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Effect of Empagliflozin on Cardiovascular and Renal Outcomes in Patients With Heart Failure by Baseline Diabetes Status: Results From the EMPEROR-Reduced Trial.
Anker, Stefan D; Butler, Javed; Filippatos, Gerasimos; Khan, Muhammad Shahzeb; Marx, Nikolaus; Lam, Carolyn S P; Schnaidt, Sven; Ofstad, Anne Pernille; Brueckmann, Martina; Jamal, Waheed; Bocchi, Edimar A; Ponikowski, Piotr; Perrone, Sergio V; Januzzi, James L; Verma, Subodh; Böhm, Michael; Ferreira, João Pedro; Pocock, Stuart J; Zannad, Faiez; Packer, Milton.
Afiliación
  • 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.).
  • Butler J; Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B., M.S.K.).
  • Filippatos G; National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, Greece (G.F.).
  • Khan MS; Department of Medicine, University of Mississippi School of Medicine, Jackson (J.B., M.S.K.).
  • Marx N; Department of Internal Medicine I, University Hospital Aachen, RWTH Aachen University, Germany (N.M.).
  • Lam CSP; National Heart Centre Singapore & Duke-National University of Singapore (C.S.P.L.).
  • Schnaidt S; Boehringer Ingelheim Pharma GmbH & Co KG, Biberach, Germany (S.S.).
  • Ofstad AP; Medical Department, Boehringer Ingelheim Norway KS, Asker, Norway (A.P.O.).
  • Brueckmann M; Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B., W.J.).
  • Jamal W; Faculty of Medicine Mannheim, University of Heidelberg, Germany (M.B.).
  • Bocchi EA; Klinik für Innere Medizin III, Saarland University, Homburg/Saar, Germany (M.B.).
  • Ponikowski P; Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B., W.J.).
  • Perrone SV; Heart Institute of the University of Sao Paulo (InCor), Brazil (E.A.B.).
  • Januzzi JL; Wroclaw Medical University, Poland (P.P.).
  • Verma S; Hospital de Alta Complejidad El Cruce "Nestor Kirchner," Florencio Varela, Buenos Aires, Argentina (S.V.P.).
  • Böhm M; Harvard Medical School, Massachusetts General Hospital, Boston (J.L.J.).
  • Ferreira JP; Division of Cardiac Surgery, St Michael's Hospital, University of Toronto, Canada (S.V.).
  • Pocock SJ; Boehringer Ingelheim International GmbH, Ingelheim, Germany (M.B., W.J.).
  • Zannad F; Faculty of Medicine Mannheim, University of Heidelberg, Germany (M.B.).
  • Packer M; Klinik für Innere Medizin III, Saarland University, Homburg/Saar, Germany (M.B.).
Circulation ; 143(4): 337-349, 2021 01 26.
Article en En | MEDLINE | ID: mdl-33175585
ABSTRACT

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, P-interaction=0.57). Patients with and without diabetes also did not differ with respect to the effect of empagliflozin on total hospitalizations for heart failure, on the decline in estimated glomerular filtration rate over time, and on the risk of serious adverse renal outcomes. Among these end points, the effects of the drug did not differ in patients with prediabetes or normoglycemia. When analyzed as a continuous variable, baseline HbA1c did not significantly modify the benefits of empagliflozin on the primary outcome (P-interaction=0.40). Empagliflozin did not lower HbA1c in patients with prediabetes or normoglycemia and was not associated with increased risk of hypoglycemia.

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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Compuestos de Bencidrilo / Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Insuficiencia Renal Crónica / Inhibidores del Cotransportador de Sodio-Glucosa 2 / Glucósidos / Insuficiencia Cardíaca Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: Circulation Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Compuestos de Bencidrilo / Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Insuficiencia Renal Crónica / Inhibidores del Cotransportador de Sodio-Glucosa 2 / Glucósidos / Insuficiencia Cardíaca Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: Circulation Año: 2021 Tipo del documento: Article