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HBV ‐Specific T Cell Responses for Short‐Term Hepatitis Progression Prediction: A Comparative, Interpretable Machine Learning Study

机器学习 医学 人工智能 队列 标杆管理 临床实习 预测建模 限制 接收机工作特性 丙型肝炎 病毒性肝炎 内科学 特征(语言学) 丙型肝炎病毒 疾病 肝炎 乙型肝炎 乙型肝炎病毒 病毒载量 队列研究 支持向量机 试验预测值 临床试验 肿瘤科 恩替卡韦 丙氨酸转氨酶 丙氨酸转氨酶 曲线下面积 免疫系统 朴素贝叶斯分类器 梅德林
作者
Sidu Feng,Y N Wu,Xueyin Mei,Ying Zhou,Tianzhang Zhai,Li J,Chuanlai Shen
出处
期刊:Liver International [Wiley]
卷期号:46 (8): e70758-e70758
标识
DOI:10.1111/liv.70758
摘要

BACKGROUND & AIMS: As central determinants of viral control and immunopathology, hepatitis B virus (HBV)-specific T-cell responses provide more clinically meaningful information than routine biochemical and virological markers. Nevertheless, most existing prediction models rely primarily on clinical parameters and rarely incorporate HBV-specific T-cell responses, potentially limiting their predictive performance and biological interpretability. To develop an accurate and interpretable model for predicting hepatitis progression, we evaluated diverse machine learning (ML) methods integrating multisource data. METHODS: We enrolled a cohort of 479 patients and divided them into training and testing cohorts based on admission time. Clinical data, treatment regimens, and HBV-specific T-cell immune responses were collected. A comprehensive benchmarking of 10 ML models was conducted through 5-fold cross-validation on the training cohort across varying feature combinations and algorithmic performances. The ML models were independently evaluated on the testing cohort, and significant predictive factors were identified. RESULTS: Based on alanine aminotransferase (ALT) levels at 6- and 12-month follow-ups, the patients were stratified into hepatitis (ALT > 40 U/L) and non-hepatitis (ALT ≤ 40 U/L) groups. The predictive performance was significantly improved after integrating clinical indicator features (CIF) and HBV-specific T-cell features (STCF). An XGBoost model based on six selected features (three CIF and three STCF) demonstrated especially robust performance, achieving AUCs of 0.874 (validation) and 0.880 (testing) at 6 months follow up and 0.851 (validation) and 0.845 (testing) at 12 months. To facilitate clinical application, a web-based tool was developed for personalized risk assessment. CONCLUSIONS: Incorporating HBV-specific T-cell responses into the predictive framework improves the prediction of disease progression among HBV-infected individuals. The developed interpretable model is a potentially valuable tool for early risk stratification, facilitating proactive monitoring.
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