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Updated: Sep 10, 2025

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Published on: August 2, 2024
Sodium glucose cotransporter 2 inhibitor use after heart transplant: Current knowledge and potential applications
Lisa M Raven1, Lina Brinker2, Konstantinos Sideris2
1Department of Diabetes and Endocrinology, St Vincent's Hospital Sydney, Sydney, New South Wales, Australia; School of Clinical Medicine, St Vincent's Campus, Faculty of Medicine and Health, University of New South Wales, Sydney, New South Wales, Australia.
Insights
Sodium glucose cotransporter 2 inhibitors (SGLT2i) show promise for heart transplant (HTx) recipients. These drugs may improve cardiovascular, kidney, and metabolic health, addressing key long-term complications post-transplant.
Area of Science:
- Cardiology
- Nephrology
- Endocrinology
Background:
- Heart transplant (HTx) improves survival for end-stage heart failure but long-term outcomes are limited by comorbidities.
- Comorbidities like cardiovascular, kidney, and metabolic diseases pose significant risks post-HTx.
- Transplant recipients are often excluded from clinical trials, limiting evidence for beneficial treatments.
Purpose of the Study:
- To review the potential benefits of Sodium-glucose cotransporter 2 inhibitors (SGLT2i) in heart transplant recipients.
- To explore the mechanistic pathways through which SGLT2i may mitigate post-HTx morbidities.
- To summarize existing experimental and retrospective data and highlight the need for prospective trials.
Main Methods:
- Review of mechanistic rationale for SGLT2i use in HTx recipients.
- Summary of experimental studies on SGLT2i in reversing calcineurin inhibitor-induced injury.
- Analysis of retrospective studies assessing SGLT2i effects in HTx patients.
Main Results:
- SGLT2i possess renoprotective, glycemic, vascular, anti-inflammatory, and erythropoietic effects.
- Experimental studies show SGLT2i can reverse calcineurin inhibitor-associated kidney and pancreatic injury.
- Retrospective studies indicate SGLT2i improve glycemia, weight, and renal function in HTx recipients.
Conclusions:
- SGLT2i offer potential benefits for managing long-term complications in heart transplant recipients.
- Further prospective clinical trials are essential to confirm the efficacy and safety of SGLT2i in this population.
- Ongoing registered trials are crucial for advancing evidence-based care for HTx survivors.
Abstract:
Heart transplant (HTx) markedly improves survival and quality of life in patients with stage D heart failure. However, long-term survival post-HTx is limited by increased risk and progression of cardiovascular disease, chronic kidney disease, and metabolic disease. There is a lack of proven mitigating treatments for these morbidities, and transplant recipients are frequently excluded from clinical trials of novel agents, which could be of benefit in this population. Sodium glucose cotransporter 2 inhibitors (SGLT2i), initially a treatment for type 2 diabetes, are now established treatments for heart failure or chronic kidney disease, with or without type 2 diabetes. There are strong mechanistic reasons that suggest HTx recipients should derive specific benefits from SGLT2i. However, prospective data to confirm these hypotheses in transplant recipient populations are limited. In this review, we present mechanisms through which SGLT2i may benefit HTx recipients, including renoprotective, glycemic, vascular, anti-inflammatory, and erythropoietic effects. We present a summary of experimental studies of SGLT2i in reversal of calcineurin inhibitor-associated kidney and pancreatic injury, and retrospective studies of SGLT2i in HTx recipients demonstrating improvement in glycaemia, weight, and renal function. Prospective trials of SGLT2i in HTx recipients are required, and the currently registered trials are highlighted.
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Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Glucose Absorption Into the Small Intestine

