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

D Dinh Thanh Anh Pham (BHF CARDIOVASCULAR RESEARCH CENTRE, Glasgow, United Kingdom) M Mingming Yang A ARZU KALAYCI (Brigham and Women's Hospital, Boston, Massachusetts, United States) A Alasdair David Henderson (British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom) I Inder Anand (VA SAN DIEGO HEATHCARE SYSTEM, La Jolla, California, United States) A Akshay Desai (Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States) A Aldo Pietro Maggioni F Felipe Martinez (INSTITUTO DAMIC, Cordoba, Argentina) M Marc Pfeffer (BRIGHAM and WOMENS HOSPITAL, Boston, Massachusetts, United States) J Jean Rouleau (Montreal Heart Institute, Montreal, Quebec, Canada) K Karl Swedberg (Department of Emergency and Cardiovascular Medicine, Groningen, Netherlands) M Muthiah Vaduganathan (Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).) D Dirk van Veldhuisen (University Hospital Groningen, Groningen, Netherlands) F Faiez Zannad M Michael Zile (RHJ Department of Veterans Affairs, Charleston, South Carolina, United States) M 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.).) A Adel Rizkala (Novartis Pharmaceuticals Corporation, East Hanover, New Jersey, United States) P Pardeep Jhund (British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom) S Scott Solomon (Brigham and Women's Hospital, Boston, Massachusetts, United States) J John McMurray (British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom)

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

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (20)

D

Dinh Thanh Anh Pham

BHF CARDIOVASCULAR RESEARCH CENTRE, Glasgow, United Kingdom

M

Mingming Yang

A

ARZU KALAYCI

Brigham and Women's Hospital, Boston, Massachusetts, United States

A

Alasdair David Henderson

British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom

I

Inder Anand

VA SAN DIEGO HEATHCARE SYSTEM, La Jolla, California, United States

A

Akshay Desai

Cardiovascular Division, Brigham And Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States

A

Aldo Pietro Maggioni

F

Felipe Martinez

INSTITUTO DAMIC, Cordoba, Argentina

M

Marc Pfeffer

BRIGHAM and WOMENS HOSPITAL, Boston, Massachusetts, United States

J

Jean Rouleau

Montreal Heart Institute, Montreal, Quebec, Canada

K

Karl Swedberg

Department of Emergency and Cardiovascular Medicine, Groningen, Netherlands

M

Muthiah Vaduganathan

Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).

D

Dirk van Veldhuisen

University Hospital Groningen, Groningen, Netherlands

F

Faiez Zannad

M

Michael Zile

RHJ Department of Veterans Affairs, Charleston, South Carolina, United States

M

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.).

A

Adel Rizkala

Novartis Pharmaceuticals Corporation, East Hanover, New Jersey, United States

P

Pardeep Jhund

British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom

S

Scott Solomon

Brigham and Women's Hospital, Boston, Massachusetts, United States

J

John McMurray

British Heart Foundation Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom