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Liver function and prognosis, and influence of sacubitril/valsartan in patients with heart failure with reduced ejection fraction.
Suzuki, Kota; Claggett, Brian; Minamisawa, Masatoshi; Packer, Milton; Zile, Michael R; Rouleau, Jean; Swedberg, Karl; Lefkowitz, Martin; Shi, Victor; McMurray, John J V; Zucker, Stephen D; Solomon, Scott D.
Afiliação
  • Suzuki K; Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Claggett B; Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Minamisawa M; Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Packer M; Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX, USA.
  • Zile MR; Medical University of South Carolina and Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston, SC, USA.
  • Rouleau J; University of Montreal, Montreal, Quebec, Canada.
  • Swedberg K; University of Gothenburg, Gothenburg, Sweden.
  • Lefkowitz M; Novartis, East Hanover, NJ, USA.
  • Shi V; Novartis, East Hanover, NJ, USA.
  • McMurray JJV; University of Glasgow, Glasgow, UK.
  • Zucker SD; Division of Gastroenterology, Hepatology, and Endoscopy, Brigham and Women's Hospital, Boston, MA, USA.
  • Solomon SD; Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Eur J Heart Fail ; 22(9): 1662-1671, 2020 09.
Article em En | MEDLINE | ID: mdl-32407608
ABSTRACT

AIMS:

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. METHODS AND

RESULTS:

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).

CONCLUSION:

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antagonistas de Receptores de Angiotensina / Insuficiência Cardíaca Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antagonistas de Receptores de Angiotensina / Insuficiência Cardíaca Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article