Literature DB >> 22958432

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

Heather M Shapiro1, Yukari Takarae, Danielle J Harvey, Margarita H Cabaral, Tony J Simon.   

Abstract

BACKGROUND: Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megabase deletion on the long arm of chromosome 22 and occurs in approximately 1 in 4000 live births. Previous studies indicate that children with 22q11.2DS are impaired on tasks involving spatial attention. However, the degree to which these impairments are due to volitionally generated (endogenous) or reflexive (exogenous) orienting of attention is unclear. Additionally, the efficacy of these component attention processes throughout child development in 22q11.2DS has yet to be examined.
METHODS: Here we compared the performance of a wide age range (7 to 14 years) of children with 22q11.2DS to typically developing (TD) children on a comprehensive visual cueing paradigm to dissociate the contributions of endogenous and exogenous attentional impairments. Paired and two-sample t-tests were used to compare outcome measures within a group or between groups. Additionally, repeated measures regression models were fit to the data in order to examine effects of age on performance.
RESULTS: We found that children with 22q11.2DS were impaired on a cueing task with an endogenous cue, but not on the same task with an exogenous cue. Additionally, it was younger children exclusively who were impaired on endogenous cueing when compared to age-matched TD children. Older children with 22q11.2DS performed comparably to age-matched TD peers on the endogenous cueing task.
CONCLUSIONS: These results suggest that endogenous but not exogenous orienting of attention is selectively impaired in children with 22q11.2DS. Additionally, the age effect on cueing in children with 22q11.2DS suggests a possible altered developmental trajectory of endogenous cueing.

Entities:  

Year:  2012        PMID: 22958432      PMCID: PMC3374293          DOI: 10.1186/1866-1955-4-5

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


  46 in total

1.  Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome.

Authors:  Joel P Bish; Renee Chiodo; Victoria Mattei; Tony J Simon
Journal:  Brain Cogn       Date:  2007-05-11       Impact factor: 2.310

2.  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
Journal:  Biol Psychiatry       Date:  2001-04-15       Impact factor: 13.382

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

Authors:  Linda E Campbell; Eileen Daly; Fiona Toal; Angela Stevens; Rayna Azuma; Marco Catani; Virginia Ng; Therese van Amelsvoort; Xavier Chitnis; William Cutter; Declan G M Murphy; Kieran C Murphy
Journal:  Brain       Date:  2006-03-28       Impact factor: 13.501

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

Authors:  T van Amelsvoort; E Daly; D Robertson; J Suckling; V Ng; H Critchley; M J Owen; J Henry; K C Murphy; D G Murphy
Journal:  Br J Psychiatry       Date:  2001-05       Impact factor: 9.319

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

Authors:  Joel Stoddard; Laurel Beckett; Tony J Simon
Journal:  J Neurodev Disord       Date:  2010-12-23       Impact factor: 4.025

6.  Rethinking attentional development: reflexive and volitional orienting in children and adults.

Authors:  Jelena Ristic; Alan Kingstone
Journal:  Dev Sci       Date:  2009-03

7.  Bisecting the mental number line in near and far space.

Authors:  Matthew R Longo; Stella F Lourenco
Journal:  Brain Cogn       Date:  2009-12-01       Impact factor: 2.310

8.  Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome.

Authors:  Therese van Amelsvoort; Jayne Henry; Robin Morris; Michael Owen; Don Linszen; Kieran Murphy; Declan Murphy
Journal:  Schizophr Res       Date:  2004-10-01       Impact factor: 4.939

Review 9.  Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.

Authors:  Bert De Smedt; Ann Swillen; Lieven Verschaffel; Pol Ghesquière
Journal:  Dev Disabil Res Rev       Date:  2009

10.  Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome.

Authors:  Tony J Simon; Zhongle Wu; Brian Avants; Hui Zhang; James C Gee; Glenn T Stebbins
Journal:  Behav Brain Funct       Date:  2008-06-17       Impact factor: 3.759

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  13 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.  Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology.

Authors:  Ashley F P Sanders; Diana A Hobbs; David D Stephenson; Robert D Laird; Elliott A Beaton
Journal:  J Autism Dev Disord       Date:  2017-04

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

5.  A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation.

Authors:  Ling M Wong; Naomi J Goodrich-Hunsaker; Yingratana A McLennan; Flora Tassone; Susan M Rivera; Tony J Simon
Journal:  J Neurodev Disord       Date:  2014-12-11       Impact factor: 4.025

6.  A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome.

Authors:  Heather M Shapiro; Ling M Wong; Tony J Simon
Journal:  Front Psychiatry       Date:  2013-08-07       Impact factor: 4.157

Review 7.  22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.

Authors:  Chiara Squarcione; Maria Chiara Torti; Fabio Di Fabio; Massimo Biondi
Journal:  Neuropsychiatr Dis Treat       Date:  2013-12-04       Impact factor: 2.570

8.  The Importance of Understanding Individual Differences of Emotion Regulation Abilities in 22q11.2 Deletion Syndrome.

Authors:  L E Campbell; L Swaab; E E Freeman; L McCormack; T J Simon; K Angkustsiri; K L McCabe
Journal:  J Autism Dev Disord       Date:  2021-07-12

9.  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.  Seeing Eye to Eye With Threat: Atypical Threat Bias in Children With 22q11.2 Deletion Syndrome.

Authors:  Abbie M Popa; Joshua R Cruz; Ling M Wong; Danielle J Harvey; Kathleen Angkustsiri; Ingrid N Leckliter; Koraly Perez-Edgar; Tony J Simon
Journal:  Am J Intellect Dev Disabil       Date:  2019-11
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