Evidence map›Paper›PMID 40640910›Full record

ArticleVirology journal2025

Reevaluating antiviral thresholds in HBV DNA-negative inactive HBsAg carriers: a multicenter histopathological analysis.

Shan Ren, Sujun Zheng, Xinyang Zhang, Junliang Fu, Rongshan Fan, Qingfa Ruan, Wenqi Huang, Haibing Gao, Xiulan Xue, Fang Yang and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Shan RenFirst Department of Liver Disease Center, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, P. R. China.
Sujun ZhengFirst Department of Liver Disease Center, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, P. R. China.
Xinyang ZhangFirst Department of Liver Disease Center, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, P. R. China.
Junliang FuDepartment of Infectious Diseases, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, P. R. China.
Rongshan FanShenzhen Hospital of Integrated Traditional Chinese and Western Medicine, Shenzhen, 518101, Guangdong, P. R. China.
Qingfa RuanXiamen Hospital of T.C.M, Xiamen, 361000, Fujian, P. R. China.
Wenqi HuangXiamen Humanity Hospital, Xiamen, 361000, Fujian, P. R. China.
Haibing GaoMengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, 350007, Fujian, P. R. China.
Xiulan XueThe First Affiliated Hospital of Xiamen University, Xiamen, 361001, Fujian, P. R. China.
Fang YangShenyang Sixth People's Hospital, Shenyang, 110006, Liaoning, P. R. China.
Yao XieLiver Disease Center, Beijing Ditan Hospital, Capital Medical University, Beijing, 100069, P. R. China.
Minghui LiLiver Disease Center, Beijing Ditan Hospital, Capital Medical University, Beijing, 100069, P. R. China.
Xinyue ChenFirst Department of Liver Disease Center, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, P. R. China. chenxydoc@163.com.

Funding

Capital Clinical Diagnostic Techniques and Translational Application Projects Z211100002921059Capital's Funds for Health Improvement and Research 2024-2-2184High-level public health technical talents construction project of Beijing Municipal Health Commission Academic Leader -02-14National Key Research and Development Program of Ministry of Science and Technology 2023YFC2308100
6 · The paper itself

Abstract

backgroundThe definition of inactive HBsAg carriers (IHC) varies globally, particularly regarding HBV DNA thresholds. Whether HBV DNA negativity reliably predicts histological quiescence remains uncertain.

aimsThis study evaluated liver pathology in IHC patients to reassess antiviral therapy thresholds.

methodsThis multi-center, retrospective study included 231IHCs(2018-2023) stratified by HBV DNA negativity (< 20IU/mL). Liver biopsies assessed inflammation (G ≥ 2) and fibrosis (F ≥ 2); evident hepatic injury (EHI) was defined as G ≥ 2 and/or F ≥ 2. Multivariable models evaluated predictors.

resultsAmong 231 IHC patients(median age:43 years old; 95.2% ≥30 years old), 35.9%(83/231) were HBV DNA negative. The median HBsAg and HBV DNA level were 132 IU/ml and 94 IU/ml, respectively. Notably, EHI prevalence was significantly higher in HBV DNA negative patients than positive ones(44.9% vs. 31%, P = 0.04), driven by fibrosis (F ≥ 2: 42.2% vs. 21.6%, P < 0.001), challenging the assumption that HBV DNA negativity ensures low histological risk. Male sex, HBV DNA negativity, and elevated liver stiffness measurement(LSM) independently predicted EHI (OR = 3.37, AUC = 0.747).

conclusionHBV DNA negativity does not guarantee histological quiescence in inactive HBsAg carriers aged ≥ 30 years, with 44.9% exhibiting significant liver injury. In this population, LSM > 6.4 Kpa should prompt consideration of liver biopsy and/or initiation of antiviral therapy.

Indexed as

Antiviral AgentsCarrier StateDNA, ViralHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B virusAdultAgedBiopsyFemaleHumansLiverLiver CirrhosisMaleMiddle AgedRetrospective StudiesAntiviral AgentsDNA, ViralHepatitis B Surface AntigensAntiviral thresholdsChronic hepatitis BFibrosisInactive HBsAg carriersLiver histopathologyNon-invasive biomarkers

Identifiers

PMID40640910
PMCPMC12243403

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.