Antibody to hepatitis B core antigen is associated with the development of hepatocellular carcinoma in hepatitis C virus-infected persons: A 12-year prospective study

被引:0
作者
Tanaka, K
Nagao, Y
Ide, T
Kumashiro, R
Sata, M
机构
[1] Kurume Univ, Sch Med, Dept Med 2, Kurume, Fukuoka 8300011, Japan
[2] Kurume Univ, Sch Med, Dept Digest Dis Informat & Res, Kurume, Fukuoka 8300011, Japan
关键词
antibody to hepatitis B core antigen; occult hepatitis B virus; hepatitis C virus; hepatocellular carcinoma; HCV hyper epidemic area;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Several studies have reported that antibody to hepatitis B core antigen (anti-HBc) positivity may influence the development of hepatocellular carcinoma (HCC) in chronic hepatitis C patients, but the evidence is still not conclusive. In this study, we examined whether the presence of anti-HBc positive was associated with the development of HCC in hepatitis C virus (HCV)-infected subjects among the residents in an HCV hyperepidemic area who were followed up for 12 years. In an HCV hyperendemic area (positive rate of anti-HCV: 23.4%), 509 residents were examined by health screening in 1990. After 12 years of follow-up, we evaluated the risk factors for HCC. The incidence of HCC was compared between anti-HBc positive and anti-HBc negative subjects after 12 years of prospective observation. Univariate and multivariate analyses were conducted to determine risk factors for the development of HCC. The incidence of HCC was significantly higher in the anti-HBc positive group (13 subjects) than in the anti-HBc negative group (0 subjects) (P=0.012). Multivariate analysis identified positivity for anti-HBc and HCV RNA, history of icterus, and female gender as independent determinants of the development of HCC. Our findings provide clear evidence in a prospective study that presence of anti-HBc, that is, past hepatitis B virus (HBV) infection, is a risk factor for the development of HCC in HCV-infected people.
引用
收藏
页码:827 / 832
页数:6
相关论文
共 48 条
[1]   High frequency of HCV infection in individuals with isolated antibody to hepatitis B core antigen [J].
Berger, A ;
Doerr, HW ;
Rabenau, HF ;
Weber, B .
INTERVIROLOGY, 2000, 43 (02) :71-76
[2]   Occult hepatitis B virus after acute self-limited infection persisting for 30 years without sequence variation [J].
Bläckberg, J ;
Kidd-Ljunggren, K .
JOURNAL OF HEPATOLOGY, 2000, 33 (06) :992-997
[3]   Occult hepatitis B virus infection in patients with chronic hepatitis C liver disease [J].
Cacciola, I ;
Pollicino, T ;
Squadrito, G ;
Cerenzia, G ;
Orlando, ME ;
Raimondo, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (01) :22-26
[4]   Hepatitis B virus infection and hepatocellular carcinoma: Molecular genetics and clinical perspectives [J].
Chen, PJ ;
Chen, DS .
SEMINARS IN LIVER DISEASE, 1999, 19 (03) :253-262
[5]   Multivariate analysis of risk factors for hepatocellular carcinoma in patients with hepatitis C virus-related liver cirrhosis [J].
Chiba, T ;
Matsuzaki, Y ;
Abei, M ;
Shoda, J ;
Aikawa, T ;
Tanaka, N ;
Osuga, T .
JOURNAL OF GASTROENTEROLOGY, 1996, 31 (04) :552-558
[6]   Transmission of hepatitis B by transplantation of livers from donors positive for antibody to hepatitis B core antigen [J].
Dickson, RC ;
Everhart, JE ;
Lake, JR ;
Wei, YL ;
Seaberg, EC ;
Wiesner, RH ;
Zetterman, RK ;
Pruett, TL ;
Ishitani, MB ;
Hoofnagle, JH ;
Detre, KM ;
Demetris, AJ ;
Lombardero, M ;
Seaberg, E ;
Lawlor, S ;
Fitzgerald, S ;
Haber, J ;
Swanson, GL ;
Wiesner, R ;
Krom, R ;
Porayko, MK ;
Schwerman, L ;
Groettum, C ;
Shaw, B ;
Taylor, K ;
Ascher, N ;
Lake, J ;
BremerKamp, C ;
Everhart, J ;
Shores, S ;
Broccoli, A ;
Hausman, G ;
Shepard, B ;
Carrol, N ;
McGory, R ;
Stevenson, WC ;
McCullough, C ;
Caldwell, S .
GASTROENTEROLOGY, 1997, 113 (05) :1668-1674
[7]  
Feitelson MA, 1997, AM J PATHOL, V150, P1141
[8]   PERSISTENCE OF HEPATITIS-B VIRUS-DNA IN THE LIVER AFTER LOSS OF HBSAG IN CHRONIC HEPATITIS-B [J].
FONG, TL ;
DIBISCEGLIE, AM ;
GERBER, MA ;
WAGGONER, JG ;
HOOFNAGLE, JH .
HEPATOLOGY, 1993, 18 (06) :1313-1318
[9]  
Fukuda R, 1999, J MED VIROL, V58, P201, DOI 10.1002/(SICI)1096-9071(199907)58:3&lt
[10]  
201::AID-JMV3&gt