Evidence map›Paper›PMID 41291666›Full record

SynthesisBMC urology2025

Effect of GLP-1 agonists on testosterone levels: a systematic review and meta-analysis.

Soraya Hussein Orra, Juan Victor Nabhan Martinez, Breno Cordeiro Porto, Carlo Camargo Passerotti, Rodrigo A S Sardenberg, Jose Arnaldo Shiomi Da Cruz

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC urology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 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.

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

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
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

6 authors.

Soraya Hussein OrraNinth of July University, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0002-0136-8432
Juan Victor Nabhan MartinezNinth of July University, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0008-0609-5799
Breno Cordeiro PortoSurgical Technique and Experimental Surgery Department, University of São Paulo School of Medicine, Cincinato Braga St. 37 - Cj 32 , São Paulo, SP, 01333-011, Brazil.ORCID http://orcid.org/0000-0002-4004-4089
Carlo Camargo PasserottiSurgical Technique and Experimental Surgery Department, University of São Paulo School of Medicine, Cincinato Braga St. 37 - Cj 32 , São Paulo, SP, 01333-011, Brazil.
Rodrigo A S SardenbergInternational Teaching and Research Institute, Hapvida NotreDame Intermédica, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-6010-1829
Jose Arnaldo Shiomi Da CruzSurgical Technique and Experimental Surgery Department, University of São Paulo School of Medicine, Cincinato Braga St. 37 - Cj 32 , São Paulo, SP, 01333-011, Brazil. arnaldoshiomi@yahoo.com.br.ORCID http://orcid.org/0000-0003-4203-3196

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTestosterone plays a central role in endocrine and metabolic functions. Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), widely prescribed for type 2 diabetes and obesity, have been proposed to modulate testosterone levels. Although this association is not yet covered by clinical guidelines, emerging studies suggest favorable effects, possibly due to weight loss and improved insulin sensitivity. This systematic review and meta-analysis aim to synthesize current evidence on how GLP-1 RAs influence testosterone levels and highlight areas for future investigation. MATERIALS AND

methodsA systematic search was conducted using Embase, PubMed, Scopus, Cochrane, and Google Scholar databases through December 2024. Eligible studies included RCTs, cohort studies, and retrospective analyses comparing testosterone levels before and after GLP-1 RA administration. Primary and secondary outcomes included total, free, and bioavailable testosterone, SHBG, and HbA1c. All included studies reported baseline hormone values and used validated measurement techniques. Data analysis was performed using RStudio.

resultsFour studies comprising 219 patients pre-treatment and 216 post-treatment were included. GLP-1 RA use was significantly associated with increased bioavailable testosterone (MD -57.18; 95% CI -87.60 to -26.76; p < 0.001; I

conclusionsGLP-1 RAs appear to elevate bioavailable testosterone and improve glycemic control, while effects on free testosterone and SHBG remain inconclusive. These findings suggest possible endocrine benefits of GLP-1 therapy; however, further well-powered studies are warranted.

Indexed as

Diabetes Mellitus, Type 2Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsTestosteroneHumansGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsTestosteroneErectile DysfunctionFunctional HypogonadismGlucagon-like Peptide-1 Receptor Agonists

Identifiers

PMID41291666
PMCPMC12752444

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.