Abnormalities in electroencephalographic microstates are state and trait markers of major depressive disorder

地方政府 重性抑郁障碍 静息状态功能磁共振成像 心理学 神经影像学 特质 脑电图 神经科学 精神科 内科学 医学 认知 计算机科学 程序设计语言
作者
Michael Murphy,Alexis E. Whitton,Stephanie Deccy,Manon L. Ironside,Ashleigh Rutherford,Miranda Beltzer,Matthew D. Sacchet,Diego A. Pizzagalli
出处
期刊:Neuropsychopharmacology [Springer Nature]
卷期号:45 (12): 2030-2037 被引量:77
标识
DOI:10.1038/s41386-020-0749-1
摘要

Neuroimaging studies have shown that major depressive disorder (MDD) is characterized by abnormal neural activity and connectivity. However, hemodynamic imaging techniques lack the temporal resolution needed to resolve the dynamics of brain mechanisms underlying MDD. Moreover, it is unclear whether putative abnormalities persist after remission. To address these gaps, we used microstate analysis to study resting-state brain activity in major depressive disorder (MDD). Electroencephalographic (EEG) "microstates" are canonical voltage topographies that reflect brief activations of components of resting-state brain networks. We used polarity-insensitive k-means clustering to segment resting-state high-density (128-channel) EEG data into microstates. Data from 79 healthy controls (HC), 63 individuals with MDD, and 30 individuals with remitted MDD (rMDD) were included. The groups produced similar sets of five microstates, including four widely-reported canonical microstates (A-D). The proportion of microstate D was decreased in MDD and rMDD compared to the HC group (Cohen's d = 0.63 and 0.72, respectively) and the duration and occurrence of microstate D was reduced in the MDD group compared to the HC group (Cohen's d = 0.43 and 0.58, respectively). Among the MDD group, proportion and duration of microstate D were negatively correlated with symptom severity (Spearman's rho = -0.34 and -0.46, respectively). Finally, microstate transition probabilities were nonrandom and the MDD group, relative to the HC and the rMDD groups, exhibited multiple distinct transition probabilities, primarily involving microstates A and C. Our findings highlight both state and trait abnormalities in resting-state brain activity in MDD.
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