| Literature DB >> 16166793 |
Chuan-Mo Lee1, Chao-Hung Hung, Sheng-Nan Lu, Jing-Houng Wang, Hung-Da Tung, Wu-Shiung Huang, Chao-Long Chen, Wei-Jen Chen, Chi-Sin Changchien.
Abstract
Etiologic variations of hepatocellular carcinoma (HCC) exist in different geographic areas of the world. Hepatitis B virus infection is associated with HCC. However, hepatitis C virus (HCV) infection plays an increasingly more important role in the development of HCC and is associated with more than 30% of HCC in Taiwan. The prevalence of HCV infection and HCV genotypes vary in different geographic areas. The prevalence of HCV genotype 1b (HCV-1b) was around 50-70% in Taiwan and even varied in different townships. In addition to host factors, HCV genotypes may be associated with the development of HCC. In our study, the prevalence of HCV-1b in patients with HCC was significantly higher than in those with liver cirrhosis and chronic hepatitis; multivariate analysis revealed that the disease severity was significantly correlated with age and HCV-1b. Furthermore, HCV-1b was associated with a lower response rate to interferon (IFN) therapy than HCV-2. Our study has demonstrated that mutations in the IFN sensitivity-determining region, spanning nucleotides 2,209-2,248 in the NS5A region, correlate with the sustained virological response to combination therapy with IFN and ribavirin in patients with chronic HCV-1b infection in Taiwan. A third-generation enzyme immunoassay for antibody to HCV can be used to predict viremia and monitor the virological response. Copyright (c) 2006 S. Karger AG, Basel.Entities:
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Year: 2006 PMID: 16166793 DOI: 10.1159/000087267
Source DB: PubMed Journal: Intervirology ISSN: 0300-5526 Impact factor: 1.763