Related Experiment Video
Updated: Jan 14, 2026

A Rat Orthotopic Renal Transplantation Model for Renal Allograft Rejection
Published on: February 2, 2022
Efficacy and Safety of Sglt-2 Inhibitors In Renal Allograft Recipients: an Open-Label, Single-Center Prospective
M S Novikova1, L O Minushkina2, S S Allazova3
1Central State Medical Academy of the Administrative Directorate of the President of the Russian Federation; Endocrinology Dispensary of the Moscow Department of Health.
Sodium-glucose cotransporter-2 inhibitors (SGLT-2i) significantly reduced mortality and adverse cardiovascular and renal outcomes in kidney transplant recipients (KTRs). This therapy also slowed chronic kidney disease progression, irrespective of post-transplant diabetes mellitus (PTDM) status.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Kidney transplant recipients (KTRs) face significant risks of cardiovascular and renal complications.
- Post-transplant diabetes mellitus (PTDM) is a common complication in KTRs, further increasing morbidity and mortality.
- Evaluating the efficacy of novel therapies like sodium-glucose cotransporter-2 inhibitors (SGLT-2i) in this population is crucial.
Purpose of the Study:
- To assess the safety and effectiveness of SGLT-2i therapy in KTRs.
- To compare outcomes in KTRs with and without PTDM receiving SGLT-2i.
- To evaluate the impact of SGLT-2i on cardiovascular, renal, and overall mortality.
Main Methods:
- A prospective, single-center study included 2146 KTRs transplanted over one year prior with stable graft function.
- 107 KTRs were prescribed SGLT-2i (empagliflozin or dapagliflozin).
- Pseudo-randomization created an experimental group (n=78) with SGLT-2i and a control group (n=78) without SGLT-2i, with comparable baseline characteristics.
Main Results:
- SGLT-2i therapy was associated with a 60% reduction in all-cause mortality (RR 0.40; p=0.04).
- Adverse coronary and renal outcomes were significantly reduced by 75% (RR 0.25; p=0.03) and 72% (RR 0.28; p=0.02), respectively.
- The GFR decline was slower in the SGLT-2i group (-1.29 ml/min/1.73 m2/year vs. -3.33 ml/min/1.73 m2/year; p=0.047).
Conclusions:
- SGLT-2i therapy is safe and effective in reducing cardiovascular and renal mortality in KTRs.
- SGLT-2i therapy mitigates the risk of adverse cardiovascular and renal events.
- The benefits of SGLT-2i in KTRs, including slowing CKD progression, are independent of PTDM status.
Related Concept Videos
Kidney Transplant II: Surgical Procedure
Kidney Transplant I: Introduction
Kidney Transplant III: Nursing Management

