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Ann Hepatol ; 13(6): 771-80, 2014.
Article in English | MEDLINE | ID: mdl-25332263

ABSTRACT

INTRODUCTION: The intrahepatic hepatitis B surface antigens (HBsAg) expression is related to disease progression of chronic hepatitis B. We examined the features of intrahepatic HBsAg expression. MATERIAL AND METHODS: A total of 181 patients with e antigen positive chronic hepatitis B were enrolled. Patterns and semi-quantitative measurement of intrahepatic HBsAg expression were analyzed. The association of intrahepatic hepatitis HBsAg expression with clinical, viral, and histological characteristics was evaluated. RESULTS: Higher necroinflammation grade and greater fibrosis stage accompanied with lower serum HBV DNA and HBsAg levels were observed in patients with type II ground glass hepatocytes and 2+/3+ scales of intrahepatic HBsAg expression. Basal core promoter T1762/A1764 mutations were strongly associated with the pattern of type II ground glass hepatocytes expression (P < 0.001) and higher level of HBsAg expression (9.3 ± 8.0% vs. 4.3 ± 5.0%, P = 0.008). In multivariate analysis, basal core promoter mutations (Odds ratio: 6.356, 95% confidence interval: 1.204 ~ 33.356, P = 0.029) was associated with 2+/3+ scale of HBsAg expression. CONCLUSION: Both pattern and levels of intrahepatic HBsAg expression were associated with severity of liver disease in e antigen positive chronic hepatitis B. Strong relationship between intrahepatic HBsAg expression and basal core promoter 1762/A1764 mutations indicated that HBsAg expression may be the histological manifestation of hepatitis B virus genomic evolution under host immune surveillance.


Subject(s)
DNA, Viral/blood , Hepatitis B Surface Antigens/metabolism , Hepatitis B virus/genetics , Hepatitis B, Chronic/metabolism , Hepatocytes/pathology , Liver/metabolism , Virus Replication , Adult , Disease Progression , Female , Genotype , Hepatitis B Surface Antigens/genetics , Hepatitis B virus/immunology , Hepatitis B virus/physiology , Hepatitis B, Chronic/blood , Hepatitis B, Chronic/pathology , Humans , Liver/pathology , Male , Middle Aged , Mutation , Promoter Regions, Genetic , Viral Load
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