Evidence map›Paper›PMID 41249755›Full record

ArticleHepatology international2025

Machine learning prediction of rapid HBsAg seroclearance at week 24 in inactive carriers treated with pegylated interferon.

Jianxia Dong, Shan Ren, Pengxuan Wu, Haitian Yu, Xinyue Meng, Jing Zhao, Xiangyang Ye, Yan Huang, Zujiang Yu, Wenhua Zhang and 7 more

Abstract readMulticenter Study
In one paragraph

Article in Hepatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 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.
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.
Xinyue MengThe 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.
Xiangyang YeThe Affiliated Hospital of Putian University, Putian, China.
Yan HuangXiangya Hospital of Central South University, Changsha, China.
Zujiang YuThe First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Wenhua ZhangGansu Wuwei Tumor Hospital, Wuwei, China.
Yilan ZengPublic Health Clinical Center of Chengdu, Chengdu, China.
Xiaozhong WangXinjiang Uygur Autonomous Region Hospital of Traditional Chinese Medicine, Urumqi, China.
Haibing GaoMengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, China.
Shuangsuo DangThe Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital), Xi'an, China.
Jiabin LiThe First Affiliated Hospital of Anhui Medical University, Hefei, China.
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.
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.

Funding

Capital Clinical Diagnostic Techniques and Translational Application Projects Z211100002921059National Key Research and Development Program of Ministry of Science and Technology 2023YFC2308100Natural Science Foundation of Beijing Municipality 7222093Project of High-level Teachers in Beijing Municipal Universities in the Period of 13th Five-year Plan Academic Leader-02-14
6 · The paper itself

Abstract

BACKGROUND AND

aimTo identify predictive factors for rapid hepatitis B surface antigen (HBsAg) seroclearance at week 24 in inactive HBsAg carriers (IHC) receiving pegylated interferon alpha-2b (Peg-IFN) therapy, and to develop a machine learning-based model to optimize individualized treatment strategies.

methodsThis retrospective analysis was based on a multicenter, prospective cohort study involving 2882 IHC patients treated with Peg-IFN and followed for at least 24 weeks. Predictive variables for week 24 HBsAg seroclearance were selected using both LASSO regression and the Boruta algorithm. Nine machine learning models were developed, including logistic regression (LR), decision tree (DT), and random forest (RF), with performance assessed via tenfold cross-validation. External validation was conducted in an independent cohort (n = 167) from three medical centers in Beijing. SHapley Additive Explanations (SHAP) were used to interpret model predictions and feature importance.

resultsThe overall HBsAg seroclearance rate at week 24 was 18.7% (541/2,882). Key predictive factors included baseline HBsAg level, ≥ 1 log IU/mL decline in HBsAg at week 12, the ratio of alanine aminotransferase (ALT) to HBsAg at week 12, the ratio of week 12 ALT to baseline HBsAg, week 12 hepatitis B virus (HBV) DNA level, and week 12 hepatitis B surface antibody (HBsAb) level. The Light Gradient Boosting Machine (Light GBM) model demonstrated the best performance, achieving an area under the receiver operating characteristic curve (AUC) of 0.902 (95% CI 0.881-0.923) and a sensitivity of 0.889 in the training cohort, and an AUC of 0.917 (95% CI 0.850-0.983) with a sensitivity of 0.879 in the external validation cohort. SHAP analysis revealed that the week 12 ALT/ HBsAg ratio was the most impactful feature.

conclusionsWe developed a LightGBM-based machine learning model that accurately predicts rapid HBsAg seroclearance at week 24 among IHC patients receiving Peg-IFN therapy. This model offers a valuable tool for early identification of rapid responders, personalized treatment planning, and potential discontinuation strategies. The individualized stopping rules derived from model-predicted probabilities provide an evidence-based approach to precision therapy in IHC patients.

Indexed as

Antiviral AgentsCarrier StateHepatitis B, ChronicHepatitis B Surface AntigensInterferon-alphaMachine LearningPolyethylene GlycolsAdultAlanine TransaminaseFemaleHepatitis B virusHumansInterferon alpha-2MaleMiddle AgedProspective StudiesAlanine TransaminaseAntiviral AgentsHepatitis B Surface AntigensInterferon-alphaInterferon alpha-2peginterferon alfa-2bPolyethylene GlycolsRecombinant ProteinsInactive HBsAg carrierLight gradient boosting machineMachine learningPrediction modelRapid HBsAg seroclearance

Identifiers

PMID41249755
PMCPMC12715036

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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.