用可解释神经网络分析脑龄差距,揭示多种神经退行性疾病独特脑区模式。
Explainable Brain Age Gap Prediction in Neurodegenerative Conditions using coVariance Neural Networks
- 基于协方差神经网络,通过解构脑结构协方差矩阵的特征谱进行建模。
- 在阿尔茨海默病等三类疾病中发现差异化的脑龄差距空间分布模式。
- 模型结果与特征谱利用方式直接关联,实现从机制到结果的可解释性。
脑龄是通过机器学习从神经影像数据中估算出的生物年龄。脑龄差距(即脑龄高于实际年龄)越大,表明神经退行性病变和认知衰退风险越高,因此是监测脑健康的重要生物标志物。然而,传统黑箱机器学习方法缺乏可解释性,限制了其实际应用。最近提出的协方差神经网络(VNN)提供了一种相对透明的深度学习流程,具备两个关键特性:(i) 推导出的生物标志物具有解剖学可解释性;(ii) 方法论上可通过与解剖协方差矩阵的特征向量关联实现可解释性。本文将VNN方法应用于多种常见神经退行性疾病,基于皮层厚度特征研究脑龄差距。结果揭示了阿尔茨海默病、额颞叶痴呆及非典型帕金森综合征中脑龄差距存在显著不同的解剖模式。进一步表明,这些差异模式与VNN对解剖协方差矩阵特征谱的利用方式相关,从而为结果提供了可解释性支持。
原文摘要 · Abstract (English)
Brain age is the estimate of biological age derived from neuroimaging datasets using machine learning algorithms. Increasing \textit{brain age gap} characterized by an elevated brain age relative to the chronological age can reflect increased vulnerability to neurodegeneration and cognitive decline. Hence, brain age gap is a promising biomarker for monitoring brain health. However, black-box machine learning approaches to brain age gap prediction have limited practical utility. Recent studies on coVariance neural networks (VNN) have proposed a relatively transparent deep learning pipeline for neuroimaging data analyses, which possesses two key features: (i) inherent \textit{anatomically interpretablity} of derived biomarkers; and (ii) a methodologically interpretable perspective based on \textit{linkage with eigenvectors of anatomic covariance matrix}. In this paper, we apply the VNN-based approach to study brain age gap using cortical thickness features for various prevalent neurodegenerative conditions. Our results reveal distinct anatomic patterns for brain age gap in Alzheimer's disease, frontotemporal dementia, and atypical Parkinsonian disorders. Furthermore, we demonstrate that the distinct anatomic patterns of brain age gap are linked with the differences in how VNN leverages the eigenspectrum of the anatomic covariance matrix, thus lending explainability to the reported results.
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