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Published on: May 26, 2022
Sodium glucose cotransporter 2 inhibitors are associated with renal stabilization in heart transplantation
Lisa M Raven1,2,3, Jerry R Greenfield1,2,3, Andrew Jabbour3,4,5
1Department of Diabetes and Endocrinology, St Vincent's Hospital, 390 Victoria Street, Darlinghurst, Sydney, Australia.
Insights
Sodium glucose cotransporter 2 inhibitors (SGLT2i) may preserve kidney function in heart transplant recipients with diabetes. This study found stable estimated glomerular filtration rate in SGLT2i users versus a decline in non-users.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Heart transplant (HTx) recipients face elevated risks for type 2 diabetes mellitus and chronic kidney disease (CKD).
- Both diabetes and CKD are independent risk factors for increased mortality in HTx patients.
- Sodium glucose cotransporter 2 inhibitors (SGLT2i) are established treatments for diabetes, heart failure, and CKD.
Purpose of the Study:
- To evaluate the impact of SGLT2 inhibitors on renal function in heart transplant recipients with diabetes.
- To assess the association between SGLT2 inhibitor use and renal function changes post-heart transplantation.
Main Methods:
- Retrospective analysis of 104 heart transplant recipients diagnosed with diabetes.
- Comparison of renal function (estimated glomerular filtration rate) at 3 years post-transplant between SGLT2 inhibitor users (n=23) and non-users (n=81).
- Survival analysis adjusted for diabetes type and baseline creatinine.
Main Results:
- SGLT2 inhibitor treatment was associated with stable renal function (median eGFR change: 0 ml/min/1.73 m²).
- Patients not exposed to SGLT2 inhibitors showed a significant decline in renal function (median eGFR change: -15 ml/min/1.73 m²; p=0.02).
- No significant difference in survival was observed based on SGLT2 inhibitor exposure (adjusted HR 0.34, p=0.06).
Conclusions:
- SGLT2 inhibitors may help preserve renal function in heart transplant recipients with diabetes.
- Further prospective studies are warranted to confirm these findings and explore renal outcomes.
- Investigating SGLT2i's role in managing comorbidities in HTx recipients is crucial.
Abstract:
Sodium glucose cotransporter 2 inhibitors (SGLT2i) are standard of care for type 2 diabetes mellitus, heart failure, and chronic kidney disease (CKD). Heart transplant (HTx) recipients are at increased risk of diabetes and CKD, and both are independently associated with increased mortality. In a retrospective analysis of 104 HTx recipients with diabetes (23 exposed to SGLT2i, 81 not exposed), SGLT2i treatment was associated with stable renal function at 3 years post-HTx, measured by estimated glomerular filtration rate change from baseline (median change of 0 ml/min/1.73 m2 (interquartile range [IQR] -13 to +11)), compared to a change of -15 ml/min/1.73 m2 (IQR -27 to +1) in patients not exposed to SGLT2i (p = 0.02). There was no significant difference in survival by SGLT2i exposure, adjusted for diabetes type and baseline creatinine (hazard ratio 0.34, confidence intervals 0.11-1.06, p = 0.06). Further investigation of SGLT2i in HTx recipients, particularly focusing on renal outcomes, is required.
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