Literature DB >> 27702912

Frontal Hypoactivation During a Working Memory Task in Children With 22q11 Deletion Syndrome.

Waverly Harrell1, Ling Zou2,3, Zoe Englander2, Stephen R Hooper4,5, Matcheri S Keshavan6, Allen Song2,7, Vandana Shashi1.   

Abstract

Impairments in executive function, such as working memory, are almost universal in children with chromosome 22q11.2 deletion syndrome. Delineating the neural underpinnings of these functions would enhance understanding of these impairments. In this study, children and adolescents with 22q11 deletion syndrome were compared with healthy control participants in a functional magnetic resonance imaging (MRI) study of working memory. When the 2-back condition was contrasted with the 1-back and 0-back conditions, the participants with 22q11 deletion syndrome showed lower activation in several brain areas involved in working memory-notably dorsolateral prefrontal cortex, anterior cingulate, and precuneus. This hypoactivation may be due to reduced gray matter volumes or white matter connectivity in the frontal and parietal regions, differences that have previously been documented in children with 22q11 deletion syndrome. Understanding differences in brain function will provide a foundation for future interventions to address the wide range of neurodevelopmental deficits observed in 22q11 deletion syndrome.

Entities:  

Keywords:  22q; DiGeorge; fMRI; velocardiofacial

Mesh:

Year:  2016        PMID: 27702912      PMCID: PMC5852670          DOI: 10.1177/0883073816670813

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  29 in total

1.  Maturation of widely distributed brain function subserves cognitive development.

Authors:  B Luna; K R Thulborn; D P Munoz; E P Merriam; K E Garver; N J Minshew; M S Keshavan; C R Genovese; W F Eddy; J A Sweeney
Journal:  Neuroimage       Date:  2001-05       Impact factor: 6.556

2.  Improved optimization for the robust and accurate linear registration and motion correction of brain images.

Authors:  Mark Jenkinson; Peter Bannister; Michael Brady; Stephen Smith
Journal:  Neuroimage       Date:  2002-10       Impact factor: 6.556

3.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 4.  Neuroimaging studies of working memory: a meta-analysis.

Authors:  Tor D Wager; Edward E Smith
Journal:  Cogn Affect Behav Neurosci       Date:  2003-12       Impact factor: 3.282

5.  Robust group analysis using outlier inference.

Authors:  Mark Woolrich
Journal:  Neuroimage       Date:  2008-03-06       Impact factor: 6.556

6.  Developmental differences in sustained and transient activity underlying working memory.

Authors:  Shefali B Brahmbhatt; Desirée A White; Deanna M Barch
Journal:  Brain Res       Date:  2010-07-24       Impact factor: 3.252

7.  Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.

Authors:  Kathryn Eve Lewandowski; Vandana Shashi; Peggy M Berry; Thomas R Kwapil
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2007-01-05       Impact factor: 3.568

8.  Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion Syndrome.

Authors:  Edith M Jolin; Ronald A Weller; Naushad R Jessani; Elaine H Zackai; Donna M McDonald-McGinn; Elizabeth B Weller
Journal:  J Affect Disord       Date:  2009-03-09       Impact factor: 4.839

9.  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
Journal:  J Child Neurol       Date:  2004-05       Impact factor: 1.987

Review 10.  Velo-cardio-facial syndrome: 30 Years of study.

Authors:  Robert J Shprintzen
Journal:  Dev Disabil Res Rev       Date:  2008
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