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GLP-1 receptor agonists in kidney transplant recipients with type 2 diabetes mellitus: a systematic review and meta-analysis on mortality and major adverse kidney events

dc.contributor.coauthorNatche, Julia
dc.contributor.coauthorJiakponna, Enyinnaya Calistus
dc.contributor.coauthorAhmad, Feras
dc.contributor.coauthorEze, Belinda
dc.contributor.coauthorNawaz, Usama Hassan
dc.contributor.coauthorEl-Amri, Imane
dc.contributor.coauthorShrestha, Sheelu
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.kuauthorAliyeva, Türkan
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.date.accessioned2026-02-26T07:11:53Z
dc.date.available2026-02-25
dc.date.issued2026
dc.description.abstractBackground Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are increasingly used in patients with type 2 diabetes mellitus and chronic kidney disease. However, their safety and efficacy in kidney transplant recipients remain uncertain. This study aims to evaluate the impact of GLP-1 RAs on all-cause mortality, major adverse cardiovascular events (MACE), and major adverse kidney events (MAKE) in adult kidney transplant recipients. Methods We conducted a systematic review and meta-analysis of retrospective cohort studies reporting outcomes in adult kidney transplant recipients treated with GLP-1 RAs. A comprehensive search of PubMed, Embase and Cochrane Library was performed up to July 2025. Studies were included if they reported on at least one of the following outcomes: all-cause mortality, MACE, or MAKE. Pooled hazard ratios (HRs) with 95% confidence intervals (CIs) were calculated using a random-effects model. Results A total of four retrospective cohort studies involving 27,153 were included. A total of 5,479 (20.2%) patients received GLP-1 RAs. The median follow-up period across studies ranged from 1.38 to 3.1 years. GLP-1 RAs treatment was associated with a significant reduction in all-cause mortality, with an aHR of 0.52 (95% CI: 0.32-0.85, I-2 = 86%; p = 0.009). Similarly, a significant reduction in MAKEs was observed, with a pooled aHR of 0.62 (95% CI, 0.53-0.73; I-2 = 15%; p < 0.00001). Conclusions In kidney transplant recipients with type 2 DM, GLP-1 RAs appear to be associated with reduced risks of all-cause mortality and MAKEs. However, given the high heterogeneity across studies and the influence of a single large cohort, these findings should be interpreted with caution and considered exploratory. Prospective studies are needed to confirm the long-term safety and efficacy of GLP-1 RAs in this population.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessGreen OA
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionN/A
dc.identifier.doi10.1007/s40200-025-01801-7
dc.identifier.eissn2251-6581
dc.identifier.embargoNo
dc.identifier.issue1
dc.identifier.pubmed41522206
dc.identifier.quartileQ4
dc.identifier.scopus2-s2.0-105027219030
dc.identifier.urihttps://doi.org/10.1007/s40200-025-01801-7
dc.identifier.urihttps://hdl.handle.net/20.500.14288/32433
dc.identifier.volume25
dc.identifier.wos001656776700003
dc.keywordsGLP-1 RAs
dc.keywordsKidney transplantation
dc.keywordsMortality
dc.keywordsMACE
dc.keywordsMAKE
dc.language.isoeng
dc.publisherSpringer
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofJournal of Diabetes and Metabolic Disorders
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.uriAttribution, Non-commercial, No Derivative Works (CC-BY-NC-ND)
dc.subjectEndocrinology
dc.subjectMetabolism
dc.titleGLP-1 receptor agonists in kidney transplant recipients with type 2 diabetes mellitus: a systematic review and meta-analysis on mortality and major adverse kidney events
dc.typeJournal Article
dspace.entity.typePublication
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