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Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection

OBJECTIVE: Liver inflammatory activity staging is critical to guide the treatment of chronic hepatitis B virus (CHB) infection. Here, we aimed to identify practical clinical biomarkers of moderate inflammatory activity in hepatitis B e-antigen (HBeAg)-negative CHB patients. METHODS: Treatment-naïve...

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Autores principales: Hu, Jianhua, Wang, Yong, Jiang, Gongying, Zheng, Jie, Chen, Tuxiang, Chen, Zhiping, Yang, Meifang, Zhang, Xuan, Zhao, Hong, Li, Lanjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673054/
https://www.ncbi.nlm.nih.gov/pubmed/33179557
http://dx.doi.org/10.1177/0300060520969582
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author Hu, Jianhua
Wang, Yong
Jiang, Gongying
Zheng, Jie
Chen, Tuxiang
Chen, Zhiping
Yang, Meifang
Zhang, Xuan
Zhao, Hong
Li, Lanjuan
author_facet Hu, Jianhua
Wang, Yong
Jiang, Gongying
Zheng, Jie
Chen, Tuxiang
Chen, Zhiping
Yang, Meifang
Zhang, Xuan
Zhao, Hong
Li, Lanjuan
author_sort Hu, Jianhua
collection PubMed
description OBJECTIVE: Liver inflammatory activity staging is critical to guide the treatment of chronic hepatitis B virus (CHB) infection. Here, we aimed to identify practical clinical biomarkers of moderate inflammatory activity in hepatitis B e-antigen (HBeAg)-negative CHB patients. METHODS: Treatment-naïve HBeAg-negative CHB patients who underwent liver biopsy at our hospital from 1 January 2013 to 31 December 2016 were enrolled. Markers of inflammatory activity were analyzed using binary logistic regression. The area under the receiver operator characteristic curve (AUROCC) was used to assess diagnostic accuracy. RESULTS: A total of 106 HBeAg-negative treatment-naive CHB patients were enrolled. According to their METAVIR inflammatory scores, 30.2% of patients were in stage ≥A2. Total triiodothyronine (TT3) and hepatitis B virus (HBV) DNA levels were predictors of moderate inflammatory activity (A ≥ 2). The AUROCCs of TT3 and HBV DNA levels were 0.651 and 0.797, respectively. The optimal cut-off values for TT3 and HBV DNA were 1.755 nmol/L and 4.61 log10 IU/mL, respectively. CONCLUSIONS: A sizable proportion of treatment-naive HBeAg-negative CHB patients required antiviral treatment (30.2%) after undergoing liver biopsy. TT3 and HBV DNA helps identify patients with moderate inflammatory activity (A ≥ 2), potentially reducing the need for liver biopsies and helping guide treatment of CHB patients.
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spelling pubmed-76730542020-11-24 Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection Hu, Jianhua Wang, Yong Jiang, Gongying Zheng, Jie Chen, Tuxiang Chen, Zhiping Yang, Meifang Zhang, Xuan Zhao, Hong Li, Lanjuan J Int Med Res Retrospective Clinical Research Report OBJECTIVE: Liver inflammatory activity staging is critical to guide the treatment of chronic hepatitis B virus (CHB) infection. Here, we aimed to identify practical clinical biomarkers of moderate inflammatory activity in hepatitis B e-antigen (HBeAg)-negative CHB patients. METHODS: Treatment-naïve HBeAg-negative CHB patients who underwent liver biopsy at our hospital from 1 January 2013 to 31 December 2016 were enrolled. Markers of inflammatory activity were analyzed using binary logistic regression. The area under the receiver operator characteristic curve (AUROCC) was used to assess diagnostic accuracy. RESULTS: A total of 106 HBeAg-negative treatment-naive CHB patients were enrolled. According to their METAVIR inflammatory scores, 30.2% of patients were in stage ≥A2. Total triiodothyronine (TT3) and hepatitis B virus (HBV) DNA levels were predictors of moderate inflammatory activity (A ≥ 2). The AUROCCs of TT3 and HBV DNA levels were 0.651 and 0.797, respectively. The optimal cut-off values for TT3 and HBV DNA were 1.755 nmol/L and 4.61 log10 IU/mL, respectively. CONCLUSIONS: A sizable proportion of treatment-naive HBeAg-negative CHB patients required antiviral treatment (30.2%) after undergoing liver biopsy. TT3 and HBV DNA helps identify patients with moderate inflammatory activity (A ≥ 2), potentially reducing the need for liver biopsies and helping guide treatment of CHB patients. SAGE Publications 2020-11-12 /pmc/articles/PMC7673054/ /pubmed/33179557 http://dx.doi.org/10.1177/0300060520969582 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Hu, Jianhua
Wang, Yong
Jiang, Gongying
Zheng, Jie
Chen, Tuxiang
Chen, Zhiping
Yang, Meifang
Zhang, Xuan
Zhao, Hong
Li, Lanjuan
Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection
title Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection
title_full Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection
title_fullStr Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection
title_full_unstemmed Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection
title_short Predictors of inflammatory activity in treatment-naive hepatitis B e-antigen-negative patients with chronic hepatitis B infection
title_sort predictors of inflammatory activity in treatment-naive hepatitis b e-antigen-negative patients with chronic hepatitis b infection
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673054/
https://www.ncbi.nlm.nih.gov/pubmed/33179557
http://dx.doi.org/10.1177/0300060520969582
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