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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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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. |
format | Online Article Text |
id | pubmed-6589917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
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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