Prevalence of HBV precore/core promoter variants in the United States

被引:171
作者
Chu, CJ
Keeffe, EB
Han, SH
Perrillo, RP
Min, AD
Soldevila-Pico, C
Carey, W
Brown, RS
Luketic, VA
Terrault, N
Lok, ASF
机构
[1] Univ Michigan, Med Ctr, Div Gastroenterol, Ann Arbor, MI 48109 USA
[2] Stanford Univ, Stanford, CA 94305 USA
[3] Univ Calif Los Angeles, Los Angeles, CA USA
[4] Mt Sinai Sch Med, New York, NY USA
[5] Ochsner Clin & Alton Ochsner Med Fdn, New York, NY USA
[6] Univ Florida, Gainesville, FL USA
[7] Cleveland Clin, Cleveland, OH 44106 USA
[8] Columbia Presbyterian Med Ctr, New York, NY 10032 USA
[9] Univ Calif San Francisco, San Francisco, CA 94143 USA
[10] Virginia Commonwealth Univ, Richmond, VA USA
关键词
D O I
10.1053/jhep.2003.50352
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Variants in the precore (G(1896)A) and core promoter (A(1762)T, G(1764)A) regions of hepatitis B virus (HBV) may be related to serum HBV DNA levels and severity of liver disease. The aims of this nationwide study were to determine the prevalence of HBV precore/core promoter variants in the United States and the association between these variants and patient demographics, HBV genotypes, serum HBV DNA level, and severity of liver disease. A total of 694 consecutive chronic HBV-infected patients seen in 17 U.S. liver centers during a 1-year period were enrolled. Demographic, clinical, and laboratory data were collected. Sera were tested for HBV genotypes as well as precore and core promoter variants by line-probe assays. Quantitative HBV DNA levels were determined using Cobas Amplicor HBV Monitor kits. Precore and core promoter variants were found in 27% and 44% of patients with chronic HBV infection in the United States. Precore and core promoter variants were more common in hepatitis B e antigen (HBeAg)-negative than in HBeAg-positive patients (precore, 38% vs. 9%; core promoter, 51% vs. 36%; respectively, P < .001). The prevalence of these variants was related to ethnicity, place of birth, and HBV genotypes. Patients with core promoter variants were more likely to have hepatic decompensation. Precore and/or core promoter variants were associated with higher serum HBV DNA levels in HBeAg-negative but not in HBeAg-positive patients. In conclusion, HBV precore and core promoter variants are not rare in the United States. Physicians should be aware of the existence of HBV precore and core promoter variants and the clinical condition of "HBeAg-negative chronic hepatitis."
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页码:619 / 628
页数:10
相关论文
共 45 条
[1]   CHRONIC ACTIVE HEPATITIS WITH HEPATITIS-B VIRUS-DNA AND ANTIBODY AGAINST E-ANTIGEN IN THE SERUM - DISTURBED SYNTHESIS AND SECRETION OF E-ANTIGEN FROM HEPATOCYTES DUE TO A POINT MUTATION IN THE PRECORE REGION [J].
AKAHANE, Y ;
YAMANAKA, T ;
SUZUKI, H ;
SUGAI, Y ;
TSUDA, F ;
YOTSUMOTO, S ;
OMI, S ;
OKAMOTO, H ;
MIYAKAWA, Y ;
MAYUMI, M .
GASTROENTEROLOGY, 1990, 99 (04) :1113-1119
[2]   High prevalence of 1762T 1764A mutations in the basic core promoter of hepatitis B virus isolated from black Africans with hepatocellular carcinoma compared with asymptomatic carriers [J].
Baptista, M ;
Kramvis, A ;
Kew, MC .
HEPATOLOGY, 1999, 29 (03) :946-953
[3]   WILD-TYPE AND E-ANTIGEN-MINUS HEPATITIS-B VIRUSES AND COURSE OF CHRONIC HEPATITIS [J].
BRUNETTO, MR ;
GIARIN, MM ;
OLIVERI, F ;
CHIABERGE, E ;
BALDI, M ;
ALFARANO, A ;
SERRA, A ;
SARACCO, G ;
VERME, G ;
WILL, H ;
BONINO, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (10) :4186-4190
[4]   Effects of a naturally occurring mutation in the hepatitis B virus basal core promoter on precore gene expression and viral replication [J].
Buckwold, VE ;
Xu, ZC ;
Chen, M ;
Yen, TSB ;
Ou, JH .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5845-5851
[5]   Effects of a frequent double-nucleotide basal core promoter mutation and its putative single-nucleotide precursor mutations on hepatitis B virus gene expression and replication [J].
Buckwold, VE ;
Xu, ZC ;
Yen, TSB ;
Ou, JH .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :2055-2065
[6]  
CARMAN WF, 1989, LANCET, V2, P588
[7]   Hepatitis B e antigen-negative chronic hepatitis B in Hong Kong [J].
Chan, HLY ;
Leung, NWY ;
Hussain, M ;
Wong, ML ;
Lok, ASF .
HEPATOLOGY, 2000, 31 (03) :763-768
[8]   Quantitative serum HBV DNA levels during different stages of chronic hepatitis B infection [J].
Chu, CJ ;
Hussain, M ;
Lok, ASF .
HEPATOLOGY, 2002, 36 (06) :1408-1415
[9]   Hepatitis B virus genotype B is associated with earlier HBeAg seroconversion compared with hepatitis B virus genotype C [J].
Chu, CJ ;
Hussain, M ;
Lok, ASF .
GASTROENTEROLOGY, 2002, 122 (07) :1756-1762
[10]  
CHU CJ, 2003, IN PRESS GASTROENTER