Genome-wide association study of panic disorder in the Japanese population

被引:83
作者
Otowa, Takeshi [2 ]
Yoshida, Eiji [3 ]
Sugaya, Nagisa [3 ]
Yasuda, Shin [3 ,4 ]
Nishimura, Yukika [5 ]
Inoue, Ken [6 ]
Tochigi, Mamoru [2 ]
Umekage, Tadashi [1 ]
Miyagawa, Taku [7 ]
Nishida, Nao [7 ]
Tokunaga, Katsushi [7 ]
Tanii, Hisashi [5 ]
Sasaki, Tsukasa [1 ]
Kaiya, Hisanobu [3 ,4 ]
Okazaki, Yuji [8 ]
机构
[1] Univ Tokyo, Hlth Serv Ctr, Sect Mental Hlth, Tokyo 1138655, Japan
[2] Univ Tokyo, Dept Neuropsychiat, Grad Sch Med, Tokyo 1138655, Japan
[3] Akasaka Mental Clin, Outpatient Clin Anxiety Disorders, Tokyo, Japan
[4] Nagoya Mental Clin, Res Ctr Pan Disorder, Nagoya, Aichi, Japan
[5] Mie Univ, Dept Neuropsychiat, Grad Sch Med, Tsu, Mie 514, Japan
[6] Fujita Hlth Univ, Sch Med, Dept Publ Hlth, Aichi, Japan
[7] Univ Tokyo, Grad Sch Med, Dept Human Genet, Tokyo 1138655, Japan
[8] Tokyo Metropolitan Matsuzawa Hosp, Dept Neurol, Tokyo, Japan
关键词
BRLMM; genome-wide association study; Japanese; panic disorder; 500K SNP chip; RECEPTOR GENE POLYMORPHISM; FREQUENCY; GENOTYPE; POWER;
D O I
10.1038/jhg.2008.17
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Panic disorder (PD) is an anxiety disorder characterized by panic attacks and anticipatory anxiety. Although a number of association studies have been conducted, no gene has been identified as a susceptibility locus. In this study, we conducted a genome-wide association study of PD in 200 Japanese patients and the same number of controls, using the GeneChip Human Mapping 500 K Array Set. Genotypes were determined using the Bayesian Robust Linear Model with Mahalanobis (BRLMM) genotype calling algorithm. The genotype data were data-cleaned using criteria for SNP call rate (>= 95%), Hardy-Weinberg equilibrium (P >= 0.1%) and minor allele frequency (>= 5%). The significance level of the allele P-value was set at 1.0 x 10(-6), to make false discovery rate (FDR) <0.05. As a result, seven SNPs were significantly associated with PD, which were located in or adjacent to genes including PKP1, PLEKHG1, TMEM16B, CALCOCO1, SDK2 and CLU (or APO-J). Studies with other samples are required to confirm the results.
引用
收藏
页码:122 / 126
页数:5
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