基于机器学习的肝移植术后不同时期胆道并发症预测模型的开发和验证:一项多中心研究。

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Clinical and Translational Gastroenterology Pub Date : 2025-04-18 eCollection Date: 2025-06-01 DOI:10.14309/ctg.0000000000000843
Feng Hu, Yuancheng Li, Hongfei Zeng, Renhua Ju, Di Jiang, Leida Zhang, Jun Li, Xingchao Liu, Guangyi Liu, Chengcheng Zhang
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引用次数: 0

摘要

背景:肝移植术后胆道并发症(BCs)的危险因素尚未全面确定。bc在发病时间上也各不相同。机器学习(Machine learning, ML)可以基于大规模数据揭示规律进行预测,并在lt中表现良好。但ML能否成为BC预测的有效工具还未确定。方法:来自两个中心的517例患者入组。患者按3:1的比例随机分为训练组和验证组。采用K-fold交叉验证和合成少数过采样技术(SMOTE)对模型进行调试,并通过受试者工作特征(ROC)曲线对模型进行评价。应用Shapley加性解释(SHAP)值和Sankey图将结果可视化。采用7种ML算法建立3、6和12个月时的bc预测模型。结果:在所有模型中,支持向量机(SVM)预测bc的曲线下面积最高(3个月= 0.916;6个月= 0.892;12个月= 0.885)。根据SVM分析,BCs的3个月危险因素及相应的SHAP值范围为供体年龄(-0.13,0.21)、终末期肝病模型(MELD)评分(-0.15,0.18)、肿瘤(-0.14,0.28)、糖尿病(-0.12,0.27)、高血压(-0.13,0.21)、术中输血(-0.09,0.25),6个月危险因素为供体年龄(-0.14,0.16)、供体体重指数(BMI)(-0.10, 0.13)、供体BMI(-0.13, 0.23)、糖尿病(-0.12,0.43)。12个月的危险因素为受体年龄(-0.14,0.19)、糖尿病(-0.13,0.25)和basiliximab(-0.16, 0.24)。Sankey图能够清晰地显示个体风险因素在不同bc发病时间对模型的贡献。结论:ML算法能够在术后所有时期识别bc的危险因素,这为患者管理提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Machine Learning Model for Predicting Biliary Complications After Liver Transplantation.

Machine Learning Model for Predicting Biliary Complications After Liver Transplantation.

Machine Learning Model for Predicting Biliary Complications After Liver Transplantation.

Machine Learning Model for Predicting Biliary Complications After Liver Transplantation.

Introduction: The risk factors of biliary complications (BCs) after liver transplantation are not comprehensively determined. BCs also vary in times of onset. Machine learning (ML) can reveal regularities based on large-scale data to make predictions and have demonstrated good performance in liver transplantation. However, whether ML can be an efficient tool for BC prediction was not determined.

Methods: Five hundred seventeen patients from 2 centers were enrolled. Patients were randomly divided into training and validation sets at 3:1 ratio. K-fold cross-validation and the synthetic minority oversampling technique were used to debug the models, which were evaluated by receiver operating characteristic curves. SHapley Additive exPlanation values and Sankey diagrams were applied to visualize the results. Seven ML algorithms were administrated to build models for BCs prediction at 3, 6, and 12 months.

Results: Among all the models, support vector machine produced the highest area under curve values in predicting BCs (3-month = 0.916; 6-month = 0.892; 12-month = 0.885). According to the analysis of support vector machine, the 3-month risk factors of BCs and corresponding SHapley Additive exPlanation value ranges were donor age (-0.13, 0.21), Model for End-Stage Liver Disease score (-0.15, 0.18), neoplastic disease (-0.14, 0.28), diabetes (-0.12, 0.27), hypertension (-0.13, 0.21), and intraoperative blood transfusion (-0.09, 0.25), whereas 6-month factors were recipient age (-0.14, 0.16), donor body mass index (-0.10, 0.13), recipient body mass index (-0.13, 0.23), and diabetes (-0.12, 0.43). The 12-month risk factors were recipient age (-0.14, 0.19), diabetes (-0.13, 0.25), and basiliximab (-0.16, 0.24). The Sankey diagram enabled clear visualization of the contribution of individual risk factors to the model in different times of BCs onset.

Discussion: The ML algorithm was able to identify risk factors of BCs in all postoperative periods and this supplied insights in patient management.

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来源期刊
Clinical and Translational Gastroenterology
Clinical and Translational Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.00
自引率
0.00%
发文量
114
审稿时长
16 weeks
期刊介绍: Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease. Colon and small bowel Endoscopy and novel diagnostics Esophagus Functional GI disorders Immunology of the GI tract Microbiology of the GI tract Inflammatory bowel disease Pancreas and biliary tract Liver Pathology Pediatrics Preventative medicine Nutrition/obesity Stomach.
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