Literature DB >> 17964762

Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia.

Mechteld L C Hoogendoorn1, Jacob A S Vorstman, Gholam R Jalali, Jean-Paul Selten, Richard J Sinke, Beverly S Emanuel, René S Kahn.   

Abstract

UNLABELLED: The objectives of this study were 1) to examine whether the prevalence of 22q11.2 deletion syndrome (22q11DS) in schizophrenia patients with the Deficit syndrome is higher than the reported approximately 2% for the population of schizophrenia patients as a whole, and 2) to estimate the overall prevalence of 22q11DS among schizophrenia patients by combining all available studies. Our sample, enriched for patients with the Deficit syndrome, had 88% power to detect an estimated prevalence of 5% of 22q11.2 deletions. No 22q11.2 deletions were detected in 311 schizophrenia patients, 146 of whom met criteria for the Deficit syndrome. Our literature research revealed that in eight studies sixteen deletions were identified in 2133 patients with schizophrenia. This corresponds to a prevalence of 0.75% (95%CI: 0.5%-1.2%). IN
CONCLUSION: The prevalence of 22q11.2DS in schizophrenia patients with the Deficit syndrome is not higher than in the population of schizophrenia patients as a whole. The prevalence of 22q11.2DS in schizophrenia patients is lower than the frequently reported prevalence of 2% or more.

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Year:  2007        PMID: 17964762      PMCID: PMC2810966          DOI: 10.1016/j.schres.2007.09.025

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


  31 in total

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Authors:  S I Usiskin; R Nicolson; D M Krasnewich; W Yan; M Lenane; M Wudarsky; S D Hamburger; J L Rapoport
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1999-12       Impact factor: 8.829

Review 2.  Childhood-onset schizophrenia: research update.

Authors:  S Kumra; M Shaw; P Merka; E Nakayama; R Augustin
Journal:  Can J Psychiatry       Date:  2001-12       Impact factor: 4.356

3.  A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients.

Authors:  Anat Horowitz; Sagiv Shifman; Nechama Rivlin; Anne Pisanté; Ariel Darvasi
Journal:  Schizophr Res       Date:  2005-03-01       Impact factor: 4.939

4.  Family characteristics of deficit and nondeficit schizophrenia in the Roscommon Family Study.

Authors:  B Kirkpatrick; D E Ross; D Walsh; L Karkowski; K S Kendler
Journal:  Schizophr Res       Date:  2000-09-29       Impact factor: 4.939

5.  The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

Authors:  Jacob A S Vorstman; Monique E J Morcus; Sasja N Duijff; Petra W J Klaassen; Josien A Heineman-de Boer; Frits A Beemer; Hanna Swaab; René S Kahn; Herman van Engeland
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2006-09       Impact factor: 8.829

6.  Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.

Authors:  T H Shaikh; H Kurahashi; S C Saitta; A M O'Hare; P Hu; B A Roe; D A Driscoll; D M McDonald-McGinn; E H Zackai; M L Budarf; B S Emanuel
Journal:  Hum Mol Genet       Date:  2000-03-01       Impact factor: 6.150

7.  Screening for 22q11 deletions in a schizophrenia population.

Authors:  T Arinami; T Ohtsuki; K Takase; H Shimizu; T Yoshikawa; H Horigome; J Nakayama; M Toru
Journal:  Schizophr Res       Date:  2001-12-01       Impact factor: 4.939

Review 8.  A separate disease within the syndrome of schizophrenia.

Authors:  B Kirkpatrick; R W Buchanan; D E Ross; W T Carpenter
Journal:  Arch Gen Psychiatry       Date:  2001-02

9.  Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia.

