Abstract 4370556: SGLT2 Inhibitors Are Associated with Improved Outcomes in HFpEF Patients with ESRD

B Bernard Evenhuis (Emory University School of Medicine, Morrow, Georgia, United States) A Allison Weiss (Emory University School of Medicine, Atlanta, Georgia, United States) A Austin Rim (Emory University, Atlanta, Georgia, United States) T Taha Ahmed (Emory University School of Medicine, Morrow, Georgia, United States) D David Kaelber P Puja Mehta (EMORY UNIVERSITY, Atlanta, Georgia, United States)

Abstract

Introduction: Heart failure with preserved ejection fraction (HFpEF) commonly coexists with end-stage renal disease (ESRD, together increasing cardiovascular risk [1,2,3,4,5]. While SGLT2 inhibitors (SGLT2i) reduce HF hospitalizations and cardiovascular death in trials like EMPEROR-Preserved and DELIVER, patients with very low eGFR or on dialysis were excluded [6,7]. While trials are ongoing, data on SGLT2i in this high-risk population remain limited. Hypothesis: SGLT2i is associated with improved cardiovascular outcomes in HFpEF patients with ESRD. Methods: We conducted a retrospective cohort analysis of deidentified, aggregate patient data from the TriNetX research network. Patients with HFpEF and ESRD between age 18-85 were included. Patients were stratified by SGLT2i use and propensity matched by demographics, baseline cardiac risk factors, DM medications, and etiology of HFpEF. Outcomes were evaluated within 18-months from the HFpEF + ESRD diagnosis. Primary endpoints included acute decompensated heart failure (ADHF) events, all-cause mortality, hospitalizations for any cause, and emergency department visits for any cause. Z-tests were used to calculate risk difference and Cox regression was used to compute hazard ratios over an 18-month period. Results: The study cohort included 7,238 patients (n = 3,619 per group; mean age 65.3 ± 11.0 years; 40.9% female; 47.3% White). In time-to-event analysis, the SGLT2i group had reduced risk of all-cause mortality (HR=0.49, 95%CI 0.43-0.55, p<0.001) and ADHF events (HR=0.72, 95%CI 0.67-0.77, p < 0.001). At 18 months SGLT2i group had lower rates of all-cause mortality (11.8% vs. 24.4%; RD -12.6%, p < 0.001), ADHF events (39.8% vs. 50.1%; RD -10.4%, p < 0.001) [Figure 1], hospitalizations (51.3% vs. 65.0%; RD -13.8%, p < 0.001) [Figure 1], and at least one ED visit (35.9% vs. 40.6%; RD -4.7%; p < 0.001). Conclusion: In this retrospective propensity-matched analysis, SGLT2i use in HFpEF with ESRD was associated with reduced mortality, ADHF, hospitalizations, and ED visits. Further investigation is needed to clarify mechanisms and guide clinical recommendations.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (6)

B

Bernard Evenhuis

Emory University School of Medicine, Morrow, Georgia, United States

A

Allison Weiss

Emory University School of Medicine, Atlanta, Georgia, United States

A

Austin Rim

Emory University, Atlanta, Georgia, United States

T

Taha Ahmed

Emory University School of Medicine, Morrow, Georgia, United States

D

David Kaelber

P

Puja Mehta

EMORY UNIVERSITY, Atlanta, Georgia, United States