Evidence map›Paper›PMID 42577490›Full record

ArticleFrontiers in cellular and infection microbiology2026

Development and validation of a machine learning-derived dual-indicator tool for identification of hepatitis B virus-related pre-acute-on-chronic liver failure.

Tianyi Zhang, Shaoli You, Jinjin Luo, Jun Ling, Sa Lv, Yiwen Xu, Shaojie Xin, Xiaohe Xiao, Jun Li, Bing Zhu

Abstract readValidation Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Tianyi Zhang *Chinese PLA General Hospital, Beijing, China.
Shaoli You *Senior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Jinjin LuoState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jun LingSenior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Sa LvSenior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Yiwen XuSenior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Shaojie XinSenior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiaohe XiaoChinese PLA General Hospital, Beijing, China.
Jun LiState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Bing ZhuSenior Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & aims: Patients who do not meet the criteria for Acute-on-Chronic Liver Failure (ACLF) at admission still face a high risk of disease progression and mortality. This study aimed to develop and validate a machine learning-derived clinical tool for the early identification of HBV-pre-ACLF. Methods: We analyzed 1,682 patients experiencing acute deterioration of HBV-related chronic liver disease but without ACLF. By random forest and SHAP analysis, we identified key predictors of ACLF onset within a 7-day window. We then validated the diagnostic thresholds in a test cohort of 260 patients. Results: Total bilirubin (TBIL) and INR were identified as the most critical predictors of ACLF progression. We established optimal diagnostic thresholds at TBIL ≥131.5 μmol/L and INR ≥1.35. Two sequential criteria were developed: pre-ACLF-O (meeting either threshold) for highly sensitive screening, and pre-ACLF-A (meeting both thresholds) for risk confirmation. In the derivation cohort, pre-ACLF-O achieved 98.3% sensitivity, while pre-ACLF-A predicted a 33.09% positive predictive value. These results were successfully validated in the test cohort, where pre-ACLF-O maintained 100% sensitivity and pre-ACLF-A demonstrated a 37.04% positive predictive value. Conclusions: This dual-indicator tool easily and effectively identifies HBV-pre-ACLF. Using these criteria sequentially provides a practical strategy for early risk stratification, allowing clinicians to initiate timely interventions for high-risk patients.

Indexed as

Acute-On-Chronic Liver FailureHepatitis B, ChronicMachine LearningAdultBilirubinBiomarkersDisease ProgressionFemaleHepatitis B virusHumansMaleMiddle AgedRandom ForestSensitivity and SpecificityBilirubinBiomarkersACLF (acute-on-chronic liver failure)early prognosisHBV related pre-acute on chronic liver failuremachine learninguser-friendly tool

Identifiers

PMID42577490
PMCPMC13454397

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