Effects of Empagliflozin in Women and Men With Heart Failure and Preserved Ejection Fraction

Author:

Butler Javed12ORCID,Filippatos Gerasimos3ORCID,Siddiqi Tariq Jamal1,Ferreira João Pedro456ORCID,Brueckmann Martina7ORCID,Bocchi Edimar8ORCID,Böhm Michael9ORCID,Chopra Vijay K.10ORCID,Giannetti Nadia11ORCID,Iwata Tomoko12,Januzzi James L.13ORCID,Kaul Sanjay14ORCID,Piña Ileana L.15ORCID,Ponikowski Piotr16ORCID,Rauch-Kröhnert Ursula1718ORCID,Shah Sanjiv J.19ORCID,Senni Michele20,Sumin Mikhail21ORCID,Verma Subodh22,Zhang Jian23ORCID,Pocock Stuart J.24,Zannad Faiez45ORCID,Packer Milton2526ORCID,Anker Stefan D.272829ORCID

Affiliation:

1. Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B., T.J.S.).

2. Baylor Scott and White Research Institute, Dallas, TX (J.B).

3. National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, Greece (G.F.).

4. Université de Lorraine, Inserm, Centre d’Investigations Cliniques, Nancy, France (J.P.F., F.Z.).

5. Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France (J.P.F., F.Z.).

6. Cardiovascular Research and Development Center, Department of Surgery and Physiology, Faculty of Medicine of the University of Porto, Portugal (J.P.F.).

7. Boehringer Ingelheim International GmbH, Ingelheim, Germany, and First Department of Medicine, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany (M. Brueckmann).

8. Heart Failure Department, Heart Institute (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Brazil (E.B.).

9. Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, Saarland University, Homburg/Saar, Germany (M. Böhm).

10. Max Superspeciality Hospital, Saket, New Delhi, India (V.K.C.).

11. Division of Cardiology, McGill University Health Centre, Montreal, QC, Canada (N.G.).

12. Boehringer Ingelheim Pharma GmbH & Co KG, Biberach, Germany (T.I.).

13. Massachusetts General Hospital and Baim Institute for Clinical Research, Boston (J.L.J.).

14. Cedars-Sinai Medical Center, Los Angeles, CA (S.K.).

15. Central Michigan University, Mount Pleasant (I.L.P.).

16. Wroclaw Medical University, Poland (P.P.).

17. Department of Cardiology, Charité University Medicine Berlin, Campus Benjamin-Franklin, Germany (U.R.-K.).

18. German Centre for Cardiovascular Research partner site Berlin (U.R.-K.).

19. Northwestern University Feinberg School of Medicine, Chicago, IL (S.J.S.).

20. Cardiovascular Department, Cardiology Division, Papa Giovanni XXIII Hospital, Bergamo, Italy (M. Senni).

21. Boehringer Ingelheim International GmbH, Ingelheim, Germany (M. Sumin).

22. Division of Cardiac Surgery, St. Michael’s Hospital, University of Toronto, ON, Canada (S.V.)

23. Fuwai Hospital Chinese Academic of Medical Science, Beijing, China (J.Z.).

24. Department of Medical Statistics, London School of Hygiene and Tropical Medicine, UK (S.J.P.).

25. Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX (M.P.).

26. Imperial College, London, UK (M.P.).

27. Department of Cardiology and Berlin Institute of Health Center for Regenerative Therapies, Germany (S.D.A.).

28. German Centre for Cardiovascular Research partner site Berlin (S.D.A.).

29. Charité Universitätsmedizin Berlin, Germany (S.D.A.).

Abstract

Background: Women and men with heart failure (HF) and preserved ejection fraction may differ in their clinical characteristics and their response to therapy. The aim of this study was to evaluate the influence of sex on the effects of empagliflozin in patients with HF and preserved ejection fraction enrolled in the EMPEROR-Preserved trial (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Preserved Ejection Fraction). Methods: The effects of empagliflozin on the primary outcome of cardiovascular death or hospitalization for HF and on secondary outcomes (including total HF hospitalization, cardiovascular and all-cause mortality, and Kansas City Cardiomyopathy Questionnaire scores) were compared in women and men in the overall cohort and in subgroups defined by left ventricular ejection fraction (41%–49%, 50%–59%, and ≥60%). The effects of empagliflozin on physiological measures, including changes in systolic blood pressure, uric acid, hemoglobin, body weight, and natriuretic peptide levels, were also assessed. Results: Of the 5988 patients randomized, 2676 (44.7%) were women. In the placebo arm, women tended to have lower risk for adverse outcomes, including a lower risk of all-cause mortality (hazard ratio, 0.69 [95% CI, 0.56, 0.84]). Compared with placebo, empagliflozin reduced the risk of cardiovascular death or hospitalization for HF to a similar degree in both sexes (hazard ratio, 0.81 [95% CI, 0.69, 0.96] for men; and hazard ratio, 0.75 [95% CI, 0.61, 0.92] for women; P interaction =0.54). Sex did not modify the relationship between empagliflozin and outcomes across ejection fraction groups. Similar results were seen for secondary outcomes and physiological measures. Compared with placebo, empagliflozin improved the Kansas City Cardiomyopathy Questionnaire Clinical Summary Score to a similar extent in both sexes (1.38 for men versus 1.63 for women at 52 weeks; P interaction =0.77); the results were similar for Kansas City Cardiomyopathy Questionnaire overall summary score and total summary score. Conclusions: Empagliflozin produced similar benefits on outcomes and health status in women and men with HF and preserved ejection fraction. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03057951.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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