Loading…
Hepatitis B and C virus and hepatocellular carcinoma
Antibody to hepatitis C virus (anti-HCV) was detected in 18·7% of patients with hepatocellular carcinoma (HCC) and in 10·9% of controls ( P < 0·001). The corresponding prevalences of hepatitis B surface antigen (HBsAg) were 59·3% and 50·0% ( P < 0·001). Using patients with non-hepatic disease...
Saved in:
Published in: | Transactions of the Royal Society of Tropical Medicine and Hygiene 1997, Vol.91 (1), p.38-41 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Antibody to hepatitis C virus (anti-HCV) was detected in 18·7% of patients with hepatocellular carcinoma (HCC) and in 10·9% of controls (
P < 0·001). The corresponding prevalences of hepatitis B surface antigen (HBsAg) were 59·3% and 50·0% (
P < 0·001). Using patients with non-hepatic disease as controls, stepwise logistic regression analysis indicated that both anti-HCV (odds ratio 6·88%; 95% confidence interval [CI] 1·63–9·77) and HBsAg (odds ratio 6·46; 95% CI 1·68–18·13) were independent risk factors for HCC. Calculation of the incremental odds ratio indicated no interaction between hepatitis B virus (HBV) and HCV. Blood transfusion was a significant risk factor for acquiring HCV infection with odds ratios of 5·48 (95% CI 1·07–29·0) and 2·86 (95% CI 1·31–22·72) for HCC cases and controls, respectively. The mean age of HCC cases with HBsAg and anti-HCV was lower than that of HCC patients with anti-HCV alone (
P < 0·01). It is concluded that there is a high rate of HBV infection, and a low rate of HCV infection, among Nigerian patients with HCC. However, HBV and HCV are independent risk factors for the development of HCC, with HBV having an effect more rapidly. Screening of blood products for transfusion might minimize the risk of HCV transmission. |
---|---|
ISSN: | 0035-9203 1878-3503 |
DOI: | 10.1016/S0035-9203(97)90387-4 |