 kg, 95% CI 1.0-2.4kg) compared with older adults (10.9 kg, 95% CI 0.8-1.1 kg), although both groups benefited (62).”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > Impact of Age
What the sources say
- Not checked — no full text of the sourcecites [62] Lopez, 2022, Moderators of resistance training effects in overweight and obese adults: a systematic review and meta-analysis, Med Sci Sports Exerc source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“While incretin pharmacotherapies are very effective for inducing weight loss, extensive diet literature indicates that weight is rapidly regained on cessation of energy intake restriction (80).This also appears to be true of incretin therapies.”
§ Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? > CAN MAINTENANCE OF LM PREVENT REBOUND WEIGHT GAIN AFTER INCRETIN THERAPY?
What the sources say
- Not checked — no full text of the sourcecites [80] Machado, 2022, Understanding weight regain after a nutritional weight loss intervention: systematic review and meta-analysis, Clin Nutr ESPEN source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper relies on this without support.
The mechanisms by which resistance exercise preserves lean mass in obesity, sarcopenia, and type 2 diabetes are similar enough to those in patients receiving incretin therapy for the effects to translate.
“Based on well-established effects on LM in obesity, sarcopenia, and type 2 diabetes, it is plausible that RT would mitigate LM loss, and perhaps promote greater fat mass loss, in participants administered incretin therapy.”
The paper relies on this without support.
Resistance exercise training can be feasibly and safely adopted by patients receiving incretin therapy.
“We propose that tailored resistance exercise training be recommended as an adjunct to incretin therapy to optimize changes in body composition by preserving lean mass while achieving fat loss.”
The authors state this as an assumption.
Incretin therapies produce an average weight loss of about 17%.
“Here, we assume that incretin therapies induce an average of $17% weight loss (combined data from Wilding et al. [17] and Jastreboff et al. [20])”
The paper relies on this without support.
Lean mass is highly metabolically active.
“LM is highly metabolically active, so its retention during incretin therapy may also result in less fat regain after treatment cessation.”
The paper relies on this without support.
Resistance training increases skeletal muscle mass and strength and prevents muscle loss caused by dieting and disease.
“RT increases skeletal muscle mass and strength and prevents muscle loss that results from dieting and disease.”
The paper relies on this without support.
Exercise is nonpharmacological, has multiple health benefits, and has evidence of effectiveness in other contexts.
“However, exercise is nonpharmacological and has multiple health benefits, and there is evidence for its effectiveness as an intervention in other contexts.”
The paper relies on this without support.
Effective loss of excess weight conveys multiple health benefits, including reduced cardiovascular risk.
“In summary, effective loss of excess weight conveys multiple health benefits, including a reduction in cardiovascular risk.”
The paper relies on this without support.
In the Australian health care system, exercise provision for type 2 diabetes yields total well-being benefits of about $8,000 per person treated at a cost of $580.
“it was calculated that total well-being benefits amounted to $8,000 per person treated, while the cost of exercise provision was $580.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“the well-documented decline in lean mass and BMD associated with that degree of weight loss must be considered.”
From The Benefits of Exercise Training in Combination With Weight Loss Therapies (2025) · cites this paper as [43]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Among other factors, exercise and targeted nutritional intakes have been proposed to influence body composition outcomes during treatment with incretin-based medications, although these practices have been minimally examined in this context.7,12,13”
From Preservation of lean soft tissue during weight loss induced by GLP-1 and GLP-1/GIP receptor agonists: A case series (2025) · cites this paper as [12]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, these benefits are accompanied by concerns about side effects, cost, long-term sustainability and, above all, the loss of lean mass, which may be mitigated by concurrent exercise (16–20).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Recent randomized controlled trials and meta-analyses suggest that combining GLP-1RAs with exercise may yield additive or synergistic effects on weight loss and metabolic syndrome severity as well as on oxidative stress and inflammation.”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Direct comparisons reveal that GLP-1RAs generally produce greater short-term weight loss than exercise alone, but exercise is superior for maintaining lean mass and cardiorespiratory fitness (16, 17, 19).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
Experimental — accuracy not yet measured
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Exercise, particularly resistance training, is crucial for preserving lean mass and functional health, especially during weight loss (11, 17, 18).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Recent randomized controlled trials show that combining GLP-1RAs with exercise yields additive benefits, including greater reductions in metabolic syndrome severity, abdominal obesity, oxidative stress and inflammation, and improved weight loss maintenance after cessation of pharmacotherapy (16, 17, 19, 21).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, these pharmacologic benefits are tempered by important trade-offs, including gastrointestinal side effects, treatment cost, and loss of lean mass, which may have long-term functional implications if not counteracted by concurrent resistance exercise (17–19).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The adverse effects of weight reduction on muscle and bone mass—particularly among individuals with insufficient physical activity or protein intake or at older ages [63, 158]—have highlighted the interrelated priorities to preserve muscle mass, muscle quality, bone mass, and physical function.”
