Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

In people with velo-cardio-facial syndrome [or 22q11.2 deletion syndrome (22qDS)], a single interstitial deletion of chromosome 22q11.2 causes a wide spectrum of cognitive deficits ranging from global learning difficulties to specific cognitive deficits. People with 22qDS are also at high risk of developing attention-deficit/hyperactivity disorder and autism spectrum disorders in childhood, and schizophrenia in adolescence or adult life. However, the neurobiology of 22qDS, and the relationship between abnormalities in brain anatomy and behaviour, is poorly understood. Thus, we studied the neuroanatomy of 22qDS children using fully automated voxel-based morphometry (VBM) and manually traced single region-of-interest (ROI) analysis. Also, we investigated whether those brain regions that differed significantly between groups were related to behavioural differences within children with 22qDS. We compared the brain morphometry of 39 children and adolescents with 22qDS (mean age: 11 years, SD +/-3, IQ = 67, SD +/-10) and 26 sibling controls (mean age: 11 years, SD +/-3, IQ = 102, SD +/-12). Using VBM, we found, after correction for IQ, that individuals with 22qDS compared with controls had a significant reduction in cerebellar grey matter, and white matter reductions in the frontal lobe, cerebellum and internal capsule. Using single ROI analysis, we found that people with 22qDS had a significant (P < 0.05) reduction in bulk volume bilaterally in the occipital-parietal lobes, but a larger right caudate nucleus and lateral ventricles. Further, within people with 22qDS, there was a significant positive correlation between severity of (i) schizotypy score and grey matter volume of the temporo-occipital regions and the corpus striatum; (ii) emotional problems and grey matter volume of frontostriatal regions; and (iii) social behavioural difficulties and grey matter in frontostriatal regions. Thus, subjects with 22qDS have widespread changes in brain anatomy, particularly affecting white matter, basal ganglia and cerebellum. Also, within 22qDS, regionally specific differences in brain development may partially underpin behavioural differences. We suggest that there is preliminary evidence for specific vulnerability of the frontostriatal and cerebellar-cortical networks in 22qDS.

[1]  S. Maier,et al.  Microstructural Development of Human Newborn Cerebral White Matter Assessed in Vivo by Diffusion Tensor Magnetic Resonance Imaging , 1998, Pediatric Research.

[2]  K. Devriendt,et al.  The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. , 1999, Genetic counseling.

[3]  David J Mikulis,et al.  Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia , 1999, Biological Psychiatry.

[4]  C. Cytrynbaum,et al.  Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders. , 2001, American journal of medical genetics.

[5]  P. Hüppi,et al.  Diffusion tensor imaging of normal and injured developing human brain ‐ a technical review , 2002, NMR in biomedicine.

[6]  M. Torrens Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268 , 1990 .

[7]  R. Royall,et al.  Improving sterological estimates for the volume of structures identified in three-dimensional arrays of spatial data , 1997, Journal of Neuroscience Methods.

[8]  E. Zackai,et al.  Autism Spectrum Disorders and Symptoms in Children with Molecularly Confirmed 22q11.2 Deletion Syndrome , 2005, Journal of autism and developmental disorders.

[9]  Eileen Daly,et al.  Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. , 2004, Archives of general psychiatry.

[10]  P I Andrews,et al.  22q11 deletion and polymicrogyria--cause or coincidence? , 2000, Clinical dysmorphology.

[11]  D. Skuse,et al.  Adolescents and young adults with 22qll deletion syndrome: psychopathology in an at-risk group , 2005, British Journal of Psychiatry.

[12]  Karl J. Friston,et al.  Voxel-Based Morphometry—The Methods , 2000, NeuroImage.

[13]  Y. Sheline 3D MRI studies of neuroanatomic changes in unipolar major depression: the role of stress and medical comorbidity , 2000, Biological Psychiatry.

[14]  R. Shprintzen,et al.  Brain anomalies in velo-cardio-facial syndrome. , 1994, American journal of medical genetics.

[15]  Ron Kikinis,et al.  Cavum septi pellucidi in first-episode schizophrenia and first-episode affective psychosis: an MRI study , 2004, Schizophrenia Research.

[16]  R Kucherlapati,et al.  Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? , 1996, The American journal of psychiatry.

[17]  K. Devriendt,et al.  Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS. , 1997, Journal of medical genetics.

[18]  E. Zackai,et al.  Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion , 2001, Genetics in Medicine.

[19]  S. Strakowski,et al.  The functional neuroanatomy of bipolar disorder: a review of neuroimaging findings , 2005, Molecular Psychiatry.

[20]  T. Sigmundsson,et al.  Brain anatomy and sensorimotor gating in Asperger's syndrome. , 2002, Brain : a journal of neurology.

[21]  S. Tezenas du Montcel,et al.  Prevalence of 22q11 microdeletion. , 1996, Journal of medical genetics.

[22]  James C. Gee,et al.  Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study , 2005, NeuroImage.

[23]  J. Lieberman,et al.  Increase in caudate nuclei volumes of first-episode schizophrenic patients taking antipsychotic drugs. , 1994, The American journal of psychiatry.

[24]  M. Owen,et al.  Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia , 2001, British Journal of Psychiatry.

[25]  Mark H Johnson,et al.  Neuroimaging of typical and atypical development: A perspective from multiple levels of analysis , 2002, Development and Psychopathology.

[26]  R. McCarley,et al.  A review of MRI findings in schizophrenia , 2001, Schizophrenia Research.

