Evidence map›Paper›PMID 41498523›Full record

SynthesisThe journal of sexual medicine2026

Effects of glucagon-like peptide-1 receptor agonists on male reproductive hormones, semen parameters, and metabolic outcomes: a systematic review.

Mohammad Ghassab Deameh, Mohamed Ramez, Rashed Rowaiee, Baha' Aldeen Bani Irshid, Hamza Mohamed, Abdelrahman Abdelshafi, Mohammad Ali Al-Osoufi, Tarek Mohamed, Safa Botros Hegazin, Omer Raheem

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in The journal of sexual medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

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

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Mohammad Ghassab DeamehDepartment of Urology, Faculty of Medicine, Al-Balqa Applied University, As-Salt 19117, Jordan.ORCID 0009-0005-6197-3273
Mohamed RamezDepartment of Urology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Rashed RowaieeDepartment of Urology, Cleveland Clinic Abu Dhabi, Abu Dhabi 112412, UAE.
Baha' Aldeen Bani IrshidDepartment of Urology, Princess Basma Teaching Hospital, Irbid 21110, Jordan.
Hamza MohamedDepartment of Urology, Faculty of Medicine, Assiut University, Assiut 71515, Egypt.
Abdelrahman AbdelshafiDepartment of Urology, Faculty of Medicine, Assiut University, Assiut 71515, Egypt.
Mohammad Ali Al-OsoufiDepartment of Urology, Prince Hamzah Hospital, Amman 11947, Jordan.
Tarek MohamedUrology Department, United Lincolnshire Hospitals NHS Trust, Lincoln LN2 5QY, United Kingdom.
Safa Botros HegazinDepartment of General Surgery, Cleveland Clinic Abu Dhabi, Abu Dhabi 112412, UAE.
Omer RaheemDepartment of Urology, Cleveland Clinic Abu Dhabi, Abu Dhabi 112412, UAE.ORCID 0000-0001-6117-116X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGlucagon-like peptide-1 receptor agonists (GLP-1RAs) are antidiabetic agents that also induce weight loss. Their widespread use has prompted investigation of potential benefits beyond glycemic control, including effects on male sexual and reproductive function. Emerging evidence suggests that they may improve male reproductive parameters, particularly in men with metabolic dysfunction.

objectivesTo systematically evaluate the effects of GLP-1RAs (liraglutide, semaglutide, dulaglutide, and exenatide) on male reproductive hormones, semen parameters, and metabolic outcomes.

methodsWe conducted a systematic review following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We searched in PubMed, Embase, Scopus, and Web of Science up to April 2025. Eligible studies included randomized controlled trials (RCTs) and cohort studies evaluating the effects of GLP-1RAs in adult men. Assessed the risk of bias with the risk of bias 2 tool for RCT and the Risk Of Bias In Non-Randomized Studies of Interventions (ROBINS-I) tool for observational studies.

resultsTen studies involving a total of 639 men were included. GLP-1RAs were consistently associated with increased total testosterone, particularly in men with obesity, type 2 diabetes, or functional hypogonadism. Free testosterone changes were inconsistent, often offset by concurrent rises in sex hormone-binding globulin. Luteinizing hormone and follicle-stimulating hormone levels were preserved or increased with GLP-1RA use, in contrast to the suppression observed in testosterone therapy comparator groups. Improvements in semen parameters were reported in obese or hypogonadal men; however, no significant changes were found in healthy individuals.

conclusionGLP-1RAs may improve testosterone levels and potentially enhance semen quality in men with metabolic issues, while maintaining gonadotropin function. They could serve as fertility-sparing alternatives to testosterone therapy in some obesity-related hypogonadism cases. More long-term, controlled studies with standardized fertility measures are needed to confirm their role in male reproductive health.

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsSemenExenatideGlucagon-Like PeptidesHumansImmunoglobulin Fc FragmentsLiraglutideLuteinizing HormoneMaleRecombinant Fusion ProteinsSemaglutideSemen AnalysisSex Hormone-Binding GlobulinTestosteronedulaglutideExenatideGlucagon-Like Peptide-1 Receptor AgonistsGlucagon-Like PeptidesHypoglycemic AgentsImmunoglobulin Fc FragmentsLiraglutideLuteinizing HormoneRecombinant Fusion ProteinsSemaglutideSex Hormone-Binding GlobulinTestosteroneGLP-1 agonistshypogonadismmale infertilitysemen analysistestosterone

Identifiers

PMID41498523

What OpenQuestion holds

Textmetadata
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.