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High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder
Brain functional network (BFN) based on electroencephalography (EEG) has been widely used to diagnose brain diseases, such as major depressive disorder (MDD). However, most existing BFNs only consider the correlation between two channels, ignoring the high-level interaction among multiple channels t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396245/ https://www.ncbi.nlm.nih.gov/pubmed/36017184 http://dx.doi.org/10.3389/fnins.2022.976229 |
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author | Zhao, Feng Pan, Hongxin Li, Na Chen, Xiaobo Zhang, Haicheng Mao, Ning Ren, Yande |
author_facet | Zhao, Feng Pan, Hongxin Li, Na Chen, Xiaobo Zhang, Haicheng Mao, Ning Ren, Yande |
author_sort | Zhao, Feng |
collection | PubMed |
description | Brain functional network (BFN) based on electroencephalography (EEG) has been widely used to diagnose brain diseases, such as major depressive disorder (MDD). However, most existing BFNs only consider the correlation between two channels, ignoring the high-level interaction among multiple channels that contain more rich information for diagnosing brain diseases. In such a sense, the BFN is called low-order BFN (LO-BFN). In order to fully explore the high-level interactive information among multiple channels of the EEG signals, a scheme for constructing a high-order BFN (HO-BFN) based on the “correlation’s correlation” strategy is proposed in this paper. Specifically, the entire EEG time series is firstly divided into multiple epochs by sliding window. For each epoch, the short-term correlation between channels is calculated to construct a LO-BFN. The correlation time series of all channel pairs are formulated by these LO-BFNs obtained from all epochs to describe the dynamic change of short-term correlation along the time. To construct HO-BFN, we cluster all correlation time series to avoid the problems caused by high dimensionality, and the correlation of the average correlation time series from different clusters is calculated to reflect the high-order correlation among multiple channels. Experimental results demonstrate the efficiency of the proposed HO-BFN in MDD identification, and its integration with the LO-BFN can further improve the recognition rate. |
format | Online Article Text |
id | pubmed-9396245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93962452022-08-24 High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder Zhao, Feng Pan, Hongxin Li, Na Chen, Xiaobo Zhang, Haicheng Mao, Ning Ren, Yande Front Neurosci Neuroscience Brain functional network (BFN) based on electroencephalography (EEG) has been widely used to diagnose brain diseases, such as major depressive disorder (MDD). However, most existing BFNs only consider the correlation between two channels, ignoring the high-level interaction among multiple channels that contain more rich information for diagnosing brain diseases. In such a sense, the BFN is called low-order BFN (LO-BFN). In order to fully explore the high-level interactive information among multiple channels of the EEG signals, a scheme for constructing a high-order BFN (HO-BFN) based on the “correlation’s correlation” strategy is proposed in this paper. Specifically, the entire EEG time series is firstly divided into multiple epochs by sliding window. For each epoch, the short-term correlation between channels is calculated to construct a LO-BFN. The correlation time series of all channel pairs are formulated by these LO-BFNs obtained from all epochs to describe the dynamic change of short-term correlation along the time. To construct HO-BFN, we cluster all correlation time series to avoid the problems caused by high dimensionality, and the correlation of the average correlation time series from different clusters is calculated to reflect the high-order correlation among multiple channels. Experimental results demonstrate the efficiency of the proposed HO-BFN in MDD identification, and its integration with the LO-BFN can further improve the recognition rate. Frontiers Media S.A. 2022-08-09 /pmc/articles/PMC9396245/ /pubmed/36017184 http://dx.doi.org/10.3389/fnins.2022.976229 Text en Copyright © 2022 Zhao, Pan, Li, Chen, Zhang, Mao and Ren. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Zhao, Feng Pan, Hongxin Li, Na Chen, Xiaobo Zhang, Haicheng Mao, Ning Ren, Yande High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
title | High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
title_full | High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
title_fullStr | High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
title_full_unstemmed | High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
title_short | High-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
title_sort | high-order brain functional network for electroencephalography-based diagnosis of major depressive disorder |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396245/ https://www.ncbi.nlm.nih.gov/pubmed/36017184 http://dx.doi.org/10.3389/fnins.2022.976229 |
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