TY - JOUR
T1 - Transdiagnostic time-varying dysconnectivity across major psychiatric disorders
AU - Li, Chao
AU - Dong, Mengshi
AU - Womer, Fay Y.
AU - Han, Shaoqiang
AU - Yin, Yi
AU - Jiang, Xiaowei
AU - Wei, Yange
AU - Duan, Jia
AU - Feng, Ruiqi
AU - Zhang, Luheng
AU - Zhang, Xizhe
AU - Wang, Fei
AU - Tang, Yanqing
AU - Xu, Ke
N1 - Publisher Copyright:
© 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
PY - 2021/3
Y1 - 2021/3
N2 - 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.
AB - 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.
KW - bipolar disorder
KW - dynamic functional connectivity
KW - major depressive disorder
KW - schizophrenia
KW - transdiagnostic study
UR - http://www.scopus.com/inward/record.url?scp=85096807084&partnerID=8YFLogxK
U2 - 10.1002/hbm.25285
DO - 10.1002/hbm.25285
M3 - Article
C2 - 33210798
AN - SCOPUS:85096807084
SN - 1065-9471
VL - 42
SP - 1182
EP - 1196
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 4
ER -