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

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 charact...

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Autores principales: Zhang, Zhan-Qing, Zhang, Xiao-Nan, Lu, Wei, Wang, Yan-Bing, Weng, Qi-Cheng, Feng, Yan-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716365/
https://www.ncbi.nlm.nih.gov/pubmed/29202690
http://dx.doi.org/10.1186/s12876-017-0703-9
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author Zhang, Zhan-Qing
Zhang, Xiao-Nan
Lu, Wei
Wang, Yan-Bing
Weng, Qi-Cheng
Feng, Yan-Ling
author_facet Zhang, Zhan-Qing
Zhang, Xiao-Nan
Lu, Wei
Wang, Yan-Bing
Weng, Qi-Cheng
Feng, Yan-Ling
author_sort Zhang, Zhan-Qing
collection PubMed
description 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.
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spelling pubmed-57163652017-12-08 Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B Zhang, Zhan-Qing Zhang, Xiao-Nan Lu, Wei Wang, Yan-Bing Weng, Qi-Cheng Feng, Yan-Ling BMC Gastroenterol Research Article 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. BioMed Central 2017-12-04 /pmc/articles/PMC5716365/ /pubmed/29202690 http://dx.doi.org/10.1186/s12876-017-0703-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Zhan-Qing
Zhang, Xiao-Nan
Lu, Wei
Wang, Yan-Bing
Weng, Qi-Cheng
Feng, Yan-Ling
Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B
title Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B
title_full Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B
title_fullStr Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B
title_full_unstemmed Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B
title_short Distinct patterns of serum hepatitis B core-related antigen during the natural history of chronic hepatitis B
title_sort distinct patterns of serum hepatitis b core-related antigen during the natural history of chronic hepatitis b
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716365/
https://www.ncbi.nlm.nih.gov/pubmed/29202690
http://dx.doi.org/10.1186/s12876-017-0703-9
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