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Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis

Alexithymia is a personality construct denoting emotion processing problems. It has been suggested to encompass two dimensions: a cognitive and affective dimension. The cognitive dimension is characterized by difficulties in identifying, verbalizing and analyzing emotions, while the affective dimens...

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Autores principales: van der Velde, Jorien, Swart, Marte, van Rijn, Sophie, van der Meer, Lisette, Wunderink, Lex, Wiersma, Durk, Krabbendam, Lydia, Bruggeman, Richard, Aleman, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451258/
https://www.ncbi.nlm.nih.gov/pubmed/26030357
http://dx.doi.org/10.1371/journal.pone.0124803
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author van der Velde, Jorien
Swart, Marte
van Rijn, Sophie
van der Meer, Lisette
Wunderink, Lex
Wiersma, Durk
Krabbendam, Lydia
Bruggeman, Richard
Aleman, André
author_facet van der Velde, Jorien
Swart, Marte
van Rijn, Sophie
van der Meer, Lisette
Wunderink, Lex
Wiersma, Durk
Krabbendam, Lydia
Bruggeman, Richard
Aleman, André
author_sort van der Velde, Jorien
collection PubMed
description Alexithymia is a personality construct denoting emotion processing problems. It has been suggested to encompass two dimensions: a cognitive and affective dimension. The cognitive dimension is characterized by difficulties in identifying, verbalizing and analyzing emotions, while the affective dimension reflects the level of emotional arousal and imagination. Alexithymia has been previously proposed as a risk factor for developing psychosis. More specifically, the two alexithymia dimensions might be differentially related to the vulnerability for psychosis. Therefore, we examined the two dimensions of alexithymia, measured with the BVAQ in 94 siblings of patients with schizophrenia, 52 subjects at ultra-high risk (UHR) for developing psychosis, 38 patients with schizophrenia and 109 healthy controls. The results revealed that siblings and patients had higher levels of cognitive alexithymia compared to controls. In addition, subjects at UHR for psychosis had even higher levels of cognitive alexithymia compared to the siblings. The levels of affective alexithymia in siblings and patients were equal to controls. However, UHR individuals had significantly lower levels of affective alexithymia (i.e. higher levels of emotional arousal and fantasizing) compared to controls. Alexithymia was further related to subclinical levels of negative and depressive symptoms. These findings indicate that alexithymia varies parametrically with the degree of risk for psychosis. More specifically, a type-II alexithymia pattern, with high levels of cognitive alexithymia and normal or low levels of affective alexithymia, might be a vulnerability factor for psychosis.
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spelling pubmed-44512582015-06-09 Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis van der Velde, Jorien Swart, Marte van Rijn, Sophie van der Meer, Lisette Wunderink, Lex Wiersma, Durk Krabbendam, Lydia Bruggeman, Richard Aleman, André PLoS One Research Article Alexithymia is a personality construct denoting emotion processing problems. It has been suggested to encompass two dimensions: a cognitive and affective dimension. The cognitive dimension is characterized by difficulties in identifying, verbalizing and analyzing emotions, while the affective dimension reflects the level of emotional arousal and imagination. Alexithymia has been previously proposed as a risk factor for developing psychosis. More specifically, the two alexithymia dimensions might be differentially related to the vulnerability for psychosis. Therefore, we examined the two dimensions of alexithymia, measured with the BVAQ in 94 siblings of patients with schizophrenia, 52 subjects at ultra-high risk (UHR) for developing psychosis, 38 patients with schizophrenia and 109 healthy controls. The results revealed that siblings and patients had higher levels of cognitive alexithymia compared to controls. In addition, subjects at UHR for psychosis had even higher levels of cognitive alexithymia compared to the siblings. The levels of affective alexithymia in siblings and patients were equal to controls. However, UHR individuals had significantly lower levels of affective alexithymia (i.e. higher levels of emotional arousal and fantasizing) compared to controls. Alexithymia was further related to subclinical levels of negative and depressive symptoms. These findings indicate that alexithymia varies parametrically with the degree of risk for psychosis. More specifically, a type-II alexithymia pattern, with high levels of cognitive alexithymia and normal or low levels of affective alexithymia, might be a vulnerability factor for psychosis. Public Library of Science 2015-06-01 /pmc/articles/PMC4451258/ /pubmed/26030357 http://dx.doi.org/10.1371/journal.pone.0124803 Text en © 2015 van der Velde et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
van der Velde, Jorien
Swart, Marte
van Rijn, Sophie
van der Meer, Lisette
Wunderink, Lex
Wiersma, Durk
Krabbendam, Lydia
Bruggeman, Richard
Aleman, André
Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis
title Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis
title_full Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis
title_fullStr Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis
title_full_unstemmed Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis
title_short Cognitive Alexithymia Is Associated with the Degree of Risk for Psychosis
title_sort cognitive alexithymia is associated with the degree of risk for psychosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451258/
https://www.ncbi.nlm.nih.gov/pubmed/26030357
http://dx.doi.org/10.1371/journal.pone.0124803
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