Effect of Incretin-Based and Nonpharmacologic Weight Loss on Body Composition

BACKGROUND: Incretin-based therapies induce substantial weight loss and are widely prescribed; disproportionate losses in fat-free mass (FFM) and skeletal muscle are a concern. PURPOSE: To evaluate body composition changes associated with incretin therapies in adults with obesity. DATA SOURCES: Scopus, Embase (Elsevier), PubMed (National Institutes of Health, National Library of Medicine), CINAHL, PsycINFO (EBSCOhost), and ClinicalTrials.gov from January 2003 to February 2026. STUDY SELECTION: English-language randomized controlled trials reporting body composition outcomes of liraglutide, semaglutide, tirzepatide, or dulaglutide therapy in adults (aged ≥18 years). DATA EXTRACTION: Primary outcomes included changes in fat mass, FFM, lean soft tissue (LST), muscle-related indices, and visceral adiposity measured by bioelectrical impedance analysis (BIA), dual-energy x-ray absorptiometry (DXA), computed tomography (CT), or magnetic resonance imaging (MRI). Prespecified benchmarks were applied to contextualize expected muscle-related losses (about 25% of total weight loss for FFM or LST derived from BIA or DXA, and about 15% for skeletal muscle measured by CT or MRI). DATA SYNTHESIS: . Weight loss was consistently larger in the incretin intervention groups than in placebo or lifestyle intervention comparators and was consistently accompanied by reductions in total fat mass and visceral adiposity. The degree of muscle-based losses varied widely; no study reported objective physical function outcomes. Within the incretin groups across agents and measurement methods, the median proportion of total weight loss attributable to reductions in muscle-based indices was 34.9% (IQR, 19.0% to 48.2%), with 68% exceeding the benchmark of about 25%; among studies using BIA or DXA, the median was about 34.9% (IQR, 17.0% to 46.9%) of total weight loss, with 65% exceeding the 25% benchmark, and in studies using CT or MRI, the median was about 35.8% (IQR, 29.8% to 50.4%), all exceeding the 15% benchmark. In contrast, the 14 studies reporting weight loss in the lifestyle or placebo comparator groups accounted for a median weight loss of -2.4% (IQR, -4.4% to 1.0%), 50% of which exceeded the respective benchmark. LIMITATION: Heterogeneous body composition methods and reporting precluded meta-analysis. CONCLUSION: Loss of muscle-related indices exceeded prespecified benchmarks in two thirds of incretin-based interventions and half of nonpharmacologic interventions that produced weight loss. Future trials are needed to better understand mechanisms underlying these changes and their clinical implications. PRIMARY FUNDING SOURCE: None. (Open Science Framework: https://doi.org/10.17605/OSF.IO/S3A5E).

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Publication Details

Journal
Annals of Internal Medicine
Published
2026-04-17
DOI
https://doi.org/10.7326/annals-25-00478
Citations
1
Primary Topic
Pharmacology and Obesity Treatment
Type
article
Field-Weighted Citation Impact
18.40
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article

Effect of Incretin-Based and Nonpharmacologic Weight Loss on Body Composition

Emily P. Jones, Danae C. Gross, Carla M. Prado, John A. Batsis et al.
1 citations
Annals of Internal Medicine
Pharmacology and Obesity Treatment
18.40
article

Effect of Incretin-Based and Nonpharmacologic Weight Loss on Body Composition

Emily P. Jones, Danae C. Gross, Carla M. Prado, John A. Batsis, Mauro Zamboni, C Ray Cheever, Alessandro Gavras, Luiz Fernando Meira Filho, Dakota Batchek, Bruna R. da Silva, Bilal Awkal, Annamarie Pape, Rohan Patel, Simone Khandpekar, Marianne Bahna
article en
1 citations

Abstract

BACKGROUND: Incretin-based therapies induce substantial weight loss and are widely prescribed; disproportionate losses in fat-free mass (FFM) and skeletal muscle are a concern. PURPOSE: To evaluate body composition changes associated with incretin therapies in adults with obesity. DATA SOURCES: Scopus, Embase (Elsevier), PubMed (National Institutes of Health, National Library of Medicine), CINAHL, PsycINFO (EBSCOhost), and ClinicalTrials.gov from January 2003 to February 2026. STUDY SELECTION: English-language randomized controlled trials reporting body composition outcomes of liraglutide, semaglutide, tirzepatide, or dulaglutide therapy in adults (aged ≥18 years). DATA EXTRACTION: Primary outcomes included changes in fat mass, FFM, lean soft tissue (LST), muscle-related indices, and visceral adiposity measured by bioelectrical impedance analysis (BIA), dual-energy x-ray absorptiometry (DXA), computed tomography (CT), or magnetic resonance imaging (MRI). Prespecified benchmarks were applied to contextualize expected muscle-related losses (about 25% of total weight loss for FFM or LST derived from BIA or DXA, and about 15% for skeletal muscle measured by CT or MRI). DATA SYNTHESIS: . Weight loss was consistently larger in the incretin intervention groups than in placebo or lifestyle intervention comparators and was consistently accompanied by reductions in total fat mass and visceral adiposity. The degree of muscle-based losses varied widely; no study reported objective physical function outcomes. Within the incretin groups across agents and measurement methods, the median proportion of total weight loss attributable to reductions in muscle-based indices was 34.9% (IQR, 19.0% to 48.2%), with 68% exceeding the benchmark of about 25%; among studies using BIA or DXA, the median was about 34.9% (IQR, 17.0% to 46.9%) of total weight loss, with 65% exceeding the 25% benchmark, and in studies using CT or MRI, the median was about 35.8% (IQR, 29.8% to 50.4%), all exceeding the 15% benchmark. In contrast, the 14 studies reporting weight loss in the lifestyle or placebo comparator groups accounted for a median weight loss of -2.4% (IQR, -4.4% to 1.0%), 50% of which exceeded the respective benchmark. LIMITATION: Heterogeneous body composition methods and reporting precluded meta-analysis. CONCLUSION: Loss of muscle-related indices exceeded prespecified benchmarks in two thirds of incretin-based interventions and half of nonpharmacologic interventions that produced weight loss. Future trials are needed to better understand mechanisms underlying these changes and their clinical implications. PRIMARY FUNDING SOURCE: None. (Open Science Framework: https://doi.org/10.17605/OSF.IO/S3A5E).

Annals of Internal Medicine
University of North Carolina at Chapel Hill (US), University of Verona (IT), University of Alberta (CA)
Zero hunger
Openalex Percentile: Top 1%
Pharmacology and Obesity Treatment
18.40
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