Large‐scale dynamic causal modeling of major depressive disorder based on resting‐state functional magnetic resonance imaging
Major depressive disorder (MDD) is a serious mental illness characterized by dysfunctional connectivity among distributed brain regions. Previous connectome studies based on functional magnetic resonance imaging (fMRI) have focused primarily on undirected functional connectivity and existing directe...
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Published in | Human brain mapping Vol. 41; no. 4; pp. 865 - 881 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.03.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Major depressive disorder (MDD) is a serious mental illness characterized by dysfunctional connectivity among distributed brain regions. Previous connectome studies based on functional magnetic resonance imaging (fMRI) have focused primarily on undirected functional connectivity and existing directed effective connectivity (EC) studies concerned mostly task‐based fMRI and incorporated only a few brain regions. To overcome these limitations and understand whether MDD is mediated by within‐network or between‐network connectivities, we applied spectral dynamic causal modeling to estimate EC of a large‐scale network with 27 regions of interests from four distributed functional brain networks (default mode, executive control, salience, and limbic networks), based on large sample‐size resting‐state fMRI consisting of 100 healthy subjects and 100 individuals with first‐episode drug‐naive MDD. We applied a newly developed parametric empirical Bayes (PEB) framework to test specific hypotheses. We showed that MDD altered EC both within and between high‐order functional networks. Specifically, MDD is associated with reduced excitatory connectivity mainly within the default mode network (DMN), and between the default mode and salience networks. In addition, the network‐averaged inhibitory EC within the DMN was found to be significantly elevated in the MDD. The coexistence of the reduced excitatory but increased inhibitory causal connections within the DMNs may underlie disrupted self‐recognition and emotional control in MDD. Overall, this study emphasizes that MDD could be associated with altered causal interactions among high‐order brain functional networks. |
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Bibliography: | Funding information China Scholarship Council; Innovation and Strong School Project of Guangdong Provincial Education Department, Grant/Award Number: 2014GKXM034; National Institute of Biomedical Imaging and Bioengineering, Grant/Award Number: EB022880; National Institute of Mental Health, Grant/Award Number: MH108560; National Institute on Aging, Grant/Award Numbers: AG041721, AG042599, AG049371; National Institute on Deafness and Other Communication Disorders, Grant/Award Number: DC013872; National Natural Science Foundation of China, Grant/Award Numbers: 81920108019, 81471251, 81771344, 91649117; Science and Technology Plan Project of Guangzhou, Grant/Award Number: 2018‐1002‐SF‐0442; Excellent Doctoral and PhD Thesis Research Papers Project of Guangzhou University of Chinese Medicine, Grant/Award Number: A1‐AFD018181A55 Guoshi Li and Yujie Liu contributed equally to this study. Funding information China Scholarship Council; Innovation and Strong School Project of Guangdong Provincial Education Department, Grant/Award Number: 2014GKXM034; National Institute of Biomedical Imaging and Bioengineering, Grant/Award Number: EB022880; National Institute of Mental Health, Grant/Award Number: MH108560; National Institute on Aging, Grant/Award Numbers: AG041721, AG042599, AG049371; National Institute on Deafness and Other Communication Disorders, Grant/Award Number: DC013872; National Natural Science Foundation of China, Grant/Award Numbers: 81920108019, 81471251, 81771344, 91649117; Science and Technology Plan Project of Guangzhou, Grant/Award Number: 2018‐1002‐SF‐0442; Excellent Doctoral and PhD Thesis Research Papers Project of Guangzhou University of Chinese Medicine, Grant/Award Number: A1‐AFD018181A55 |
ISSN: | 1065-9471 1097-0193 |
DOI: | 10.1002/hbm.24845 |