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

被引:27
作者
Azuma, Rayna [1 ,2 ]
Deeley, Quinton [2 ,3 ]
Campbell, Linda E. [4 ]
Daly, Eileen M. [2 ]
Giampietro, Vincent [5 ]
Brammer, Michael J. [5 ]
Murphy, Kieran C. [6 ]
Murphy, Declan G. M. [2 ,7 ]
机构
[1] Waseda Univ, Sch Int Liberal Studies, Tokyo, Japan
[2] Kings Coll London, Inst Psychiat, Dept Forens & Neurodev Sci, London WC2R 2LS, England
[3] SLAM NHS Fdn Trust, Bethlem Royal Hosp, Natl Autism Unit, London, England
[4] Univ Newcastle, Sch Psychol, Newcastle, NSW 2300, Australia
[5] Kings Coll London, Inst Psychiat, Dept Neuroimaging, London WC2R 2LS, England
[6] Beaumont Hosp, Royal Coll Surg Ireland, Dept Psychiat, Dublin 9, Ireland
[7] Kings Coll London, Sackler Inst Translat Neurodev, Inst Psychiat, London WC2R 2LS, England
基金
英国惠康基金;
关键词
Velo-cardio-facial syndrome (VCFS); 22q11.2 deletion syndrome (22q11DS); Emotion; fMRI; Children; Social cognition; DIFFICULTIES QUESTIONNAIRE SDQ; GENERIC BRAIN ACTIVATION; AUTISM-SPECTRUM; VELOCARDIOFACIAL SYNDROME; PSYCHIATRIC-DISORDERS; HUMAN AMYGDALA; NEUROPSYCHIATRIC DISORDERS; CORTICAL ACTIVATION; SOCIAL COGNITION; NEURAL BASIS;
D O I
10.1186/1866-1955-7-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
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页数:16
相关论文
共 132 条
[1]   Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome [J].
Andersson, Frederic ;
Glaser, Bronwyn ;
Spiridon, Mona ;
Debbane, Martin ;
Vuilleumier, Patrik ;
Eliez, Stephan .
BIOLOGICAL PSYCHIATRY, 2008, 63 (01) :49-57
[2]  
[Anonymous], 2013, Diagnostic and statistical manual of mental disorders
[3]  
[Anonymous], 1994, AM PSYCHIATR ASSOC
[4]   Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study [J].
Azuma, Rayna ;
Daly, Eileen M. ;
Campbell, Linda E. ;
Stevens, Angela F. ;
Deeley, Quinton ;
Giampietro, Vincent ;
Brammer, Michael J. ;
Glaser, Beate ;
Ambery, Fiona Z. ;
Morris, Robin G. ;
Williams, Steven C. R. ;
Owen, Michael J. ;
Murphy, Declan G. M. ;
Murphy, Kieran C. .
JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2009, 1 (01) :46-60
[5]   Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP) [J].
Baird, Gillian ;
Simonoff, Emily ;
Pickles, Andrew ;
Chandler, Susie ;
Loucas, Tom ;
Meldrum, David ;
Charman, Tony .
LANCET, 2006, 368 (9531) :210-215
[6]   Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome? [J].
Baker, Kate ;
Vorstman, Jacob A. S. .
CURRENT OPINION IN NEUROLOGY, 2012, 25 (02) :131-137
[7]   Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome [J].
Bearden, CE ;
Jawad, AF ;
Lynch, DR ;
Monterossso, JR ;
Sokol, S ;
McDonald-McGinn, DM ;
Saitta, SC ;
Harris, SE ;
Moss, E ;
Wang, PP ;
Zackai, E ;
Emanuel, BS ;
Simon, TJ .
CHILD NEUROPSYCHOLOGY, 2005, 11 (01) :109-117
[8]   Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome [J].
Bearden, CE ;
Jawad, AF ;
Lynch, DR ;
Sokol, S ;
Kanes, SJ ;
McDonald-McGinn, DM ;
Saitta, SC ;
Harris, SE ;
Moss, E ;
Wang, PP ;
Zackai, E ;
Emanuel, BS ;
Simon, TJ .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (09) :1700-1702
[9]   The functional neuroanatomy of major depression: an fMRI study using an emotional activation paradigm [J].
Beauregard, M ;
Leroux, JM ;
Bergman, S ;
Arzoumanian, Y ;
Beaudoin, G ;
Bourgouin, P ;
Stip, E .
NEUROREPORT, 1998, 9 (14) :3253-3258
[10]   Autism screening questionnaire: diagnostic validity [J].
Berument, SK ;
Rutter, M ;
Lord, C ;
Pickles, A ;
Bailey, A .
BRITISH JOURNAL OF PSYCHIATRY, 1999, 175 :444-451