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A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion
Siblings of individuals with autism have over 20 times the population risk of autism. Evidence of comparable, but less marked, cognitive and social communication deficits in siblings suggests a role for these traits in the search for biomarkers of familial risk. However, no neuroimaging biomarkers o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309518/ https://www.ncbi.nlm.nih.gov/pubmed/22832521 http://dx.doi.org/10.1038/tp.2011.18 |
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author | Spencer, M D Holt, R J Chura, L R Suckling, J Calder, A J Bullmore, E T Baron-Cohen, S |
author_facet | Spencer, M D Holt, R J Chura, L R Suckling, J Calder, A J Bullmore, E T Baron-Cohen, S |
author_sort | Spencer, M D |
collection | PubMed |
description | Siblings of individuals with autism have over 20 times the population risk of autism. Evidence of comparable, but less marked, cognitive and social communication deficits in siblings suggests a role for these traits in the search for biomarkers of familial risk. However, no neuroimaging biomarkers of familial risk have been identified to date. Here we show, for the first time, that the neural response to facial expression of emotion differs between unaffected siblings and healthy controls with no family history of autism. Strikingly, the functional magnetic resonance imaging (fMRI) response to happy versus neutral faces was significantly reduced in unaffected siblings compared with controls within a number of brain areas implicated in empathy and face processing. The response in unaffected siblings did not differ significantly from the response in autism. Furthermore, investigation of the response to faces versus fixation crosses suggested that, within the context of this study, an atypical response specifically to happy faces, rather than to faces in general, accounts for the observed sibling versus controls difference and is a clear biomarker of familial risk. Our findings suggest that an atypical implicit response to facial expression of emotion may form the basis of impaired emotional reactivity in autism and in the broader autism phenotype in relatives. These results demonstrate that the fMRI response to facial expression of emotion is a candidate neuroimaging endophenotype for autism, and may offer far-reaching insights into the etiology of autism. |
format | Online Article Text |
id | pubmed-3309518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33095182012-04-03 A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion Spencer, M D Holt, R J Chura, L R Suckling, J Calder, A J Bullmore, E T Baron-Cohen, S Transl Psychiatry Original Article Siblings of individuals with autism have over 20 times the population risk of autism. Evidence of comparable, but less marked, cognitive and social communication deficits in siblings suggests a role for these traits in the search for biomarkers of familial risk. However, no neuroimaging biomarkers of familial risk have been identified to date. Here we show, for the first time, that the neural response to facial expression of emotion differs between unaffected siblings and healthy controls with no family history of autism. Strikingly, the functional magnetic resonance imaging (fMRI) response to happy versus neutral faces was significantly reduced in unaffected siblings compared with controls within a number of brain areas implicated in empathy and face processing. The response in unaffected siblings did not differ significantly from the response in autism. Furthermore, investigation of the response to faces versus fixation crosses suggested that, within the context of this study, an atypical response specifically to happy faces, rather than to faces in general, accounts for the observed sibling versus controls difference and is a clear biomarker of familial risk. Our findings suggest that an atypical implicit response to facial expression of emotion may form the basis of impaired emotional reactivity in autism and in the broader autism phenotype in relatives. These results demonstrate that the fMRI response to facial expression of emotion is a candidate neuroimaging endophenotype for autism, and may offer far-reaching insights into the etiology of autism. Nature Publishing Group 2011-07 2011-07-12 /pmc/articles/PMC3309518/ /pubmed/22832521 http://dx.doi.org/10.1038/tp.2011.18 Text en Copyright © 2011 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Article Spencer, M D Holt, R J Chura, L R Suckling, J Calder, A J Bullmore, E T Baron-Cohen, S A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
title | A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
title_full | A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
title_fullStr | A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
title_full_unstemmed | A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
title_short | A novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
title_sort | novel functional brain imaging endophenotype of autism: the neural response to facial expression of emotion |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309518/ https://www.ncbi.nlm.nih.gov/pubmed/22832521 http://dx.doi.org/10.1038/tp.2011.18 |
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