Validation of APRI and FIB-4 score in an Antwerp cohort of chronic hepatitis C patients

Acta Gastroenterol Belg. 2015 Dec;78(4):373-80.

Abstract

Background and aims: Evaluation of liver fibrosis in chronic hepatitis C patients guides clinical decision-making. The aim of this study is to validate APRI and FIB-4, two easily calculated noninvasive tests to predict fibrosis, in chronic HCV patients using biopsy as a gold standard and to compare accuracy between HCV monoinfected and HIV/HCV coinfected patients.

Patients and methods: We retrospectively studied HCV patients of two centres who underwent liver biopsy. Liver fibrosis was staged according to METAVIR.

Results: 136 patients were included. The AUROC of FIB-4 (0.896) to discriminate F0-F2 vs. F3-F4 was significantly higher (p=0.0186) than the AUROC of APRI (0.842). The difference in AUROC between HIV-negative and positive patients was not significant for APRI (p=0.471), nor for FIB-4 (p=0.495). Performance status was lower in HIV-positive patients with 46.7% and 69.0% of patients correctly classified using APRI and FIB-4, compared to 56.6% and 73.6% in HIV-negative patients, respectively. Conversion of transaminase values from one hospital to the other did not significantly change the AUROC of FIB-4 (p=0.928).

Conclusions: APRI and FIB-4 have a better performance status in HCV monoinfected patients compared to HIV/HCV coinfected patients. FIB-4 has a better AUROC compared to APRI and is the preferred noninvasive fibrosis score to discriminate between F0-F2 and F3-F4. Different hospitals should use their local absolute serum transaminase values without conversion.

MeSH terms

  • Adult
  • Age Factors
  • Alanine Transaminase / metabolism
  • Aspartate Aminotransferases / metabolism
  • Cohort Studies
  • Female
  • Hepatitis C, Chronic / metabolism*
  • Hepatitis C, Chronic / pathology*
  • Humans
  • Liver Cirrhosis / diagnosis*
  • Liver Cirrhosis / virology
  • Male
  • Middle Aged
  • Platelet Count
  • Predictive Value of Tests
  • Retrospective Studies

Substances

  • Aspartate Aminotransferases
  • Alanine Transaminase