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EEG Microstates and Psychosocial Stress During an Exchange Year
The well-known stress vulnerability model of psychosis assumes that psychotic episodes result from the coincidence of individual trait dispositions and triggering stressors. We thus hypothesized that a transient psychosocial stressor would not only increase the number of and stress caused by psychos...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892813/ https://www.ncbi.nlm.nih.gov/pubmed/33169276 http://dx.doi.org/10.1007/s10548-020-00806-0 |
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author | Kadier, Nursija Stein, Maria Koenig, Thomas |
author_facet | Kadier, Nursija Stein, Maria Koenig, Thomas |
author_sort | Kadier, Nursija |
collection | PubMed |
description | The well-known stress vulnerability model of psychosis assumes that psychotic episodes result from the coincidence of individual trait dispositions and triggering stressors. We thus hypothesized that a transient psychosocial stressor would not only increase the number of and stress caused by psychosis-like symptoms (like delusion-like symptoms or auditory hallucinations) in healthy subjects but also elicit changes in EEG microstates that have been related to the presence of psychotic symptoms in patients with schizophrenia. Considering a radical change of one’s psychosocial environment as a significant stressor, we analyzed psychotic symptoms and EEG microstate data in teenage exchange-students at an early and a later phase of their stay. The subjects experienced a small and transient, but significant increase of stress by psychosis-like symptoms. These changes in mental state were associated with increases in microstate class A, which has previously been related to unspecific stress. microstate classes C and D, which have consistently been found to be altered in patients with psychosis, were found unaffected by the time of the recording and the subjective stress experiences. Therefore, we conclude that microstate class A appears to be a psychosis independent and rather general correlate of psychosocial stress, whereas changes in microstate classes C and D seem to be more specifically tied to the presence of psychotic symptoms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10548-020-00806-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7892813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-78928132021-03-03 EEG Microstates and Psychosocial Stress During an Exchange Year Kadier, Nursija Stein, Maria Koenig, Thomas Brain Topogr Brief Communication The well-known stress vulnerability model of psychosis assumes that psychotic episodes result from the coincidence of individual trait dispositions and triggering stressors. We thus hypothesized that a transient psychosocial stressor would not only increase the number of and stress caused by psychosis-like symptoms (like delusion-like symptoms or auditory hallucinations) in healthy subjects but also elicit changes in EEG microstates that have been related to the presence of psychotic symptoms in patients with schizophrenia. Considering a radical change of one’s psychosocial environment as a significant stressor, we analyzed psychotic symptoms and EEG microstate data in teenage exchange-students at an early and a later phase of their stay. The subjects experienced a small and transient, but significant increase of stress by psychosis-like symptoms. These changes in mental state were associated with increases in microstate class A, which has previously been related to unspecific stress. microstate classes C and D, which have consistently been found to be altered in patients with psychosis, were found unaffected by the time of the recording and the subjective stress experiences. Therefore, we conclude that microstate class A appears to be a psychosis independent and rather general correlate of psychosocial stress, whereas changes in microstate classes C and D seem to be more specifically tied to the presence of psychotic symptoms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10548-020-00806-0) contains supplementary material, which is available to authorized users. Springer US 2020-11-09 2021 /pmc/articles/PMC7892813/ /pubmed/33169276 http://dx.doi.org/10.1007/s10548-020-00806-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Brief Communication Kadier, Nursija Stein, Maria Koenig, Thomas EEG Microstates and Psychosocial Stress During an Exchange Year |
title | EEG Microstates and Psychosocial Stress During an Exchange Year |
title_full | EEG Microstates and Psychosocial Stress During an Exchange Year |
title_fullStr | EEG Microstates and Psychosocial Stress During an Exchange Year |
title_full_unstemmed | EEG Microstates and Psychosocial Stress During an Exchange Year |
title_short | EEG Microstates and Psychosocial Stress During an Exchange Year |
title_sort | eeg microstates and psychosocial stress during an exchange year |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7892813/ https://www.ncbi.nlm.nih.gov/pubmed/33169276 http://dx.doi.org/10.1007/s10548-020-00806-0 |
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