From Nutritional priorities to support GLP ‐1 therapy for obesity: A joint Advisory from the American College of Lifestyle Medicine, the American Society for Nutrition, the Obesity Medicine Association, and The Obesity Society (2025) · cites this paper as [158]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, in patients receiving GLP-1 receptor agonists, serial measurements of creatinine-based eGFR may be confounded by an effect of these drugs to reduce muscle mass,89 and the resulting decline in serum creatinine may imply an improvement in kidney function that has not taken place.53,56”
From Interplay of Chronic Kidney Disease and the Effects of Tirzepatide in Patients With Heart Failure, Preserved Ejection Fraction, and Obesity (2025) · cites this paper as [89]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“RT, in particular, is poised to play a similarly vital role for patients losing weight on incretin therapy (43).”
From The Benefits of Exercise Training in Combination With Weight Loss Therapies (2025) · cites this paper as [43]
The cited source says what the claim attributes to it.
In the citing paper
“tirzepatide and retatrutide induce even greater degrees of weight loss, at 20.9% over 72 weeks and 24.2% over 48 weeks, respectively (43).”
From The Benefits of Exercise Training in Combination With Weight Loss Therapies (2025) · cites this paper as [43]
The cited source says what the claim attributes to it.
In the citing paper
“The amount of lean mass lost in such a short time frame even exceeds the loss experienced by patients actively undergoing chemotherapy for certain cancers (43).”
From The Benefits of Exercise Training in Combination With Weight Loss Therapies (2025) · cites this paper as [43]
The cited source says what the claim attributes to it.
In the citing paper
“treatment with tirzepatide in its phase III trial led to a significant decline in lean mass, of 6.0 kg, or 10.9%, over the 72-week trial period (43).”
From The Benefits of Exercise Training in Combination With Weight Loss Therapies (2025) · cites this paper as [43]
The cited source says what the claim attributes to it.
In the citing paper
“However, long-term weight maintenance is more successful when exercise is included, as stopping GLP-1 therapy alone often leads to weight regain, while exercise helps preserve muscle mass and sustain weight loss.”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
The cited source says what the claim attributes to it.
In the citing paper
“Moreover, exercise may help maintain weight loss after cessation of pharmacotherapy (16, 17, 19, 21).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
The cited source says what the claim attributes to it.
In the citing paper
“However, gastrointestinal side effects and loss of lean mass are notable concerns (5, 10, 17, 18).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [17]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“A nearly identical pattern of response was seen in patients with diabetes with tirzepatide in the SURPASS-4 trial (A Study of Tirzepatide [LY3298176] Once a Week Versus Insulin Glargine Once a Day in Participants With Type 2 Diabetes and Increased Cardiovascular Risk),89 which also relied on eGFR-creatinine.”
From Interplay of Chronic Kidney Disease and the Effects of Tirzepatide in Patients With Heart Failure, Preserved Ejection Fraction, and Obesity (2025) · cites this paper as [89]
Experimental — accuracy not yet measuredIn the citing paper
“Tailored resistance exercise training can optimize changes in body composition by preserving lean mass while achieving fat loss when associated to hypocaloric diet or incretin therapy [38, 39].”
