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e-Article

Relationship between three commonly used non‐invasive fibrosis biomarkers and improvement in fibrosis stage in patients with non‐alcoholic steatohepatitis
Document Type
article
Source
Liver International. 39(5)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Digestive Diseases
Hepatitis
Clinical Trials and Supportive Activities
Chronic Liver Disease and Cirrhosis
Clinical Research
Liver Disease
Evaluation of treatments and therapeutic interventions
6.1 Pharmaceuticals
Oral and gastrointestinal
Good Health and Well Being
Adult
Biomarkers
Biopsy
Chenodeoxycholic Acid
Female
Humans
Liver
Liver Cirrhosis
Logistic Models
Male
Middle Aged
Non-alcoholic Fatty Liver Disease
United States
biomarkers
fibrosis
non-alcoholic steatohepatitis
non-invasive
Gastroenterology & Hepatology
Clinical sciences
Language
Abstract
Background & aimsNon-invasive biomarkers are needed for monitoring changes in liver histology in patients with non-alcoholic steatohepatitis (NASH). Obeticholic acid (OCA) was shown to improve fibrosis in patients with NASH in the FLINT trial; a post hoc analysis of these data was performed to determine the relationship between 3 non-invasive fibrosis markers and liver fibrosis improvement.MethodsIn the Phase 2b FLINT trial, patients were randomised (1:1) to receive 25 mg OCA or placebo once daily for 72 weeks. Aspartate aminotransferase:platelet ratio index (APRI), fibrosis-4 (FIB-4) index and non-alcoholic fatty liver disease fibrosis score (NFS) were evaluated in serum at baseline and weeks 24, 48, 72 and 96. Liver biopsies were obtained at baseline and 72 weeks.ResultsIn patients with fibrosis improvement at week 24, scores were reduced by a median of 34% for APRI, 10% for FIB-4 and 4% for NFS. Reductions in APRI (P = 0.015) and FIB-4 (P = 0.036), but not NFS (P = 0.201) at week 24, significantly correlated with ≥1-stage improvement in histologic fibrosis at week 72. Reductions in APRI at week 72 were significantly correlated with fibrosis improvement at week 72 (P = 0.012). Patients receiving OCA had significant reductions in all markers compared with patients receiving placebo at week 72 [APRI and FIB-4 (P