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Neural self-representation in autistic women and association with ‘compensatory camouflaging’

Prior work has revealed sex/gender-dependent autistic characteristics across behavioural and neural/biological domains. It remains unclear whether and how neural sex/gender differences are related to behavioural sex/gender differences in autism. Here, we examined whether atypical neural responses du...

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Autores principales: Lai, Meng-Chuan, Lombardo, Michael V, Chakrabarti, Bhismadev, Ruigrok, Amber NV, Bullmore, Edward T, Suckling, John, Auyeung, Bonnie, Happé, Francesca, Szatmari, Peter, Baron-Cohen, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589917/
https://www.ncbi.nlm.nih.gov/pubmed/30354191
http://dx.doi.org/10.1177/1362361318807159
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author Lai, Meng-Chuan
Lombardo, Michael V
Chakrabarti, Bhismadev
Ruigrok, Amber NV
Bullmore, Edward T
Suckling, John
Auyeung, Bonnie
Happé, Francesca
Szatmari, Peter
Baron-Cohen, Simon
author_facet Lai, Meng-Chuan
Lombardo, Michael V
Chakrabarti, Bhismadev
Ruigrok, Amber NV
Bullmore, Edward T
Suckling, John
Auyeung, Bonnie
Happé, Francesca
Szatmari, Peter
Baron-Cohen, Simon
author_sort Lai, Meng-Chuan
collection PubMed
description Prior work has revealed sex/gender-dependent autistic characteristics across behavioural and neural/biological domains. It remains unclear whether and how neural sex/gender differences are related to behavioural sex/gender differences in autism. Here, we examined whether atypical neural responses during mentalizing and self-representation are sex/gender-dependent in autistic adults and explored whether ‘camouflaging’ (acting as if behaviourally neurotypical) is associated with sex/gender-dependent neural responses. In total, N = 119 adults (33 typically developing males, 29 autistic males, 29 typically developing females and 28 autistic females) participated in a task-related functional magnetic resonance imaging paradigm to assess neural activation within right temporo-parietal junction and ventromedial prefrontal cortex during mentalizing and self-representation. Camouflaging in autism was quantified as the discrepancy between extrinsic behaviour in social–interpersonal contexts and intrinsic status. While autistic men showed hypoactive right temporo-parietal junction mentalizing and ventromedial prefrontal cortex self-representation responses compared to typically developing men, such neural responses in autistic women were not different from typically developing women. In autistic women only, increasing camouflaging was associated with heightened ventromedial prefrontal cortex self-representation response. There is a lack of impaired neural self-representation and mentalizing in autistic women compared to typically developing women. Camouflaging is heightened in autistic women and may relate to neural self-representation response. These results reveal brain-behaviour relations that help explain sex/gender-heterogeneity in social brain function in autism.
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spelling pubmed-65899172019-07-01 Neural self-representation in autistic women and association with ‘compensatory camouflaging’ Lai, Meng-Chuan Lombardo, Michael V Chakrabarti, Bhismadev Ruigrok, Amber NV Bullmore, Edward T Suckling, John Auyeung, Bonnie Happé, Francesca Szatmari, Peter Baron-Cohen, Simon Autism Original Articles Prior work has revealed sex/gender-dependent autistic characteristics across behavioural and neural/biological domains. It remains unclear whether and how neural sex/gender differences are related to behavioural sex/gender differences in autism. Here, we examined whether atypical neural responses during mentalizing and self-representation are sex/gender-dependent in autistic adults and explored whether ‘camouflaging’ (acting as if behaviourally neurotypical) is associated with sex/gender-dependent neural responses. In total, N = 119 adults (33 typically developing males, 29 autistic males, 29 typically developing females and 28 autistic females) participated in a task-related functional magnetic resonance imaging paradigm to assess neural activation within right temporo-parietal junction and ventromedial prefrontal cortex during mentalizing and self-representation. Camouflaging in autism was quantified as the discrepancy between extrinsic behaviour in social–interpersonal contexts and intrinsic status. While autistic men showed hypoactive right temporo-parietal junction mentalizing and ventromedial prefrontal cortex self-representation responses compared to typically developing men, such neural responses in autistic women were not different from typically developing women. In autistic women only, increasing camouflaging was associated with heightened ventromedial prefrontal cortex self-representation response. There is a lack of impaired neural self-representation and mentalizing in autistic women compared to typically developing women. Camouflaging is heightened in autistic women and may relate to neural self-representation response. These results reveal brain-behaviour relations that help explain sex/gender-heterogeneity in social brain function in autism. SAGE Publications 2018-10-24 2019-07 /pmc/articles/PMC6589917/ /pubmed/30354191 http://dx.doi.org/10.1177/1362361318807159 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Lai, Meng-Chuan
Lombardo, Michael V
Chakrabarti, Bhismadev
Ruigrok, Amber NV
Bullmore, Edward T
Suckling, John
Auyeung, Bonnie
Happé, Francesca
Szatmari, Peter
Baron-Cohen, Simon
Neural self-representation in autistic women and association with ‘compensatory camouflaging’
title Neural self-representation in autistic women and association with ‘compensatory camouflaging’
title_full Neural self-representation in autistic women and association with ‘compensatory camouflaging’
title_fullStr Neural self-representation in autistic women and association with ‘compensatory camouflaging’
title_full_unstemmed Neural self-representation in autistic women and association with ‘compensatory camouflaging’
title_short Neural self-representation in autistic women and association with ‘compensatory camouflaging’
title_sort neural self-representation in autistic women and association with ‘compensatory camouflaging’
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589917/
https://www.ncbi.nlm.nih.gov/pubmed/30354191
http://dx.doi.org/10.1177/1362361318807159
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