From Muscle loss and GLP-1R agonists use (2025) · cites this paper as [38]
In the citing paper
“The adverse effects of weight reduction on muscle and bone mass—particularly among individuals with insufficient physical activity or protein intake or at older ages [59,149]—have highlighted the interrelated priorities to preserve muscle mass, muscle quality, bone mass, and physical function.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Fat-loss percentages differ between the text and Table 1
MinorFor the same liraglutide-and-exercise study, the text gives fat-loss percentages of 3.5%, 1.8%, and 1.6% for the combination, exercise-only, and liraglutide-only groups. Table 1 gives 12.1%, 3.8%, and 5.3%, respectively, while reporting the same kilogram losses.
“Better results in the combined group were also found in terms of fat loss, with a reduction of 3.5% (À4.7 kg), approximately twice the decrease in the exercise group (À1.8% or À1.4 kg) and the Lira group (À1.6% or À2.0 kg) (77).”
“| Lira 3.0 mg | 42 ± 12 years | | À0.7 (À0.7) | À2 (À5.3) | 0 | | Lira 3.0 mg 1 exercise | | | À3.4 (À3.5) | À4.7 (À12.1) | 0.5 (0.8) | | Exercise | | | 2 (À2.1) | À1.4 (À3.8) | 2.1 (3.4) |”
Citations
Cites
James, S. L., Abate, D., Abate, K. H., Abay, S. M., Abbafati, C., Abbasi, N., Abbastabar, H., Abd-Allah, F., Abdela, J., Abdelalim, A., et al. (2018) · The Lancet · doi:10.1016/s0140-6736(18)32279-7 · Cited by 13,867
Sarcopenia: revised European consensus on definition and diagnosis
Cruz-Jentoft, A. J., Bahat, G., Bauer, J., Boirie, Y., Bruyère, O., Cederholm, T., Cooper, C., Landi, F., Rolland, Y., Sayer, A. A., et al. (2019) · Age and Ageing · doi:10.1093/ageing/afy169 · Cited by 13,818
Global Burden of Cardiovascular Diseases and Risk Factors, 1990–2019
Roth, G. A., Mensah, G. A., Johnson, C. O., Addolorato, G., Ammirati, E., Baddour, L. M., Barengo, N. C., Beaton, A. Z., Benjamin, E. J., Benziger, C. P., et al. (2020) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2020.11.010 · Cited by 11,449
Garber, C. E., Blissmer, B., Deschenes, M. R., Franklin, B. A., Lamonte, M. J., Lee, I.-M., Nieman, D. C., & Swain, D. P. (2011) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e318213fefb · Cited by 9,319
Once-Weekly Semaglutide in Adults with Overweight or Obesity
Wilding, J. P. H., Batterham, R. L., Calanna, S., Davies, M., Van Gaal, L. F., Lingvay, I., McGowan, B. M., Rosenstock, J., Tran, M. T. D., Wadden, T. A., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2032183 · Cited by 5,205
Tirzepatide Once Weekly for the Treatment of Obesity
Jastreboff, A. M., Aronne, L. J., Ahmad, N. N., Wharton, S., Connery, L., Alves, B., Kiyosue, A., Zhang, S., Liu, B., Bunck, M. C., et al. (2022) · New England Journal of Medicine · doi:10.1056/nejmoa2206038 · Cited by 3,838
Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes
Lincoff, A. M., Brown-Frandsen, K., Colhoun, H. M., Deanfield, J., Emerson, S. S., Esbjerg, S., Hardt-Lindberg, S., Hovingh, G. K., Kahn, S. E., Kushner, R. F., et al. (2023) · New England Journal of Medicine · doi:10.1056/nejmoa2307563 · Cited by 3,236
Goodpaster, B. H., Park, S. W., Harris, T. B., Kritchevsky, S. B., Nevitt, M., Schwartz, A. V., Simonsick, E. M., Tylavsky, F. A., Visser, M., Newman, A. B., et al. (2006) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/61.10.1059 · Cited by 3,083
