Liver function and prognosis, and influence of sacubitril/valsartan in patients with heart failure with reduced ejection fraction.


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:
09 2020
Historique:
received: 07 04 2020
revised: 11 04 2020
accepted: 16 04 2020
pubmed: 15 5 2020
medline: 19 5 2021
entrez: 15 5 2020
Statut: ppublish

Résumé

The prevalence of liver function abnormalities is common in patients with heart failure (HF) with reduced ejection fraction (HFrEF). We assessed the impact of liver function on prognosis and the effect of sacubitril/valsartan on measures of liver function in patients with HFrEF. The PARADIGM-HF trial was a randomized, double-blind, active treatment-controlled trial. We included 8232 HFrEF patients with available measures of liver function, including transaminases, alkaline phosphatase (ALP) and bilirubin; the primary endpoint was a composite of HF hospitalization and cardiovascular (CV) death. At screening, 11.6% of study patients had total bilirubin above the upper limit of normal (20.5 μmol/L) and 9.2% had ALP above the upper limit of normal (123 IU/L). Although ALP and albumin were associated with an increased risk of outcomes, among conventional test of liver function, total bilirubin was the strongest predictor for the primary endpoint [hazard ratio (HR) 1.10; 95% confidence interval (CI) 1.04-1.15; P < 0.001], HF hospitalization (HR 1.14; 95% CI 1.07-1.22; P < 0.001); CV death (HR 1.07; 95% CI 1.00-1.14; P = 0.040), and all-cause death (HR 1.08; 95% CI 1.02-1.14; P = 0.009). All conventional measures of liver function were significantly improved in the sacubitril/valsartan group compared with the enalapril group after randomization (between-group reduction: total bilirubin 2.4%, 95% CI 0.7-4.2%, P = 0.007; aspartate aminotransferase 7.9%, 95% CI 6.7-9.0%, P < 0.001; alanine aminotransferase 7.7%; 95% CI 6.2-9.3%, P < 0.001; ALP 5.4%, 95% CI 4.4-6.4%, P < 0.001). Total bilirubin was a significant and independent predictor of CV death or HF hospitalization and all-cause mortality in patients with HFrEF enrolled in PARADIGM-HF. Sacubitril/valsartan improved measures of liver function compared with enalapril.

Identifiants

pubmed: 32407608
doi: 10.1002/ejhf.1853
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1662-1671

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 European Society of Cardiology.

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Auteurs

Kota Suzuki (K)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.

Brian Claggett (B)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.

Masatoshi Minamisawa (M)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.

Milton Packer (M)

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX, USA.

Michael R Zile (MR)

Medical University of South Carolina and Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston, SC, USA.

Jean Rouleau (J)

University of Montreal, Montreal, Quebec, Canada.

Karl Swedberg (K)

University of Gothenburg, Gothenburg, Sweden.

Martin Lefkowitz (M)

Novartis, East Hanover, NJ, USA.

Victor Shi (V)

Novartis, East Hanover, NJ, USA.

John J V McMurray (JJV)

University of Glasgow, Glasgow, UK.

Stephen D Zucker (SD)

Division of Gastroenterology, Hepatology, and Endoscopy, Brigham and Women's Hospital, Boston, MA, USA.

Scott D Solomon (SD)

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.

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