Glucagon-like peptide 1 receptor agonists and renal outcomes in kidney transplant recipients with diabetes mellitus

被引:1
作者
Cohen, Talia Diker [1 ,5 ]
Rudman, Yaron [1 ,5 ]
Turjeman, Adi [2 ,5 ]
Akirov, Amit [1 ,5 ]
Steinmetz, Tali [3 ,5 ]
Calvarysky, Bronya [4 ,6 ]
Dotan, Idit [1 ,5 ]
机构
[1] Beilinson Med Ctr, Inst Endocrinol Diabet & Metab, Rabin Med Ctr, 39 Jabotinski St, IL-4941492 Petah Tiqwa, Israel
[2] Beilinson Med Ctr, Rabin Med Ctr, Res author, Petah Tiqwa, Israel
[3] Beilinson Med Ctr, Inst Nephrol, Rabin Med Ctr, Petah Tiqwa, Israel
[4] Beilinson Med Ctr, Rabin Med Ctr, Pharm, Petah Tiqwa, Israel
[5] Tel Aviv Univ, Fac Med, Tel Aviv, Israel
[6] Hebrew Univ Jerusalem, Fac Med, Jerusalem, Israel
关键词
GLP1 receptor agonists; Kidney transplantation; Post-transplant diabetes; LIRAGLUTIDE; RISK;
D O I
10.1016/j.diabet.2025.101624
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: Glucagon-like peptide-1 receptor agonists (GLP1-RAs) show reno-protective effects in type 2 diabetes. Limited data is available on their use in post-transplant diabetes mellitus. We aimed to explore the effect of GLP1RAs on renal outcomes in diabetic kidney transplant recipients (KTR). Methods: We conducted a cohort retrospective study on adult KTR with diabetes mellitus. KTR treated with GLP1RAs were matched with non-users. The primary outcome was the first occurrence of graft rejection, start of dialysis, re-transplantation or all-cause mortality. Other outcomes included a composite of the first occurrence of a genitourinary infection or all-cause mortality, and all-cause mortality. Metabolic effects of GLP1-RA treatment and risk for biliopancreatic adverse events were also explored. Results: We included 272 patients (69 % males, average age 58.3 +/- 11.0 years) with a 3.1-year median follow-up. The use of GLP1-RAs lowered the incidence of the composite renal outcome after adjustment for independent risk factors (114 versus 68 events per 1000-patient years in controls versus GLP1-RA users, HR 0.489, 95 % CI 0.271-0.883). GLP-RA users had improved glycemic control, lipid profile and a decrease in body mass index. The treatment was safe without increased genitourinary infections or biliopancreatic events. Conclusion: The use of GLP1-RAs decreased the risk of a composite outcome of renal dysfunction and mortality, improved metabolic control and showed safety of use in a large cohort of diabetic KTR, suggesting renoprotective effects in this high-risk population. Prospective data is further needed in KTR who are excluded from large RCTs.
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页数:7
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