Empagliflozin for Heart Failure With Preserved Left Ventricular Ejection Fraction With and Without Diabetes

Author:

Filippatos Gerasimos1ORCID,Butler Javed23ORCID,Farmakis Dimitrios4ORCID,Zannad Faiez5ORCID,Ofstad Anne Pernille67ORCID,Ferreira João Pedro58ORCID,Green Jennifer B.9ORCID,Rosenstock Julio10,Schnaidt Sven11,Brueckmann Martina1213ORCID,Pocock Stuart J.14,Packer Milton1516ORCID,Anker Stefan D.1718ORCID,

Affiliation:

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

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

3. Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B.).

4. University of Cyprus Medical School, Nicosia (D.F.).

5. Centre d’Investigations Cliniques Plurithématique 14-33, Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Université de Lorraine, Nancy, France (F.Z., J.P.F.).

6. Medical Department, Boehringer Ingelheim Norway KS, Asker (A.P.O.).

7. Oslo Diabetes Research Center, Norway (A.P.O.).

8. Cardiovascular Research and Development Center, Faculty of Medicine of the University of Porto, Portugal (J.P.F.).

9. Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (J.B.G.).

10. Dallas Diabetes Research Center at Medical City, TX (J.R.).

11. Boehringer Ingelheim Pharma GmbH & Co KG, Biberach, Germany (S.S.).

12. Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B.).

13. First Department of Medicine, Faculty of Medicine Mannheim, University of Heidelberg, Germany (M.B.).

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

15. Baylor University Medical Center, Dallas, TX (M.P.).

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

17. Department of Cardiology and Berlin Institute of Health Center for Regenerative Therapies, German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin, Berlin, Germany (S.D.A.).

18. Institute of Heart Diseases, Wrocław Medical University, Poland (S.D.A.).

Abstract

Background: Empagliflozin improves outcomes in patients with heart failure with a preserved ejection fraction, but whether the effects are consistent in patients with and without diabetes remains to be elucidated. Methods: Patients with class II through IV heart failure and a left ventricular ejection fraction >40% were randomized to receive empagliflozin 10 mg or placebo in addition to usual therapy. We undertook a prespecified analysis comparing the effects of empagliflozin versus placebo in patients with and without diabetes. Results: Of the 5988 patients enrolled, 2938 (49%) had diabetes. The risk of the primary outcome (first hospitalization for heart failure or cardiovascular death), total hospitalizations for heart failure, and estimated glomerular filtration rate decline was higher in patients with diabetes. Empagliflozin reduced the rate of the primary outcome irrespective of diabetes status (hazard ratio, 0.79 [95% CI, 0.67, 0.94] for patients with diabetes versus hazard ratio, 0.78 [95% CI, 0.64, 0.95] in patients without diabetes; P interaction =0.92). The effect of empagliflozin to reduce total hospitalizations for heart failure was also consistent in patients with and without diabetes. The effect of empagliflozin to attenuate estimated glomerular filtration rate decline during double-blind treatment was also present in patients with and without diabetes, although more pronounced in patients with diabetes (1.77 in diabetes versus 0.98 mL/min/1.73m 2 in patients without diabetes; P interaction =0.01). Across these 3 end points, the effect of empagliflozin did not differ in patients with prediabetes or normoglycemia (33% and 18% of the patient population, respectively). When investigated as a continuous variable, baseline hemoglobin A1c did not modify the effects on the primary outcome ( P interaction =0.26). There was no increased risk of hypoglycemic events in either subgroup as compared with placebo. Conclusions: In patients with heart failure and a preserved ejection fraction enrolled in the EMPEROR-Preserved (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Preserved Ejection Fraction), empagliflozin significantly reduced the risk of heart failure outcomes irrespective of diabetes status at baseline. 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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