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


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
30 08 2022
Historique:
pubmed: 29 6 2022
medline: 1 9 2022
entrez: 28 6 2022
Statut: ppublish

Résumé

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. 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. 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; 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. URL: https://www. gov; Unique identifier: NCT03057951.

Sections du résumé

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;
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.

Identifiants

pubmed: 35762322
doi: 10.1161/CIRCULATIONAHA.122.059785
pmc: PMC9422757
doi:

Substances chimiques

Benzhydryl Compounds 0
Glucosides 0
Sodium-Glucose Transporter 2 Inhibitors 0
empagliflozin HDC1R2M35U

Banques de données

ClinicalTrials.gov
['NCT03057951']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

676-686

Commentaires et corrections

Type : CommentIn

Références

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Auteurs

Gerasimos Filippatos (G)

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

Javed Butler (J)

Baylor Scott and White Research Institute, Dallas, TX (J.B.).
Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B.).

Dimitrios Farmakis (D)

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

Faiez Zannad (F)

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.).

Anne Pernille Ofstad (AP)

Medical Department, Boehringer Ingelheim Norway KS, Asker (A.P.O.).
Oslo Diabetes Research Center, Norway (A.P.O.).

João Pedro Ferreira (JP)

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

Jennifer B Green (JB)

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

Julio Rosenstock (J)

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

Sven Schnaidt (S)

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

Martina Brueckmann (M)

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

Stuart J Pocock (SJ)

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

Milton Packer (M)

Baylor University Medical Center, Dallas, TX (M.P.).
Imperial College, London, UK (M.P.).

Stefan D Anker (SD)

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

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Classifications MeSH