Hepatic stellate cells and fibrosis progression in patients with nonalcoholic fatty liver disease

Ariel E. Feldstein, Bettina G. Papouchado, Paul Angulo, Schyler Sanderson, Leon Adams, Gregory J. Gores

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

Background & Aims: Many patients with nonalcoholic fatty liver disease (NAFLD) have a benign clinical course, but a subgroup of patients progress to advanced fibrosis and cirrhosis. However, there are no available clinical tools to predict fibrosis progression in this population. Activated hepatic stellate cells (HSCs) are the source of collagen deposition in the liver. We aimed at determining whether an HSC activation score predicts fibrosis progression in NAFLD patients. Methods: The cohort consisted of 39 untreated patients with NAFLD with paired liver biopsies performed 5-59 months apart (mean, 22 months). Patients were divided into 2 groups on the basis of whether fibrosis progression was noted on their second liver biopsy. Liver tissue was immunostained for α-smooth muscle actin, and the HSC score was determined independently by 2 pathologists in the NAFLD population and in control subjects without liver disease. Results: The HSC activation score was significantly increased in patients with fibrosis progression versus patients in whom no fibrosis progression was observed (4.8 ± 0.5 vs 1.8 ± 0.6, respectively; P <. 001). The HSC score was accurate in predicting fibrosis progression, with a positive predictive value of 90%, specificity of 94%, and an area under the receiver operating characteristic curve of 0.82. However, the negative predictive value and sensitivity were 56% and 41%, respectively. The inter-pathologist agreement for the HSC score was excellent (kappa coefficient, 0.95). Conclusions: These findings suggest that the HSC activation score is a suitable clinical tool to determine the risk of fibrosis progression in patients with NAFLD.

Original languageEnglish (US)
Pages (from-to)384-389
Number of pages6
JournalClinical Gastroenterology and Hepatology
Volume3
Issue number4
DOIs
StatePublished - Apr 1 2005

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

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