Effective Connectivity in Depression
Resting-state functional connectivity reflects correlations in the activity between brain areas, whereas effective connectivity between different brain areas measures directed influences of brain regions on each other. Using the latter approach, we compare effective connectivity results in patients...
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Published in | Biological psychiatry : cognitive neuroscience and neuroimaging Vol. 3; no. 2; pp. 187 - 197 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.02.2018
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Abstract | Resting-state functional connectivity reflects correlations in the activity between brain areas, whereas effective connectivity between different brain areas measures directed influences of brain regions on each other. Using the latter approach, we compare effective connectivity results in patients with major depressive disorder (MDD) and control subjects.
We used a new approach to the measurement of effective connectivity, in which each brain area has a simple dynamical model, and known anatomical connectivity is used to provide constraints. This helps the approach to measure the effective connectivity between the 94 brain areas parceled in the automated anatomical labeling (AAL2) atlas, using resting-state functional magnetic resonance imaging. Moreover, we show how the approach can be used to measure the differences in effective connectivity between different groups of individuals, using as an example effective connectivity in the healthy brain and in individuals with depression. The first brainwide resting-state effective-connectivity neuroimaging analysis of depression, with 350 healthy individuals and 336 patients with major depressive disorder, is described.
Key findings are that the medial orbitofrontal cortex, implicated in reward and subjective pleasure, has reduced effective connectivity from temporal lobe input areas in depression; that the lateral orbitofrontal cortex, implicated in nonreward, has increased activity (variance) in depression, with decreased effective connectivity to and from cortical areas contralateral to language-related areas; and that the hippocampus, implicated in memory, has increased activity (variance) in depression and increased effective connectivity from the temporal pole.
Measurements of effective connectivity made using the new method provide a new approach to causal mechanisms in the brain in depression. |
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AbstractList | Resting-state functional connectivity reflects correlations in the activity between brain areas, whereas effective connectivity between different brain areas measures directed influences of brain regions on each other. Using the latter approach, we compare effective connectivity results in patients with major depressive disorder (MDD) and control subjects.BACKGROUNDResting-state functional connectivity reflects correlations in the activity between brain areas, whereas effective connectivity between different brain areas measures directed influences of brain regions on each other. Using the latter approach, we compare effective connectivity results in patients with major depressive disorder (MDD) and control subjects.We used a new approach to the measurement of effective connectivity, in which each brain area has a simple dynamical model, and known anatomical connectivity is used to provide constraints. This helps the approach to measure the effective connectivity between the 94 brain areas parceled in the automated anatomical labeling (AAL2) atlas, using resting-state functional magnetic resonance imaging. Moreover, we show how the approach can be used to measure the differences in effective connectivity between different groups of individuals, using as an example effective connectivity in the healthy brain and in individuals with depression. The first brainwide resting-state effective-connectivity neuroimaging analysis of depression, with 350 healthy individuals and 336 patients with major depressive disorder, is described.METHODSWe used a new approach to the measurement of effective connectivity, in which each brain area has a simple dynamical model, and known anatomical connectivity is used to provide constraints. This helps the approach to measure the effective connectivity between the 94 brain areas parceled in the automated anatomical labeling (AAL2) atlas, using resting-state functional magnetic resonance imaging. Moreover, we show how the approach can be used to measure the differences in effective connectivity between different groups of individuals, using as an example effective connectivity in the healthy brain and in individuals with depression. The first brainwide resting-state effective-connectivity neuroimaging analysis of depression, with 350 healthy individuals and 336 patients with major depressive disorder, is described.Key findings are that the medial orbitofrontal cortex, implicated in reward and subjective pleasure, has reduced effective connectivity from temporal lobe input areas in depression; that the lateral orbitofrontal cortex, implicated in nonreward, has increased activity (variance) in depression, with decreased effective connectivity to and from cortical areas contralateral to language-related areas; and that the hippocampus, implicated in memory, has increased activity (variance) in depression and increased effective connectivity from the temporal pole.RESULTSKey findings are that the medial orbitofrontal cortex, implicated in reward and subjective pleasure, has reduced effective connectivity from temporal lobe input areas in depression; that the lateral orbitofrontal cortex, implicated in nonreward, has increased activity (variance) in depression, with decreased effective connectivity to and from cortical areas contralateral to language-related areas; and that the hippocampus, implicated in memory, has increased activity (variance) in depression and increased effective connectivity from the temporal pole.Measurements of effective connectivity