Machine Learning-Driven Noninvasive Prediction of Liver Fibrosis in Unclassified Liver Disease.

IF 14.1 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2026-10-04 eCollection Date: 2026-10-01 DOI:10.1002/mco2.70990
Ye Yang, Yirui Hu, Ting Wei, Yue Chen, Wenkang Gao, Yupin Tan, Yuanqing Zhu, Yonggang Yuan, Zhuang Cao, Yunfei Zhao, Zexuan Li, Jiake Che, Yue Yang, Xinyang Wang, Shengqi Yan, Weiyan Huang, Shuyan Wang, Fuyu Yang, Lijia Yin, Xiaotong Du, Jiahao Liu, Rong Lin, Ling Yang, Huikuan Chu
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Abstract

Chronic liver diseases (CLDs) frequently progress silently to advanced fibrosis or cirrhosis, yet existing predictive models have largely been developed for patients with clearly defined etiologies. Here, we asked whether a noninvasive machine-learning model based on routine clinical variables and liver stiffness measurement (LSM) could accurately identify significant liver fibrosis in patients with CLD of uncertain etiology, and whether such a model would add value beyond conventional fibrosis scores for clinical decision-making. We retrospectively analyzed 503 patients who underwent liver biopsy at Union Hospital, Tongji Medical College, Huazhong University of Science and Technology. Twelve machine-learning algorithms were trained to predict significant hepatic fibrosis, and model interpretability was assessed using SHapley Additive exPlanations. The best-performing model was then compared with four established noninvasive tools: FIB-4, GPR, Forns Index, and LSM alone. Among all candidate models, Categorical Boosting delivered the most favorable overall diagnostic performance, achieving the highest discriminative accuracy (AUC, 0.827; 95% CI, 0.754-0.900) and outperforming all conventional comparators across key classification metrics. We therefore establish an interpretable and clinically applicable panel integrating serological markers, age, LSM for noninvasive fibrosis assessment in patients with undefined or clinically ambiguous liver disease, with potential to reduce unnecessary biopsy and enable earlier intervention.

机器学习驱动的无创预测未分类肝病肝纤维化。
慢性肝病(CLDs)通常会悄无声息地发展为晚期纤维化或肝硬化,然而现有的预测模型主要是针对病因明确的患者开发的。在这里,我们询问基于常规临床变量和肝硬度测量(LSM)的无创机器学习模型是否可以准确识别病因不确定的CLD患者的显著肝纤维化,以及这种模型是否可以在常规纤维化评分之外为临床决策增加价值。我们回顾性分析在华中科技大学同济医学院协和医院行肝活检的503例患者。训练了12种机器学习算法来预测显著的肝纤维化,并使用SHapley加法解释评估模型的可解释性。然后将表现最佳的模型与四种已建立的无创工具进行比较:FIB-4、GPR、Forns Index和单独LSM。在所有候选模型中,Categorical Boosting提供了最有利的整体诊断性能,实现了最高的判别准确率(AUC, 0.827; 95% CI, 0.754-0.900),并且在关键分类指标上优于所有传统比较器。因此,我们建立了一个可解释且临床适用的小组,整合血清学标志物、年龄、LSM,用于对未明确或临床不明确肝病患者进行无创纤维化评估,有可能减少不必要的活检并使早期干预成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.70
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0.00%
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10 weeks
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