乙型肝炎表面抗原
共感染
基因型
医学
持久性(不连续性)
乙型肝炎病毒
免疫学
内科学
慢性感染
病毒学
乙型肝炎
病毒
肝病学
生物
基因
免疫系统
生物化学
岩土工程
工程类
作者
Kiyoaki Ito,Hiroshi Yotsuyanagi,Hiroshi Yatsuhashi,Yoshiyasu Karino,Yasuhiro Takikawa,Takafumi Saito,Yasuji Arase,Fumio Imazeki,Masayuki Kurosaki,Takeji Umemura,Takafumi Ichida,Hidenori Toyoda,Masashi Yoneda,Eiji Mita,Kazuhide Yamamoto,Kojiro Michitaka,Tatsuji Maeshiro,Junko Tanuma,Yasuhito Tanaka,Masaya Sugiyama
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2013-07-29
卷期号:59 (1): 89-97
被引量:89
摘要
The proportion of patients who progress to chronicity following acute hepatitis B (AHB) varies widely worldwide. Moreover, the association between viral persistence after AHB and hepatitis B virus (HBV) genotypes in adults remains unclear. A nationwide multicenter study was conducted throughout Japan to evaluate the influence of clinical and virological factors on chronic outcomes in patients with AHB. For comparing factors between AHB patients with viral persistence and those with self-limited infection, 212 AHB patients without human immunodeficiency virus (HIV) coinfection were observed in 38 liver centers until serum hepatitis B surface antigen (HBsAg) disappeared or a minimum of 6 months in cases where HBsAg persisted. The time to disappearance of HBsAg was significantly longer for genotype A patients than that of patients infected with non-A genotypes. When chronicity was defined as the persistence of HBsAg positivity for more than 6 or 12 months, the rate of progression to chronicity was higher in patients with genotype A, although many cases caused by genotype A were prolonged cases of AHB, rather than chronic infection. Multivariate logistic regression analysis revealed only genotype A was independently associated with viral persistence following AHB. A higher peak level of HBV DNA and a lower peak of alanine aminotransferase (ALT) levels were characteristics of AHB caused by genotype A. Treatment with nucleotide analogs (NAs) did not prevent progression to chronic infection following AHB overall. Subanalysis suggested early NA initiation may enhance the viral clearance.Genotype A was an independent risk factor for progression to chronic infection following AHB. Our data will be useful in elucidating the association between viral persistence after AHB, host genetic factors, and treatment with NAs in future studies.
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