Diagnosis of Autism Spectrum Disorder Using Central-Moment Features From Low- and High-Order Dynamic Resting-State Functional Connectivity Networks
- Authors
- Zhao, Feng; Chen, Zhiyuan; Rekik, Islem; Lee, Seong-Whan; Shen, Dinggang
- Issue Date
- 28-4월-2020
- Publisher
- FRONTIERS MEDIA SA
- Keywords
- autism spectrum disorder; dynamic functional connectivity networks; resting-state functional MRI; central-moment features; conventional FC network
- Citation
- FRONTIERS IN NEUROSCIENCE, v.14
- Indexed
- SCIE
SCOPUS
- Journal Title
- FRONTIERS IN NEUROSCIENCE
- Volume
- 14
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/56269
- DOI
- 10.3389/fnins.2020.00258
- ISSN
- 1662-4548
- Abstract
- The sliding-window-based dynamic functional connectivity networks (D-FCNs) derived from resting-state functional magnetic resonance imaging (rs-fMRI) are effective methods for diagnosing various neurological diseases, including autism spectrum disorder (ASD). However, traditional D-FCNs are low-order networks based on pairwise correlation between brain regions, thus overlooking high-level interactions across multiple regions of interest (ROIs). Moreover, D-FCNs suffer from the temporal mismatching issue, i.e., subnetworks in the same temporal window do not have temporal correspondence across different subjects. To address the above problems, we first construct a novel high-order D-FCNs based on the principle of "correlation's correlation" to further explore the higher level and more complex interaction relationships among multiple ROIs. Furthermore, we propose to use a central-moment method to extract temporal-invariance properties contained in either low- or high-order D-FCNs. Finally, we design and train an ensemble classifier by fusing the features extracted from conventional FCN, low-order D-FCNs, and high-order D-FCNs for the diagnosis of ASD and normal control subjects. Our method achieved the best ASD classification accuracy (83%), and our results revealed the features extracted from different networks fingerprinting the autistic brain at different connectional levels.
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Collections - Graduate School > Department of Artificial Intelligence > 1. Journal Articles
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