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Cardio-Vasculo-Renal Benefits of SGLT2 Inhibitors in Heart Failure: A Retrospective Study from a Lower-Resource
Olivia-Maria Bodea1,2, Gabriel Florin Răzvan Mogoș3, Nilima Rajpal Kundnani2,4
1Doctoral School, "Victor Babes" University of Medicine and Pharmacy, 3000041 Timisoara, Romania.
Insights
Sodium glucose cotransporter 2 (SGLT2) inhibitors may reduce adverse cardio-renal events in heart failure patients with reduced ejection fraction. Real-world data suggest SGLT2 inhibitors slow kidney function decline and decrease heart failure hospitalizations.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Heart failure (HF) and chronic kidney disease (CKD) frequently coexist, worsening patient prognosis through cardio-renal interactions.
- Sodium glucose cotransporter 2 (SGLT2) inhibitors show promise for cardiovascular and renal benefits, but real-world data in lower-resource settings are scarce.
Purpose of the Study:
- To evaluate the real-world effectiveness of SGLT2 inhibitors in patients with chronic heart failure and reduced ejection fraction (LVEF ≤ 45%).
- To assess the impact of SGLT2 inhibitors on cardio-vasculo-renal outcomes and kidney function trajectory in this population.
Main Methods:
- Retrospective single-center cohort study of 240 adult patients with chronic HF and LVEF ≤ 45% (2021-2024).
- Patients were stratified based on SGLT2 inhibitor use.
- Primary endpoint: composite of cardiovascular death, HF hospitalization, or ≥40% sustained eGFR decline/KRT initiation. Annual eGFR slope analyzed.
Main Results:
- SGLT2 inhibitor use was linked to a reduced risk of the composite cardio-vasculo-renal endpoint (adjusted HR 0.70, 95% CI 0.50-0.98).
- This reduction was mainly driven by fewer heart failure hospitalizations.
- Longitudinal analyses indicated a slower decline in kidney function among SGLT2 inhibitor-treated patients.
Conclusions:
- In this observational study, SGLT2 inhibitors were associated with improved cardio-renal outcomes and preserved kidney function in HF patients.
- Findings are hypothesis-generating due to observational design and potential residual confounding.
- Results provide implementation-relevant signals supporting further prospective research on SGLT2 inhibitors in HF and CKD.
Abstract:
Background and Objectives: Heart failure frequently coexists with CKD, compounding prognosis via cardio-renal interplay. Sodium glucose cotransporter 2 (SGLT2) inhibitors have demonstrated cardiovascular and renal benefits in randomized trials, but data remain limited in real-world lower-resource settings. Materials and Methods: We conducted a retrospective single-center cohort study at a tertiary university hospital in western Romania, including adults with chronic HF and LVEF ≤ 45%, monitored between 2021-2024. Patients were stratified based on receipt of SGLT2 inhibitors. The primary endpoint was a composite of cardiovascular death, HF hospitalization, or ≥40% sustained decline in eGFR/initiation of KRT. Annual eGFR slope was analyzed to assess renal trajectory. Results: Among 240 patients, treatment with SGLT2 inhibitors was associated with a lower risk of the composite cardio-vasculo-renal endpoint compared with no treatment (adjusted HR 0.70, 95% CI 0.50-0.98). The reduction was primarily driven by fewer heart failure hospitalizations. Decline in kidney function was slower among SGLT2 inhibitor-treated patients in longitudinal mixed-effects analyses. Conclusions: In this retrospective cohort, SGLT2 inhibitor use was associated with fewer cardio-renal events and a slower decline in kidney function. Given the observational design and residual confounding risk, these findings should be considered hypothesis-generating but provide implementation-relevant signals supporting further prospective evaluation.
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