Literature DB >> 15823984

Gender-moderated dorsolateral prefrontal reductions in 22q11.2 Deletion Syndrome: implications for risk for schizophrenia.

Wendy R Kates1, Kevin Antshel, Rachael Willhite, Brandy A Bessette, Nuria AbdulSabur, Anne Marie Higgins.   

Abstract

To investigate the impact of the microdeletion on morphology of the prefrontal cortex in 22q11.2 Deletion Syndrome (22q11.2 DS), high-resolution, anatomic magnetic resonance imaging was performed on 19 children and adolescents with 22q11.2 DS (11 females, 8 males) and 18 unaffected controls (10 females, 8 males). Tissue volumes of the dorsolateral, dorsomedial, orbitolateral, and orbitomedial prefrontal cortex were measured. Tasks of executive function and working memory were administered to investigate the association between anatomy and function. Whole brain volume and frontal lobe tissue volume were preserved in girls but reduced in boys with 22q11.2 DS relative to age-matched controls. Dorsolateral prefrontal cortex (DLPFC) volumes were reduced in participants with 22q11.2 DS, although the gender-by-diagnosis effect found for frontal lobe was not as robust for DLPFC. DLPFC volumes were associated with performance on tasks of planning and emotional facial recognition. Longitudinal studies are needed to clarify whether gender differences in frontal lobe and DLPFC persist with development, and whether the volumes of the DLPFC are associated with eventual deterioration in adaptive/psychosocial function that may presage the onset of schizophrenia, for which individuals with 22q11.2 DS are at a disproportionately high risk.

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Year:  2005        PMID: 15823984     DOI: 10.1080/09297040590911211

Source DB:  PubMed          Journal:  Child Neuropsychol        ISSN: 0929-7049            Impact factor:   2.500


  13 in total

1.  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
Journal:  Schizophr Res       Date:  2014-07-25       Impact factor: 4.939

2.  Attentional functioning in individuals with 22q11 deletion syndrome: insight from ERPs.

Authors:  Daniela Mannarelli; Caterina Pauletti; Tommaso Accinni; Luca Carlone; Marianna Frascarelli; Guido Maria Lattanzi; Antonio Currà; Francesco Fattapposta
Journal:  J Neural Transm (Vienna)       Date:  2018-03-08       Impact factor: 3.575

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.  Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

Authors:  Kevin M Antshel; Alka Aneja; Leslie Strunge; Jena Peebles; Wanda P Fremont; Kimberly Stallone; Nuria Abdulsabur; Anne Marie Higgins; Robert J Shprintzen; Wendy R Kates
Journal:  J Autism Dev Disord       Date:  2006-12-19

5.  Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study.

Authors:  Wendy R Kates; Kevin M Antshel; Stephen V Faraone; Wanda P Fremont; Anne Marie Higgins; Robert J Shprintzen; Jo-Anna Botti; Lauren Kelchner; Christopher McCarthy
Journal:  Biol Psychiatry       Date:  2010-12-31       Impact factor: 13.382

Review 6.  Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Authors:  Daniel W Meechan; Thomas M Maynard; Eric S Tucker; Alejandra Fernandez; Beverly A Karpinski; Lawrence A Rothblat; Anthony-S LaMantia
Journal:  Prog Neurobiol       Date:  2015-04-09       Impact factor: 11.685

7.  Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study.

Authors:  Vandana Shashi; Aravindhan Veerapandiyan; Matcheri S Keshavan; Michael Zapadka; Kelly Schoch; Thomas R Kwapil; Stephen R Hooper; Jeffrey A Stanley
Journal:  Biol Psychiatry       Date:  2012-05-25       Impact factor: 13.382

8.  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

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

Authors:  Vandana Shashi; Thomas R Kwapil; Jessica Kaczorowski; Margaret N Berry; Cesar S Santos; Timothy D Howard; Dhruman Goradia; Konasale Prasad; Diwadkar Vaibhav; Rajaprabhakaran Rajarethinam; Edward Spence; Matcheri S Keshavan
Journal:  Psychiatry Res       Date:  2010-01-30       Impact factor: 3.222

10.  A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).

Authors:  Wendy R Kates; Kevin M Antshel; Nuria Abdulsabur; Deirdre Colgan; Birgit Funke; Wanda Fremont; Anne Marie Higgins; Raju Kucherlapati; Robert J Shprintzen
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2006-04-05       Impact factor: 3.568

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