An exploratory machine learning model for predicting advanced liver fibrosis in autoimmune hepatitis patients: A preliminary study.

IF 3.7 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Annals of hepatology Pub Date : 2024-12-12 DOI:10.1016/j.aohep.2024.101754
Qinglin Wei, Wen Li, Shubei He, Hongbo Wu, Qiaoling Xie, Ying Peng, Xingyue Zhang
{"title":"An exploratory machine learning model for predicting advanced liver fibrosis in autoimmune hepatitis patients: A preliminary study.","authors":"Qinglin Wei, Wen Li, Shubei He, Hongbo Wu, Qiaoling Xie, Ying Peng, Xingyue Zhang","doi":"10.1016/j.aohep.2024.101754","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction and objectives: </strong>Advanced fibrosis is a crucial stage in the progression of autoimmune hepatitis (AIH), where fibrosis can either regress or advance. This study aims to leverage machine learning (ML) models for the assessment of advanced liver fibrosis in AIH patients using routine clinical features.</p><p><strong>Patients and methods: </strong>A total of 233 patients diagnosed with AIH and underwent liver biopsy were included in the discovery cohort. The dataset was randomly split into training and testing sets. Patients were categorized into groups with no/minimal/moderate fibrosis and advanced fibrosis. Six ML models were employed to identify the optimal model. Subsequently, the predictive capability of the best ML model was validated in an additional cohort (n = 33) and compared with conventional noninvasive fibrosis scores.</p><p><strong>Results: </strong>Three key clinical features, including prothrombin time (PT), albumin (ALB), and ultrasound spleen thickness (UTST), were analyzed by least absolute shrinkage and selection operator (LASSO) regression. In the training set, the random forest (RF) model showed the highest diagnostic performance in predicting advanced fibrosis stage (AUC=0.951). In the testing cohort and validation cohort, the RF model maintained high accuracy (AUC = 0.863 and AUC = 0.843). Additionally, the random forest model outperformed the conventional noninvasive fibrosis scores.</p><p><strong>Conclusions: </strong>ML models, particularly the RF model, can help improve the discrimination of advanced liver fibrosis in patients with AIH.</p>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":" ","pages":"101754"},"PeriodicalIF":3.7000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of hepatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.aohep.2024.101754","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction and objectives: Advanced fibrosis is a crucial stage in the progression of autoimmune hepatitis (AIH), where fibrosis can either regress or advance. This study aims to leverage machine learning (ML) models for the assessment of advanced liver fibrosis in AIH patients using routine clinical features.

Patients and methods: A total of 233 patients diagnosed with AIH and underwent liver biopsy were included in the discovery cohort. The dataset was randomly split into training and testing sets. Patients were categorized into groups with no/minimal/moderate fibrosis and advanced fibrosis. Six ML models were employed to identify the optimal model. Subsequently, the predictive capability of the best ML model was validated in an additional cohort (n = 33) and compared with conventional noninvasive fibrosis scores.

Results: Three key clinical features, including prothrombin time (PT), albumin (ALB), and ultrasound spleen thickness (UTST), were analyzed by least absolute shrinkage and selection operator (LASSO) regression. In the training set, the random forest (RF) model showed the highest diagnostic performance in predicting advanced fibrosis stage (AUC=0.951). In the testing cohort and validation cohort, the RF model maintained high accuracy (AUC = 0.863 and AUC = 0.843). Additionally, the random forest model outperformed the conventional noninvasive fibrosis scores.

Conclusions: ML models, particularly the RF model, can help improve the discrimination of advanced liver fibrosis in patients with AIH.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
预测自身免疫性肝炎患者晚期肝纤维化的探索性机器学习模型:初步研究
简介和目的:晚期纤维化是自身免疫性肝炎(AIH)进展的关键阶段,在此阶段纤维化可退可进。本研究旨在利用机器学习(ML)模型,利用常规临床特征评估AIH患者的晚期肝纤维化。患者和方法:共有233名确诊为AIH并接受肝活检的患者被纳入发现队列。数据集随机分为训练集和测试集。患者分为无/轻度/中度纤维化组和晚期纤维化组。采用6个ML模型来确定最优模型。随后,在另一个队列中验证了最佳ML模型的预测能力(n = 33),并与传统的非侵入性纤维化评分进行了比较。结果:采用最小绝对收缩和选择算子(LASSO)回归分析凝血酶原时间(PT)、白蛋白(ALB)和超声脾厚度(UTST) 3个关键临床特征。在训练集中,随机森林(RF)模型预测纤维化晚期的诊断性能最高(AUC=0.951)。在检验队列和验证队列中,RF模型保持较高的准确性(AUC = 0.863,AUC = 0.843)。此外,随机森林模型优于传统的非侵入性纤维化评分。结论:ML模型,尤其是RF模型有助于提高AIH患者晚期肝纤维化的鉴别能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Annals of hepatology
Annals of hepatology 医学-胃肠肝病学
CiteScore
7.90
自引率
2.60%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.
期刊最新文献
From gut to liver: Exploring the crosstalk between gut-liver axis and oxidative stress in metabolic dysfunction-associated steatotic liver disease. The rationale for the aggressive progression of MASLD in patients with type 2 diabetes. The promoting effect of the POU3F2/METTL16/PFKM cascade on glycolysis and tumorigenesis of hepatocellular carcinoma. Mechanisms and therapeutic targets of mitochondria in the progression of metabolic dysfunction-associated steatotic liver disease. The role of inflammasomes in hepatocellular carcinoma: Mechanisms and therapeutic insights.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1