Feature aggregation graph convolutional network based on imaging genetic data for diagnosis and pathogeny identification of Alzheimer's disease

被引:11
|
作者
Bi, Xia-an [3 ,4 ]
Zhou, Wenyan [4 ]
Luo, Sheng [4 ]
Mao, Yuhua [4 ]
Hu, Xi [4 ]
Zeng, Bin [1 ]
Xu, Luyun [2 ]
机构
[1] Hunan YouDao Informat Technol Co Ltd, Changsha 410000, Peoples R China
[2] Hunan Normal Univ, Coll Business, Changsha 410081, Peoples R China
[3] Hunan Normal Univ, Hunan Prov Key Lab Intelligent Comp & Language In, Changsha, Peoples R China
[4] Hunan Normal Univ, Coll Informat Sci & Engn, Changsha, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
imaging genetics; Alzheimer's disease; deep learning; feature aggregation graph convolutional network; CANONICAL CORRELATION-ANALYSIS; FUNCTIONAL CONNECTIVITY; BRAIN;
D O I
10.1093/bib/bbac137
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The roles of brain regions activities and gene expressions in the development of Alzheimer's disease (AD) remain unclear. Existing imaging genetic studies usually has the problem of inefficiency and inadequate fusion of data. This study proposes a novel deep learning method to efficiently capture the development pattern of AD. First, we model the interaction between brain regions and genes as node-to-node feature aggregation in a brain region-gene network. Second, we propose a feature aggregation graph convolutional network (FAGCN) to transmit and update the node feature. Compared with the trivial graph convolutional procedure, we replace the input from the adjacency matrix with a weight matrix based on correlation analysis and consider common neighbor similarity to discover broader associations of nodes. Finally, we use a full-gradient saliency graph mechanism to score and extract the pathogenetic brain regions and risk genes. According to the results, FAGCN achieved the best performance among both traditional and cutting-edge methods and extracted AD-related brain regions and genes, providing theoretical and methodological support for the research of related diseases.
引用
收藏
页数:15
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