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.

JHLT Open
|April 18, 2025
PubMed

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.

Related Concept Videos

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
305
Secondary Active Transport01:55

Secondary Active Transport

One example of how cells use the energy contained in electrochemical gradients is demonstrated by glucose transport into cells. The ion vital to this process is sodium (Na+), which is typically present in higher concentrations extracellularly than in the cytosol. Such a concentration difference is due, in part, to the action of an enzyme “pump” embedded in the cellular membrane that actively expels Na+ from a cell. Importantly, as this pump contributes to the high concentration of...
116.8K
Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
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:
22.2K