Evidence mapPaperPMID 38937282Full record

ReviewDiabetes, obesity & metabolism2024

Changes in lean body mass with glucagon-like peptide-1-based therapies and mitigation strategies.

Ian J Neeland, Jennifer Linge, Andreas L Birkenfeld

2 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Diabetes, obesity & metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 165 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed, 4 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06811324 phase2recruitingstarted 2026, after this paper: background citation

The Effects of Tirzepatide Use on Muscle and Vascular Function Among Obese Older Adults

Ran2026Enrolled20Registered outcomes3Posted comparisons0ConditionsCardiovascular Function, GLP - 1, Obesity Prevention, Sarcopenia in ElderlyArmsTirzepatide
Open the trial in the graph
NCT07702461 recruitingstarted 2026, after this paper: background citation

Determination of Resistance Training Status for Patients on Glucagon-Like Peptide-1 Receptor Agonists

Ran2026Enrolled300Registered outcomes2Posted comparisons0ConditionsDiabetes (DM), Obesity & OverweightArmsGlucagon-Like Peptide-1 Agonist (GLP-1)
Open the trial in the graph
3 · Its place in the literature

Who cites it

165 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Effects of GLP-1 Receptor Agonists on Muscle Mass, Strength, and Quality in MASLD: A Systematic Review.Liver international : official journal of the International Association for the Study of the Liver · 2026
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  13. The evolving landscape of obesity pharmacotherapy.Nature reviews. Drug discovery · 2026
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  18. Lower fall and femoral fracture risks with semaglutide and tirzepatide compared with DPP-4 inhibitors in older adults with type 2 diabetes.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
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105 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ian J NeelandDepartment of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.ORCID 0000-0003-2831-3618
Jennifer LingeAMRA Medical AB, Linköping, Sweden.
Andreas L BirkenfeldInstitute for Diabetes Research and Metabolic Diseases (IDM) of the Helmholtz Center Munich at the Eberhard Karls University Tübingen, Tübingen, Germany.ORCID 0000-0003-1407-9023

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Weight loss induced by glucagon-like peptide-1 receptor agonists (GLP-1RAs) and dual glucagon-like peptide-1 receptor (GLP-1R)/glucose-dependent insulinotropic polypeptide receptor agonists is coming closer to the magnitudes achieved with surgery. However, with greater weight loss there is concern about potential side effects on muscle quantity (mass), health and function. There is heterogeneity in the reported effects of GLP-1-based therapies on lean mass changes in clinical trials: in some studies, reductions in lean mass range between 40% and 60% as a proportion of total weight lost, while other studies show lean mass reductions of approximately 15% or less of total weight lost. There are several potential reasons underlying this heterogeneity, including population, drug-specific/molecular, and comorbidity effects. Furthermore, changes in lean mass may not always reflect changes in muscle mass as the former measure includes not only muscle but also organs, bone, fluids, and water in fat tissue. Based on contemporary evidence with the addition of magnetic resonance imaging-based studies, skeletal muscle changes with GLP-1RA treatments appear to be adaptive: reductions in muscle volume seem to be commensurate with what is expected given ageing, disease status, and weight loss achieved, and the improvement in insulin sensitivity and muscle fat infiltration likely contributes to an adaptive process with improved muscle quality, lowering the probability for loss in strength and function. Nevertheless, factors such as older age and severity of disease may influence the selection of appropriate candidates for these therapies due to risk of sarcopenia. To further improve muscle health during weight loss, several pharmacological treatments to maintain or improve muscle mass designed in combination with GLP-1-based therapies are under development. Future research on GLP-1-based and other therapies designed for weight loss should focus on more accurate and meaningful assessments of muscle mass, composition, as well as function, mobility or strength, to better define their impact on muscle health for the substantial number of patients who will likely be taking these medications well into the future.

Indexed as

Body CompositionGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsMuscle, SkeletalWeight LossDiabetes Mellitus, Type 2FemaleHumansHypoglycemic AgentsObesityGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic Agentscardiovascular diseaseGLP‐1 receptor agonistinsulin resistancemuscleobesitysarcopeniatype 2 diabetes

Identifiers

PMID38937282

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.