Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss

Abstract Background/Aims It is unclear whether nucleos(t)ide analogs (NUCs) continuation provides clinical benefits following HBsAg seroclearance with pegylated interferon (PEG-IFN)-based therapy. This study aims to investigate the role of NUCs continuation in HBsAg seroreversion. Methods Patients w...

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Main Authors: Na Gao, Haishi Wu, Bin Li, Huiying Yu, Lili Wu, Jing Zhang, Nan Zhang, Bingliang Lin, Qiyi Zhao, Zhiliang Gao
Format: Article
Language:English
Published: BMC 2025-03-01
Series:Virology Journal
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Online Access:https://doi.org/10.1186/s12985-025-02700-2
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author Na Gao
Haishi Wu
Bin Li
Huiying Yu
Lili Wu
Jing Zhang
Nan Zhang
Bingliang Lin
Qiyi Zhao
Zhiliang Gao
author_facet Na Gao
Haishi Wu
Bin Li
Huiying Yu
Lili Wu
Jing Zhang
Nan Zhang
Bingliang Lin
Qiyi Zhao
Zhiliang Gao
author_sort Na Gao
collection DOAJ
description Abstract Background/Aims It is unclear whether nucleos(t)ide analogs (NUCs) continuation provides clinical benefits following HBsAg seroclearance with pegylated interferon (PEG-IFN)-based therapy. This study aims to investigate the role of NUCs continuation in HBsAg seroreversion. Methods Patients who experienced serum HBsAg loss after PEG-IFN-based therapy were enrolled and followed up for 96 weeks. Propensity score matching (PSM) was performed using a 1:1 ratio to adjust for the associated factors. A multivariate logistic regression analysis was used to determine the factors associated with HBsAg seroreversion. Results In total, 220 patients with HBsAg seroclearance were divided into NUCs (n = 54) and non-NUCs (n = 166) consolidation therapy groups. At week 96, the HBsAg seroreversion (12/54 vs. 31/166, P = 0.709) and virological relapse (2/54 vs. 10/166, P = 0.759) rates were similar in the NUCs and non-NUCs groups. After PSM, HBsAg seroreversion (12/53 vs. 13/53; P = 1.000) and virological relapse (2/53 vs. 4/53; P = 0.674) rates were not significantly different between the two groups. Serum hepatitis B surface antibody titer (odds ratio, 0.388; 95% confidence interval, 0.245–0.616; P < 0.001) was found to be associated with HBsAg seroreversion, while NUCs continuation was not related to HBsAg seroreversion. Conclusions NUCs continuation is not associated with a lower risk of HBsAg seroreversion in patients with serum HBsAg loss following PEG-IFN-based therapy.
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spelling doaj-art-8f667c495ae84e56a0e1b8edbe5d3a0a2025-08-20T03:22:08ZengBMCVirology Journal1743-422X2025-03-012211910.1186/s12985-025-02700-2Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg lossNa Gao0Haishi Wu1Bin Li2Huiying Yu3Lili Wu4Jing Zhang5Nan Zhang6Bingliang Lin7Qiyi Zhao8Zhiliang Gao9Department of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen UniversityAbstract Background/Aims It is unclear whether nucleos(t)ide analogs (NUCs) continuation provides clinical benefits following HBsAg seroclearance with pegylated interferon (PEG-IFN)-based therapy. This study aims to investigate the role of NUCs continuation in HBsAg seroreversion. Methods Patients who experienced serum HBsAg loss after PEG-IFN-based therapy were enrolled and followed up for 96 weeks. Propensity score matching (PSM) was performed using a 1:1 ratio to adjust for the associated factors. A multivariate logistic regression analysis was used to determine the factors associated with HBsAg seroreversion. Results In total, 220 patients with HBsAg seroclearance were divided into NUCs (n = 54) and non-NUCs (n = 166) consolidation therapy groups. At week 96, the HBsAg seroreversion (12/54 vs. 31/166, P = 0.709) and virological relapse (2/54 vs. 10/166, P = 0.759) rates were similar in the NUCs and non-NUCs groups. After PSM, HBsAg seroreversion (12/53 vs. 13/53; P = 1.000) and virological relapse (2/53 vs. 4/53; P = 0.674) rates were not significantly different between the two groups. Serum hepatitis B surface antibody titer (odds ratio, 0.388; 95% confidence interval, 0.245–0.616; P < 0.001) was found to be associated with HBsAg seroreversion, while NUCs continuation was not related to HBsAg seroreversion. Conclusions NUCs continuation is not associated with a lower risk of HBsAg seroreversion in patients with serum HBsAg loss following PEG-IFN-based therapy.https://doi.org/10.1186/s12985-025-02700-2Chronic hepatitis BNucleos(t)ide analogsSeroreversionFunctional cure
spellingShingle Na Gao
Haishi Wu
Bin Li
Huiying Yu
Lili Wu
Jing Zhang
Nan Zhang
Bingliang Lin
Qiyi Zhao
Zhiliang Gao
Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss
Virology Journal
Chronic hepatitis B
Nucleos(t)ide analogs
Seroreversion
Functional cure
title Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss
title_full Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss
title_fullStr Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss
title_full_unstemmed Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss
title_short Nucleos(t)ide analogs continuation is not associated with a lower risk of HBsAg seroreversion following PEG-IFN-induced HBsAg loss
title_sort nucleos t ide analogs continuation is not associated with a lower risk of hbsag seroreversion following peg ifn induced hbsag loss
topic Chronic hepatitis B
Nucleos(t)ide analogs
Seroreversion
Functional cure
url https://doi.org/10.1186/s12985-025-02700-2
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