Abstract 4365699: Liver fibrosis as assessed by the fibrosis-5 (FIB-5) index in patients with heart failure: Insights from the PARADIGM-HF and PARAGON-HF trials
Abstract
Background: By causing systemic venous congestion and hypoperfusion, heart failure can lead to liver dysfunction and these processes along with neurohumoral activation, inflammation, and metabolic dysfunction may lead to liver fibrosis. The fibrosis-5 (FIB-5) index, which incorporates serum albumin, alkaline phosphatase, aspartate transaminase, alanine aminotransferase and platelet count, is a marker of possible liver fibrosis. We evaluated the prevalence of an abnormal FIB-5 index in heart failure with reduced ejection fraction (HFrEF), compared with (HFpEF), and the association between FIB-5 index and outcomes in these two types of HF. Research Questions: What is the prognostic value of the FIB-5 index in patients with HF across the range of left ventricular ejection fraction (LVEF)? Methods: The PARADIGM-HF and PARAGON-HF trials were randomized, double-blind, active treatment-controlled trials which included 8442 HFrEF patients and 4822 HFpEF patients, respectively. The primary endpoint examined in this analysis was the composite of HF hospitalization or cardiovascular (CV) death. We compared outcomes according to quartiles of FIB-5 index. A low FIB-5 index is associated with hepatic fibrosis. Results: Overall, 44% of HFrEF patients and 42% of HFpEF patients had possible liver fibrosis as identified by a FIB-5 index <0 (which is reported to have a high specificity, positive predictive value, and negative predictive value for liver fibrosis in other diseases). Lower FIB-5 index was associated with adverse outcomes in both HF phenotypes (Figures). Comparing Quartile 1 to Quartile 4 of the FIB-5 index, gave a hazard ratio (HR) for the primary endpoint of 1.87 (95% CI 1.64-2.13) in PARADIGM-HF and 1.55 (95% CI 1.32-1.83) in PARAGON-HF. The corresponding HRs for CV death were 1.90 (95% CI 1.61–2.23) in PARADIGM-HF and 1.70 (95% CI 1.23-2.3) in PARAGON-HF. The benefit of sacubitril/valsartan was not modified by FIB-5 index. Conclusion: The FIB-5 index suggests liver fibrosis is common in both HFrEF and HFpEF and is prognostically important, regardless of ejection fraction phenotype.
Article Details
Authors (20)
Dinh Thanh Anh Pham
BHF CARDIOVASCULAR RESEARCH CENTRE, Glasgow, United Kingdom
Mingming Yang
ARZU KALAYCI
Brigham and Women's Hospital, Boston, Massachusetts, United States
Alasdair David Henderson
British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom
Inder Anand
VA SAN DIEGO HEATHCARE SYSTEM, La Jolla, California, United States
Akshay Desai
Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States
Aldo Pietro Maggioni
Felipe Martinez
INSTITUTO DAMIC, Cordoba, Argentina
Marc Pfeffer
BRIGHAM and WOMENS HOSPITAL, Boston, Massachusetts, United States
Jean Rouleau
Montreal Heart Institute, Montreal, Quebec, Canada
Karl Swedberg
Department of Emergency and Cardiovascular Medicine, Groningen, Netherlands
Muthiah Vaduganathan
Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).
Dirk van Veldhuisen
University Hospital Groningen, Groningen, Netherlands
Faiez Zannad
Michael Zile
RHJ Department of Veterans Affairs, Charleston, South Carolina, United States
Milton Packer
From Baylor University Medical Center, Dallas (M.P.); Imperial College, London (M.P.); RHJ Department of Veterans Affairs, Health System and Medical University of South Carolina, Charleston (M.R.Z., S.E.L.); the Cardiovascular Division, Department of Medicine, University of Virginia Health System, Charlottesville (C.M.K.); Flourish Research, Boca Raton, FL (S.J.B.); the Department of Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland (V.M.); the Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China (J.G.); Eli Lilly, Indianapolis (G.J.W., Y.O., M.C.B., K.C.H., M.M.); and the Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN (B.A.B.).
Adel Rizkala
Novartis Pharmaceuticals Corporation, East Hanover, New Jersey, United States
Pardeep Jhund
British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom
Scott Solomon
Brigham and Women's Hospital, Boston, Massachusetts, United States
John McMurray
British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom