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Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders
BACKGROUND: Atypical sensory processing is a common clinical observation in autism spectrum disorder (ASD). Neural hyperexcitability has been suggested as the cause for sensory hypersensitivity, a frequently reported clinical observation in ASD. We examined visual evoked responses to parametric incr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976475/ https://www.ncbi.nlm.nih.gov/pubmed/27504143 http://dx.doi.org/10.1186/s11689-016-9162-9 |
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author | Takarae, Yukari Sablich, Savanna R. White, Stormi P. Sweeney, John A. |
author_facet | Takarae, Yukari Sablich, Savanna R. White, Stormi P. Sweeney, John A. |
author_sort | Takarae, Yukari |
collection | PubMed |
description | BACKGROUND: Atypical sensory processing is a common clinical observation in autism spectrum disorder (ASD). Neural hyperexcitability has been suggested as the cause for sensory hypersensitivity, a frequently reported clinical observation in ASD. We examined visual evoked responses to parametric increases in stimulus contrast in order to model neural responsivity of sensory systems in ASD. METHODS: Thirteen high-functioning individuals with ASD and 12 typically developing (TD) individuals completed a steady-state visual evoked potential study. Stimuli were vertical circular gratings oscillating at 3.76 Hz at varying contrasts (5, 10, 20,…, 90 % contrast, 10 levels). The average spectral power at the stimulus oscillation frequency was calculated for each contrast level. RESULTS: The magnitude of evoked sensory responses increased at a significantly greater rate and resulted in disproportionately elevated activation with higher contrasts in the ASD group. Approximately 45 % of ASD participants had rates of response increases greater than any TD participant. This alteration was highly associated with parental reports of these participants’ sensory difficulties. CONCLUSIONS: Greater increases in visual responses over contrast manipulation suggest heightened excitability in the sensory cortex in ASD participants. Heightened neural excitability was observed in a substantial portion but not all of the ASD participants. This pattern suggests that individuals with higher excitability may constitute a neurobiologically distinct subgroup requiring individualized treatment interventions. |
format | Online Article Text |
id | pubmed-4976475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49764752016-08-09 Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders Takarae, Yukari Sablich, Savanna R. White, Stormi P. Sweeney, John A. J Neurodev Disord Research BACKGROUND: Atypical sensory processing is a common clinical observation in autism spectrum disorder (ASD). Neural hyperexcitability has been suggested as the cause for sensory hypersensitivity, a frequently reported clinical observation in ASD. We examined visual evoked responses to parametric increases in stimulus contrast in order to model neural responsivity of sensory systems in ASD. METHODS: Thirteen high-functioning individuals with ASD and 12 typically developing (TD) individuals completed a steady-state visual evoked potential study. Stimuli were vertical circular gratings oscillating at 3.76 Hz at varying contrasts (5, 10, 20,…, 90 % contrast, 10 levels). The average spectral power at the stimulus oscillation frequency was calculated for each contrast level. RESULTS: The magnitude of evoked sensory responses increased at a significantly greater rate and resulted in disproportionately elevated activation with higher contrasts in the ASD group. Approximately 45 % of ASD participants had rates of response increases greater than any TD participant. This alteration was highly associated with parental reports of these participants’ sensory difficulties. CONCLUSIONS: Greater increases in visual responses over contrast manipulation suggest heightened excitability in the sensory cortex in ASD participants. Heightened neural excitability was observed in a substantial portion but not all of the ASD participants. This pattern suggests that individuals with higher excitability may constitute a neurobiologically distinct subgroup requiring individualized treatment interventions. BioMed Central 2016-08-08 /pmc/articles/PMC4976475/ /pubmed/27504143 http://dx.doi.org/10.1186/s11689-016-9162-9 Text en © The Author(s). 2016 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 Takarae, Yukari Sablich, Savanna R. White, Stormi P. Sweeney, John A. Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
title | Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
title_full | Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
title_fullStr | Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
title_full_unstemmed | Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
title_short | Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
title_sort | neurophysiological hyperresponsivity to sensory input in autism spectrum disorders |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976475/ https://www.ncbi.nlm.nih.gov/pubmed/27504143 http://dx.doi.org/10.1186/s11689-016-9162-9 |
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