Relationship Between Alcoholic Liver Disease and Hcv Infection
Shujiro Takase, Nobuo Takada, Makoto Sawada, Mikihiro Tsutsumi, Akira Takada
Abstract
Shujiro Takase, Nobuo Takada, Makoto Sawada, Mikihiro Tsutsumi, Akira Takada
Abstract
The high prevalence of hepatitis C virus (HCV) markers in alcoholic liver cirrhosis (AL-LC) and hepatocellular carcinoma (HCC) suggests a close aetiopathogenic relationship between alcoholic liver disease (ALD) and HCV infection. In the present study, HCV markers in ALD were measured by the highly sensitive methods, and the changes of sequential HCV markers after abstinence in ALD patients were analysed in order to elucidate the effect of alcohol on HCV. Antibodies to HCV-related antigen were determined using the first or second generation test kit. HCV-RNA genomes encoding the NS-5 region were detected using the RT-PCR method. In the HCV-NS5 negative serum, HCV genomes of the 5′-noncoding region were detected using the two-stage PCR method. Titres of HCV-RNA were measured by multiple cyclic PCR and cDNA dot blotting. Typing of HCV genomes was carried out on the PCR product from the NS-5 region by slot blot hybridization using type-specific cDNA probes, or by restriction fragment length polymorphisms analysis. In alcoholic fibrosis and alcoholic hepatitis, the prevalence of HCV markers was low, suggesting that the main aetiological factor is alcohol but not HCV in these types of ALD. HCV markers were positive in the half of the patients with AL-LC, and in more than 80%of patients with AL-CH and AL-HCC, indicating that HCV infection closely relates to these types of ALD. The ratio of the K1 type to the K2 type of HCV genomes was 4:1 in all types of NANB liver disease. On the other hand, the prevalence of the K1 type was significantly higher than that of the K2 type in AL-HCC, suggesting a possibility that alcohol misuse may modify the development of HCC caused by the K1 type of HCV. Disappearance of HCV-NS5 from blood was observed in four out of eight patients who were sequentially determined HCV-NS5 following abstinence. In one patient, the titres of HCV-RNA changed in parallel with drinking or abstinence, suggesting that alcohol misuse enhances the replication of HCV. These results indicate that the HCV-marker positive ALD patients had a high risk of developing HCC.
OpenAlex reports 33 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The high prevalence of hepatitis C virus (HCV) markers in alcoholic liver cirrhosis (AL-LC) and hepatocellular carcinoma (HCC) suggests a close aetiopathogenic relationship between alcoholic liver disease (ALD) and HCV infection. In the present study, HCV markers in ALD were measured by the highly sensitive methods, and the changes of sequential HCV markers after abstinence in ALD patients were analysed in order to elucidate the effect of alcohol on HCV. Antibodies to HCV-related antigen were determined using the first or second generation test kit. HCV-RNA genomes encoding the NS-5 region were detected using the RT-PCR method. In the HCV-NS5 negative serum, HCV genomes of the 5′-noncoding region were detected using the two-stage PCR method. Titres of HCV-RNA were measured by multiple cyclic PCR and cDNA dot blotting. Typing of HCV genomes was carried out on the PCR product from the NS-5 region by slot blot hybridization using type-specific cDNA probes, or by restriction fragment length polymorphisms analysis. In alcoholic fibrosis and alcoholic hepatitis, the prevalence of HCV markers was low, suggesting that the main aetiological factor is alcohol but not HCV in these types of ALD. HCV markers were positive in the half of the patients with AL-LC, and in more than 80%of patients with AL-CH and AL-HCC, indicating that HCV infection closely relates to these types of ALD. The ratio of the K1 type to the K2 type of HCV genomes was 4:1 in all types of NANB liver disease. On the other hand, the prevalence of the K1 type was significantly higher than that of the K2 type in AL-HCC, suggesting a possibility that alcohol misuse may modify the development of HCC caused by the K1 type of HCV. Disappearance of HCV-NS5 from blood was observed in four out of eight patients who were sequentially determined HCV-NS5 following abstinence. In one patient, the titres of HCV-RNA changed in parallel with drinking or abstinence, suggesting that alcohol misuse enhances the replication of HCV. These results indicate that the HCV-marker positive ALD patients had a high risk of developing HCC.
Key concepts: Alcoholic liver disease, Hepatitis C virus, Hepatocellular carcinoma, Cirrhosis, Hepatitis C, Liver disease, Alcoholic hepatitis, Virology