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Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B

Authors :
Zhan-Qing Zhang
Xiao-Nan Zhang
Wei Lu
Yan-Bing Wang
Qi-Cheng Weng
Yan-Ling Feng
Source :
BMC Gastroenterology, Vol 17, Iss 1, Pp 1-8 (2017)
Publication Year :
2017
Publisher :
BMC, 2017.

Abstract

Abstract Background The current clinical practice on chronic hepatitis B (CHB) requires better on-treatment monitoring of viral persistence. Quantified assays for hepatitis B surface antigen (HBsAg) and core-related antigen (HBcrAg) hold promise for further optimization of therapy. Here, we aimed to characterize HBcrAg during the natural course of CHB. Methods Four-hundred and forty four treatment naïve CHB patients, who all underwent liver histology examination, were enrolled in this cross-sectional study. Their HBV DNA, HBsAg, HBeAg and HBcrAg titres were quantified and analyzed in the context of four distinct clinical phases. Correlation of HBcrAg and HBsAg with other markers were performed. The relationship between liver and serum antigen levels were also assessed. Results HBcrAg, like HBsAg, exhibited high degree of correlation with HBV DNA. However, a more significant linear relationship was found between HBcrAg and HBeAg titre in immune tolerant (IT) and immune clearance (IC) phases, while in HBeAg negative hepatitis (ENH) group, HBV DNA is a major determinant of HBcrAg. Significant difference was observed in liver HBcAg score and HBcrAg level in both IT and IC phases whereas barely significant positive correlations between liver HBsAg score and HBsAg titre was documented. Conclusion HBcrAg titre exhibited distinct correlative profile in a phase-specific manner. In addition, its level is well-related to the intrahepatic expression of core antigen. It has a considerable utility in monitoring and refining antiviral therapy.

Details

Language :
English
ISSN :
1471230X
Volume :
17
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Gastroenterology
Publication Type :
Academic Journal
Accession number :
edsdoj.667ab6f650cf4a0690e7103fd9875e72
Document Type :
article
Full Text :
https://doi.org/10.1186/s12876-017-0703-9