Hepatic iron, liver steatosis and viral genotypes in patients with chronic hepatitis C

• Published in: Journal of viral hepatitis Vol. 13; no. 3; pp. 199 - 205
• Main Authors: Sebastiani, G., Vario, A., Ferrari, A., Pistis, R., Noventa, F., Alberti, A.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.03.2006
• Subjects: Adult; Fatty Liver - etiology; Fatty Liver - metabolism; Female; Ferritins - blood; Genotype; HCV genotypes; Hepacivirus - classification; Hepacivirus - genetics; hepatic iron; hepatitis C; Hepatitis C virus; Hepatitis C, Chronic - complications; Hepatitis C, Chronic - metabolism; Hepatitis C, Chronic - pathology; Hepatitis C, Chronic - virology; Humans; Iron - blood; Iron - metabolism; Liver - metabolism; Liver - pathology; Liver Cirrhosis - complications; Liver Cirrhosis - metabolism; Male; Middle Aged; Multivariate Analysis; Predictive Value of Tests; RNA, Viral - genetics; serum ferritin; Statistics as Topic; steatosis; Transferrin - analysis
• ISSN: 1352-0504; 1365-2893
• DOI: 10.1111/j.1365-2893.2005.00662.x

Hepatic iron has been described in hepatitis C virus (HCV) infection as an important cofactor of disease outcome. The mechanisms leading to hepatic iron deposits (HIDs) in HCV patients are partially understood. We investigated HIDs in the liver biopsies of a consecutive series of 242 HCV‐infected patients with well‐compensated liver disease. Serum ferritin was elevated in 20.7% and transferrin saturation in 19.0%, while 38.8% had stainable HIDs indicating that serum markers of systemic iron overload have low sensitivity in predicting HIDs in hepatitis C. A cut‐off value of serum ferritin (350 μg/L in females and 450 μg/L in males) had good negative predictive value in excluding presence of mild–moderate HIDs (grade II–III). Hepatic iron deposits correlated by multivariate analysis with serum ferritin [odds ratio (OR) 1.008, 95% confidence interval (CI) 1.005–1.011] and albumin (OR 1.15, 95% CI 1.02–1.297). Hepatic iron deposits were more frequent in HCV‐3‐infected cases than in other genotypes (P = 0.027) while raised serum iron indices were more frequent in non‐HCV‐3 genotypes (P = 0.02). Furthermore, advanced fibrosis (F3–F4 by METAVIR) was more frequent in non‐HCV‐3 genotypes (P = 0.04). In HCV‐3 cases there was a close association between HIDs and severe (grade II–III) steatosis (P < 0.00001). These results indicate that in well‐compensated chronic hepatitis C HIDs are strongly associated with HCV‐3 and viral‐induced hepatic steatosis, while in the presence of other genotypes they might merely reflect a more advanced stage of liver disease and/or a systemic iron overload. Serum ferritin could identify a subgroup of patients in which the need of venesection could be excluded without liver biopsy.