4.4 Article

Resting-state connectivity in the prodromal phase of schizophrenia: Insights from EEG microstates

期刊

SCHIZOPHRENIA RESEARCH
卷 152, 期 2-3, 页码 513-520

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.schres.2013.12.008

关键词

Schizophrenia; At-risk mental state; Resting-state; Microstates; EEG; Connectivity

资金

  1. German Research Foundation [SFB 936]

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Introduction: Resting-state EEG microstates are thought to reflect the momentary local states and interactions of distributed neural networks in the brain. Several changes in resting-state EEG microstates have been described in acutely ill patients with schizophrenia, but it is not known whether these represent trait or state abnormalities. The present study aimed to investigate this issue by assessing EEG microstate characteristics in high-risk individuals (HR) and clinically stable first-episode patients with schizophrenia (SZ) with low symptom levels, compared to each other and healthy controls (HC). Method: Participants were 18 HR, 18 SZ, and 22 HC subjects. 64-channel resting-state EEG recordings were used for microstate analyses. Microstates were clustered into four classes (A-D) according to their topography. Temporal parameters and topographies of microstates were compared among groups. Results: Microstate class A displayed higher coverage and occurrence in HR than SZ and HC, while microstate class B covered significantly more time in SZ compared to both HR and HC. Microstate class B displayed an aberrant spatial configuration in SZ, and to a lesser extent also in HR, compared to HC, with patients exhibiting significantly higher activity in the vicinity of the left posterior cingulate. Discussion: Microstate abnormalities observed in HR were similar to those previously reported in acutely ill patients with schizophrenia. Moreover, there was evidence that HR and SZ might share specific disturbances in brain functional connectivity. These findings raise the possibility that certain abnormalities in resting-state EEG microstates might be associated with an increased risk for psychosis. (C) 2013 Elsevier B.V. All rights reserved.

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