Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.

Abstract:

:Chromosome 22q11.2 deletion syndrome (22q11DS) is associated with cognitive deficits and morphometric brain abnormalities in childhood and a markedly elevated risk of schizophrenia in adolescence/early adulthood. Determining the relationship between neurocognition and neuroimaging findings would yield crucial information about childhood neurodevelopment and provide a basis for the study of the trajectory that occurs on the pathway to psychosis. We compared morphometric brain findings between non-psychotic children with 22q11DS (n = 22) and healthy controls (n = 16), and examined the association between neurocognitive functioning and morphometric brain findings. Volumetric regional gray matter differences between the 22q11DS and control subjects were measured, and correlations of the regional gray matter volumes and neurocognition were performed. Children with 22q11DS demonstrated reductions in gray matter in several brain regions, chiefly the frontal cortices, the cingulate gyrus and the cerebellum. The volumetric reductions in these salient areas were associated with poor performance in sustained attention, executive function and verbal memory; however, the relation of brain volume with cognitive performance did not differ between the patient and control groups. Thus, children with 22q11DS demonstrate gray matter reductions in multiple brain regions that are thought to be relevant to schizophrenia. The correlation of these volumetric reductions with poor neurocognition indicates that these brain regions may mediate higher neurocognitive functions implicated in schizophrenia.

journal_name

Psychiatry Res

journal_title

Psychiatry research

authors

Shashi V,Kwapil TR,Kaczorowski J,Berry MN,Santos CS,Howard TD,Goradia D,Prasad K,Vaibhav D,Rajarethinam R,Spence E,Keshavan MS

doi

10.1016/j.pscychresns.2009.07.003

subject

Has Abstract

pub_date

2010-01-30 00:00:00

pages

1-8

issue

1

eissn

0165-1781

issn

1872-7123

pii

S0925-4927(09)00168-1

journal_volume

181

pub_type

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