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Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders

Severe symptoms of anxiety add substantial additional burden to many individuals diagnosed with Autism Spectrum Disorder (ASD). Improved understanding of specific factors that contribute to anxiety in ASD can aid research regarding the causes of autism and also provide targets for more effective int...

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Autores principales: South, Mikle, Rodgers, Jacqui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5258728/
https://www.ncbi.nlm.nih.gov/pubmed/28174531
http://dx.doi.org/10.3389/fnhum.2017.00020
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author South, Mikle
Rodgers, Jacqui
author_facet South, Mikle
Rodgers, Jacqui
author_sort South, Mikle
collection PubMed
description Severe symptoms of anxiety add substantial additional burden to many individuals diagnosed with Autism Spectrum Disorder (ASD). Improved understanding of specific factors that contribute to anxiety in ASD can aid research regarding the causes of autism and also provide targets for more effective intervention. This mini-review article focuses on emerging evidence for three concepts that appear to be related to each other and which also strongly predict anxiety in ASD samples. Atypical sensory function is included in the diagnostic criteria for ASD and is likely an important contributor to anxiety. Difficulties in understanding and labeling emotions (alexithymia), although a co-morbidity, may arise in part from atypical sensory function and can lead to confusion and uncertainty about how to respond to social and emotional situations. Intolerance of uncertainty (IU) describes people who have a particularly hard time with ambiguity and is known to be a key mechanism underlying some anxiety disorders. While evidence for linking these ideas is to date incomplete, we put forward a model including each concept as a framework for future studies. Specifically, we propose that IU is a critical mediator for anxiety in ASD, and explore the relationships between sensory function, alexithymia and IU. We further explore the role of the medial prefrontal cortex (mPFC) in regulating emotional response, in connection with limbic and insula-based networks, and suggest that disrupted integration in these networks underlies difficulties with habituation to strong emotional stimuli, which results in an enhanced perception of threat in many people with ASD. Behavioral and biologically-based treatments for anxiety in ASD will benefit from attending to these specific mechanisms as adjunct to traditional interventions.
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spelling pubmed-52587282017-02-07 Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders South, Mikle Rodgers, Jacqui Front Hum Neurosci Neuroscience Severe symptoms of anxiety add substantial additional burden to many individuals diagnosed with Autism Spectrum Disorder (ASD). Improved understanding of specific factors that contribute to anxiety in ASD can aid research regarding the causes of autism and also provide targets for more effective intervention. This mini-review article focuses on emerging evidence for three concepts that appear to be related to each other and which also strongly predict anxiety in ASD samples. Atypical sensory function is included in the diagnostic criteria for ASD and is likely an important contributor to anxiety. Difficulties in understanding and labeling emotions (alexithymia), although a co-morbidity, may arise in part from atypical sensory function and can lead to confusion and uncertainty about how to respond to social and emotional situations. Intolerance of uncertainty (IU) describes people who have a particularly hard time with ambiguity and is known to be a key mechanism underlying some anxiety disorders. While evidence for linking these ideas is to date incomplete, we put forward a model including each concept as a framework for future studies. Specifically, we propose that IU is a critical mediator for anxiety in ASD, and explore the relationships between sensory function, alexithymia and IU. We further explore the role of the medial prefrontal cortex (mPFC) in regulating emotional response, in connection with limbic and insula-based networks, and suggest that disrupted integration in these networks underlies difficulties with habituation to strong emotional stimuli, which results in an enhanced perception of threat in many people with ASD. Behavioral and biologically-based treatments for anxiety in ASD will benefit from attending to these specific mechanisms as adjunct to traditional interventions. Frontiers Media S.A. 2017-01-24 /pmc/articles/PMC5258728/ /pubmed/28174531 http://dx.doi.org/10.3389/fnhum.2017.00020 Text en Copyright © 2017 South and Rodgers. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
South, Mikle
Rodgers, Jacqui
Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders
title Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders
title_full Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders
title_fullStr Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders
title_full_unstemmed Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders
title_short Sensory, Emotional and Cognitive Contributions to Anxiety in Autism Spectrum Disorders
title_sort sensory, emotional and cognitive contributions to anxiety in autism spectrum disorders
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5258728/
https://www.ncbi.nlm.nih.gov/pubmed/28174531
http://dx.doi.org/10.3389/fnhum.2017.00020
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