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Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning

BACKGROUND: Prevalence estimates of autistic traits in individuals with psychotic disorders (PD) vary greatly and it is unclear whether individuals with a familial risk (FR) for psychosis have an increased propensity to display autistic traits. Furthermore, it is unknown whether the presence of como...

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Autores principales: Ziermans, Tim B., Schirmbeck, Frederike, Oosterwijk, Floor, Geurts, Hilde M., de Haan, Lieuwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327624/
https://www.ncbi.nlm.nih.gov/pubmed/32151297
http://dx.doi.org/10.1017/S0033291720000458
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author Ziermans, Tim B.
Schirmbeck, Frederike
Oosterwijk, Floor
Geurts, Hilde M.
de Haan, Lieuwe
author_facet Ziermans, Tim B.
Schirmbeck, Frederike
Oosterwijk, Floor
Geurts, Hilde M.
de Haan, Lieuwe
author_sort Ziermans, Tim B.
collection PubMed
description BACKGROUND: Prevalence estimates of autistic traits in individuals with psychotic disorders (PD) vary greatly and it is unclear whether individuals with a familial risk (FR) for psychosis have an increased propensity to display autistic traits. Furthermore, it is unknown whether the presence of comorbid autism traits disproportionally affects the cognitive and behavioral aspects of social functioning in PD. METHODS: In total, 504 individuals with PD, 587 unaffected siblings with FR, and 337 typical comparison (TC) individuals (16–50 years) were included. Autistic and psychotic traits were measured with the Autism Spectrum Quotient (AQ) and the Community Assessment of Psychic Experiences (CAPE). Social cognition was assessed with the Picture Sequencing Task (PST) and social behavior with the Social Functioning Scale (SFS). RESULTS: For PD 6.5% scored above AQ clinical cut-off (⩾32), 1.0% for FR, and 1.2% for TC. After accounting for age, sex, and IQ, the PD group showed significantly more autistic traits and alterations in social behavior and cognition, while FR and TC only displayed marginal differences. Within the PD group autistic traits were a robust predictor of social behavior and there were no interactions with positive psychotic symptoms. CONCLUSIONS: Levels of autistic traits are substantially elevated in PD and have a profoundly negative association with social functioning. In contrast, autistic traits above the clinical cut-off are not elevated in those with FR, and only marginally on a dimensional level. These findings warrant specific clinical guidelines for psychotic patients who present themselves with autistic comorbidity to help address their social needs.
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spelling pubmed-83276242021-08-11 Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning Ziermans, Tim B. Schirmbeck, Frederike Oosterwijk, Floor Geurts, Hilde M. de Haan, Lieuwe Psychol Med Original Article BACKGROUND: Prevalence estimates of autistic traits in individuals with psychotic disorders (PD) vary greatly and it is unclear whether individuals with a familial risk (FR) for psychosis have an increased propensity to display autistic traits. Furthermore, it is unknown whether the presence of comorbid autism traits disproportionally affects the cognitive and behavioral aspects of social functioning in PD. METHODS: In total, 504 individuals with PD, 587 unaffected siblings with FR, and 337 typical comparison (TC) individuals (16–50 years) were included. Autistic and psychotic traits were measured with the Autism Spectrum Quotient (AQ) and the Community Assessment of Psychic Experiences (CAPE). Social cognition was assessed with the Picture Sequencing Task (PST) and social behavior with the Social Functioning Scale (SFS). RESULTS: For PD 6.5% scored above AQ clinical cut-off (⩾32), 1.0% for FR, and 1.2% for TC. After accounting for age, sex, and IQ, the PD group showed significantly more autistic traits and alterations in social behavior and cognition, while FR and TC only displayed marginal differences. Within the PD group autistic traits were a robust predictor of social behavior and there were no interactions with positive psychotic symptoms. CONCLUSIONS: Levels of autistic traits are substantially elevated in PD and have a profoundly negative association with social functioning. In contrast, autistic traits above the clinical cut-off are not elevated in those with FR, and only marginally on a dimensional level. These findings warrant specific clinical guidelines for psychotic patients who present themselves with autistic comorbidity to help address their social needs. Cambridge University Press 2021-07 2020-03-10 /pmc/articles/PMC8327624/ /pubmed/32151297 http://dx.doi.org/10.1017/S0033291720000458 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ziermans, Tim B.
Schirmbeck, Frederike
Oosterwijk, Floor
Geurts, Hilde M.
de Haan, Lieuwe
Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
title Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
title_full Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
title_fullStr Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
title_full_unstemmed Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
title_short Autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
title_sort autistic traits in psychotic disorders: prevalence, familial risk, and impact on social functioning
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327624/
https://www.ncbi.nlm.nih.gov/pubmed/32151297
http://dx.doi.org/10.1017/S0033291720000458
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