Dynamic multi-site graph convolutional network for autism spectrum disorder identification

被引:4
|
作者
Cui, Weigang [1 ]
Du, Junling [2 ]
Sun, Mingyi [2 ]
Zhu, Shimao [4 ]
Zhao, Shijie [5 ]
Peng, Ziwen [6 ]
Tan, Li [7 ]
Li, Yang [2 ,3 ]
机构
[1] Beihang Univ, Sch Engn Med, Beijing 100191, Peoples R China
[2] Beihang Univ, Dept Automat Sci & Elect Engn, Beijing 100191, Peoples R China
[3] Beihang Univ, State Key Lab Virtual Real Technol & Syst, Beijing 100191, Peoples R China
[4] Shenzhen Univ, South China Hosp, Shenzhen 518111, Peoples R China
[5] Northwestern Polytech Univ, Sch Automation, Xian 710072, Shaanxi, Peoples R China
[6] Shenzhen Univ, Shenzhen Kangning Hosp, Dept Child Psychiat, Sch Med, Shenzhen 518020, Peoples R China
[7] Beijing Technol & Business Univ, Sch Comp Sci & Engn, Beijing 100048, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Austim spectrum disorder; Graph convolutional network; Functional magnetic resonance imaging; Sliding window; Multi-site learning; FUNCTIONAL CONNECTIVITY; TENSOR;
D O I
10.1016/j.compbiomed.2023.106749
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multi-site learning has attracted increasing interests in autism spectrum disorder (ASD) identification tasks by its efficacy on capturing data heterogeneity of neuroimaging taken from different medical sites. However, existing multi-site graph convolutional network (MSGCN) often ignores the correlations between different sites, and may obtain suboptimal identification results. Moreover, current feature extraction methods characterizing temporal variations of functional magnetic resonance imaging (fMRI) signals require the time series to be of the same length and cannot be directly applied to multi-site fMRI datasets. To address these problems, we propose a dual graph based dynamic multi-site graph convolutional network (DG-DMSGCN) for multi-site ASD identification. First, a sliding-window dual-graph convolutional network (SW-DGCN) is introduced for feature extraction, simultaneously capturing temporal and spatial features of fMRI data with different series lengths. Then we aggregate the features extracted from multiple medical sites through a novel dynamic multi-site graph con-volutional network (DMSGCN), which effectively considers the correlations between different sites and is beneficial to improve identification performance. We evaluate the proposed DG-DMSGCN on public ABIDE I dataset containing data from 17 medical sites. The promising results obtained by our framework outperforms the state-of-the-art methods with increase in identification accuracy, indicating that it has a potential clinical prospect for practical ASD diagnosis. Our codes are available on https://github.com/Junling-Du/DG-DMSGCN.
引用
收藏
页数:10
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