Serum hepatitis B core-related antigen as a surrogate marker of hepatitis B e antigen seroconversion in chronic hepatitis B.

Correlation Detection Hepatitis B core antigen Hepatitis B virus Hepatitis B virus DNA Liver biopsy Pregenomic RNA Quantitative hepatitis B core-related antigen Receiver operating characteristic Seroconversion

Journal

World journal of gastroenterology
ISSN: 2219-2840
Titre abrégé: World J Gastroenterol
Pays: United States
ID NLM: 100883448

Informations de publication

Date de publication:
28 Oct 2021
Historique:
received: 11 03 2021
revised: 06 05 2021
accepted: 01 09 2021
entrez: 18 11 2021
pubmed: 19 11 2021
medline: 20 11 2021
Statut: ppublish

Résumé

Quantitative hepatitis B core-related antigen (qHBcrAg) has a better correlation with intrahepatic hepatitis B virus (HBV) covalently closed circular DNA (cccDNA) than HBV DNA or hepatitis B e antigen (HBeAg), but data are still lacking for its clinical application. The aim was to investigate serum qHBcrAg levels in patients with chronic hepatitis B and assess the correlation of serum qHBcrAg with pregenomic RNA (pgRNA), cccDNA, and HBeAg seroconversion. This study was a secondary analysis of patients who underwent percutaneous liver biopsy between July 2014 and June 2019 in two multicenter randomized controlled clinical trials of peginterferon A total of 139 patients were included. The mean qHBcrAg levels were 5.32 ± 1.18 log Serum HBcrAg levels were correlated with HBV virological markers and could be used to predict HBeAg seroconversion.

Sections du résumé

BACKGROUND BACKGROUND
Quantitative hepatitis B core-related antigen (qHBcrAg) has a better correlation with intrahepatic hepatitis B virus (HBV) covalently closed circular DNA (cccDNA) than HBV DNA or hepatitis B e antigen (HBeAg), but data are still lacking for its clinical application.
AIM OBJECTIVE
The aim was to investigate serum qHBcrAg levels in patients with chronic hepatitis B and assess the correlation of serum qHBcrAg with pregenomic RNA (pgRNA), cccDNA, and HBeAg seroconversion.
METHODS METHODS
This study was a secondary analysis of patients who underwent percutaneous liver biopsy between July 2014 and June 2019 in two multicenter randomized controlled clinical trials of peginterferon
RESULTS RESULTS
A total of 139 patients were included. The mean qHBcrAg levels were 5.32 ± 1.18 log
CONCLUSION CONCLUSIONS
Serum HBcrAg levels were correlated with HBV virological markers and could be used to predict HBeAg seroconversion.

Identifiants

pubmed: 34790015
doi: 10.3748/wjg.v27.i40.6927
pmc: PMC8567480
doi:

Substances chimiques

Antiviral Agents 0
Biomarkers 0
DNA, Viral 0
Hepatitis B Core Antigens 0
Hepatitis B Surface Antigens 0
Hepatitis B e Antigens 0

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

6927-6938

Informations de copyright

©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: The authors declare that they have no conflicting interests.

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Auteurs

Xiu-Mei Chi (XM)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Xiao-Mei Wang (XM)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Zhong-Feng Wang (ZF)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Rui-Hong Wu (RH)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Xiu-Zhu Gao (XZ)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Hong-Qin Xu (HQ)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Yan-Hua Ding (YH)

Phase I Clinical Trials Unit, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.

Jun-Qi Niu (JQ)

Department of Hepatology, Key Laboratory of Zoonosis Research, Ministry Education, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China. junqiniu@jlu.edu.cn.

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