利用可解释图卷积网络对阿尔茨海默病进行多模式诊断

Houliang Zhou, Lifang He, Brian Y Chen, Li Shen, Yu Zhang
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引用次数: 0

摘要

神经系统疾病中大脑区域之间的相互联系为生物标记和诊断的发展提供了重要信息。虽然图卷积网络被广泛应用于发现指向疾病状况的大脑连接模式,但多种成像模式产生的连接模式的潜力尚未得到充分发挥。在本文中,我们提出了一种多模态稀疏可解释 GCN 框架(SGCN),用于检测阿尔茨海默病(AD)及其前驱阶段,即轻度认知障碍(MCI)。在我们的实验中,SGCN 学习了稀疏区域重要性概率以找到特征感兴趣区域(ROI),并学习了连接重要性概率以揭示特定疾病的大脑网络连接。我们在阿尔茨海默病神经影像倡议数据库的多模态脑图像上对 SGCN 进行了评估,结果表明,SGCN 学习到的 ROI 特征能有效增强对阿尔茨海默病状态的识别。识别出的异常与阿兹海默症相关临床症状明显相关。我们进一步从大尺度神经系统和与性别相关的连接异常层面解释了所发现的 AD/MCI 脑功能障碍。SGCN所解释的突出ROI和明显的大脑连接异常对于开发新型生物标记物相当重要。这些发现有助于通过多模态诊断更好地了解基于网络的疾病,并为精准诊断提供了潜力。源代码见 https://github.com/Houliang-Zhou/SGCN。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-Modal Diagnosis of Alzheimer's Disease using Interpretable Graph Convolutional Networks.

The interconnection between brain regions in neurological disease encodes vital information for the advancement of biomarkers and diagnostics. Although graph convolutional networks are widely applied for discovering brain connection patterns that point to disease conditions, the potential of connection patterns that arise from multiple imaging modalities has yet to be fully realized. In this paper, we propose a multi-modal sparse interpretable GCN framework (SGCN) for the detection of Alzheimer's disease (AD) and its prodromal stage, known as mild cognitive impairment (MCI). In our experimentation, SGCN learned the sparse regional importance probability to find signature regions of interest (ROIs), and the connective importance probability to reveal disease-specific brain network connections. We evaluated SGCN on the Alzheimer's Disease Neuroimaging Initiative database with multi-modal brain images and demonstrated that the ROI features learned by SGCN were effective for enhancing AD status identification. The identified abnormalities were significantly correlated with AD-related clinical symptoms. We further interpreted the identified brain dysfunctions at the level of large-scale neural systems and sex-related connectivity abnormalities in AD/MCI. The salient ROIs and the prominent brain connectivity abnormalities interpreted by SGCN are considerably important for developing novel biomarkers. These findings contribute to a better understanding of the network-based disorder via multi-modal diagnosis and offer the potential for precision diagnostics. The source code is available at https://github.com/Houliang-Zhou/SGCN.

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