Chooi, Y. C., Ding, C., & Magkos, F. (2018) · Metabolism · doi:10.1016/j.metabol.2018.09.005 · Cited by 2,997
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–147 of 147
Cardamone, K., Byham-Gray, L. D., Sackey, J. D., & Brody, R. A. (2026) · Journal of the Academy of Nutrition and Dietetics · doi:10.1016/j.jand.2026.156432
Targeting the gut microbiota as a treatment for obesity and cancer cachexia
Giannakogeorgou, A., van den Ende, T., Verhaar, B. J. H., de Clercq, N. C., van Laarhoven, H. W. M., & Nieuwdorp, M. (2025) · Expert Opinion on Emerging Drugs · doi:10.1080/14728214.2026.2650180
Jin, C. A., Many, G. M., Spurrier, C. S. R., Borsellino, P., Wheeler, M. T., Adkins, J., Snyder, M. P., Newgard, C. B., Radom‐Aizik, S., Cooper, D. M., et al. (2026) · Physiological Genomics · doi:10.1152/physiolgenomics.00171.2026
Zhang, Z., Liu, S., Xian, J., Zhang, Y., Zhang, C., Wang, Z., Deng, H., Feng, J., & Yao, L. (2025) · Reviews in Cardiovascular Medicine · doi:10.31083/rcm26154
Yetgin, M. K., Gletsu-Miller, N. A., Chapman, R. F., Gelber, E., Snyder, J., Gregg, D., & Nabhan, D. C. (2026) · Obesity Pillars · doi:10.1016/j.obpill.2026.100335
Mallardo, M., Messina, A., Monda, V., Marra, M. L., Monda, A., Allocca, S., Casillo, M., Maio, G. D., Perrone, P., Daniele, A., et al. (2026) · Nutrients · doi:10.3390/nu18172748 · Cited by 1
Damasio, N. M. A., Freccia, G. W., Fortes, M. D. S. R., Gomes, M. G. Z., & de Lira, C. A. B. (2026) · Obesity Medicine · doi:10.1016/j.obmed.2026.100743
Kavsara, H. K. (2026) · Journal of Medical Topics and Updates · doi:10.58651/jomtu.1980569
Hill, C. K., Rattenborg, J., Martens, A., Houchlei, S., Vleisides, B., Verkler, A., Mclean, A., Buehler, S., Smith, C. R., Goddard, S., et al. (2026) · Obesities · doi:10.3390/obesities6050067
Semaglutide and weight management in the Arab countries: Focus on the United Arab Emirates
Semiz, S. (2025) · Health Sciences Review · doi:10.1016/j.hsr.2025.100244 · Cited by 1
Davies, A. P., Hesketh, K. L., Apperley, L. J., Clarke, E., Crozier, A., Russon, C. L., Sprung, V. S., Jones, H., Kinnafick, F., Senniappan, S., et al. (2026) · Archives of Disease in Childhood · doi:10.1136/archdischild-2025-329092 · Cited by 1
Fouad, Y. M., Abdelghany, W. A., & Sheemy, R. Y. E. (2026) · World Journal of Hepatology · doi:10.4254/wjh.v18.i5.118303
Prokopidis, K., Cacciatore, S., Anton, S. D., & Batsis, J. A. (2026) · Advances in Therapy · doi:10.1007/s12325-026-03750-w · Cited by 2
Zhang, X., Tian, Y., Ren, X., Tian, J., Liu, J., & Wang, G. (2026) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.71185
Medeot, M. (2026) · Biomedicine Advances · doi:10.34172/bma.74
Feraco, A., Camajani, E., Muscogiuri, G., Barrea, L., Colao, A., & Caprio, M. (2026) · Current Obesity Reports · doi:10.1007/s13679-026-00695-7 · Cited by 2
Fuentes-Barría, H., Aguilera-Eguía, R. A., Alarcón-Rivera, M., & Flores-Fernández, C. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48080850 · Cited by 1
Michielsen, M., Gojevic, T., Bekhuis, Y., Claes, J., Machado, F. V. C., Claessen, G., Goetschalckx, K., Hansen, D., Craemer, M. D., & Cornelissen, V. (2026) · European Journal of Preventive Cardiology · doi:10.1093/eurjpc/zwag150
