Evidence map›Paper›PMID 41276798›Full record

ArticleVirology journal2025

Machine learning model for HBsAg seroclearance after 48-week pegylated interferon therapy in inactive HBsAg carriers: a retrospective study.

Jianxia Dong, Shan Ren, Jing Zhao, Pengxuan Wu, Haitian Yu, Yao Xie, Junliang Fu, Xiaorong Mao, Zhiliang Gao, Bingliang Lin and 8 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

18 authors.

Jianxia Dong *The First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China.
Shan Ren *The First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China.
Jing ZhaoThe First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China.
Pengxuan WuThe First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China.
Haitian YuThe First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China.
Yao XieBeijing Ditan Hospital, Capital Medical University, Beijing, China.
Junliang FuSenior Department of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Xiaorong MaoThe First Hospital of Lanzhou University, Lanzhou, China.
Zhiliang GaoThe Third Affiliated Hospital of Sun Yat-sen university, Guangzhou, China.
Bingliang LinThe Third Affiliated Hospital of Sun Yat-sen university, Guangzhou, China.
Qingfa RuanXiamen Hospital of Traditional Chinese Medicine, Xiamen, China.
Yongfang JiangThe Second Xiangya Hospital of Central South University, Changsha, China.
Xiulan XueThe First Affiliated Hospital of Xiamen University, Xiamen, China.
Yueyong ZhuThe First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Haidong ZhaoXiamen Chang Gung Hospital, Xiamen, China.
Haifang CaoQinghai Provincial Fourth People's Hospital, Xining, China.
Xinyue ChenThe First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China. chenxydoc@ccmu.edu.cn.
Sujun ZhengThe First Unit, Department of Hepatology, Beijing Youan Hospital, Capital Medical University, 8 Xitoutiao, Youan men wai, Fengtai District, Beijing, 100069, China. zhengsujun@ccmu.edu.cn.

Funding

Capital Clinical Diagnostic Techniques and Translational Application Projects Z211100002921059High-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 2023YFC2308100Natural Science Foundation of Beijing Municipality 7222093
6 · The paper itself

Abstract

purposeTo identify early predictive factors for hepatitis B surface antigen (HBsAg) clearance at week 48 following pegylated interferon (Peg-IFN) therapy in inactive HBsAg carriers (IHC), and to develop an early machine learning-based model to assist clinical decision-making.

methodsThis retrospective analysis was based on a multicenter, prospective cohort and included 777 IHC patients who received at least 48 weeks of Peg-IFN therapy. Least Absolute Shrinkage and Selection Operator (LASSO) regression and the Boruta algorithm were applied to select predictive variables. Nine machine learning models-including logistic regression (LR), decision tree (DT), and random forest (RF)-were constructed and evaluated using 10-fold cross-validation. An external validation cohort (n = 167) from three medical centers in Beijing was used for model validation. SHapley Additive exPlanations (SHAP) values were used to interpret variable contributions.

resultsThe overall HBsAg clearance rate at week 48 was 29.9% (232/777). Key predictors included baseline HBsAg level, HBsAg decline > 1 log IU/mL at week 12, and the ratio of alanine aminotransferase (ALT) to HBsAg at week 12. The RF model demonstrated the best performance with an area under the curve (AUC) of 0.829 (95% CI: 0.784-0.874) and specificity of 0.774 in the training set, and an AUC of 0.838 (95% CI: 0.759-0.917) with specificity of 0.968 in the external validation set. SHAP analysis showed that baseline HBsAg had the highest predictive importance.

conclusionsThe RF-based model accurately predicts HBsAg clearance in IHC patients undergoing Peg-IFN therapy and offers a promising tool for early identification of candidates for individualized treatment strategies.

Indexed as

Antiviral AgentsCarrier StateHepatitis B, ChronicHepatitis B Surface AntigensInterferon-alphaMachine LearningPolyethylene GlycolsAdultAgedFemaleHepatitis B virusHumansMaleMiddle AgedRecombinant ProteinsRetrospective StudiesAntiviral AgentsHepatitis B Surface AntigensInterferon-alphaPolyethylene GlycolsRecombinant ProteinsHBsAg clearanceInactive HBsAg carrierMachine learningPredictive modelRandom forest

Identifiers

PMID41276798
PMCPMC12781715

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.