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Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder
The clinical misdiagnosis ratio of bipolar disorder (BD) patients to major depressive disorder (MDD) patients is high. Recent findings hypothesize that the ability to flexibly recruit functional neural networks is differently altered in BD and MDD patients. This study aimed to explore distinct aberr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375077/ https://www.ncbi.nlm.nih.gov/pubmed/32400932 http://dx.doi.org/10.1002/hbm.25017 |
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author | Han, Shaoqiang Cui, Qian Wang, Xiao Li, Liang Li, Di He, Zongling Guo, Xiaonan Fan, Yun‐Shuang Guo, Jing Sheng, Wei Lu, Fengmei Chen, Huafu |
author_facet | Han, Shaoqiang Cui, Qian Wang, Xiao Li, Liang Li, Di He, Zongling Guo, Xiaonan Fan, Yun‐Shuang Guo, Jing Sheng, Wei Lu, Fengmei Chen, Huafu |
author_sort | Han, Shaoqiang |
collection | PubMed |
description | The clinical misdiagnosis ratio of bipolar disorder (BD) patients to major depressive disorder (MDD) patients is high. Recent findings hypothesize that the ability to flexibly recruit functional neural networks is differently altered in BD and MDD patients. This study aimed to explore distinct aberrance of network flexibility during dynamic networks configuration in BD and MDD patients. Resting state functional magnetic resonance imaging of 40 BD patients, 61 MDD patients, and 61 matched healthy controls were recruited. Dynamic functional connectivity matrices for each subject were constructed with a sliding window method. Then, network switching rate of each node was calculated and compared among the three groups. BD and MDD patients shared decreased network switching rate of regions including left precuneus, bilateral parahippocampal gyrus, and bilateral dorsal medial prefrontal cortex. Apart from these regions, MDD patients presented specially decreased network switching rate in the bilateral anterior insula, left amygdala, and left striatum. Taken together, BD and MDD patients shared decreased network switching rate of key hubs in default mode network and MDD patients presented specially decreased switching rate in salience network and striatum. We found shared and distinct aberrance of network flexibility which revealed altered adaptive functions during dynamic networks configuration of BD and MDD. |
format | Online Article Text |
id | pubmed-7375077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73750772020-07-22 Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder Han, Shaoqiang Cui, Qian Wang, Xiao Li, Liang Li, Di He, Zongling Guo, Xiaonan Fan, Yun‐Shuang Guo, Jing Sheng, Wei Lu, Fengmei Chen, Huafu Hum Brain Mapp Research Articles The clinical misdiagnosis ratio of bipolar disorder (BD) patients to major depressive disorder (MDD) patients is high. Recent findings hypothesize that the ability to flexibly recruit functional neural networks is differently altered in BD and MDD patients. This study aimed to explore distinct aberrance of network flexibility during dynamic networks configuration in BD and MDD patients. Resting state functional magnetic resonance imaging of 40 BD patients, 61 MDD patients, and 61 matched healthy controls were recruited. Dynamic functional connectivity matrices for each subject were constructed with a sliding window method. Then, network switching rate of each node was calculated and compared among the three groups. BD and MDD patients shared decreased network switching rate of regions including left precuneus, bilateral parahippocampal gyrus, and bilateral dorsal medial prefrontal cortex. Apart from these regions, MDD patients presented specially decreased network switching rate in the bilateral anterior insula, left amygdala, and left striatum. Taken together, BD and MDD patients shared decreased network switching rate of key hubs in default mode network and MDD patients presented specially decreased switching rate in salience network and striatum. We found shared and distinct aberrance of network flexibility which revealed altered adaptive functions during dynamic networks configuration of BD and MDD. John Wiley & Sons, Inc. 2020-05-13 /pmc/articles/PMC7375077/ /pubmed/32400932 http://dx.doi.org/10.1002/hbm.25017 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. 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 Han, Shaoqiang Cui, Qian Wang, Xiao Li, Liang Li, Di He, Zongling Guo, Xiaonan Fan, Yun‐Shuang Guo, Jing Sheng, Wei Lu, Fengmei Chen, Huafu Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
title | Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
title_full | Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
title_fullStr | Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
title_full_unstemmed | Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
title_short | Resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
title_sort | resting state functional network switching rate is differently altered in bipolar disorder and major depressive disorder |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375077/ https://www.ncbi.nlm.nih.gov/pubmed/32400932 http://dx.doi.org/10.1002/hbm.25017 |
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