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

被引:25
作者
Hoogendoorn, Mechteld L. C. [1 ]
Vorstman, Jacob A. S. [1 ,3 ]
Jalali, Gholam R. [3 ]
Selten, Jean-Paul [1 ]
Sinke, Richard J. [2 ]
Emanuel, Beverly S. [3 ]
Kahn, Rene S. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Psychiat, Rudolf Magnus Inst Neurosci, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Biomed Genet, Complex Genet Sect, NL-3584 CG Utrecht, Netherlands
[3] Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
关键词
22q11 deletion syndrome; 22q11DS; schizophrenia; VCFS; deficit syndrome; prevalence;
D O I
10.1016/j.schres.2007.09.025
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
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 similar to 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. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 88
页数:5
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