Seroreversion of hepatitis B surface antigen among subjects with resolved hepatitis B virus infection: A community‐based cohort study
Background and Aim Hepatitis B virus (HBV) surface antigen (HBsAg) seroreversion usually occurs during immunosuppressive therapy. The risk and factors of HBsAg seroreversion from resolved HBV infection in the general population remained unclear. Methods This retrospective study enrolled subjects wit...
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Published in | Journal of gastroenterology and hepatology Vol. 36; no. 11; pp. 3239 - 3246 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Australia
Wiley Subscription Services, Inc
01.11.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Background and Aim
Hepatitis B virus (HBV) surface antigen (HBsAg) seroreversion usually occurs during immunosuppressive therapy. The risk and factors of HBsAg seroreversion from resolved HBV infection in the general population remained unclear.
Methods
This retrospective study enrolled subjects with resolved HBV infection and who had received at least two times of screening in a longitudinal community screening program. HBsAg, hepatitis B surface antibody (anti‐HBs), and hepatitis C virus antibody (anti‐HCV) were tested every time in all subjects. The primary endpoint was HBsAg seroreversion.
Results
Of the 7630 subjects enrolled, 5158 (67.6%) subjects had positive anti‐HBs at baseline. HBsAg seroreversion occurred in 84 subjects during 42 815‐person‐year follow‐up with an annual incidence of 0.2% and a 10‐year cumulative risk of 1.9%. Anti‐HBV treatment‐experienced subjects had a significantly higher risk of HBsAg seroreversion than anti‐HBV treatment‐naive subjects (83/310 [26.8%] vs 1/7320 [0.01%], P < 0.001). Lower rates of positive anti‐HBs and anti‐HCV were observed in anti‐HBV treatment‐experienced subjects who developed HBsAg seroreversion. Both positive anti‐HBs (hazard ratio/95% confidence interval: 0.56/0.348–0.903, P = 0.017) and positive anti‐HCV (hazard ratio/95% confidence interval: 0.08/0.030–0.234, P < 0.001) were independent factors of HBsAg seroreversion in anti‐HBV treatment‐experienced subjects. Less than 5% of the HBsAg seroreverters had clinical hepatitis flare at HBsAg seroreversion. The HBsAg titer was low, and only transient reappeared in most of the HBsAg seroreverters.
Conclusions
Subjects with resolved HBV infection were at a minimal risk of HBsAg seroreversion, unless with prior anti‐HBV treatment experience. Fortunately, even with a reappearance of HBsAg, it was transient and clinically non‐relevant. |
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Bibliography: | Author contribution Guarantor of the article Declaration of conflict of interest This study was funded in part by grants from Kaohsiung Medical University (grant numbers MOST 108‐2314‐B‐037‐101, KMU‐K1110002, MOST 108‐2314‐B‐037‐066‐MY3, KMU‐TC108B06, KMU‐TC108B07, KMU‐DK109002, KMU‐TC109B05, and 105KMUOR08) and Kaohsiung Medical University Chung‐Ho Memorial Hospital (grant numbers KMUH109‐9R06 and KMUH109‐9M05). Financial support Ming‐Lun Yeh and Ming‐Lung Yu contributed in the conception and design of the study; Ming‐Lun Yeh, Po‐Cheng Liang, Ching‐I Huang, Meng‐Hsuan Hsieh, Yi‐Hung Lin, Tyng‐Yuan Jang, Yu‐Ju Wei, Po‐Yao Hsu, Cheng‐Ting Hsu, Chih‐Wen Wang, Ming‐Yen Hsieh, Zu‐Yau Lin, Shinn‐Cherng Chen, Chung‐Feng Huang, Jee‐Fu Huang, Chia‐Yen Dai, Wan‐Long Chuang, and Ming‐Lung Yu in the acquisition of data; Ming‐Lun Yeh and Ming‐Lung Yu in the data analysis and interpretation and in drafting and critically revising the manuscript; and all authors in the critical review and approval of the manuscript. Ming‐Lung Yu has received research support from Abbott, BMS, Gilead, and Merck; served as a consultant of Abbvie, Abbott, Ascletis, BMS, Gilead, Merck, and Roche; and served as a speaker of Abbvie, Abbott, BMS, Gilead, Merck, and Ipsen. Chia‐Yen Dai has served as a consultant of Abbvie, BMS, Gilead, Merck, and Pharmaessential and served as a speaker of Abbvie, BMS, Gilead, Merck, and Pharmaessential. Wan‐Long Chuang served as a consultant of Gilead, AbbVie, BMS, and PharmaEssentia and served as a speaker of Gilead, AbbVie, BMS, and PharmaEssentia. The other authors have nothing to disclose. Ming‐Lung Yu. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0815-9319 1440-1746 1440-1746 |
DOI: | 10.1111/jgh.15640 |