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An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome

BACKGROUND: 22q11.2 deletion syndrome (22q11DS, velo-cardio-facial syndrome [VCFS]) is a genetic disorder associated with interstitial deletions of chromosome 22q11.2. In addition to high rates of neuropsychiatric disorders, children with 22q11DS have impairments of face processing, as well as IQ-in...

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Autores principales: Azuma, Rayna, Deeley, Quinton, Campbell, Linda E, Daly, Eileen M, Giampietro, Vincent, Brammer, Michael J, Murphy, Kieran C, Murphy, Declan GM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429366/
https://www.ncbi.nlm.nih.gov/pubmed/25972975
http://dx.doi.org/10.1186/1866-1955-7-1
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author Azuma, Rayna
Deeley, Quinton
Campbell, Linda E
Daly, Eileen M
Giampietro, Vincent
Brammer, Michael J
Murphy, Kieran C
Murphy, Declan GM
author_facet Azuma, Rayna
Deeley, Quinton
Campbell, Linda E
Daly, Eileen M
Giampietro, Vincent
Brammer, Michael J
Murphy, Kieran C
Murphy, Declan GM
author_sort Azuma, Rayna
collection PubMed
description BACKGROUND: 22q11.2 deletion syndrome (22q11DS, velo-cardio-facial syndrome [VCFS]) is a genetic disorder associated with interstitial deletions of chromosome 22q11.2. In addition to high rates of neuropsychiatric disorders, children with 22q11DS have impairments of face processing, as well as IQ-independent deficits in visuoperceptual function and social and abstract reasoning. These face-processing deficits may contribute to the social impairments of 22q11DS. However, their neurobiological basis is poorly understood. METHODS: We used event-related functional magnetic resonance imaging (fMRI) to examine neural responses when children with 22q11DS (aged 9–17 years) and healthy controls (aged 8–17 years) incidentally processed neutral expressions and mild (50%) and intense (100%) expressions of fear and disgust. We included 28 right-handed children and adolescents: 14 with 22q11DS and 14 healthy (including nine siblings) controls. RESULTS: Within groups, contrasts showed that individuals significantly activated ‘face responsive’ areas when viewing neutral faces, including fusiform-extrastriate cortices. Further, within both groups, there was a significant positive linear trend in activation of fusiform-extrastriate cortices and cerebellum to increasing intensities of fear. There were, however, also between-group differences. Children with 22q11DS generally showed reduced activity as compared to controls in brain regions involved in social cognition and emotion processing across emotion types and intensities, including fusiform-extrastriate cortices, anterior cingulate cortex (Brodmann area (BA) 24/32), and superomedial prefrontal cortices (BA 6). Also, an exploratory correlation analysis showed that within 22q11DS children reduced activation was associated with behavioural impairment—social difficulties (measured using the Total Difficulties Score from the Strengths and Difficulties Questionnaire [SDQ]) were significantly negatively correlated with brain activity during fear and disgust processing (respectively) in the left precentral gyrus (BA 4) and in the left fusiform gyrus (FG, BA 19), right lingual gyrus (BA 18), and bilateral cerebellum. CONCLUSIONS: Regions involved in face processing, including fusiform-extrastriate cortices, anterior cingulate gyri, and superomedial prefrontal cortices (BA 6), are activated by facial expressions of fearful, disgusted, and neutral expressions in children with 22q11DS but generally to a lesser degree than in controls. Hypoactivation in these regions may partly explain the social impairments of children with 22q11DS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1866-1955-7-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-44293662015-05-14 An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome Azuma, Rayna Deeley, Quinton Campbell, Linda E Daly, Eileen M Giampietro, Vincent Brammer, Michael J Murphy, Kieran C Murphy, Declan GM J Neurodev Disord Research BACKGROUND: 22q11.2 deletion syndrome (22q11DS, velo-cardio-facial syndrome [VCFS]) is a genetic disorder associated with interstitial deletions of chromosome 22q11.2. In addition to high rates of neuropsychiatric disorders, children with 22q11DS have impairments of face processing, as well as IQ-independent deficits in visuoperceptual function and social and abstract reasoning. These face-processing deficits may contribute to the social impairments of 22q11DS. However, their neurobiological basis is poorly understood. METHODS: We used event-related functional magnetic resonance imaging (fMRI) to examine neural responses when children with 22q11DS (aged 9–17 years) and healthy controls (aged 8–17 years) incidentally processed neutral expressions and mild (50%) and intense (100%) expressions of fear and disgust. We included 28 right-handed children and adolescents: 14 with 22q11DS and 14 healthy (including nine siblings) controls. RESULTS: Within groups, contrasts showed that individuals significantly activated ‘face responsive’ areas when viewing neutral faces, including fusiform-extrastriate cortices. Further, within both groups, there was a significant positive linear trend in activation of fusiform-extrastriate cortices and cerebellum to increasing intensities of fear. There were, however, also between-group differences. Children with 22q11DS generally showed reduced activity as compared to controls in brain regions involved in social cognition and emotion processing across emotion types and intensities, including fusiform-extrastriate cortices, anterior cingulate cortex (Brodmann area (BA) 24/32), and superomedial prefrontal cortices (BA 6). Also, an exploratory correlation analysis showed that within 22q11DS children reduced activation was associated with behavioural impairment—social difficulties (measured using the Total Difficulties Score from the Strengths and Difficulties Questionnaire [SDQ]) were significantly negatively correlated with brain activity during fear and disgust processing (respectively) in the left precentral gyrus (BA 4) and in the left fusiform gyrus (FG, BA 19), right lingual gyrus (BA 18), and bilateral cerebellum. CONCLUSIONS: Regions involved in face processing, including fusiform-extrastriate cortices, anterior cingulate gyri, and superomedial prefrontal cortices (BA 6), are activated by facial expressions of fearful, disgusted, and neutral expressions in children with 22q11DS but generally to a lesser degree than in controls. Hypoactivation in these regions may partly explain the social impairments of children with 22q11DS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1866-1955-7-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-02 2015 /pmc/articles/PMC4429366/ /pubmed/25972975 http://dx.doi.org/10.1186/1866-1955-7-1 Text en © Azuma et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. 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
Azuma, Rayna
Deeley, Quinton
Campbell, Linda E
Daly, Eileen M
Giampietro, Vincent
Brammer, Michael J
Murphy, Kieran C
Murphy, Declan GM
An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
title An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
title_full An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
title_fullStr An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
title_full_unstemmed An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
title_short An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
title_sort fmri study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429366/
https://www.ncbi.nlm.nih.gov/pubmed/25972975
http://dx.doi.org/10.1186/1866-1955-7-1
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