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Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders
Dynamic functional connectivity (DFC) analysis can capture time‐varying properties of connectivity. However, studies on large samples using DFC to investigate transdiagnostic dysconnectivity across schizophrenia (SZ), bipolar disorder (BD), and major depressive disorder (MDD) are rare. In this study...
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/PMC7856647/ https://www.ncbi.nlm.nih.gov/pubmed/33210798 http://dx.doi.org/10.1002/hbm.25285 |
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author | Li, Chao Dong, Mengshi Womer, Fay Y. Han, Shaoqiang Yin, Yi Jiang, Xiaowei Wei, Yange Duan, Jia Feng, Ruiqi Zhang, Luheng Zhang, Xizhe Wang, Fei Tang, Yanqing Xu, Ke |
author_facet | Li, Chao Dong, Mengshi Womer, Fay Y. Han, Shaoqiang Yin, Yi Jiang, Xiaowei Wei, Yange Duan, Jia Feng, Ruiqi Zhang, Luheng Zhang, Xizhe Wang, Fei Tang, Yanqing Xu, Ke |
author_sort | Li, Chao |
collection | PubMed |
description | Dynamic functional connectivity (DFC) analysis can capture time‐varying properties of connectivity. However, studies on large samples using DFC to investigate transdiagnostic dysconnectivity across schizophrenia (SZ), bipolar disorder (BD), and major depressive disorder (MDD) are rare. In this study, we used resting‐state functional magnetic resonance imaging and a sliding‐window method to study DFC in a total of 610 individuals (150 with SZ, 100 with BD, 150 with MDD, and 210 healthy controls [HC]) at a single site. Using k‐means clustering, DFCs were clustered into three functional connectivity states: one was a more frequent state with moderate positive and negative connectivity (State 1), and the other two were less frequent states with stronger positive and negative connectivity (State 2 and State 3). Significant 4‐group differences (SZ, BD, MDD, and HC groups; q < .05, false‐discovery rate [FDR]‐corrected) in DFC were nearly only in State 1. Post hoc analyses (q < .05, FDR‐corrected) in State 1 showed that transdiagnostic dysconnectivity patterns among SZ, BD and MDD featured consistently decreased connectivity within most networks (the visual, somatomotor, salience and frontoparietal networks), which was most obvious in both range and extent for SZ. Our findings suggest that there is more common dysconnectivity across SZ, BD and MDD than we previously expected and that such dysconnectivity is state‐dependent, which provides new insights into the pathophysiological mechanism of major psychiatric disorders. |
format | Online Article Text |
id | pubmed-7856647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78566472021-02-05 Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders Li, Chao Dong, Mengshi Womer, Fay Y. Han, Shaoqiang Yin, Yi Jiang, Xiaowei Wei, Yange Duan, Jia Feng, Ruiqi Zhang, Luheng Zhang, Xizhe Wang, Fei Tang, Yanqing Xu, Ke Hum Brain Mapp Research Articles Dynamic functional connectivity (DFC) analysis can capture time‐varying properties of connectivity. However, studies on large samples using DFC to investigate transdiagnostic dysconnectivity across schizophrenia (SZ), bipolar disorder (BD), and major depressive disorder (MDD) are rare. In this study, we used resting‐state functional magnetic resonance imaging and a sliding‐window method to study DFC in a total of 610 individuals (150 with SZ, 100 with BD, 150 with MDD, and 210 healthy controls [HC]) at a single site. Using k‐means clustering, DFCs were clustered into three functional connectivity states: one was a more frequent state with moderate positive and negative connectivity (State 1), and the other two were less frequent states with stronger positive and negative connectivity (State 2 and State 3). Significant 4‐group differences (SZ, BD, MDD, and HC groups; q < .05, false‐discovery rate [FDR]‐corrected) in DFC were nearly only in State 1. Post hoc analyses (q < .05, FDR‐corrected) in State 1 showed that transdiagnostic dysconnectivity patterns among SZ, BD and MDD featured consistently decreased connectivity within most networks (the visual, somatomotor, salience and frontoparietal networks), which was most obvious in both range and extent for SZ. Our findings suggest that there is more common dysconnectivity across SZ, BD and MDD than we previously expected and that such dysconnectivity is state‐dependent, which provides new insights into the pathophysiological mechanism of major psychiatric disorders. John Wiley & Sons, Inc. 2020-11-19 /pmc/articles/PMC7856647/ /pubmed/33210798 http://dx.doi.org/10.1002/hbm.25285 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-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Li, Chao Dong, Mengshi Womer, Fay Y. Han, Shaoqiang Yin, Yi Jiang, Xiaowei Wei, Yange Duan, Jia Feng, Ruiqi Zhang, Luheng Zhang, Xizhe Wang, Fei Tang, Yanqing Xu, Ke Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
title | Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
title_full | Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
title_fullStr | Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
title_full_unstemmed | Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
title_short | Transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
title_sort | transdiagnostic time‐varying dysconnectivity across major psychiatric disorders |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856647/ https://www.ncbi.nlm.nih.gov/pubmed/33210798 http://dx.doi.org/10.1002/hbm.25285 |
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