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Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study

BACKGROUND: Humans can easily grasp the affective meaning of touch when observing social interactions. Several neural systems support this ability, including the theory of mind (ToM) network and the somatosensory system linked to embodied resonance, but it is unclear how these systems are affected i...

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Autores principales: Lee Masson, Haemy, Pillet, Ineke, Amelynck, Steffie, Van De Plas, Stien, Hendriks, Michelle, Op de Beeck, Hans, Boets, Bart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881998/
https://www.ncbi.nlm.nih.gov/pubmed/31798816
http://dx.doi.org/10.1186/s13229-019-0294-0
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author Lee Masson, Haemy
Pillet, Ineke
Amelynck, Steffie
Van De Plas, Stien
Hendriks, Michelle
Op de Beeck, Hans
Boets, Bart
author_facet Lee Masson, Haemy
Pillet, Ineke
Amelynck, Steffie
Van De Plas, Stien
Hendriks, Michelle
Op de Beeck, Hans
Boets, Bart
author_sort Lee Masson, Haemy
collection PubMed
description BACKGROUND: Humans can easily grasp the affective meaning of touch when observing social interactions. Several neural systems support this ability, including the theory of mind (ToM) network and the somatosensory system linked to embodied resonance, but it is unclear how these systems are affected in autism spectrum disorder (ASD). Individuals with ASD exhibit impairments in the use of nonverbal communication such as social and reciprocal touch. Despite the importance of touch in social communication and the reported touch aversion in ASD, surprisingly little is known about the neural systems underlying impairments in touch communication in ASD. METHODS: The present study applies a dynamic and socially meaningful stimulus set combined with functional magnetic resonance imaging (fMRI) to pinpoint atypicalities in the neural circuitry underlying socio-affective touch observation in adults with ASD. Twenty-one adults with ASD and 21 matched neurotypical adults evaluated the valence and arousal of 75 video fragments displaying touch interactions. Subsequently, they underwent fMRI while watching the same videos. Using multi-voxel pattern analysis (MVPA) and multiple regression analysis, we examined which brain regions represent the socio-affective meaning of observed touch. To further understand the brain-behavior relationship, we correlated the strength of affective representations in the somatosensory cortex with individuals’ attitude towards social touch in general and with a quantitative index of autism traits as measured by the Social Responsiveness Scale. RESULTS: Results revealed that the affective meaning of touch was well represented in the temporoparietal junction, a core mentalizing area, in both groups. Conversely, only the neurotypical group represented affective touch in the somatosensory cortex, a region involved in self-experienced touch. Lastly, irrespective of the group, individuals with a more positive attitude towards receiving, witnessing, and providing social touch and with a higher score on social responsivity showed more differentiated representations of the affective meaning of touch in these somatosensory areas. CONCLUSIONS: Together, our findings imply that male adults with ASD show intact cognitive understanding (i.e., “knowing”) of observed socio-affective touch interactions, but lack of spontaneous embodied resonance (i.e., “feeling”).
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spelling pubmed-68819982019-12-03 Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study Lee Masson, Haemy Pillet, Ineke Amelynck, Steffie Van De Plas, Stien Hendriks, Michelle Op de Beeck, Hans Boets, Bart Mol Autism Research BACKGROUND: Humans can easily grasp the affective meaning of touch when observing social interactions. Several neural systems support this ability, including the theory of mind (ToM) network and the somatosensory system linked to embodied resonance, but it is unclear how these systems are affected in autism spectrum disorder (ASD). Individuals with ASD exhibit impairments in the use of nonverbal communication such as social and reciprocal touch. Despite the importance of touch in social communication and the reported touch aversion in ASD, surprisingly little is known about the neural systems underlying impairments in touch communication in ASD. METHODS: The present study applies a dynamic and socially meaningful stimulus set combined with functional magnetic resonance imaging (fMRI) to pinpoint atypicalities in the neural circuitry underlying socio-affective touch observation in adults with ASD. Twenty-one adults with ASD and 21 matched neurotypical adults evaluated the valence and arousal of 75 video fragments displaying touch interactions. Subsequently, they underwent fMRI while watching the same videos. Using multi-voxel pattern analysis (MVPA) and multiple regression analysis, we examined which brain regions represent the socio-affective meaning of observed touch. To further understand the brain-behavior relationship, we correlated the strength of affective representations in the somatosensory cortex with individuals’ attitude towards social touch in general and with a quantitative index of autism traits as measured by the Social Responsiveness Scale. RESULTS: Results revealed that the affective meaning of touch was well represented in the temporoparietal junction, a core mentalizing area, in both groups. Conversely, only the neurotypical group represented affective touch in the somatosensory cortex, a region involved in self-experienced touch. Lastly, irrespective of the group, individuals with a more positive attitude towards receiving, witnessing, and providing social touch and with a higher score on social responsivity showed more differentiated representations of the affective meaning of touch in these somatosensory areas. CONCLUSIONS: Together, our findings imply that male adults with ASD show intact cognitive understanding (i.e., “knowing”) of observed socio-affective touch interactions, but lack of spontaneous embodied resonance (i.e., “feeling”). BioMed Central 2019-11-27 /pmc/articles/PMC6881998/ /pubmed/31798816 http://dx.doi.org/10.1186/s13229-019-0294-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lee Masson, Haemy
Pillet, Ineke
Amelynck, Steffie
Van De Plas, Stien
Hendriks, Michelle
Op de Beeck, Hans
Boets, Bart
Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
title Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
title_full Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
title_fullStr Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
title_full_unstemmed Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
title_short Intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
title_sort intact neural representations of affective meaning of touch but lack of embodied resonance in autism: a multi-voxel pattern analysis study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881998/
https://www.ncbi.nlm.nih.gov/pubmed/31798816
http://dx.doi.org/10.1186/s13229-019-0294-0
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