TY - JOUR
T1 - The Role of Chronic Viral Hepatitis in Hepatocellular Carcinoma in the United States
AU - Di Bisceglie, Adrian M.
AU - Order, Stanley E.
AU - Klein, Jerry L.
AU - Waggoner, Jeanne G.
AU - Sjogren, Maria H.
AU - Kuo, George
AU - Houghton, Michael
AU - Choo, Q. ‐L
AU - Hoofnagle, Jay H.
PY - 1991/3
Y1 - 1991/3
N2 - Although hepatocellular carcinoma is a relatively uncommon tumor in the United States, it is quite common in sub‐Saharan Africa and the Far East, where most cases are associated with infection with the hepatitis B virus. We have studied 99 American patients with hepatocellular carcinoma for evidence of hepatitis B or hepatitis C viral infection and compared these findings to those in a group of matched controls with other cancers. The two groups differed in proportion, with hepatitis B surface antigen in serum being significantly higher in patients with hepatocellular carcinoma (7% vs. 0%, p = 0.009). Antibody to hepatitis C virus was also found more frequently in patients with hepatocellular carcinoma (13% vs. 2%, p = 0.002). The relative risk for hepatocellular carcinoma in hepatitis B surface antigen‐positive patients was calculated to be 17.3 and for antibody to hepatitis C virus to be 7.3. The attributable fraction of cases related to the hepatitis B surface antigen carrier state was 6.7% and for patients infected with the hepatitis C virus was 11.4%. Approximately three quarters of cases of hepatocellular carcinoma did not have evidence of either hepatitis C or hepatitis B virus infection. These findings provide strong evidence that hepatitis C virus infection is associated with the development of hepatocellular carcinoma, and in the United States may even play a more important role than the hepatitis B virus.
AB - Although hepatocellular carcinoma is a relatively uncommon tumor in the United States, it is quite common in sub‐Saharan Africa and the Far East, where most cases are associated with infection with the hepatitis B virus. We have studied 99 American patients with hepatocellular carcinoma for evidence of hepatitis B or hepatitis C viral infection and compared these findings to those in a group of matched controls with other cancers. The two groups differed in proportion, with hepatitis B surface antigen in serum being significantly higher in patients with hepatocellular carcinoma (7% vs. 0%, p = 0.009). Antibody to hepatitis C virus was also found more frequently in patients with hepatocellular carcinoma (13% vs. 2%, p = 0.002). The relative risk for hepatocellular carcinoma in hepatitis B surface antigen‐positive patients was calculated to be 17.3 and for antibody to hepatitis C virus to be 7.3. The attributable fraction of cases related to the hepatitis B surface antigen carrier state was 6.7% and for patients infected with the hepatitis C virus was 11.4%. Approximately three quarters of cases of hepatocellular carcinoma did not have evidence of either hepatitis C or hepatitis B virus infection. These findings provide strong evidence that hepatitis C virus infection is associated with the development of hepatocellular carcinoma, and in the United States may even play a more important role than the hepatitis B virus.
UR - http://www.scopus.com/inward/record.url?scp=0025761253&partnerID=8YFLogxK
U2 - 10.1111/j.1572-0241.1991.tb05359.x
DO - 10.1111/j.1572-0241.1991.tb05359.x
M3 - Article
C2 - 1847790
AN - SCOPUS:0025761253
SN - 0002-9270
VL - 86
SP - 335
EP - 338
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 3
ER -