Literature DB >> 16753283

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.

Eva W C Chow1, Mark Watson, Donald A Young, Anne S Bassett.   

Abstract

OBJECTIVE: Schizophrenia is associated with neurocognitive deficits, but its etiologic heterogeneity may complicate the delineation of a neurocognitive profile. Schizophrenia associated with 22q11 Deletion Syndrome (22qDS) represents a more genetically homogeneous subtype for study. We hypothesized that in adults with 22qDS the neurocognitive profiles would differ between those with and without schizophrenia.
METHOD: Using a comprehensive battery of tests, we compared the neurocognitive performance profiles in those with schizophrenia (n=27; 14 M, 13 F; mean age=30.6 years, SD=7.7 years) and those with no history of psychosis (n=29; 16 M, 13 F; mean age=25.0 years, SD=9.0 years).
RESULTS: The 22qDS groups with and without schizophrenia had similar mean estimated IQ (71.6, SD=8.2 and 74.8, SD=6.1, respectively) and academic achievement, however the neurocognitive profiles of the two groups differed significantly on multivariate analysis (F(24,31)=2.25, p=0.017). The group with schizophrenia performed significantly more poorly on tests of motor skills, verbal learning, and social cognition (effect sizes>or=0.8) after correction for multiple comparisons. Other tests, but not the attentional measures used, showed nominally significant differences.
CONCLUSIONS: In adults with 22qDS, the pattern of neurocognitive differences between those with and without schizophrenia appears similar to that between patients with schizophrenia and controls. Attentional dysfunction may be a more general feature of 22qDS. The findings support 22qDS-schizophrenia as a genetic model for neurodevelopmental investigations of schizophrenia.

Entities:  

Mesh:

Year:  2006        PMID: 16753283      PMCID: PMC3127863          DOI: 10.1016/j.schres.2006.04.007

Source DB:  PubMed          Journal:  Schizophr Res        ISSN: 0920-9964            Impact factor:   4.939


  37 in total

Review 1.  Genetic insights into the neurodevelopmental hypothesis of schizophrenia.

Authors:  A S Bassett; E W Chow; S O'Neill; L M Brzustowicz
Journal:  Schizophr Bull       Date:  2001       Impact factor: 9.306

2.  Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

Authors:  E M Moss; M L Batshaw; C B Solot; M Gerdes; D M McDonald-McGinn; D A Driscoll; B S Emanuel; E H Zackai; P P Wang
Journal:  J Pediatr       Date:  1999-02       Impact factor: 4.406

3.  Cognitive functioning in stabilized first-episode psychosis patients.

Authors:  L A Townsend; A K Malla; R M Norman
Journal:  Psychiatry Res       Date:  2001-11-01       Impact factor: 3.222

4.  Implications of normal brain development for the pathogenesis of schizophrenia.

Authors:  D R Weinberger
Journal:  Arch Gen Psychiatry       Date:  1987-07

5.  Base rates of WAIS-R VIQ-PIQ differences in 1593 psychiatric inpatients.

Authors:  G L Iverson; T S Woodward; P Green
Journal:  J Clin Psychol       Date:  2001-12

6.  Velo-cardio-facial syndrome: language and psychological profiles.

Authors:  K J Golding-Kushner; G Weller; R J Shprintzen
Journal:  J Craniofac Genet Dev Biol       Date:  1985

7.  Stability and course of neuropsychological deficits in schizophrenia.

Authors:  R K Heaton; J A Gladsjo; B W Palmer; J Kuck; T D Marcotte; D V Jeste
Journal:  Arch Gen Psychiatry       Date:  2001-01

8.  Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome.

Authors:  D Gothelf; A Frisch; H Munitz; R Rockah; N Laufer; T Mozes; H Hermesh; A Weizman; M Frydman
Journal:  Schizophr Res       Date:  1999-01-11       Impact factor: 4.939

9.  Heterogeneity of schizophrenia: a study of individual neuropsychological profiles.

Authors:  William S Kremen; Larry J Seidman; Stephen V Faraone; Rosemary Toomey; Ming T Tsuang
Journal:  Schizophr Res       Date:  2004-12-01       Impact factor: 4.939

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

View more
  92 in total

1.  Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.

Authors:  G Costain; E W C Chow; P N Ray; A S Bassett
Journal:  J Intellect Disabil Res       Date:  2011-12-06

Review 2.  The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.

Authors:  Liam J Drew; Gregg W Crabtree; Sander Markx; Kimberly L Stark; Florence Chaverneff; Bin Xu; Jun Mukai; Karine Fenelon; Pei-Ken Hsu; Joseph A Gogos; Maria Karayiorgou
Journal:  Int J Dev Neurosci       Date:  2010-10-08       Impact factor: 2.457

Review 3.  The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

Authors:  Rachel K Jonas; Caroline A Montojo; Carrie E Bearden
Journal:  Biol Psychiatry       Date:  2013-08-28       Impact factor: 13.382

4.  Abnormalities in white matter tracts in the fronto-striatal-thalamic circuit are associated with verbal performance in 22q11.2DS.

Authors:  Carina Heller; Saskia Steinmann; James J Levitt; Nikos Makris; Kevin M Antshel; Wanda Fremont; Ioana L Coman; Stefan R Schweinberger; Thomas Weiß; Sylvain Bouix; Marek R Kubicki; Wendy R Kates; Zora Kikinis
Journal:  Schizophr Res       Date:  2020-10-23       Impact factor: 4.939

5.  The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.

Authors:  Christina Zaleski; Anne S Bassett; Karen Tam; Andrea L Shugar; Eva W C Chow; Elizabeth McPherson
Journal:  Am J Med Genet A       Date:  2009-03       Impact factor: 2.802

6.  Premature death in adults with 22q11.2 deletion syndrome.

Authors:  A S Bassett; E W C Chow; J Husted; K A Hodgkinson; E Oechslin; L Harris; C Silversides
Journal:  J Med Genet       Date:  2009-02-25       Impact factor: 6.318

Review 7.  Mitochondria in complex psychiatric disorders: Lessons from mouse models of 22q11.2 deletion syndrome: Hemizygous deletion of several mitochondrial genes in the 22q11.2 genomic region can lead to symptoms associated with neuropsychiatric disease.

Authors:  Prakash Devaraju; Stanislav S Zakharenko
Journal:  Bioessays       Date:  2017-01-03       Impact factor: 4.345

Review 8.  Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome.

Authors:  Matthew J Schreiner; Maria T Lazaro; Maria Jalbrzikowski; Carrie E Bearden
Journal:  Neuropharmacology       Date:  2012-10-23       Impact factor: 5.250

9.  Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?

Authors:  Kathleen Angkustsiri; Beth Goodlin-Jones; Lesley Deprey; Khyati Brahmbhatt; Susan Harris; Tony J Simon
Journal:  J Autism Dev Disord       Date:  2014-04

10.  Heritability of neurocognitive traits in familial schizophrenia.

Authors:  Janice A Husted; Sooyeol Lim; Eva W C Chow; Celia Greenwood; Anne S Bassett
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-09-05       Impact factor: 3.568

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.