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Functional autonomic nervous system profile in children with autism spectrum disorder
BACKGROUND: Autonomic dysregulation has been recently reported as a feature of autism spectrum disorder (ASD). However, the nature of autonomic atypicalities in ASD remain largely unknown. The goal of this study was to characterize the cardiac autonomic profile of children with ASD across four domai...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099494/ https://www.ncbi.nlm.nih.gov/pubmed/25031832 http://dx.doi.org/10.1186/2040-2392-5-39 |
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author | Kushki, Azadeh Brian, Jessica Dupuis, Annie Anagnostou, Evdokia |
author_facet | Kushki, Azadeh Brian, Jessica Dupuis, Annie Anagnostou, Evdokia |
author_sort | Kushki, Azadeh |
collection | PubMed |
description | BACKGROUND: Autonomic dysregulation has been recently reported as a feature of autism spectrum disorder (ASD). However, the nature of autonomic atypicalities in ASD remain largely unknown. The goal of this study was to characterize the cardiac autonomic profile of children with ASD across four domains affected in ASD (anxiety, attention, response inhibition, and social cognition), and suggested to be affected by autonomic dysregulation. METHODS: We compared measures of autonomic cardiac regulation in typically developing children (n = 34) and those with ASD (n = 40) as the children performed tasks eliciting anxiety, attention, response inhibition, and social cognition. Heart rate was used to quantify overall autonomic arousal, and respiratory sinus arrhythmia (RSA) was used as an index of vagal influences. Associations between atypical autonomic findings and intellectual functioning (Weschler scale), ASD symptomatology (Social Communication Questionnaire score), and co-morbid anxiety (Revised Children’s Anxiety and Depression Scale) were also investigated. RESULTS: The ASD group had marginally elevated basal heart rate, and showed decreased heart rate reactivity to social anxiety and increased RSA reactivity to the social cognition task. In this group, heart rate reactivity to the social anxiety task was positively correlated with IQ and task performance, and negatively correlated with generalized anxiety. RSA reactivity in the social cognition task was positively correlated with IQ. CONCLUSIONS: Our data suggest overall autonomic hyperarousal in ASD and selective atypical reactivity to social tasks. |
format | Online Article Text |
id | pubmed-4099494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40994942014-07-17 Functional autonomic nervous system profile in children with autism spectrum disorder Kushki, Azadeh Brian, Jessica Dupuis, Annie Anagnostou, Evdokia Mol Autism Research BACKGROUND: Autonomic dysregulation has been recently reported as a feature of autism spectrum disorder (ASD). However, the nature of autonomic atypicalities in ASD remain largely unknown. The goal of this study was to characterize the cardiac autonomic profile of children with ASD across four domains affected in ASD (anxiety, attention, response inhibition, and social cognition), and suggested to be affected by autonomic dysregulation. METHODS: We compared measures of autonomic cardiac regulation in typically developing children (n = 34) and those with ASD (n = 40) as the children performed tasks eliciting anxiety, attention, response inhibition, and social cognition. Heart rate was used to quantify overall autonomic arousal, and respiratory sinus arrhythmia (RSA) was used as an index of vagal influences. Associations between atypical autonomic findings and intellectual functioning (Weschler scale), ASD symptomatology (Social Communication Questionnaire score), and co-morbid anxiety (Revised Children’s Anxiety and Depression Scale) were also investigated. RESULTS: The ASD group had marginally elevated basal heart rate, and showed decreased heart rate reactivity to social anxiety and increased RSA reactivity to the social cognition task. In this group, heart rate reactivity to the social anxiety task was positively correlated with IQ and task performance, and negatively correlated with generalized anxiety. RSA reactivity in the social cognition task was positively correlated with IQ. CONCLUSIONS: Our data suggest overall autonomic hyperarousal in ASD and selective atypical reactivity to social tasks. BioMed Central 2014-07-04 /pmc/articles/PMC4099494/ /pubmed/25031832 http://dx.doi.org/10.1186/2040-2392-5-39 Text en Copyright © 2014 Kushki et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Kushki, Azadeh Brian, Jessica Dupuis, Annie Anagnostou, Evdokia Functional autonomic nervous system profile in children with autism spectrum disorder |
title | Functional autonomic nervous system profile in children with autism spectrum disorder |
title_full | Functional autonomic nervous system profile in children with autism spectrum disorder |
title_fullStr | Functional autonomic nervous system profile in children with autism spectrum disorder |
title_full_unstemmed | Functional autonomic nervous system profile in children with autism spectrum disorder |
title_short | Functional autonomic nervous system profile in children with autism spectrum disorder |
title_sort | functional autonomic nervous system profile in children with autism spectrum disorder |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099494/ https://www.ncbi.nlm.nih.gov/pubmed/25031832 http://dx.doi.org/10.1186/2040-2392-5-39 |
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