To evaluate the role of oxidative stress and
aflatoxin exposure on risk of
hepatocellular carcinoma (HCC), a case-control study nested within a community-based cohort was conducted in Taiwan. Baseline urine samples, collected from a total of 74 HCC cases and 290 matched controls, were used to determine by
enzyme-linked
immunosorbent assays the level of urinary excretion of 8-oxodeoxyguanosine (8-oxodG), a
biomarker of oxidative DNA damage and urinary
aflatoxin B(1) metabolites, a
biomarker of
aflatoxin exposure. Multivariate-adjusted linear regression analysis showed that urinary
aflatoxin metabolites and gender were significantly associated with level of urinary
8-oxodG among controls. Moreover, after adjustments for potential confounding factors, there was a statistically significant positive dose-response relationship between levels of urinary
8-oxodG and urinary
aflatoxin metabolites (P < 0.0001). However, when compared with subjects in the lowest quartile of
8-oxodG, there was a decrease in risk of HCC, with adjusted odds ratios (
ORs) of 0.8 [95% confidence interval (CI) 0.3-2.0], 0.7 (95% CI 0.3-2.0) and 0.7 (95% CI 0.2-1.7) for subjects in the second, third and fourth quartile, respectively. The combination of level of urinary
8-oxodG below the median and
hepatitis B virus infection resulted in an OR of 11.4 (95% CI 3.9-33.3), compared with those with urinary
8-oxodG above the median and hepatitis B virus
surface antigen negative. These results suggest that elevated levels of urinary
8-oxodG may be related to increasing level of
aflatoxin exposure but may also indicate enhanced repair of oxidative DNA damage and therefore lower risk of HCC.