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Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder

Schizophrenia (SCH) and bipolar disorder (BD) are characterized by many types of symptoms, damaged cognitive function, and abnormal brain connections. The microstates are considered to be the cornerstones of the mental states shown in EEG data. In our study, we investigated the use of microstates as...

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Autores principales: Wang, Fanglan, Hujjaree, Khamlesh, Wang, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952514/
https://www.ncbi.nlm.nih.gov/pubmed/33716831
http://dx.doi.org/10.3389/fpsyt.2021.638722
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author Wang, Fanglan
Hujjaree, Khamlesh
Wang, Xiaoping
author_facet Wang, Fanglan
Hujjaree, Khamlesh
Wang, Xiaoping
author_sort Wang, Fanglan
collection PubMed
description Schizophrenia (SCH) and bipolar disorder (BD) are characterized by many types of symptoms, damaged cognitive function, and abnormal brain connections. The microstates are considered to be the cornerstones of the mental states shown in EEG data. In our study, we investigated the use of microstates as biomarkers to distinguish patients with bipolar disorder from those with schizophrenia by analyzing EEG data measured in an eyes-closed resting state. The purpose of this article is to provide an electron directional physiological explanation for the observed brain dysfunction of schizophrenia and bipolar disorder patients. Methods: We used microstate resting EEG data to explore group differences in the duration, coverage, occurrence, and transition probability of 4 microstate maps among 20 SCH patients, 26 BD patients, and 35 healthy controls (HCs). Results: Microstate analysis revealed 4 microstates (A–D) in global clustering across SCH patients, BD patients, and HCs. The samples were chosen to be matched. We found the greater presence of microstate B in BD patients, and the less presence of microstate class A and B, the greater presence of microstate class C, and less presence of D in SCH patients. Besides, a greater frequent switching between microstates A and B and between microstates B and A in BD patients than in SCH patients and HCs and less frequent switching between microstates C and D and between microstates D and C in BD patients compared with SCH patients. Conclusion: We found abnormal features of microstate A, B in BD patients and abnormal features of microstate A, B, C, and D in SCH patients. These features may indicate the potential abnormalities of SCH patients and BD patients in distributing neural resources and influencing opportune transitions between different states of activity.
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spelling pubmed-79525142021-03-13 Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder Wang, Fanglan Hujjaree, Khamlesh Wang, Xiaoping Front Psychiatry Psychiatry Schizophrenia (SCH) and bipolar disorder (BD) are characterized by many types of symptoms, damaged cognitive function, and abnormal brain connections. The microstates are considered to be the cornerstones of the mental states shown in EEG data. In our study, we investigated the use of microstates as biomarkers to distinguish patients with bipolar disorder from those with schizophrenia by analyzing EEG data measured in an eyes-closed resting state. The purpose of this article is to provide an electron directional physiological explanation for the observed brain dysfunction of schizophrenia and bipolar disorder patients. Methods: We used microstate resting EEG data to explore group differences in the duration, coverage, occurrence, and transition probability of 4 microstate maps among 20 SCH patients, 26 BD patients, and 35 healthy controls (HCs). Results: Microstate analysis revealed 4 microstates (A–D) in global clustering across SCH patients, BD patients, and HCs. The samples were chosen to be matched. We found the greater presence of microstate B in BD patients, and the less presence of microstate class A and B, the greater presence of microstate class C, and less presence of D in SCH patients. Besides, a greater frequent switching between microstates A and B and between microstates B and A in BD patients than in SCH patients and HCs and less frequent switching between microstates C and D and between microstates D and C in BD patients compared with SCH patients. Conclusion: We found abnormal features of microstate A, B in BD patients and abnormal features of microstate A, B, C, and D in SCH patients. These features may indicate the potential abnormalities of SCH patients and BD patients in distributing neural resources and influencing opportune transitions between different states of activity. Frontiers Media S.A. 2021-02-26 /pmc/articles/PMC7952514/ /pubmed/33716831 http://dx.doi.org/10.3389/fpsyt.2021.638722 Text en Copyright © 2021 Wang, Hujjaree and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Wang, Fanglan
Hujjaree, Khamlesh
Wang, Xiaoping
Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder
title Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder
title_full Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder
title_fullStr Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder
title_full_unstemmed Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder
title_short Electroencephalographic Microstates in Schizophrenia and Bipolar Disorder
title_sort electroencephalographic microstates in schizophrenia and bipolar disorder
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952514/
https://www.ncbi.nlm.nih.gov/pubmed/33716831
http://dx.doi.org/10.3389/fpsyt.2021.638722
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