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促肾上腺皮质激素释放激素受体2基因与惊恐障碍之间不存在关联。

Lack of association between the corticotrophin-releasing hormone receptor 2 gene and panic disorder.

作者信息

Tharmalingam Subi, King Nicole, De Luca Vincenzo, Rothe Claudia, Koszycki Diana, Bradwejn Jacques, Macciardi Fabio, Kennedy James L

机构信息

Neurogenetics Section, Centre for Addiction and Mental Health, University of Toronto, Canada.

出版信息

Psychiatr Genet. 2006 Jun;16(3):93-7. doi: 10.1097/01.ypg.0000218610.45441.c3.

Abstract

Panic disorder is classified as an anxiety disorder and affects 1-3% of the population. An individual suffering from such a disorder may experience unexpected recurrent panic attacks and fear of future attacks. Twin and family studies have pointed towards a strong heritability of the disorder. Stress response and anxiety are thought to be mediated, at least in part, by the corticotrophin-releasing hormone (CRH), which is known to be a regulator of the hypothalamic-pituitary-adrenal pathway. To search for markers conferring genetic susceptibility to panic disorder, we typed three polymorphisms of the CRHR2 gene - CRHR2(CA), CRHR2(GT), and CRHR2(GAT) - in 466 individuals, 183 of whom had DSM-IV panic disorder. Seventy-five case-controls and 101 triad families plus 13 siblings were examined. Case-control association analyses using chi(2) tests yielded no difference in the distribution of the alleles. Linkage analysis using the Transmission Disequilibrium Test showed no preferential transmission of alleles for any of the three markers. Haplotype analysis indicated that allele 7 of CRHR2 (GAT) and 8 of CRHR2 (GT) are in almost complete linkage disequilibrium (P = 0.000 000 1). Although both neurobiology and chromosomal location point to the CHRH2 receptor gene as a candidate for panic disorder, our study indicates that the CRHR2 polymorphisms examined do not confer susceptibility to panic disorder. Further studies investigating additional polymorphisms in this gene and other components of the CRH signalling system may prove useful.

摘要

惊恐障碍被归类为焦虑症,影响着1%至3%的人口。患有这种障碍的个体可能会经历意外的反复惊恐发作,并对未来的发作感到恐惧。双胞胎和家族研究表明这种障碍具有很强的遗传性。应激反应和焦虑被认为至少部分是由促肾上腺皮质激素释放激素(CRH)介导的,已知CRH是下丘脑 - 垂体 - 肾上腺途径的调节因子。为了寻找赋予惊恐障碍遗传易感性的标记物,我们对466名个体的促肾上腺皮质激素释放激素受体2(CRHR2)基因的三个多态性——CRHR2(CA)、CRHR2(GT)和CRHR2(GAT)进行了分型,其中183人患有DSM-IV惊恐障碍。研究了75个病例对照和101个三联体家庭以及13对兄弟姐妹。使用卡方检验的病例对照关联分析显示等位基因分布没有差异。使用传递不平衡检验的连锁分析表明,这三个标记物中的任何一个都没有等位基因的优先传递。单倍型分析表明,CRHR2(GAT)的等位基因7和CRHR2(GT)的等位基因8几乎完全连锁不平衡(P = 0.000 000 1)。尽管神经生物学和染色体定位都表明CHRH2受体基因是惊恐障碍的候选基因,但我们的研究表明,所检测的CRHR2多态性不会赋予惊恐障碍易感性。进一步研究该基因和CRH信号系统其他成分的额外多态性可能会有所帮助。

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