made using the new method provide a new approach to causal mechanisms in the brain in depression.CONCLUSIONSMeasurements of effective connectivity made using the new method provide a new approach to causal mechanisms in the brain in depression. Resting-state functional connectivity reflects correlations in the activity between brain areas, whereas effective connectivity between different brain areas measures directed influences of brain regions on each other. Using the latter approach, we compare effective connectivity results in patients with major depressive disorder (MDD) and control subjects. We used a new approach to the measurement of effective connectivity, in which each brain area has a simple dynamical model, and known anatomical connectivity is used to provide constraints. This helps the approach to measure the effective connectivity between the 94 brain areas parceled in the automated anatomical labeling (AAL2) atlas, using resting-state functional magnetic resonance imaging. Moreover, we show how the approach can be used to measure the differences in effective connectivity between different groups of individuals, using as an example effective connectivity in the healthy brain and in individuals with depression. The first brainwide resting-state effective-connectivity neuroimaging analysis of depression, with 350 healthy individuals and 336 patients with major depressive disorder, is described. Key findings are that the medial orbitofrontal cortex, implicated in reward and subjective pleasure, has reduced effective connectivity from temporal lobe input areas in depression; that the lateral orbitofrontal cortex, implicated in nonreward, has increased activity (variance) in depression, with decreased effective connectivity to and from cortical areas contralateral to language-related areas; and that the hippocampus, implicated in memory, has increased activity (variance) in depression and increased effective connectivity from the temporal pole. Measurements of effective connectivity made using the new method provide a new approach to causal mechanisms in the brain in depression. |
Author | Li, Yu Lin, Ching-Po Qiu, Jiang Xie, Peng Hu, Zicheng Tsai, Shih-Jen Cheng, Wei Deco, Gustavo Huang, Chu-Chung Yang, Albert C. Ruan, Hongtao Zhang, Xiaodong Gilson, Matthieu Feng, Jianfeng Rolls, Edmund T. Zhuang, Kaixiang |
Author_xml | – sequence: 1 givenname: Edmund T. surname: Rolls fullname: Rolls, Edmund T. email: Edmund.Rolls@oxcns.org organization: Department of Computer Science, University of Warwick, Coventry, United Kingdom – sequence: 2 givenname: Wei orcidid: 0000-0001-8276-0692 surname: Cheng fullname: Cheng, Wei organization: Department of Computer Science, University of Warwick, Coventry, United Kingdom – sequence: 3 givenname: Matthieu surname: Gilson fullname: Gilson, Matthieu organization: Center for Brain and Cognition, Computational Neuroscience Group, Department of Information and Communication Technologies, Universitat Pompeu Fabra, Barcelona, Spain – sequence: 4 givenname: Jiang surname: Qiu fullname: Qiu, Jiang organization: Key Laboratory of Cognition and Personality, Southwest University, Ministry of Education, Chongqing, China – sequence: 5 givenname: Zicheng orcidid: 0000-0003-3747-232X surname: Hu fullname: Hu, Zicheng organization: Institute of Neuroscience, Chongqing Medical University, Chongqing, China – sequence: 6 givenname: Hongtao surname: Ruan fullname: Ruan, Hongtao organization: Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, PR China – sequence: 7 givenname: Yu surname: Li fullname: Li, Yu organization: Department of Psychology, Southwest University, Chongqing, China – sequence: 8 givenname: Chu-Chung surname: Huang fullname: Huang, Chu-Chung organization: Institute of Neuroscience, National Yang-Ming University, Taipei, Taiwan – sequence: 9 givenname: Albert C. surname: Yang fullname: Yang, Albert C. organization: Department of Psychiatry, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 10 givenname: Shih-Jen surname: Tsai fullname: Tsai, Shih-Jen organization: Department of Psychiatry, Taipei Veterans General Hospital, Taipei, Taiwan – sequence: 11 givenname: Xiaodong surname: Zhang fullname: Zhang, Xiaodong organization: Institute of Neuroscience, Chongqing Medical University, Chongqing, China – sequence: 12 givenname: Kaixiang surname: Zhuang fullname: Zhuang, Kaixiang organization: Department of Psychology, Southwest University, Chongqing, China – sequence: 13 givenname: Ching-Po surname: Lin fullname: Lin, Ching-Po email: cplin@ym.edu.tw organization: Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, PR China – sequence: 14 givenname: Gustavo surname: Deco fullname: Deco, Gustavo organization: Center for Brain and Cognition, Computational Neuroscience Group, Department of Information and Communication Technologies, Universitat Pompeu Fabra, Barcelona, Spain – sequence: 15 givenname: Peng surname: Xie fullname: Xie, Peng email: xiepeng@cqmu.edu.cn organization: Institute of Neuroscience, Chongqing Medical University, Chongqing, China – sequence: 16 givenname: Jianfeng surname: Feng fullname: Feng, Jianfeng email: jianfeng64@gmail.com organization: Department of Computer Science, University of Warwick, Coventry, United Kingdom |
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Keywords | Functional connectivity Orbitofrontal cortex Precuneus Depression Effective connectivity Medial temporal lobe Resting-state functional neuroimaging |
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SubjectTerms | Cerebral Cortex - physiopathology Depression Depressive Disorder, Major - physiopathology Effective connectivity Female Functional connectivity Hippocampus - physiopathology Humans Magnetic Resonance Imaging - methods Male Medial temporal lobe Nerve Net - physiopathology Neural Pathways - physiopathology Orbitofrontal cortex Precuneus Prefrontal Cortex - physiopathology Resting-state functional neuroimaging Reward Temporal Lobe - physiopathology |
Title | Effective Connectivity in Depression |
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