The Association of Fibrosis-4 Index Scores with Severe Liver Outcomes in Primary Care.


Journal

Journal of general internal medicine
ISSN: 1525-1497
Titre abrégé: J Gen Intern Med
Pays: United States
ID NLM: 8605834

Informations de publication

Date de publication:
10 2022
Historique:
received: 18 06 2021
accepted: 15 12 2021
pubmed: 21 1 2022
medline: 13 10 2022
entrez: 20 1 2022
Statut: ppublish

Résumé

The Fibrosis-4 Index (FIB-4)non-invasively assesses fibrosis risk in chronic liver disease (CLD), but underdiagnosis limits FIB-4's application in primary care. To evaluate the association of FIB-4 risk with hazard of severe liver outcomes in primary care patients with and without diagnosed CLD. Retrospective cohort study of primary care data from 2007 to 2018. Adult patients with qualifying aminotransferase and platelet count results were included and a single FIB-4 score was calculated for each patient using the first of these values. Patients with a CLD diagnosis or outcome prior to their FIB-4 score were excluded. FIB-4 advanced fibrosis risk categorization (low, indeterminate, and high) was the primary predictor variable. Patients were followed from FIB-4 score to a severe liver outcome, a composite of cirrhosis, liver transplantation, and hepatocellular carcinoma. We analyzed the association of FIB-4 risk categories with hazard risk of a severe liver outcome using stratified Cox regression models, stratifying patients by known CLD. A total of 20,556 patients were followed for a mean 2,978 days (SD 1,201 days), and 4% of patients experienced a severe liver outcome. Of patients with low-, indeterminate-, and high-risk FIB-4 scores, 2%, 4%, and 20% suffered a severe liver outcome, respectively. In the overall adjusted model, high-risk FIB-4 scores were associated with hazard of severe liver disease (HR 6.64; 95% CI 5.58-7.90). High-risk FIB-4 scores were associated with severe liver outcomes for patients with known NAFLD (HR 7.32; 95% CI 3.44-15.58), other liver disease (HR 11.39; 95% CI 8.53-15.20), and no known CLD (HR 4.05; 95% CI 3.10-5.28). High-risk FIB-4 scores were strongly associated with risk of severe liver outcomes in patients with and without known CLD. Comprehensive FIB-4 application in primary care may signal silently advancing liver fibrosis.

Sections du résumé

BACKGROUND
The Fibrosis-4 Index (FIB-4)non-invasively assesses fibrosis risk in chronic liver disease (CLD), but underdiagnosis limits FIB-4's application in primary care.
OBJECTIVE
To evaluate the association of FIB-4 risk with hazard of severe liver outcomes in primary care patients with and without diagnosed CLD.
DESIGN
Retrospective cohort study of primary care data from 2007 to 2018.
PARTICIPANTS
Adult patients with qualifying aminotransferase and platelet count results were included and a single FIB-4 score was calculated for each patient using the first of these values. Patients with a CLD diagnosis or outcome prior to their FIB-4 score were excluded.
MEASURES
FIB-4 advanced fibrosis risk categorization (low, indeterminate, and high) was the primary predictor variable. Patients were followed from FIB-4 score to a severe liver outcome, a composite of cirrhosis, liver transplantation, and hepatocellular carcinoma. We analyzed the association of FIB-4 risk categories with hazard risk of a severe liver outcome using stratified Cox regression models, stratifying patients by known CLD.
KEY RESULTS
A total of 20,556 patients were followed for a mean 2,978 days (SD 1,201 days), and 4% of patients experienced a severe liver outcome. Of patients with low-, indeterminate-, and high-risk FIB-4 scores, 2%, 4%, and 20% suffered a severe liver outcome, respectively. In the overall adjusted model, high-risk FIB-4 scores were associated with hazard of severe liver disease (HR 6.64; 95% CI 5.58-7.90). High-risk FIB-4 scores were associated with severe liver outcomes for patients with known NAFLD (HR 7.32; 95% CI 3.44-15.58), other liver disease (HR 11.39; 95% CI 8.53-15.20), and no known CLD (HR 4.05; 95% CI 3.10-5.28).
CONCLUSIONS
High-risk FIB-4 scores were strongly associated with risk of severe liver outcomes in patients with and without known CLD. Comprehensive FIB-4 application in primary care may signal silently advancing liver fibrosis.

Identifiants

pubmed: 35048297
doi: 10.1007/s11606-021-07341-z
pii: 10.1007/s11606-021-07341-z
pmc: PMC9550951
doi:

Substances chimiques

Transaminases EC 2.6.1.-

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3266-3274

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK118200
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK123704
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001450
Pays : United States

Informations de copyright

© 2022. The Author(s) under exclusive licence to Society of General Internal Medicine.

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Auteurs

Andrew D Schreiner (AD)

Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA. schrein@musc.edu.

William P Moran (WP)

Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.

Jingwen Zhang (J)

Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.

Sherry Livingston (S)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, 29425, USA.

Justin Marsden (J)

Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.

Patrick D Mauldin (PD)

Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.

David Koch (D)

Department of Medicine, Medical University of South Carolina, Charleston, SC, 29425, USA.

Mulugeta Gebregziabher (M)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, 29425, USA.

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