[27]  A Pickles,et al.  Autism screening questionnaire: Diagnostic validity , 1999, British Journal of Psychiatry.

[28]  Y. Finkelstein,et al.  Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome , 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[29]  R. Vataja,et al.  Midline brain anomalies and schizophrenia in people with CATCH 22 syndrome , 1998, British Journal of Psychiatry.

[30]  M. Mehmet Haznedar,et al.  Striatal Volume on Magnetic Resonance Imaging and Repetitive Behaviors in Autism , 2005, Biological Psychiatry.

[31]  A. Kanner,et al.  Is major depression a neurologic disorder with psychiatric symptoms? , 2004, Epilepsy & Behavior.

[32]  J J Bartko,et al.  ON THE METHODS AND THEORY OF RELIABILITY , 1976, The Journal of nervous and mental disease.

[33]  M. Owen,et al.  An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS) , 2000, Neuropsychologia.

[34]  B Horwitz,et al.  White matter hyperintensities in dementia of Alzheimer's type and in healthy subjects without cerebrovascular risk factors. A magnetic resonance imaging study. , 1990, Archives of neurology.

[35]  J. Plese,et al.  Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment. , 2004, Journal of neuroradiology. Journal de neuroradiologie.

[36]  S Eliez,et al.  Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. , 2000, The American journal of psychiatry.

[37]  E. Zackai,et al.  Polymicrogyria in chromosome 22 deletion syndrome , 1998, Neurology.

[38]  J. Suckling,et al.  Mapping the brain in autism. A voxel-based MRI study of volumetric differences and intercorrelations in autism. , 2004, Brain : a journal of neurology.

[39]  Karl J. Friston,et al.  A Voxel-Based Morphometric Study of Ageing in 465 Normal Adult Human Brains , 2001, NeuroImage.

[40]  J B Poline,et al.  Temporal lobe dysfunction in childhood autism: a PET study. Positron emission tomography. , 2000, The American journal of psychiatry.

[41]  H. Critchley,et al.  Asperger syndrome: a proton magnetic resonance spectroscopy study of brain. , 2002, Archives of general psychiatry.

[42]  Kathryn E. Lewandowski,et al.  Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome , 2004, NeuroImage.

[43]  M. Egan,et al.  Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain. , 2004, American journal of human genetics.

[44]  R. Weksberg,et al.  22q11 deletion syndrome in adults with schizophrenia. , 1998, American journal of medical genetics.

[45]  A. Fasth,et al.  Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden , 2004, Archives of Disease in Childhood.

[46]  R. Shprintzen,et al.  Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus , 1992, The Lancet.

[47]  H. Kawame,et al.  Polymicrogyria is an uncommon manifestation in 22q11.2 deletion syndrome. , 2000, American journal of medical genetics.

[48]  Godfrey D Pearlson,et al.  Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis , 2001, Biological Psychiatry.

[49]  K. Murphy,et al.  Schizophrenia and velo-cardio-facial syndrome , 2002, The Lancet.

[50]  A. Green,et al.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. , 1997, Journal of medical genetics.

[51]  John Suckling,et al.  Global, voxel, and cluster tests, by theory and permutation, for a difference between two groups of structural MR images of the brain , 1999, IEEE Transactions on Medical Imaging.

[52]  R. Shprintzen,et al.  Velo-cardio-facial syndrome: language and psychological profiles. , 1985, Journal of craniofacial genetics and developmental biology.

[53]  Jane S. Paulsen,et al.  Relationship of neuropsychological and MRI measures to age of onset of schizophrenia a , 1998, Acta psychiatrica Scandinavica.

[54]  Tyrone D. Cannon,et al.  Regional Brain Abnormalities in 22q11.2 Deletion Syndrome: Association With Cognitive Abilities and Behavioral Symptoms , 2004, Neurocase.

[55]  J Suckling,et al.  Structural brain abnormalities associated with deletion at chromosome 22q11 , 2001, British Journal of Psychiatry.

[56]  H Meltzer,et al.  Using the Strengths and Difficulties Questionnaire (SDQ) to screen for child psychiatric disorders in a community sample , 2003, International review of psychiatry.

[57]  J. Nigg,et al.  An integrative theory of attention-deficit/ hyperactivity disorder based on the cognitive and affective neurosciences , 2005, Development and Psychopathology.

[58]  Christina Sobin,et al.  Networks of Attention in Children With the 22q11 Deletion Syndrome , 2004, Developmental neuropsychology.

[59]  Stéphane Moniotte,et al.  Polymicrogyria in chromosome 22q11 deletion syndrome. , 2002, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[60]  A. Nieoullon Dopamine and the regulation of cognition and attention , 2002, Progress in Neurobiology.

[61]  Godfrey D. Pearlson,et al.  Frontal and Caudate Alterations in Velocardiofacial Syndrome (Deletion at Chromosome 22q11.2) , 2004, Journal of child neurology.

[62]  T. Sigmundsson,et al.  Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms. , 2001, The American journal of psychiatry.

[63]  K. Devriendt,et al.  Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability? , 1999, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.

[64]  Stephan Eliez,et al.  Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study. , 2003, The American journal of psychiatry.

[65]  Abraham Weizman,et al.  Obsessive‐compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome , 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[66]  N. Makris,et al.  Structural Brain Imaging of Attention-Deficit/Hyperactivity Disorder , 2005, Biological Psychiatry.

[67]  M. Owen,et al.  High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS) , 1999, Schizophrenia Research.