Hepatitis B genotypes correlate with clinical outcomes in patients with chronic hepatitis B

被引:853
作者
Kao, JH
Chen, PJ
Lai, MY
Chen, DS
机构
[1] Natl Taiwan Univ Hosp, Hepatitis Res Ctr, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Med, Grad Inst Clin Med, Taipei 10018, Taiwan
[3] Natl Taiwan Univ, Coll Med, Hepatitis Res Ctr, Taipei 10018, Taiwan
[4] Natl Taiwan Univ, Coll Med, Dept Internal Med, Taipei 10018, Taiwan
关键词
D O I
10.1016/S0016-5085(00)70261-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Six genotypes (A-F) of hepatitis B virus (HBV) have been identified; however, the genotype-related differences in the pathogenicity of HBV remain unknown. Therefore, we investigated the prevalence of HBV genotypes in Taiwan and the association between distinct genotypes and severity of liver disease in a cross-sectional study. Methods: Using a molecular method, HBV genotypes were determined in 100 asymptomatic carriers and in 170 patients with histologically verified chronic liver disease and hepatocellular carcinoma (HCC). Results: All genotypes except genotype E were identified in Taiwan, and genotypes B and C were predominant. Genotype C was prevalent in patients with cirrhosis and in those with HCC who were older than 50 years compared with age-matched asymptomatic carriers (60% vs. 23%, P < 0.001, and 41% vs. 15%, P = 0.005, respectively). Genotype B was significantly more common in patients with HCC aged less than 50 years compared with age-matched asymptomatic carriers (80% vs. 52%, P = 0.03). This predominance was more marked in younger patients with HCC (90% in those aged less than or equal to 35 years), most of whom did not have cirrhosis. Conclusions: Our data suggest that HBV genotype C is associated with more severe liver disease and genotype B may be associated with the development of HCC in young Taiwanese. However, additional large-scale longitudinal studies are needed to confirm the relationship of HBV genotypes to liver disease severity and clinical outcomes.
引用
收藏
页码:554 / 559
页数:6
相关论文
共 32 条
[1]   FROM HEPATITIS TO HEPATOMA - LESSONS FROM TYPE-B VIRAL-HEPATITIS [J].
CHEN, DS .
SCIENCE, 1993, 262 (5132) :369-370
[2]   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
[3]   Cytotoxic T cells and viral hepatitis [J].
Chisari, FV .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (07) :1472-1477
[4]   NEW HEPATITIS-B SURFACE-ANTIGEN SUBTYPES INSIDE AD CATEGORY [J].
COUROUCEPAUTY, AM ;
LEMAIRE, JM ;
ROUX, JF .
VOX SANGUINIS, 1978, 35 (05) :304-308
[5]   DISTRIBUTION OF HBSAG SUBTYPES IN THE WORLD [J].
COUROUCEPAUTY, AM ;
PLANCON, A ;
SOULIER, JP .
VOX SANGUINIS, 1983, 44 (04) :197-211
[6]  
DESMET VJ, 1994, HEPATOLOGY, V19, P1513, DOI 10.1002/hep.1840190629
[7]   Pathogenesis of hepatitis B and C-induced hepatocellular carcinoma [J].
Idilman, R ;
De Maria, N ;
Colantoni, A ;
Van Thiel, DH .
JOURNAL OF VIRAL HEPATITIS, 1998, 5 (05) :285-299
[8]   GENOTYPES OF HEPATITIS-C VIRUS IN TAIWAN AND THE PROGRESSION OF LIVER-DISEASE [J].
KAO, JH ;
CHEN, PJ ;
LAI, MY ;
YANG, PM ;
SHEU, JC ;
WANG, TH ;
CHEN, DS .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1995, 21 (03) :233-237
[9]   AVOIDING FALSE POSITIVES WITH PCR [J].
KWOK, S ;
HIGUCHI, R .
NATURE, 1989, 339 (6221) :237-238
[10]  
LAU JYN, 1993, LANCET, V342, P1335