Literature DB >> 17618656

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome).

Wendy R Kates1, Beth R Krauss, Nuria Abdulsabur, Deirdre Colgan, Kevin M Antshel, Anne Marie Higgins, Robert J Shprintzen.   

Abstract

Velocardiofacial syndrome (VCFS), also known as 22q11.2 deletion syndrome, is a neurogenetic disorder that is associated with both learning disabilities and a consistent neuropsychological phenotype, including deficits in executive function, visuospatial perception, and working memory. Anatomic imaging studies have identified significant volumetric reductions in the parietal lobe of individuals with VCFS, but several studies have reported that the frontal lobe is relatively preserved. We used functional magnetic resonance imaging to investigate the neural correlates of non-spatial working memory in 17 youths with VCFS, 10 of their unaffected siblings, and 10 community controls (with the same proportion of learning disabilities as the VCFS youths). Task performance of siblings tended to be more accurate than children with VCFS, who did not differ from community controls. All three-study groups recruited parietal regions that were equivalent in location and magnitude. Whereas the sibling group also recruited the dorsolateral prefrontal cortex (DLPFC), Broca's area, and anterior cingulate, DLPFC activation was absent in the whole brain analyses of children with VCFS and controls. Moreover, the magnitude of frontal activation in VCFS participants was restricted relative to both siblings and controls. These findings suggest that VCFS participants exhibit frontal hypoactivation that is not attributable to performance. In addition, VCFS children and controls (many with idiopathic learning disabilities) appear to rely on phonological rehearsal to hold information on line instead of the DLPFC. Despite previous anatomic MRI reports of preserved frontal lobe volumes in VCFS therefore, these fMRI findings suggest that the frontal component of the distributed network subserving executive function and working memory may be disrupted in youth with this disorder.

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Year:  2007        PMID: 17618656      PMCID: PMC2034197          DOI: 10.1016/j.neuropsychologia.2007.05.007

Source DB:  PubMed          Journal:  Neuropsychologia        ISSN: 0028-3932            Impact factor:   3.139


  51 in total

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4.  Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.

Authors:  W R Kates; C P Burnette; E W Jabs; J Rutberg; A M Murphy; M Grados; M Geraghty; W E Kaufmann; G D Pearlson
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6.  Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?

Authors:  Renée R Lajiness-O'Neill; Isabelle Beaulieu; Jeffrey B Titus; Alexander Asamoah; Erin D Bigler; Erawati V Bawle; Rebecca Pollack
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7.  Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis.

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8.  Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

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10.  Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2).

Authors:  Wendy R Kates; Courtney P Burnette; Brandy A Bessette; Bradley S Folley; Leslie Strunge; Ethylin W Jabs; Godfrey D Pearlson
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2.  Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology.

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3.  The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion.

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4.  White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosis.

Authors:  Wendy R Kates; Amy K Olszewski; Matthew H Gnirke; Zora Kikinis; Joshua Nelson; Kevin M Antshel; Wanda Fremont; Petya D Radoeva; Frank A Middleton; Martha E Shenton; Ioana L Coman
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Review 5.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

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Review 7.  Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.

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9.  White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis.

Authors:  Matthew D Perlstein; Moeed R Chohan; Ioana L Coman; Kevin M Antshel; Wanda P Fremont; Matthew H Gnirke; Zora Kikinis; Frank A Middleton; Petya D Radoeva; Martha E Shenton; Wendy R Kates
Journal:  Schizophr Res       Date:  2013-12-08       Impact factor: 4.939

10.  Associations between performance on the Rey-Osterrieth Complex Figure and regional brain volumes in children with and without velocardiofacial syndrome.

Authors:  Kevin M Antshel; Jena Peebles; Nuria AbdulSabur; Anne Marie Higgins; Nancy Roizen; Robert Shprintzen; Wanda P Fremont; Robert Nastasi; Wendy R Kates
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