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Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome
BACKGROUND: Social impairments are described as a common feature of the 22q11.2 deletion syndrome (22q11DS). However, the neural correlates underlying these impairments are largely unknown in this population. In this study, we investigated neural substrates of socio-emotional perception. METHODS: We...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891973/ https://www.ncbi.nlm.nih.gov/pubmed/29631546 http://dx.doi.org/10.1186/s11689-018-9232-2 |
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author | Dubourg, Lydia Vrticka, Pascal Debbané, Martin Chambaz, Léa Eliez, Stephan Schneider, Maude |
author_facet | Dubourg, Lydia Vrticka, Pascal Debbané, Martin Chambaz, Léa Eliez, Stephan Schneider, Maude |
author_sort | Dubourg, Lydia |
collection | PubMed |
description | BACKGROUND: Social impairments are described as a common feature of the 22q11.2 deletion syndrome (22q11DS). However, the neural correlates underlying these impairments are largely unknown in this population. In this study, we investigated neural substrates of socio-emotional perception. METHODS: We used event-related functional magnetic resonance imaging (fMRI) to explore neural activity in individuals with 22q11DS and healthy controls during the visualization of stimuli varying in social (social or non-social) or emotional (positive or negative valence) content. RESULTS: Neural hyporesponsiveness in regions of the default mode network (inferior parietal lobule, precuneus, posterior and anterior cingulate cortex and frontal regions) in response to social versus non-social images was found in the 22q11DS population compared to controls. A similar pattern of activation for positive and negative emotional processing was observed in the two groups. No correlation between neural activation and social functioning was observed in patients with the 22q11DS. Finally, no social × valence interaction impairment was found in patients. CONCLUSIONS: Our results indicate atypical neural correlates of social perception in 22q11DS that appear to be independent of valence processing. Abnormalities in the social perception network may lead to social impairments observed in 22q11DS individuals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11689-018-9232-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5891973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58919732018-04-11 Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome Dubourg, Lydia Vrticka, Pascal Debbané, Martin Chambaz, Léa Eliez, Stephan Schneider, Maude J Neurodev Disord Research BACKGROUND: Social impairments are described as a common feature of the 22q11.2 deletion syndrome (22q11DS). However, the neural correlates underlying these impairments are largely unknown in this population. In this study, we investigated neural substrates of socio-emotional perception. METHODS: We used event-related functional magnetic resonance imaging (fMRI) to explore neural activity in individuals with 22q11DS and healthy controls during the visualization of stimuli varying in social (social or non-social) or emotional (positive or negative valence) content. RESULTS: Neural hyporesponsiveness in regions of the default mode network (inferior parietal lobule, precuneus, posterior and anterior cingulate cortex and frontal regions) in response to social versus non-social images was found in the 22q11DS population compared to controls. A similar pattern of activation for positive and negative emotional processing was observed in the two groups. No correlation between neural activation and social functioning was observed in patients with the 22q11DS. Finally, no social × valence interaction impairment was found in patients. CONCLUSIONS: Our results indicate atypical neural correlates of social perception in 22q11DS that appear to be independent of valence processing. Abnormalities in the social perception network may lead to social impairments observed in 22q11DS individuals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11689-018-9232-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-10 /pmc/articles/PMC5891973/ /pubmed/29631546 http://dx.doi.org/10.1186/s11689-018-9232-2 Text en © The Author(s). 2018 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 Dubourg, Lydia Vrticka, Pascal Debbané, Martin Chambaz, Léa Eliez, Stephan Schneider, Maude Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
title | Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
title_full | Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
title_fullStr | Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
title_full_unstemmed | Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
title_short | Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
title_sort | neural correlates of socio-emotional perception in 22q11.2 deletion syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891973/ https://www.ncbi.nlm.nih.gov/pubmed/29631546 http://dx.doi.org/10.1186/s11689-018-9232-2 |
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