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Microstate and Omega Complexity Analyses of the Resting-state Electroencephalography
Published on: June 15, 2018
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Electroencephalogram Microstate Abnormalities in Early-Course Psychosis
Michael Murphy1, Robert Stickgold2, Dost Öngür1
1Department of Psychiatry, Harvard Medical School, Boston, Massachusetts; Schizophrenia and Bipolar Disorder Research Program, McLean Hospital, Belmont, Massachusetts.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging
|September 24, 2019
Summary
Patients with early-course psychosis exhibit chaotic brain network transitions, indicated by abnormal microstate sequences. This suggests altered neural resource allocation and state transitions in psychosis.
Area of Science:
- Neuroscience
- Psychiatry
- Computational Neuroscience
Background:
- Electroencephalography (EEG) microstates reflect brain network activity.
- Abnormal microstate parameters are observed in psychotic disorders.
- Early-course psychosis presents unique challenges for understanding brain dynamics.
Purpose of the Study:
- To investigate resting-state network dynamics in early-course psychosis using microstate and sample entropy analysis.
- To identify alterations in brain network transitions associated with psychosis.
Main Methods:
- High-density EEG data from 22 early-course psychosis patients and 22 controls were analyzed.
- Microstate analysis identified characteristic scalp topographies.
- Sample entropy quantified the complexity of microstate transition sequences.
Main Results:
- Patients and controls showed similar microstate sets (A, B, C, D).
- Patients had decreased frequency of microstate A and lacked self-similarity in microstate transitions.
- Elevated entropy in unmedicated patients decreased with medication; specific transition patterns differed between groups.
Conclusions:
- Early-course psychosis is associated with abnormally chaotic brain network transitions.
- This chaos may stem from impaired neural resource allocation and state transitions.
- Microstate and entropy analysis offer insights into psychosis pathophysiology.

