Literature DB >> 21475729

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome.

Joel Stoddard, Laurel Beckett, Tony J Simon.   

Abstract

Impairment in the executive control of attention has been found in youth with chromosome 22q11.2 deletion syndrome (22q11.2DS). However, how this impairment is modified by other factors, particularly age, is unknown. Forty-six typically developing and 53 children with 22q11.2DS were tested with the attention networks task (ANT) in this cross-sectional study. We used logarithmic transform and linear modeling to assess age effects on the executive index of the ANT. Mixed modeling accounted for between subject variability, age, handedness, catecholamine-O-transferase (COMT; codon 158) genotype, and gender on performance for all experimental conditions (cue × flanker) and their two-level interactions. Children with 22q11.2DS showed a relative, age-dependent executive index impairment but not orienting or alerting network index impairments. In factorial analysis, age was a major predictor of overall performance. There was a significant effect of the 22q11.2DS on overall performance. Of note, children with 22q11.2DS are specifically vulnerable to incongruent flanker interference, especially at younger ages. We did not find an overall effect of COMT genotype or handedness. Children with 22q11.2DS demonstrated age-related impairment in the executive control of attention. Future investigation will likely reveal that there are different developmental trajectories of executive attentional function likely related to the development of schizophrenia in 22q11.2DS.

Entities:  

Keywords:  Attention networks task; Chromosome 22q11.2 deletion syndrome; Cognitive control

Year:  2010        PMID: 21475729      PMCID: PMC3056994          DOI: 10.1007/s11689-010-9070-3

Source DB:  PubMed          Journal:  J Neurodev Disord        ISSN: 1866-1947            Impact factor:   4.025


  45 in total

1.  Selective impairment of attentional networks of orienting and executive control in schizophrenia.

Authors:  Kai Wang; Jin Fan; Yi Dong; Chang-Qing Wang; Tatia M C Lee; Michael I Posner
Journal:  Schizophr Res       Date:  2005-10-15       Impact factor: 4.939

Review 2.  Anterior cingulate cortex and conflict detection: an update of theory and data.

Authors:  Cameron S Carter; Vincent van Veen
Journal:  Cogn Affect Behav Neurosci       Date:  2007-12       Impact factor: 3.282

3.  Prevalence of 22q11 microdeletion.

Authors:  S Tézenas Du Montcel; H Mendizabai; S Aymé; A Lévy; N Philip
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

Review 4.  22q11 deletion syndrome: a genetic subtype of schizophrenia.

Authors:  A S Bassett; E W Chow
Journal:  Biol Psychiatry       Date:  1999-10-01       Impact factor: 13.382

5.  Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

Authors:  A G Nackley; S A Shabalina; I E Tchivileva; K Satterfield; O Korchynskyi; S S Makarov; W Maixner; L Diatchenko
Journal:  Science       Date:  2006-12-22       Impact factor: 47.728

6.  Effect of catechol-O-methyltransferase val158met genotype on attentional control.

Authors:  Giuseppe Blasi; Venkata S Mattay; Alessandro Bertolino; Brita Elvevåg; Joseph H Callicott; Saumitra Das; Bhaskar S Kolachana; Michael F Egan; Terry E Goldberg; Daniel R Weinberger
Journal:  J Neurosci       Date:  2005-05-18       Impact factor: 6.167

Review 7.  A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.

Authors:  Tony J Simon; Joel P Bish; Carrie E Bearden; Lijun Ding; Samantha Ferrante; Vy Nguyen; James C Gee; Donna M McDonald-McGinn; Elaine H Zackai; Beverly S Emanuel
Journal:  Dev Psychopathol       Date:  2005

8.  Networks of attention in children with the 22q11 deletion syndrome.

Authors:  Christina Sobin; Karen Kiley-Brabeck; Sarah Daniels; Maude Blundell; Kwame Anyane-Yeboa; Maria Karayiorgou
Journal:  Dev Neuropsychol       Date:  2004       Impact factor: 2.253

9.  Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome.

Authors:  Yukari Takarae; Linda Schmidt; Flora Tassone; Tony J Simon
Journal:  Cogn Affect Behav Neurosci       Date:  2009-03       Impact factor: 3.282

10.  Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.

Authors:  M Woodin; P P Wang; D Aleman; D McDonald-McGinn; E Zackai; E Moss
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

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  10 in total

Review 1.  Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome.

Authors:  Kerri L Tang; Kevin M Antshel; Wanda P Fremont; Wendy R Kates
Journal:  J Dev Behav Pediatr       Date:  2015-10       Impact factor: 2.225

2.  A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome.

Authors:  Joel Stoddard; Yukari Takarae; Tony J Simon
Journal:  Schizophr Res       Date:  2012-01-14       Impact factor: 4.939

3.  Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.

Authors:  Ling M Wong; Tracy Riggins; Danielle Harvey; Margarita Cabaral; Tony J Simon
Journal:  Am J Intellect Dev Disabil       Date:  2014-03

4.  The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety.

Authors:  Julia A Scott; Naomi Goodrich-Hunsaker; Kristopher Kalish; Aaron Lee; Michael R Hunsaker; Cynthia M Schumann; Owen T Carmichael; Tony J Simon
Journal:  J Psychiatry Neurosci       Date:  2016-04       Impact factor: 6.186

Review 5.  Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Authors:  N Hiroi; T Takahashi; A Hishimoto; T Izumi; S Boku; T Hiramoto
Journal:  Mol Psychiatry       Date:  2013-08-06       Impact factor: 15.992

Review 6.  Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.

Authors:  Ann Swillen; Edward Moss; Sasja Duijff
Journal:  Am J Med Genet A       Date:  2018-04-25       Impact factor: 2.802

7.  A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome.

Authors:  Heather M Shapiro; Yukari Takarae; Danielle J Harvey; Margarita H Cabaral; Tony J Simon
Journal:  J Neurodev Disord       Date:  2012-02-15       Impact factor: 4.025

8.  The development of cognitive control in children with chromosome 22q11.2 deletion syndrome.

Authors:  Heather M Shapiro; Flora Tassone; Nimrah S Choudhary; Tony J Simon
Journal:  Front Psychol       Date:  2014-06-10

9.  Reduced fronto-temporal and limbic connectivity in the 22q11.2 deletion syndrome: vulnerability markers for developing schizophrenia?

Authors:  Marie-Christine Ottet; Marie Schaer; Leila Cammoun; Maude Schneider; Martin Debbané; Jean-Philippe Thiran; Stephan Eliez
Journal:  PLoS One       Date:  2013-03-22       Impact factor: 3.240

10.  Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes.

Authors:  Andrea I Quintero; Elliott A Beaton; Danielle J Harvey; Judith L Ross; Tony J Simon
Journal:  J Neurodev Disord       Date:  2014-03-14       Impact factor: 4.025

  10 in total

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