Precore Stop Mutant in HBeAg-Positive Patients with Chronic Hepatitis B: Clinical Characteristics and Correlation with the Course of HBeAg-to-Anti-HBe Seroconversion

Author:

Chu Chia-Ming1,Yeh Chau-Ting1,Lee Ching-Song1,Sheen I-Shyan1,Liaw Yun-Fan1

Affiliation:

1. Liver Research Unit, Chang Gung Memorial Hospital, Chang Gung University, Taipei, Taiwan

Abstract

ABSTRACT This study aimed to investigate the ratios of precore stop mutant (codon 28; TGG to TAG) to total viremia in 53 HBeAg-positive patients with chronic hepatitis B by amplification-created restriction site assays along the course of HBeAg-to-anti-HBe seroconversion. At baseline, 11% had exclusive wild-type hepatitis B virus (HBV), 15% had exclusively precore mutant, and 74% had mixed viral strains. Precore mutant ratios correlated little with age, sex, or HBV DNA levels (all P > 0.1), but correlated modestly with alanine aminotransferase (ALT) levels ( P = 0.05). The intervals from presentation to anti-HBe seroconversion correlated significantly with ALT and precore mutant ratios in univariate analysis but with only precore mutant ratios in multivariate analysis ( P = 0.003). Precore mutant ratios at baseline were significantly higher ( P < 0.001) in six patients with persistent high viremia and ALT elevation after anti-HBe seroconversion (group 1) than in 47 with remission (group 2). All group 1 patients had exclusive precore mutant after anti-HBe seroconversion, as did only 14 (30%) of the group 2 patients ( P = 0.003). Among group 2 patients, precore mutant ratios at baseline or after anti-HBe seroconversion showed no significant difference between 34 patients with sustained remission and 13 with relapse. Cirrhosis developed in 50% (5 of 10) of patients with precore mutant ratios >50% at baseline but only in 12% (5 of 43) of those with precore mutant ratios of <50% at baseline ( P < 0.05). In conclusion, precore mutant of variable ratios was frequently detected in HBeAg-positive patients with chronic hepatitis B. Precore mutant ratios tended to correlate with ALT levels and anti-HBe seroconversion, but high precore mutant ratios were associated with persistent hepatitis after anti-HBe seroconversion and increased risk of cirrhosis.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference39 articles.

1. Akahane, Y., T. Yamanaka, H. Suzuki, Y. Sugri, F. Tsuda, S. Yotsumoto, S. Omi, H. Okamoto, Y. Miyakawa, and M. Mayumi. 1990. Chronic active hepatitis with hepatitis B virus DNA and antibody against e antigen in the serum. Gastroenterology90:1113–1119.

2. Bonino, F., F. Rosina, M. Rizzetto, R. Rizzi, E. Chiaberge, R. Tardanico, F. Callea, and G. Verme. 1986. Chronic hepatitis in HBsAg carriers with serum HBV-DNA and anti-HBe. Gastroenterology90:1268–1273.

3. Brook, M. G., P. Karayiannis, and H. C. Thomas. 1989. Which patients with chronic hepatitis B virus infection will respond to alpha-interferon therapy? A statistical analysis of predictive factors. Hepatology10:761–763.

4. Brunetto, M. R., M. Stemler, F. Schodel, H. Will, A. Ottobrelli, M. Rizzetto, G. Verme, and F. Bonino. 1989. Identification of HBV variants which cannot produce precore-derived HBeAg and may be responsible for severe hepatitis. Ital. J. Gastroenterol. 21:151–154.

5. Brunetto, M. R., M. Giarin, G. Saracco, F. Oliver, P. Calvo, G. Capra, A. Randone, M. L. Abate, P. Manzini, and M. Capalbo. 1993. Hepatitis B virus unable to secrete e antigen and response to interferon in chronic hepatitis B. Gastroenterology105:846–850.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3