Authors:  Hui Liu; Simon C Heath; Christina Sobin; J Louw Roos; Brandi L Galke; Maude L Blundell; Marge Lenane; Brian Robertson; Ellen M Wijsman; Judith L Rapoport; Joseph A Gogos; Maria Karayiorgou
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

10.  Neuropsychiatric disorders in the 22q11 deletion syndrome.

Authors:  L Niklasson; P Rasmussen; S Oskarsdóttir; C Gillberg
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

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  19 in total

1.  Clinically detectable copy number variations in a Canadian catchment population of schizophrenia.

Authors:  Anne S Bassett; Gregory Costain; Wai Lun Alan Fung; Kathryn J Russell; Laura Pierce; Ronak Kapadia; Ronald F Carter; Eva W C Chow; Pamela J Forsythe
Journal:  J Psychiatr Res       Date:  2010-11       Impact factor: 4.791

Review 2.  Schizopsychotic symptom-profiles and biomarkers: beacons in diagnostic labyrinths.

Authors:  Tomas Palomo; Richard M Kostrzewa; Richard J Beninger; Trevor Archer
Journal:  Neurotox Res       Date:  2008-10       Impact factor: 3.911

3.  Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome.

Authors:  Jacob A S Vorstman; Eva W Chow; Roel A Ophoff; Herman van Engeland; Frits A Beemer; René S Kahn; Richard J Sinke; Anne S Bassett
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-04-05       Impact factor: 3.568

4.  Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

Authors:  Jacobine E Buizer-Voskamp; Jan-Willem Muntjewerff; Eric Strengman; Chiara Sabatti; Hreinn Stefansson; Jacob A S Vorstman; Roel A Ophoff
Journal:  Biol Psychiatry       Date:  2011-04-13       Impact factor: 13.382

Review 5.  Clinical perspectives on the genetics of schizophrenia: a bottom-up orientation.

Authors:  Willem M A Verhoeven; Siegfried Tuinier
Journal:  Neurotox Res       Date:  2008-10       Impact factor: 3.911

6.  Psychotic features as the first manifestation of 22q11.2 deletion syndrome.

Authors:  So Dahm Kook; Suk Kyoon An; Kyung Ran Kim; Woo Jung Kim; Eun Lee; Kee Namkoong
Journal:  Psychiatry Investig       Date:  2010-02-19       Impact factor: 2.505

7.  Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India.

Authors:  Ashutosh Halder; Manish Jain; Isha Chaudhary; Madhulika Kabra
Journal:  BMC Med Genet       Date:  2010-06-23       Impact factor: 2.103

8.  High rate of disease-related copy number variations in childhood onset schizophrenia.

Authors:  K Ahn; N Gotay; T M Andersen; A A Anvari; P Gochman; Y Lee; S Sanders; S Guha; A Darvasi; J T Glessner; H Hakonarson; T Lencz; M W State; Y Y Shugart; J L Rapoport
Journal:  Mol Psychiatry       Date:  2013-05-21       Impact factor: 15.992

9.  A genome-wide investigation of SNPs and CNVs in schizophrenia.

Authors:  Anna C Need; Dongliang Ge; Michael E Weale; Jessica Maia; Sheng Feng; Erin L Heinzen; Kevin V Shianna; Woohyun Yoon; Dalia Kasperaviciūte; Massimo Gennarelli; Warren J Strittmatter; Cristian Bonvicini; Giuseppe Rossi; Karu Jayathilake; Philip A Cola; Joseph P McEvoy; Richard S E Keefe; Elizabeth M C Fisher; Pamela L St Jean; Ina Giegling; Annette M Hartmann; Hans-Jürgen Möller; Andreas Ruppert; Gillian Fraser; Caroline Crombie; Lefkos T Middleton; David St Clair; Allen D Roses; Pierandrea Muglia; Clyde Francks; Dan Rujescu; Herbert Y Meltzer; David B Goldstein
Journal:  PLoS Genet       Date:  2009-02-06       Impact factor: 5.917

10.  Top-down or bottom-up: Contrasting perspectives on psychiatric diagnoses.

Authors:  Willem Ma Verhoeven; Siegfried Tuinier; Ineke van der Burgt
Journal:  Biologics       Date:  2008-09
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