Ilie, I. R. P., Ghibu, S., Butucă, A., Dobrea, C. M., Frum, A., Stoicescu, L., Homorodean, C., Gligor, F. G., & Morgovan, C. (2026) · BMJ Open · doi:10.1136/bmjopen-2026-120507
Shil, K. K. (2026) · European journal of medical research · doi:10.1186/s40001-026-04862-3
Tirzepatide: A Paradigm Shift in the Management of Type 2 Diabetes and Obesity
Sonawane, R. A., Gulave, O. K., Kale, P. A., & Rasal, P. B. (2026) · Journal of Bio-X Research · doi:10.34133/jbioxresearch.0092
Marmett, B., da Silva, I., Lira, F. S., & Dorneles, G. P. (2025) · Translational Exercise Biomedicine · doi:10.1515/teb-2024-0039
Anaspure, O. S., Sivaram, P., Guruprasad, P., Anaspure, A. S., Kadakia, R. J., & Anastasio, A. T. (2026) · The Journal of Foot & Ankle Surgery · doi:10.1053/j.jfas.2026.07.011 · Cited by 1
Diabetes Update 2026 – Neue Studienergebnisse und Erkenntnisse
Scherbaum, W. A. (2026) · Die Diabetologie · doi:10.1007/s11428-026-01486-3
Alawadi, F., Abdelgadir, E., Hassoun, A. A. K., Abusnana, S., Afandi, B. O., Aldahmani, K. M., Alkaabi, J., Bashier, A. M., Bayado, F., Belaila, B. A. B., et al. (2026) · Dubai Diabetes and Endocrinology Journal · doi:10.18502/ddej.v32i1.21067
Agonistes du récepteur du GLP-1 et sarcopénie : question émergente ou véritable enjeu clinique ?
Halimi, S. (2025) · Médecine des Maladies Métaboliques · doi:10.1016/j.mmm.2025.10.004
Treatment of obesity: New drugs
Berti, S., Garelli, S., & Pagotto, U. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00330-7
Phenotypic and genomic frameworks for precision pharmacotherapy in obesity: a narrative review
López-Delgado, D. S., Reyes-Zermeño, M. G., Lemus, E. D. S., Acosta-Celis, C. G., Kantún-Marín, M. A., Gomez-Lujan, M., Fallaza-Moya, K., Muñoz-Chuquilín, O., Levano, S. E. T., Gutierrez-Chavez, G., et al. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1803474 · Cited by 2
Read, D., Smith, A. C. T., Mountjoy, M. L., van Rensburg, D. C. J., Dijkstra, H. P., & Taylor, L. K. (2026) · Sports Medicine · doi:10.1007/s40279-026-02514-4
Miller, C. K., Young-Hyman, D. L., Wooldridge, J. S., Piatt, G., & Hawkins, J. (2025) · Clinical Diabetes · doi:10.2337/cd25-0020 · Cited by 1
Zhang, D., Devarakonda, S. L. S., Roberts, R. A., Greenway, F. L., & Rebello, C. J. (2026) · Current Developments in Nutrition · doi:10.1016/j.cdnut.2026.107707 · Cited by 1
Coulter, A. A., Greenway, F. L., Ramanathan, G., Hubbard, J. R., & Rebello, C. J. (2026) · Obesity Reviews · doi:10.1111/obr.70173
Liu, D., Cheng, D., Wang, Q., Zhang, Y., Kang, P., Zhao, C., Mao, H., Qu, J., Liu, S., Gao, X., et al. (2026) · 中国科学通报:英文版 · doi:10.1016/j.scib.2026.06.021
Soni, R., Goswami, D., Gani, A., Halami, P. M., & Chauhan, K. (2026) · Current Obesity Reports · doi:10.1007/s13679-026-00729-0
Gracioto, P. G. A., de Oliveira, J. C. M., & Oliveira, C. R. (2026) · Research Society and Development · doi:10.33448/rsd-v15i7.51444
Ruga, S., Matarese, E., Bava, R., Lombardi, C., Dimatteo, T., Miscio, L., Raponi, M., Giordano, A., Sansone, C., Liguori, G., et al. (2026) · Pharmaceuticals · doi:10.3390/ph19081230 · Cited by 1
Preventive Strategies to Reduce Sarcopenia Risk During GLP-1-Based Anti-Obesity Therapy
