Effects of hepatitis C and B viruses infection on the development of hepatocellular carcinoma
- PMID: 7528262
- DOI: 10.1002/jmv.1890440117
Effects of hepatitis C and B viruses infection on the development of hepatocellular carcinoma
Abstract
A case control study consisting of 102 patients with HCC, 102 sex-matched and age-matched patients with nonhepatic disease, and 204 matched healthy controls was carried out to investigate the effect of hepatitis B virus (HBV) and hepatitis C virus (HCV) infection on the development of hepatocellular carcinoma (HCC). The prevalence of antibody to HCV (anti-HCV) in HCC (34.3%) was higher than in nonhepatic disease (10.7%, P < 0.001) or in healthy controls (2.4%, P < 0.001). The prevalence of hepatitis B surface antigen (HBsAg) in HCC (77.4%) was higher than in nonhepatic disease (16.6%, P < 0.001) or in healthy controls (19.6%, P < 0.001). Anti-HCV positivity in nonhepatic disease was higher than in healthy controls (P < 0.01). Using patients with nonhepatic disease as controls, stepwise logistic regression analysis indicated that both anti-HCV (odds ratio, 3.4; 95% confidence interval, 2.1-5.6) and HBsAg (odds ratio, 5.6; 95% confidence interval, 3.6-8.5) are independent risk factors for HCC. Using healthy controls, the development of HCC was also strongly associated with anti-HCV (odds ratio, 8.0; 95% confidence interval, 4.3-14.6) and HBsAg (odds ratio, 5.5; 95% confidence interval, 3.7-8.2). Calculation of incremental odds ratio indicated that there is no interaction between HBV and HCV. In conclusion, HBV and HCV are risk factors of HCC. They act independently and without interaction.
Similar articles
-
A case-control study of hepatitis B and C virus infection as risk factors for hepatocellular carcinoma in Henan, China.Int J Epidemiol. 1998 Aug;27(4):574-8. doi: 10.1093/ije/27.4.574. Int J Epidemiol. 1998. PMID: 9758109
-
Additive effect modification of hepatitis B surface antigen and e antigen on the development of hepatocellular carcinoma.Br J Cancer. 1996 Jun;73(12):1498-502. doi: 10.1038/bjc.1996.283. Br J Cancer. 1996. PMID: 8664119 Free PMC article.
-
Hepatitis C virus infection as a risk factor for hepatocellular carcinoma in patients with cirrhosis. A case-control study.Ann Intern Med. 1992 Jan 15;116(2):97-102. doi: 10.7326/0003-4819-116-2-97. Ann Intern Med. 1992. PMID: 1309286
-
Coinfection of hepatitis B and C viruses and risk of hepatocellular carcinoma: systematic review and meta-analysis.Int J Cancer. 2011 Jan 1;128(1):176-84. doi: 10.1002/ijc.25321. Int J Cancer. 2011. PMID: 20232388 Review.
-
[Co-infection of HBV with HCV and a possible role of HBV DNA in hepatocarcinogenesis].Nihon Rinsho. 1999 Jan;57(1):213-9. Nihon Rinsho. 1999. PMID: 10036965 Review. Japanese.
Cited by
-
An IARC evaluation of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans as risk factors in human carcinogenesis.Environ Health Perspect. 1998 Apr;106 Suppl 2(Suppl 2):755-60. doi: 10.1289/ehp.98106755. Environ Health Perspect. 1998. PMID: 9599727 Free PMC article. Review.
-
p53 codon 72 polymorphism and hepatocellular carcinoma: a meta-analysis.Hepatol Int. 2013 Jun;7(2):669-75. doi: 10.1007/s12072-012-9389-9. Epub 2012 Aug 3. Hepatol Int. 2013. PMID: 26201800
-
Low prevalence of hepatitis C infection in hepatocellular carcinoma (HCC) cases and population controls in Guangxi, a hyperendemic region for HCC in the People's Republic of China.Br J Cancer. 1996 Aug;74(3):491-3. doi: 10.1038/bjc.1996.389. Br J Cancer. 1996. PMID: 8695372 Free PMC article.
-
Viral genotypes and associated risk factors of hepatocellular carcinoma in India.Cancer Biol Med. 2012 Sep;9(3):172-81. doi: 10.7497/j.issn.2095-3941.2012.03.004. Cancer Biol Med. 2012. PMID: 23691475 Free PMC article.
-
Hepatitis C viremia and genotype distribution among a sample of nonmedical prescription drug users exposed to HCV in rural Appalachia.J Med Virol. 2012 Sep;84(9):1376-87. doi: 10.1002/jmv.23252. J Med Virol. 2012. PMID: 22825816 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical