Liver tests, cardiovascular outcomes and effects of empagliflozin in patients with heart failure and preserved ejection fraction: The EMPEROR-Preserved trial.

Empagliflozin Heart failure Heart failure with preserved ejection fraction Liver fibrosis Liver steatosis SGLT2 inhibitors

Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
08 2023
Historique:
revised: 17 04 2023
received: 27 01 2023
accepted: 30 05 2023
medline: 31 8 2023
pubmed: 6 6 2023
entrez: 6 6 2023
Statut: ppublish

Résumé

The prognostic implication of elevated liver tests in heart failure with preserved ejection fraction (HFpEF) is uncertain. This analysis investigates the association of liver markers with hospitalization for heart failure (HHF) and cardiovascular death (CVD), and the treatment effect of empagliflozin across the range of liver marker levels. The double-blind, placebo-controlled EMPEROR-Preserved (EMPagliflozin outcomE tRial in Patients With chrOnic heaRt Failure with Preserved Ejection Fraction) enrolled 5988 patients with HFpEF (ejection fraction >40%). Patients in New York Heart Association class II-IV and elevated N-terminal pro-B-type natriuretic peptide were randomized to receive empagliflozin 10 mg daily or placebo in addition to usual therapy. Patients with significant liver disease were excluded. The primary endpoint was time to first adjudicated HHF or CVD. We explored the association of liver function abnormalities with heart failure outcomes in patients on placebo, the effects of empagliflozin on liver tests and the treatment effects of empagliflozin on heart failure outcomes across categories of liver laboratory values. High alkaline phosphatase (p trend < 0.0001), low albumin (p trend < 0.0001) and high bilirubin (p = 0.02) were associated with poorer outcomes for HHF or CVD, while high aspartate aminotransferase was not, and high alanine aminotransferase was associated with better outcomes. Empagliflozin had no significant effects on liver tests compared to placebo except for albumin which was significantly increased. The treatment effect of empagliflozin on outcomes was not modified by liver tests. Abnormalities of liver function tests are associated differently with heart failure outcomes. Salutary effects of empagliflozin on liver tests were not observed although albumin increased. The treatment benefits of empagliflozin were not affected by baseline values of liver parameters.

Identifiants

pubmed: 37278451
doi: 10.1002/ejhf.2922
doi:

Substances chimiques

empagliflozin HDC1R2M35U

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1375-1383

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Michael Böhm (M)

Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, Saarland University, Homburg, Germany.
Cape Heart Institute, Cape Town, South Africa.

Javed Butler (J)

Department of Medicine, University of Mississippi School of Medicine, Jackson, MS, USA.
Baylor Scott and White Research Institute, Dallas, TX, USA.

Marcin Krawczyk (M)

Klinik für Innere Medizin II, Universitätsklinikum des Saarlandes, Saarland University, Homburg, Germany.

Felix Mahfoud (F)

Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, Saarland University, Homburg, Germany.

Bernhard Haring (B)

Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, Saarland University, Homburg, Germany.
Cape Heart Institute, Cape Town, South Africa.

Gerasimos Filippatos (G)

National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, Athens, Greece.

João Pedro Ferreira (JP)

Université de Lorraine, Centre d'Investigation Clinique-Plurithématique Inserm CIC-P 1433, Nancy, France.
Inserm U1116, CHRU Nancy Brabois, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.
Cardiovascular R&D Centre - UnIC@RISE, Department of Physiology and Cardiothoracic Surgery, Faculty of Medicine of the University of Porto, Porto, Portugal.

Stuart J Pocock (SJ)

Department of Medical Statistics, London School of Hygiene & Tropical Medicine, London, UK.

Martina Brueckmann (M)

Boehringer Ingelheim International, Ingelheim, Germany.
First Department of Medicine, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.

Anne Pernille Ofstad (AP)

Medical Department, Boehringer Ingelheim Norway KS, Asker, Norway.
Oslo Diabetes Research Center, Oslo, Norway.

Elke Schüler (E)

mainanalytics GmbH, Sulzbach, Germany.

Christoph Wanner (C)

Medizinische Klinik und Poliklinik 1, Schwerpunkt Nephrologie, Universitätsklinikum Würzburg, Würzburg, Germany.

Subodh Verma (S)

Division of Cardiac Surgery, St Michael's Hospital, and Departments of Surgery, and Pharmacology and Toxicology, University of Toronto, Toronto, ONT, Canada.

Milton Packer (M)

Baylor University Medical Center, Dallas, TX, USA.
Imperial College, London, UK.

Stefan D Anker (SD)

Department of Cardiology (CVK); and Berlin Institute of Health Center for Regenerative Therapies (BCRT); German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin Berlin, Berlin, Germany.

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