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Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks

Major depressive disorder (MDD) is a leading cause of disability; its symptoms interfere with social, occupational, interpersonal, and academic functioning. However, the diagnosis of MDD is still made by phenomenological approach. The advent of neuroimaging techniques allowed numerous studies to use...

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Autores principales: Jun, Eunji, Na, Kyoung‐Sae, Kang, Wooyoung, Lee, Jiyeon, Suk, Heung‐Il, Ham, Byung‐Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643383/
https://www.ncbi.nlm.nih.gov/pubmed/32813309
http://dx.doi.org/10.1002/hbm.25175
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author Jun, Eunji
Na, Kyoung‐Sae
Kang, Wooyoung
Lee, Jiyeon
Suk, Heung‐Il
Ham, Byung‐Joo
author_facet Jun, Eunji
Na, Kyoung‐Sae
Kang, Wooyoung
Lee, Jiyeon
Suk, Heung‐Il
Ham, Byung‐Joo
author_sort Jun, Eunji
collection PubMed
description Major depressive disorder (MDD) is a leading cause of disability; its symptoms interfere with social, occupational, interpersonal, and academic functioning. However, the diagnosis of MDD is still made by phenomenological approach. The advent of neuroimaging techniques allowed numerous studies to use resting‐state functional magnetic resonance imaging (rs‐fMRI) and estimate functional connectivity for brain‐disease identification. Recently, attempts have been made to investigate effective connectivity (EC) that represents causal relations among regions of interest. In the meantime, to identify meaningful phenotypes for clinical diagnosis, graph‐based approaches such as graph convolutional networks (GCNs) have been leveraged recently to explore complex pairwise similarities in imaging/nonimaging features among subjects. In this study, we validate the use of EC for MDD identification by estimating its measures via a group sparse representation along with a structured equation modeling approach in a whole‐brain data‐driven manner from rs‐fMRI. To distinguish drug‐naïve MDD patients from healthy controls, we utilize spectral GCNs based on a population graph to successfully integrate EC and nonimaging phenotypic information. Furthermore, we devise a novel sensitivity analysis method to investigate the discriminant connections for MDD identification in our trained GCNs. Our experimental results validated the effectiveness of our method in various scenarios, and we identified altered connectivities associated with the diagnosis of MDD.
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spelling pubmed-76433832020-11-13 Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks Jun, Eunji Na, Kyoung‐Sae Kang, Wooyoung Lee, Jiyeon Suk, Heung‐Il Ham, Byung‐Joo Hum Brain Mapp Research Articles Major depressive disorder (MDD) is a leading cause of disability; its symptoms interfere with social, occupational, interpersonal, and academic functioning. However, the diagnosis of MDD is still made by phenomenological approach. The advent of neuroimaging techniques allowed numerous studies to use resting‐state functional magnetic resonance imaging (rs‐fMRI) and estimate functional connectivity for brain‐disease identification. Recently, attempts have been made to investigate effective connectivity (EC) that represents causal relations among regions of interest. In the meantime, to identify meaningful phenotypes for clinical diagnosis, graph‐based approaches such as graph convolutional networks (GCNs) have been leveraged recently to explore complex pairwise similarities in imaging/nonimaging features among subjects. In this study, we validate the use of EC for MDD identification by estimating its measures via a group sparse representation along with a structured equation modeling approach in a whole‐brain data‐driven manner from rs‐fMRI. To distinguish drug‐naïve MDD patients from healthy controls, we utilize spectral GCNs based on a population graph to successfully integrate EC and nonimaging phenotypic information. Furthermore, we devise a novel sensitivity analysis method to investigate the discriminant connections for MDD identification in our trained GCNs. Our experimental results validated the effectiveness of our method in various scenarios, and we identified altered connectivities associated with the diagnosis of MDD. John Wiley & Sons, Inc. 2020-08-19 /pmc/articles/PMC7643383/ /pubmed/32813309 http://dx.doi.org/10.1002/hbm.25175 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Jun, Eunji
Na, Kyoung‐Sae
Kang, Wooyoung
Lee, Jiyeon
Suk, Heung‐Il
Ham, Byung‐Joo
Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
title Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
title_full Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
title_fullStr Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
title_full_unstemmed Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
title_short Identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
title_sort identifying resting‐state effective connectivity abnormalities in drug‐naïve major depressive disorder diagnosis via graph convolutional networks
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643383/
https://www.ncbi.nlm.nih.gov/pubmed/32813309
http://dx.doi.org/10.1002/hbm.25175
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