BMC Nephrology
Semaglutide in adults receiving dialysis: anthropometric outcomes and transplant-access milestones in a systematic review with exploratory meta‑analysis
By Yiwei Shang, Wenfang He, Ran He and 7 others.
Abstract
Abstract Background Obesity can delay access to kidney transplantation in patients receiving dialysis, but evidence for semaglutide in this setting remains limited. We evaluated anthropometric, safety and transplant-access outcomes in adults receiving dialysis. Methods We searched PubMed, Embase, the Cochrane Library/CENTRAL, ClinicalTrials.gov and the World Health Organization International Clinical Trials Registry Platform from inception to 23 May 2026. Eligible reports evaluated semaglutide in adults receiving dialysis; mixed populations without separately extractable dialysis-specific outcomes were retained only for supportive or descriptive analyses. Mean within-cohort changes in body weight and body mass index (BMI) were pooled with random-effects models when change-score standard deviations were directly reported. Comparative estimates, transplant-access milestones and safety outcomes were synthesised separately. Results Twenty reports were included in the evidence map; seven main studies comprised 147 semaglutide-exposed participants. Four studies (89 participants) contributed to an exploratory weighted descriptive synthesis of within-cohort body-weight change, with a weighted mean change of − 7.25 kg (95% confidence interval − 10.70 to − 3.80; I² = 87%). Three studies (65 participants) contributed to the corresponding exploratory BMI synthesis, with a weighted mean change of − 2.79 kg/m² (95% confidence interval − 4.31 to − 1.27; I² = 92%). In selected transplant-candidate cohorts, waitlist activation or listing occurred in 14/29 and 13/23 previously ineligible patients; 7/29 and 8/23 were subsequently transplanted. A third cohort reported 3/41 transplants. In the early-terminated RAISE-KT registry result from a mixed advanced-CKD/dialysis population, new activation occurred in 3/5 semaglutide-treated participants versus 0/7 placebo. Gastrointestinal adverse events were reported in 59/146 participants and adverse-event-related discontinuation in 21/147. Conclusions Across dialysis cohorts, body weight and BMI decreased during follow-up after semaglutide initiation, but the evidence base was small, heterogeneous and predominantly uncontrolled. Transplant-access events were observed in selected candidates, but causal effects on listing or transplantation cannot be established. Comparative prospective studies with standardised anthropometric, transplant-access and dialysis-specific safety outcomes are needed.



