Evidence map›Paper›PMID 41211586›Full record

SynthesisJournal of obesity2025

Efficacy and Safety of Glucagon-Like Peptide-1 Receptor Agonists for Obesity Management in Adults With and Without Type 2 Diabetes: A Systematic Review.

Jena Velji-Ibrahim, Dhruvil Radadiya, Kalpit Devani, Harsh Patel, Piyush Nathani, Cesare Hassan, Nicola Pugliese, Christopher Thompson, Prateek Sharma

Erratum issuedAbstract readSystematic Review
In one paragraph

Synthesis in Journal of obesity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jena Velji-IbrahimGastroenterology and Liver Center, Prisma Health-Upstate, University of South Carolina School of Medicine, Greenville, South Carolina, USA.ORCID 0000-0002-5282-0727
Dhruvil RadadiyaGastroenterology, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Kalpit DevaniGastroenterology and Liver Center, Prisma Health-Upstate, University of South Carolina School of Medicine, Greenville, South Carolina, USA.
Harsh PatelDepartment of Gastroenterology, Hepatology and Motility, University of Kansas Medical Center, Kansas City, Kansas, USA.
Piyush NathaniDepartment of Gastroenterology, Hepatology and Motility, University of Kansas Medical Center, Kansas City, Kansas, USA.
Cesare HassanDepartment of Gastroenterology and Hepatology, Humanitas Research Hospital, Milan, Italy.
Nicola PuglieseDepartment of Gastroenterology and Hepatology, Humanitas Research Hospital, Milan, Italy.ORCID 0000-0001-6466-1412
Christopher ThompsonDepartment of Advanced Endoscopy, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Prateek SharmaDepartment of Gastroenterology, Hepatology and Motility, University of Kansas Medical Center, Kansas City, Kansas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This systematic review aimed to assess the efficacy and safety of GLP-1 RAs in adults with obesity or overweight, by comparing different GLP-1 RAs, identifying the most effective agents, and evaluating adverse effects. Methods: We systematically searched Embase, MEDLINE, and Cochrane for phase 3 and 4 randomized controlled trials (RCTs) with a minimum duration of 40 weeks. Included studies compared GLP-1 RAs to placebo or to each other in adults with obesity (BMI ≥ 30 kg/m Results: A total of 22 RCTs involving 41,757 participants were included. Among adults with T2DM, the greatest weight reductions were observed with tirzepatide 15 mg (-9.5 kg at 40 weeks; 72% lost ≥ 5% of baseline weight) and semaglutide 2.4 mg (-9.6% body weight at 68 weeks; 69% lost ≥ 5%). In participants without T2DM, semaglutide 2.4 mg (-14.9% body weight at 68 weeks) and tirzepatide 15 mg (-20.9% at 72 weeks) produced the most substantial effects, while semaglutide 50 mg was also effective in nondiabetic patients. Liraglutide 3 mg showed modest efficacy. Across trials, GLP-1 RAs were consistently associated with a higher frequency of gastrointestinal adverse events compared to placebo, including nausea (14%-28% vs. 5%-10%), vomiting (6%-12% vs. 2%-4%), and diarrhea (8%-20% vs. 4%-7%). The risk of pancreatitis and serious adverse events remained comparable to placebo. Conclusions: GLP-1 RAs, especially semaglutide and tirzepatide, are effective for weight management. Liraglutide may remain a viable, cost-effective alternative.

Indexed as

Diabetes Mellitus, Type 2Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsObesityAdultGlucagon-Like Peptide 1Glucagon-Like PeptidesHumansRandomized Controlled Trials as TopicSemaglutideTreatment OutcomeWeight LossGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsGlucagon-Like PeptidesHypoglycemic AgentsSemaglutidediabetes mellitusglucagon-like peptide-1 receptor agonistobesitytirzepatideweight loss

Identifiers

PMID41211586
PMCPMC12591819

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.