Literature DB >> 32590838

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

Michael Murphy1,2, Alexis E Whitton1,2,3, Stephanie Deccy2,4, Manon L Ironside2,5, Ashleigh Rutherford2,6, Miranda Beltzer2,7, Matthew Sacchet1,2, Diego A Pizzagalli8,9.   

Abstract

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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Year:  2020        PMID: 32590838      PMCID: PMC7547108          DOI: 10.1038/s41386-020-0749-1

Source DB:  PubMed          Journal:  Neuropsychopharmacology        ISSN: 0893-133X            Impact factor:   7.853


  1 in total

1.  Electroencephalogram Microstate Abnormalities in Early-Course Psychosis.

Authors:  Michael Murphy; Robert Stickgold; Dost Öngür
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2019-07-25
  1 in total
  14 in total

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3.  The pro-inflammatory factors contribute to the EEG microstate abnormalities in patients with major depressive disorder.

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4.  Large-scale EEG neural network changes in response to therapeutic TMS.

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5.  Alteration in Resting-State EEG Microstates Following 24 Hours of Total Sleep Deprivation in Healthy Young Male Subjects.

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Journal:  Front Hum Neurosci       Date:  2021-04-12       Impact factor: 3.169

6.  Resting-State EEG Microstates Parallel Age-Related Differences in Allocentric Spatial Working Memory Performance.

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Journal:  Brain Topogr       Date:  2021-04-19       Impact factor: 3.020

7.  Abnormalities in Electroencephalographic Microstates Among Adolescents With First Episode Major Depressive Disorder.

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10.  Dynamics of brain function in patients with chronic pain assessed by microstate analysis of resting-state electroencephalography.

Authors:  Elisabeth S May; Cristina Gil Ávila; Son Ta Dinh; Henrik Heitmann; Vanessa D Hohn; Moritz M Nickel; Laura Tiemann; Thomas R Tölle; Markus Ploner
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