Effect of Empagliflozin on Cardiovascular and Renal Outcomes in Patients With Heart Failure by Baseline Diabetes Status: Results From the EMPEROR-Reduced Trial.


Journal

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

Informations de publication

Date de publication:
26 01 2021
Historique:
pubmed: 12 11 2020
medline: 29 12 2021
entrez: 11 11 2020
Statut: ppublish

Résumé

Sodium-glucose cotransporter 2 inhibitors improve outcomes in patients with heart failure with reduced ejection fraction, but additional information is needed about whether glycemic status influences the magnitude of their benefits on heart failure and renal events. Patients with Class II-IV heart failure and a left ventricular ejection fraction ≤40% were randomized to receive empagliflozin (10 mg daily) or placebo in addition to recommended therapy. We prespecified a comparison of the effect of empagliflozin in patients with and without diabetes. Of the 3730 patients enrolled, 1856 (50%) had diabetes, 1268 (34%) had prediabetes (hemoglobin A1c [HbA1c] 5.7-6.4%), and 606 (16%) had normoglycemia (HbA1c <5.7%). The risks of the primary outcome (cardiovascular death or hospitalization for heart failure), total hospitalizations for heart failure, and adverse renal outcomes were higher in patients with diabetes, but were similar between patients with prediabetes and normoglycemia. Empagliflozin reduced the risk of the primary outcome in patients with and without diabetes (hazard ratio, 0.72 [95% CI, 0.60-0.87] and 0.78 [95% CI, 0.64-0.97], respectively, In EMPEROR-Reduced (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Reduced Ejection Fraction), empagliflozin significantly improved cardiovascular and renal outcomes in patients with heart failure and a reduced ejection fraction, independent of baseline diabetes status and across the continuum of HbA1c. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03057977.

Sections du résumé

BACKGROUND
Sodium-glucose cotransporter 2 inhibitors improve outcomes in patients with heart failure with reduced ejection fraction, but additional information is needed about whether glycemic status influences the magnitude of their benefits on heart failure and renal events.
METHODS
Patients with Class II-IV heart failure and a left ventricular ejection fraction ≤40% were randomized to receive empagliflozin (10 mg daily) or placebo in addition to recommended therapy. We prespecified a comparison of the effect of empagliflozin in patients with and without diabetes.
RESULTS
Of the 3730 patients enrolled, 1856 (50%) had diabetes, 1268 (34%) had prediabetes (hemoglobin A1c [HbA1c] 5.7-6.4%), and 606 (16%) had normoglycemia (HbA1c <5.7%). The risks of the primary outcome (cardiovascular death or hospitalization for heart failure), total hospitalizations for heart failure, and adverse renal outcomes were higher in patients with diabetes, but were similar between patients with prediabetes and normoglycemia. Empagliflozin reduced the risk of the primary outcome in patients with and without diabetes (hazard ratio, 0.72 [95% CI, 0.60-0.87] and 0.78 [95% CI, 0.64-0.97], respectively,
CONCLUSIONS
In EMPEROR-Reduced (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Reduced Ejection Fraction), empagliflozin significantly improved cardiovascular and renal outcomes in patients with heart failure and a reduced ejection fraction, independent of baseline diabetes status and across the continuum of HbA1c. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03057977.

Identifiants

pubmed: 33175585
doi: 10.1161/CIRCULATIONAHA.120.051824
pmc: PMC7834911
doi:

Substances chimiques

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

Banques de données

ClinicalTrials.gov
['NCT03057977']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

337-349

Commentaires et corrections

Type : CommentIn

Références

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Auteurs

Stefan D Anker (SD)

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

Javed Butler (J)

Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B., M.S.K.).

Gerasimos Filippatos (G)

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

Muhammad Shahzeb Khan (MS)

Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B., M.S.K.).

Nikolaus Marx (N)

Department of Internal Medicine I, University Hospital Aachen, RWTH Aachen University, Germany (N.M.).

Carolyn S P Lam (CSP)

National Heart Centre Singapore & Duke-National University of Singapore (C.S.P.L.).

Sven Schnaidt (S)

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

Anne Pernille Ofstad (AP)

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

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B., W.J.).
Faculty of Medicine Mannheim, University of Heidelberg, Germany (M.B.).
Klinik für Innere Medizin III, Saarland University, Homburg/Saar, Germany (M.B.).

Waheed Jamal (W)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B., W.J.).

Edimar A Bocchi (EA)

Heart Institute of the University of Sao Paulo (InCor), Brazil (E.A.B.).

Piotr Ponikowski (P)

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

Sergio V Perrone (SV)

Hospital de Alta Complejidad El Cruce "Nestor Kirchner," Florencio Varela, Buenos Aires, Argentina (S.V.P.).

James L Januzzi (JL)

Harvard Medical School, Massachusetts General Hospital, Boston (J.L.J.).

Subodh Verma (S)

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

Michael Böhm (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B., W.J.).
Faculty of Medicine Mannheim, University of Heidelberg, Germany (M.B.).
Klinik für Innere Medizin III, Saarland University, Homburg/Saar, Germany (M.B.).

João Pedro Ferreira (JP)

Institut Lorrain du Coeur et des Vaisseaux, Nancy, France (J.P.F., F.Z.).

Stuart J Pocock (SJ)

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

Faiez Zannad (F)

Institut Lorrain du Coeur et des Vaisseaux, Nancy, France (J.P.F., F.Z.).

Milton Packer (M)

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

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Classifications MeSH