从轻度认知障碍到阿尔茨海默病转换的多模态预测的可解释的分层机器学习方法。

IF 2 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Soheil Zarei, Mohsen Saffar, Reza Shalbaf, Peyman Hassani Abharian, Ahmad Shalbaf
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,对早期诊断和干预具有挑战性,但许多预测模型的黑箱性质限制了临床应用。在这项研究中,我们开发了一个先进的机器学习(ML)框架,该框架将分层特征选择与多个分类器集成在一起,以预测从轻度认知障碍(MCI)到AD的进展。使用来自580名阿尔茨海默病神经影像学倡议(ADNI)参与者的基线数据,将其分为稳定型MCI (sMCI)和进行性MCI (pMCI)亚组,我们分析了个体和七个关键组的特征。神经心理测试组表现出最高的预测能力,有几个最重要的个体预测来自这个领域。分层特征选择结合初始统计过滤和基于机器学习的细化,将特征集缩小到8个信息量最大的变量。为了揭开模型决策的神秘面纱,我们应用了基于shap (SHapley可加解释)的可解释性分析,量化每个特征对转换风险的贡献。基于这些特征进行优化的可解释随机森林分类器准确率达到83.79%(灵敏度84.93%,特异性83.32%),优于其他方法,并显示海马体积、延迟记忆回忆(LDELTOTAL)和功能活动问卷(FAQ)得分是转换的主要驱动因素。这些结果强调了将不同数据源与先进的ML模型相结合的有效性,并证明了透明的、shap驱动的见解与已知的AD生物标志物相一致,将我们的模型从预测黑箱转变为临床可操作的工具,用于早期诊断和患者分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Explainable hierarchical machine-learning approaches for multimodal prediction of conversion from mild cognitive impairment to Alzheimer's disease.

Alzheimer's disease (AD) is a neurodegenerative disorder that challenges early diagnosis and intervention, yet the black-box nature of many predictive models limits clinical adoption. In this study, we developed an advanced machine learning (ML) framework that integrates hierarchical feature selection with multiple classifiers to predict progression from mild cognitive impairment (MCI) to AD. Using baseline data from 580 participants in the Alzheimer's Disease Neuroimaging Initiative (ADNI), categorized into stable MCI (sMCI) and progressive MCI (pMCI) subgroups, we analyzed features both individually and across seven key groups. The neuropsychological test group exhibited the highest predictive power, with several of the top individual predictors drawn from this domain. Hierarchical feature selection combining initial statistical filtering and machine learning based refinement, narrowed the feature set to the eight most informative variables. To demystify model decisions, we applied SHAP-based (SHapley Additive exPlanations) explainability analysis, quantifying each feature's contribution to conversion risk. The explainable random forest classifier, optimized on these selected features, achieved 83.79% accuracy (84.93% sensitivity, 83.32% specificity), outperforming other methods and revealing hippocampal volume, delayed memory recall (LDELTOTAL), and Functional Activities Questionnaire (FAQ) scores as the top drivers of conversion. These results underscore the effectiveness of combining diverse data sources with advanced ML models, and demonstrate that transparent, SHAP-driven insights align with known AD biomarkers, transforming our model from a predictive black box into a clinically actionable tool for early diagnosis and patient stratification.

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来源期刊
CiteScore
8.40
自引率
4.50%
发文量
110
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