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Updated: Jun 5, 2025

Transplantation of Pancreatic Islets Into the Kidney Capsule of Diabetic Mice
Published on: October 31, 2007
Use of glucagon-like peptide type 1 receptor agonists in kidney transplant recipients
Luis Alberto Vigara1, Florentino Villanego2, Cristhian Orellana2
1Department of Nephrology, Puerta del Mar University Hospital, Cádiz, Spain; Department of Nephrology, Jerez de la Frontera University Hospital, Cádiz, Spain.
Introduction:
In kidney transplant (KT) recipients diabetes mellitus (DM) are associated with an increased mortality and a poorer graft survival. Glucagon-like peptide 1 receptor agonists (GLP1-RA) have demonstrated cardiovascular and renal benefits in the general population. However, there is lacking evidence in KT recipients.
Objective:
To analyze the efficacy and safety of glucagon-like peptide 1 receptor GLP1-RA in a cohort of KT recipients.
Methods:
Multicenter retrospective cohort study of KT patients with DM who started subcutaneous GLP1-RA in 3 hospitals in the province of Cádiz between February 2016 and July 2022. Estimated glomerular filtration rate (eGFR), proteinuria, and weight at baseline and after 6 and 12 months were collected. We analyzed glycemic control, blood pressure, lipid profile, and doses and trough levels of tacrolimus. We document episodes of acute rejection (AR), de novo donor-specific antibodies (dnDSA), and adverse effects.
Results:
During this period, 96 KT with DM started treatment with GLP1-RA, of which 84 had a minimum follow-up of 6 months and 61 were followed for 12 months. A significant reduction was observed in proteinuria (-19.1 mg/g, p = 0.000; -46.6 mg/g, p = 0.000), weight (-3.6 kg, p = 0.000; -3.6 kg, p = 0.000), glycosylated hemoglobin (-0.7%, p = 0.000; -0.9%, p = 0.000), systolic blood pressure (-7.5 mmHg, p = 0.013; -7.3 mmHg, p = 0.004), total cholesterol (-11.5 mg/dL, p = 0.001; -15.6 mg/dl, p = 0.002) and LDL cholesterol (-9.2 mg/dl, p = 0.002; -16.8 mg/dl, p = 0.000) at 6 months and 1 year of follow-up. The eGFR remained stable and the dose and trough levels of tacrolimus did not change. No episodes of AR or development of dnDSA were observed during follow-up.
Conclusions:
GLP1-RA in KT patients can be a safe and effective option for the management of DM in KT.
Insights
Glucagon-like peptide 1 receptor agonists (GLP1-RA) show promise in managing diabetes mellitus (DM) in kidney transplant (KT) recipients. This study found GLP1-RA safe and effective, improving proteinuria, weight, glycemic control, and cardiovascular risk factors without impacting graft survival.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Diabetes mellitus (DM) in kidney transplant (KT) recipients is linked to increased mortality and reduced graft survival.
- Glucagon-like peptide 1 receptor agonists (GLP1-RA) offer cardiovascular and renal benefits in the general population, but evidence in KT recipients is limited.
Purpose of the Study:
- To evaluate the efficacy and safety of GLP1-RA in KT recipients with DM.
Main Methods:
- A multicenter retrospective cohort study included 96 KT patients with DM treated with GLP1-RA between 2016 and 2022.
- Data collected included eGFR, proteinuria, weight, glycemic control, blood pressure, lipid profile, and tacrolimus levels.
- Outcomes assessed were changes in these parameters, acute rejection (AR), and de novo donor-specific antibodies (dnDSA).
Main Results:
- GLP1-RA treatment led to significant reductions in proteinuria, weight, HbA1c, systolic blood pressure, total cholesterol, and LDL cholesterol at 6 and 12 months.
- Estimated glomerular filtration rate (eGFR) remained stable, and tacrolimus levels were unchanged.
- No episodes of AR or dnDSA were observed during the follow-up period.
Conclusions:
- GLP1-RA represent a safe and effective therapeutic option for managing DM in kidney transplant recipients.
- The findings support the use of GLP1-RA to improve metabolic and cardiovascular profiles in this patient population without compromising graft integrity.
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