Poor accuracy and sustainability of the first‐step FIB4 EASL pathway for stratifying steatotic liver disease risk in the general population

Author:

De Vincentis Antonio1ORCID,Tavaglione Federica23,Namba Shinichi4,Kanai Masahiro456,Okada Yukinori478910,Kamatani Yoichiro11,Maurotti Samantha12,Pedone Claudio13,Antonelli Incalzi Raffaele1,Valenti Luca1415ORCID,Romeo Stefano31216ORCID,Vespasiani‐Gentilucci Umberto2ORCID

Affiliation:

1. Internal Medicine Unit, Department of Internal Medicine and Geriatrics Campus Bio‐Medico University Rome Italy

2. Clinical Medicine and Hepatology Unit, Department of Internal Medicine and Geriatrics Campus Bio‐Medico University Rome Italy

3. Department of Molecular and Clinical Medicine, Sahlgrenska Academy University of Gothenburg Gothenburg Sweden

4. Department of Statistical Genetics Osaka University Graduate School of Medicine Suita Japan

5. Broad Institute of MIT and Harvard Cambridge Massachusetts USA

6. Massachusetts General Hospital Boston Massachusetts USA

7. Department of Genome Informatics Graduate School of Medicine, The University of Tokyo Tokyo Japan

8. Laboratory for Systems Genetics, RIKEN Center for Integrative Medical Sciences Yokohama Japan

9. Laboratory of Statistical Immunology, Immunology Frontier Research Center (WPI‐IFReC) Osaka University Suita Japan

10. Integrated Frontier Research for Medical Science Division Institute for Open and Transdisciplinary Research Initiatives, Osaka University Suita Japan

11. Laboratory of Complex Trait Genomics, Department of Computational Biology and Medical Sciences Graduate School of Frontier Sciences, The University of Tokyo Tokyo Japan

12. Clinical Nutrition Unit, Department of Medical and Surgical Science Magna Graecia University Catanzaro Italy

13. Unit of Geriatrics, Department of Internal Medicine and Geriatrics Campus Bio‐Medico University Rome Italy

14. Department of Pathophysiology and Transplantation Università degli Studi di Milano Milano Italy

15. Translational Medicine, Biological Resource Center, Department of Transfusion Medicine Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano Italy

16. Department of Cardiology Sahlgrenska University Hospital Gothenburg Sweden

Abstract

SummaryBackground and AimsThe European Association for the Study of the Liver introduced a clinical pathway (EASL CP) for screening significant/advanced fibrosis in people at risk of steatotic liver disease (SLD). We assessed the performance of the first‐step FIB4 EASL CP in the general population across different SLD risk groups (MASLD, Met‐ALD and ALD) and various age classes.MethodsWe analysed a total of 3372 individuals at risk of SLD from the 2017–2018 National Health and Nutrition Examination Survey (NHANES17‐18), projected to 152.3 million U.S. adults, 300,329 from the UK Biobank (UKBB) and 57,644 from the Biobank Japan (BBJ). We assessed liver stiffness measurement (LSM) ≥8 kPa and liver‐related events occurring within 3 and 10 years (3/10 year‐LREs) as outcomes. We defined MASLD, MetALD, and ALD according to recent international recommendations.ResultsFIB4 sensitivity for LSM ≥ 8 kPa was low (27.7%), but it ranged approximately 80%‐90% for 3‐year LREs. Using FIB4, 22%–57% of subjects across the three cohorts were identified as candidates for vibration‐controlled transient elastography (VCTE), which was mostly avoidable (positive predictive value of FIB4 ≥ 1.3 for LSM ≥ 8 kPa ranging 9.5%–13% across different SLD categories). Sensitivity for LSM ≥ 8 kPa and LREs increased with increasing alcohol intake (ALD>MetALD>MASLD) and age classes. For individuals aged ≥65 years, using the recommended age‐adjusted FIB4 cut‐off (≥2) substantially reduced sensitivity for LSM ≥ 8 kPa and LREs.ConclusionsThe first‐step FIB4 EASL CP is poorly accurate and feasible for individuals at risk of SLD in the general population. It is crucial to enhance the screening strategy with a first‐step approach able to reduce unnecessary VCTEs and optimise their yield.

Funder

Vetenskapsrådet

Diabetesförbundet

Hjärt-Lungfonden

Knut och Alice Wallenbergs Stiftelse

Stiftelsen för Strategisk Forskning

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Publisher

Wiley

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