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Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study
Brain-to-brain synchrony has been proposed as an important mechanism underlying social interaction. While first findings indicate that it may be modulated in children with autism spectrum disorder (ASD), no study to date has investigated the influence of different interaction partners and task chara...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812623/ https://www.ncbi.nlm.nih.gov/pubmed/32685971 http://dx.doi.org/10.1093/scan/nsaa092 |
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author | Kruppa, Jana A Reindl, Vanessa Gerloff, Christian Oberwelland Weiss, Eileen Prinz, Julia Herpertz-Dahlmann, Beate Konrad, Kerstin Schulte-Rüther, Martin |
author_facet | Kruppa, Jana A Reindl, Vanessa Gerloff, Christian Oberwelland Weiss, Eileen Prinz, Julia Herpertz-Dahlmann, Beate Konrad, Kerstin Schulte-Rüther, Martin |
author_sort | Kruppa, Jana A |
collection | PubMed |
description | Brain-to-brain synchrony has been proposed as an important mechanism underlying social interaction. While first findings indicate that it may be modulated in children with autism spectrum disorder (ASD), no study to date has investigated the influence of different interaction partners and task characteristics. Using functional near-infrared spectroscopy hyperscanning, we assessed brain-to-brain synchrony in 41 male typically developing (TD) children (8–18 years; control sample), as well as 18 children with ASD and age-matched TD children (matched sample), while performing cooperative and competitive tasks with their parents and an adult stranger. Dyads were instructed either to respond jointly in response to a target (cooperation) or to respond faster than the other player (competition). Wavelet coherence was calculated for oxy- and deoxyhemoglobin brain signals. In the control sample, a widespread enhanced coherence was observed for parent–child competition, and a more localized coherence for parent–child cooperation in the frontopolar cortex. While behaviorally, children with ASD showed a lower motor synchrony than children in the TD group, no significant group differences were observed on the neural level. In order to identify biomarkers for typical and atypical social interactions in the long run, more research is needed to investigate the neurobiological underpinnings of reduced synchrony in ASD. |
format | Online Article Text |
id | pubmed-7812623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78126232021-01-25 Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study Kruppa, Jana A Reindl, Vanessa Gerloff, Christian Oberwelland Weiss, Eileen Prinz, Julia Herpertz-Dahlmann, Beate Konrad, Kerstin Schulte-Rüther, Martin Soc Cogn Affect Neurosci Original Manuscript Brain-to-brain synchrony has been proposed as an important mechanism underlying social interaction. While first findings indicate that it may be modulated in children with autism spectrum disorder (ASD), no study to date has investigated the influence of different interaction partners and task characteristics. Using functional near-infrared spectroscopy hyperscanning, we assessed brain-to-brain synchrony in 41 male typically developing (TD) children (8–18 years; control sample), as well as 18 children with ASD and age-matched TD children (matched sample), while performing cooperative and competitive tasks with their parents and an adult stranger. Dyads were instructed either to respond jointly in response to a target (cooperation) or to respond faster than the other player (competition). Wavelet coherence was calculated for oxy- and deoxyhemoglobin brain signals. In the control sample, a widespread enhanced coherence was observed for parent–child competition, and a more localized coherence for parent–child cooperation in the frontopolar cortex. While behaviorally, children with ASD showed a lower motor synchrony than children in the TD group, no significant group differences were observed on the neural level. In order to identify biomarkers for typical and atypical social interactions in the long run, more research is needed to investigate the neurobiological underpinnings of reduced synchrony in ASD. Oxford University Press 2020-07-18 /pmc/articles/PMC7812623/ /pubmed/32685971 http://dx.doi.org/10.1093/scan/nsaa092 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Manuscript Kruppa, Jana A Reindl, Vanessa Gerloff, Christian Oberwelland Weiss, Eileen Prinz, Julia Herpertz-Dahlmann, Beate Konrad, Kerstin Schulte-Rüther, Martin Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study |
title | Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study |
title_full | Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study |
title_fullStr | Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study |
title_full_unstemmed | Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study |
title_short | Brain and motor synchrony in children and adolescents with ASD—a fNIRS hyperscanning study |
title_sort | brain and motor synchrony in children and adolescents with asd—a fnirs hyperscanning study |
topic | Original Manuscript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812623/ https://www.ncbi.nlm.nih.gov/pubmed/32685971 http://dx.doi.org/10.1093/scan/nsaa092 |
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