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Published on: October 31, 2007
Benefits of Glucagon-like Peptide-1 Receptor Agonists After Kidney Transplantation
Sukhdeep S Sahi1, Oscar Garcia Valencia1, Jie Na2
1Department of Medicine, Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota.
Objective:
Benefits of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in kidney transplant (KT) recipients have not been adequately studied.
Methods:
We retrospectively examined the effects of GLP-1 RA on mortality, kidney outcomes and metabolic parameters in KT recipients with type 2 diabetes mellitus (T2DM) treated versus not treated with GLP-1 RA. A reference group of KT recipients not treated with GLP-1 RA was used for comparison. Data were analyzed using analysis of variance, χ2 tests, and generalized estimating equation models. GLP-1 RA was used as a time-dependent model in Cox regression modeling. For survival analysis, the final model fitting was stratified by race-ethnicity.
Results:
Seventy-seven KT recipients with T2DM were treated with GLP-1 RA for at least 12 months. Reference group included 2094 patients not on GLP-1 RA. The mean (SD) age at transplant was 57.9 (9.5) and 60.8 (9.5) years for the treatment and reference groups, respectively. Median follow-up time from the index date for mortality was 1.5 (IQR 0.99, 2.4) in the treatment and 5.8 (IQR 3.4, 9.1) years in the reference group. GLP-1 RA use was associated with improved survival (P = .049), decreased urine albumin to creatinine ratio (net reduction of 10.62 mg/g per year, P = .003), slower estimated glomerular filtration rate decline (1.04 vs 1.56 mL/min/1.73 m2 per year, P = .04), and lower troponin levels.
Conclusions:
GLP-1 RA in KT recipients with T2DM was associated with reduced mortality, and improved kidney function compared to the reference group. Larger, prospective studies are needed to fully evaluate the risks and benefits of GLP-1 RA therapy in KT recipients.
Insights
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) show promise in kidney transplant recipients with type 2 diabetes mellitus, improving survival and kidney function. Further research is recommended to confirm these benefits.
Area of Science:
- Nephrology
- Endocrinology
- Transplantation Immunology
Background:
- Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are increasingly used for type 2 diabetes mellitus (T2DM).
- Their benefits in kidney transplant (KT) recipients, particularly those with T2DM, remain under-investigated.
- Understanding GLP-1 RA effects in this population is crucial for optimizing post-transplant care.
Purpose of the Study:
- To evaluate the impact of GLP-1 receptor agonists (GLP-1 RAs) on mortality, kidney outcomes, and metabolic parameters in kidney transplant recipients with type 2 diabetes mellitus.
- To compare outcomes between KT recipients treated with GLP-1 RAs and a matched reference group not receiving these agents.
Main Methods:
- Retrospective analysis of KT recipients with T2DM, comparing those treated with GLP-1 RAs (n=77) versus a reference group (n=2094).
- Utilized analysis of variance, chi-squared tests, and generalized estimating equation models for data analysis.
- Employed time-dependent Cox regression modeling for GLP-1 RA use and stratified survival analysis by race-ethnicity.
Main Results:
- GLP-1 RA use was associated with significantly improved survival (P = .049).
- Treatment led to a decreased urine albumin-to-creatinine ratio (net reduction of 10.62 mg/g per year, P = .003) and slower estimated glomerular filtration rate decline (1.04 vs 1.56 mL/min/1.73 m² per year, P = .04).
- Lower troponin levels were also observed in the GLP-1 RA group.
Conclusions:
- GLP-1 receptor agonists (GLP-1 RAs) are associated with reduced mortality and improved kidney function in kidney transplant recipients with type 2 diabetes mellitus.
- These findings suggest a potential protective role for GLP-1 RAs in this vulnerable patient population.
- Larger, prospective studies are warranted to definitively establish the risks and benefits of GLP-1 RA therapy in KT recipients.
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