Diabetes mellitus (DM) is frequent in kidney transplant recipients (KTRs), reducing graft and patient survival. In recent years, hypoglycemic agents have been approved for chronic kidney disease (CKD) patients, such as sodium glucose co-transporter type 2 inhibitors (SGLT2is), glucagon-like peptide-1 receptor agonists (GLP1RAs), and nonsteroidal mineralocorticoid receptor antagonists (ns-MRAs), such as finerenone. Several studies demonstrated the ability of these drugs to reduce cardiovascular (CV) events and kidney disease progression in diabetic CKD patients. In this review, we will describe their use in KTRs with type 2 DM or post-transplant diabetes mellitus (PTDM), focusing on the potential positive effects. In particular, we will report literature data from observational studies, meta-analyses, and clinical trials. Based on their mechanism of actions, these drugs may balance the negative effects of immunosuppressive therapy on metabolic balance, reducing the risk of PTDM and CV events, that remain the first cause of death in KTRs. Generally, SGLT2is and GLP1RAs appear to be safe and efficacious in KTRs, and no interaction with immunosuppressive drugs or an increased risk of rejection has been reported. Regarding finerenone, no literature data are available and only one clinical trial is ongoing. In conclusion, although the 2022 KDIGO guidelines recommend caution in KTRs, the last meeting in Vienna on PTDM encourages their use in this population.

Bartoli, G., Dello Strologo, A., Arena, M., Josè Ceravolo, M., Mitterhofer, A.p., Pesce, F., et al. (2025). Diabetes Mellitus in Kidney Transplant Recipients and New Hypoglycemic Agent Options. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 26(13) [10.3390/ijms26135952].

Diabetes Mellitus in Kidney Transplant Recipients and New Hypoglycemic Agent Options

Giulia Bartoli;Anna Paola Mitterhofer;
2025-01-01

Abstract

Diabetes mellitus (DM) is frequent in kidney transplant recipients (KTRs), reducing graft and patient survival. In recent years, hypoglycemic agents have been approved for chronic kidney disease (CKD) patients, such as sodium glucose co-transporter type 2 inhibitors (SGLT2is), glucagon-like peptide-1 receptor agonists (GLP1RAs), and nonsteroidal mineralocorticoid receptor antagonists (ns-MRAs), such as finerenone. Several studies demonstrated the ability of these drugs to reduce cardiovascular (CV) events and kidney disease progression in diabetic CKD patients. In this review, we will describe their use in KTRs with type 2 DM or post-transplant diabetes mellitus (PTDM), focusing on the potential positive effects. In particular, we will report literature data from observational studies, meta-analyses, and clinical trials. Based on their mechanism of actions, these drugs may balance the negative effects of immunosuppressive therapy on metabolic balance, reducing the risk of PTDM and CV events, that remain the first cause of death in KTRs. Generally, SGLT2is and GLP1RAs appear to be safe and efficacious in KTRs, and no interaction with immunosuppressive drugs or an increased risk of rejection has been reported. Regarding finerenone, no literature data are available and only one clinical trial is ongoing. In conclusion, although the 2022 KDIGO guidelines recommend caution in KTRs, the last meeting in Vienna on PTDM encourages their use in this population.
2025
Pubblicato
Rilevanza internazionale
Recensione
Esperti anonimi
Settore MED/14
Settore MEDS-08/B - Nefrologia
English
chronic kidney disease; glucagon-like peptide-1 receptor agonists; hypoglycemic agent; kidney transplantation;
nonsteroidal mineralocorticoid receptor antagonist; post-transplant diabetes mellitus ; sodium glucose co-transporter type 2 inhibitors
Bartoli, G., Dello Strologo, A., Arena, M., Josè Ceravolo, M., Mitterhofer, A.p., Pesce, F., et al. (2025). Diabetes Mellitus in Kidney Transplant Recipients and New Hypoglycemic Agent Options. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 26(13) [10.3390/ijms26135952].
Bartoli, G; Dello Strologo, A; Arena, M; Josè Ceravolo, M; Mitterhofer, Ap; Pesce, F; Grandaliano, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/435523
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