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Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study

Schizotypy is associated with poor emotion regulation that is thought to contribute to the development of psychotic symptoms and to indicate a predisposition to schizophrenia. Having focused primarily on the relationship between schizotypy and explicit emotion regulation, existing studies have, unti...

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Autores principales: Hoid, Delhii, Pan, Dong-ni, Wang, Yi, Li, Xuebing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054415/
https://www.ncbi.nlm.nih.gov/pubmed/32127580
http://dx.doi.org/10.1038/s41598-020-60787-9
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author Hoid, Delhii
Pan, Dong-ni
Wang, Yi
Li, Xuebing
author_facet Hoid, Delhii
Pan, Dong-ni
Wang, Yi
Li, Xuebing
author_sort Hoid, Delhii
collection PubMed
description Schizotypy is associated with poor emotion regulation that is thought to contribute to the development of psychotic symptoms and to indicate a predisposition to schizophrenia. Having focused primarily on the relationship between schizotypy and explicit emotion regulation, existing studies have, until now, neglected to acknowledge the potentially important role of implicit emotion regulation. Our aim in the current study was to investigate implicit emotion regulation deficits in schizotypy. To this end, we used a newly developed Priming-Identification (PI) ERP paradigm, consisting of a priming phase and an emotion identification phase, to test 30 individuals with schizotypy and 30 healthy controls while also acquiring EEG data. During the priming phase, we aimed to manipulate emotion regulation goals (i.e., to bring about an intended emotional state) by presenting a category of words related to emotion regulation alongside a category of control words. Associated brain responses occurring during the subsequent stage were indexed according to three ERP components: N170, early posterior negativity (EPN) and late positive potential (LPP). Results showed that, in the control group, priming words associated with emotion regulation led to enhancements in the early N170 amplitude and the middle EPN during expression identification. The same pattern was not observed in the schizotypy group. In summary, our results suggest the presence of deficits in the early and middle stages of the implicit emotion regulation process among individuals with high schizotypal traits.
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spelling pubmed-70544152020-03-11 Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study Hoid, Delhii Pan, Dong-ni Wang, Yi Li, Xuebing Sci Rep Article Schizotypy is associated with poor emotion regulation that is thought to contribute to the development of psychotic symptoms and to indicate a predisposition to schizophrenia. Having focused primarily on the relationship between schizotypy and explicit emotion regulation, existing studies have, until now, neglected to acknowledge the potentially important role of implicit emotion regulation. Our aim in the current study was to investigate implicit emotion regulation deficits in schizotypy. To this end, we used a newly developed Priming-Identification (PI) ERP paradigm, consisting of a priming phase and an emotion identification phase, to test 30 individuals with schizotypy and 30 healthy controls while also acquiring EEG data. During the priming phase, we aimed to manipulate emotion regulation goals (i.e., to bring about an intended emotional state) by presenting a category of words related to emotion regulation alongside a category of control words. Associated brain responses occurring during the subsequent stage were indexed according to three ERP components: N170, early posterior negativity (EPN) and late positive potential (LPP). Results showed that, in the control group, priming words associated with emotion regulation led to enhancements in the early N170 amplitude and the middle EPN during expression identification. The same pattern was not observed in the schizotypy group. In summary, our results suggest the presence of deficits in the early and middle stages of the implicit emotion regulation process among individuals with high schizotypal traits. Nature Publishing Group UK 2020-03-03 /pmc/articles/PMC7054415/ /pubmed/32127580 http://dx.doi.org/10.1038/s41598-020-60787-9 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hoid, Delhii
Pan, Dong-ni
Wang, Yi
Li, Xuebing
Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study
title Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study
title_full Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study
title_fullStr Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study
title_full_unstemmed Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study
title_short Implicit emotion regulation deficits in individuals with high schizotypal traits: an ERP study
title_sort implicit emotion regulation deficits in individuals with high schizotypal traits: an erp study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054415/
https://www.ncbi.nlm.nih.gov/pubmed/32127580
http://dx.doi.org/10.1038/s41598-020-60787-9
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