Belančić, A., Skroče, K., Gkrinia, E. M. M., Glavić, M. M., & Kwok, M. K. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15155870 · Cited by 3
Yang, W., Hao, C., Wang, N., Xie, J., Zhou, B., Yang, Z., Zheng, A., Wei, J., Li, C., Xie, C., et al. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2661854 · Cited by 3
Groothof, D., Erler, N. S., & Bakker, S. J. L. (2026) · Open Research Europe · doi:10.12688/openreseurope.20428.2
Liraglutide-associated body composition change: muscle mass loss and determinants
AYHAN, İ., & Topaloğlu, Ö. (2026) · Çukurova medical journal (Online)/Çukurova medical journal · doi:10.17826/cumj.1925099
Would a weekly shot be enough to solve the obesity problem? a new denial of a complex reality
Duparc, A., Terral, P., & Lairez, O. (2025) · European Journal of Preventive Cardiology · doi:10.1093/eurjpc/zwaf002
PHARMACOLOGICAL TREATMENT FOR OBESITY: MECHANISMS OF ACTION, SAFETY AND THERAPEUTIC EFFICACY
dos Santos, R. R. L., Guasti, E. D. P., Nunes, F. M., Leopoldo, A. S., & Lima‐Leopoldo, A. P. (2026) · International Journal of Health Management Review · doi:10.47172/ijhmreview.v12i1.461
Yu, X., Jia, S., & Shen, D. (2026) · BIO Web of Conferences · doi:10.1051/bioconf/202623702005 · Cited by 1
Khoo, C. M., Tan, M. Z.-W., Eng, S. K., Leong, C. K., Bee, Y. M., Tham, K. W., Bhaskaran, K., Lee, Y. V., Wong, G., Chan, S. L., et al. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1810277
Zheng, Q., Sun, N., Yang, H., Zeng, Y., Zhang, Z., Qi, A., & Li, S. (2026) · BMC Nephrology · doi:10.1186/s12882-026-04888-z · Cited by 1
Metadata
- Authors
- Locatelli, J. C., Costa, J. G., Haynes, A., Naylor, L. H., Fegan, P. G., Yeap, B. B., & Green, D. J.
- Affiliations
- The University of Western Australia (AU)
- Curtin University (AU)
- Corresponding author
- Yeap, Bu B.
- Green, Daniel J.
- ORCID
- Venue
- Diabetes Care
- Publisher
- American Diabetes Association
- Published
- 2024-04-30
- Volume
- 47
- Issue
- 10
- Pages
- 1718-1730
- ISSN
- 0149-5992 (ISSN-L)
- 1935-5548
- OpenAlex
- W4396515179
- Cited by
- 152
- References
- 94
- Citations by year
- 2026: 67 · 2025: 72 · 2024: 13
- FWCI
- 9.49
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Diabetes Care (publishedVersion)
- PubMed (publishedVersion)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- Funders
- National Health and Medical Research Council (APP1080914)
- Western Australian State Government (Research Excellence Award)
- Topics
- Health Sciences › Medicine › Pharmacology (medical) › Pharmacology and Obesity Treatment
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Keywords
- obesity, weight loss, resistance training, lean mass preservation, body composition, sarcopenia, frailty, GLP-1 receptor agonists, GIP receptor agonist, tirzepatide, liraglutide, semaglutide, retatrutide, muscle mass, weight regain, hypocaloric diet
- MeSH terms
- Liraglutide, Body Composition, Humans, Obesity, Weight Loss, Incretins, Resistance Training
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-09-28, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-09-28 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Cited sources are checked with a language model’s help (gpt-6-sol).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review