The role of contraceptive steroids in the etiology or pathogenesis of hepatocellular carcinoma in urban South African black women was investigated in a hospital‐based case and control study. Participating were 46 women, 19 to 54 yr old, with carcinoma, and 92 matched controls. South African blacks have a high incidence of hepatocellular carcinoma, and urban black women have used contraceptive steroids fairly widely for a number of years. Use of contraceptive steroids for longer than 6 mo (mean duration 46.7 mo) was not found to pose a risk for development of hepatocellular carcinoma in this population–relative risk 0.8 (95% confidence interval [C. I.] 0.4 to 1.7). This was also true of use for longer than 8 yr–relative risk 0.6 (95% C. I. 0.2 to 2.5), and if a combination of an estrogen and a progestogen or a progestogen alone was used (relative risk 1.7 [95% C. I. 0.7 to 4.2] and 0.4 [95% C. I. 0.1 to 1.2], respectively). Chronic hepatitis B virus infection was confirmed to have an etiological association with hepatocellular carcinoma, but there was no evidence that contraceptive steroids acted as a co‐carcinogen with the virus or, conversely, that they played a causal role in patients negative for hepatitis B surface antigenemia. We cannot, however, exclude the possibility that contraceptive steroids may play a causal role in hepatocellular carcinoma in black women who have never been infected with the hepatitis B virus. Nor was there evidence that contraceptive steroids acted in concert with either cigarette smoking or chronic alcohol abuse in hepatocarcinogenesis. We conclude that contraceptive steroids cannot at present be incriminated as a risk factor for the development of hepatocellular carcinoma in South African black women. Copyright © 1990 American Association for the Study of Liver Diseases
CITATION STYLE
Kew, M. C., Song, E., Mohammed, A., & Hodkinson, J. (1990). Contraceptive steroids as a risk factor for hepatocellular carcinoma: A case/control study in south african black women. Hepatology, 11(2), 298–302. https://doi.org/10.1002/hep.1840110221
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