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首页> 外文期刊>Depression and anxiety >ASSOCIATION STUDY BETWEEN GABA RECEPTOR GENES AND ANXIETY SPECTRUM DISORDERS
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ASSOCIATION STUDY BETWEEN GABA RECEPTOR GENES AND ANXIETY SPECTRUM DISORDERS

机译:GABA受体基因与焦虑谱疾病之间的关联研究

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摘要

Background: Human anxiety disorders are complex diseases with relatively unknown etiology. Dysfunction of the Gamma-aminobutyric acid (GABA) system has been implicated in many neuropsychiatric conditions, including anxiety and depressive disorders. In this investigation, we explored four GABA receptor genes for their possible associations with genetic risk for anxiety disorders and depression. Methods: Our study sample consisted of 589 cases and 539 controls selected from a large population-based twin registry based upon a latent genetic risk factor shared by several anxiety disorders, major depression, and neuroticism. We subjected these to a two-stage protocol, in which all candidate genetic markers were screened for association in stage I (N = 3 76), the positive results of which were tested for replication in stage 2 (N = 752). We analyzed data from 26 single nucleotide polymorphisms (SNPs) from four GABA receptor genes: GABRA2, GABRA3, GABRA6, and GABRG2. Results: Of the 26 SNPs genotyped in stage 1, we identified two markers in GABRA3 that met the threshold (P <=.1) to be tested in stage 2. Phenotypic associations of these two markers failed to replicate in stage 2. Conclusions: These findings suggest that common variation in the GABRA2, GABRA3, GABRA6, and GABRG2 genes does not play a major role in liability to anxiety spectrum disorders.
机译:背景:人类焦虑症是病因相对未知的复杂疾病。 γ-氨基丁酸(GABA)系统的功能障碍已牵涉到许多神经精神疾病,包括焦虑症和抑郁症。在这项研究中,我们探讨了四个GABA受体基因与焦虑症和抑郁症的遗传风险的可能关联。方法:我们的研究样本包括589例病例和539例对照者,这些病例是从大型人群为基础的双生子登记表中选取的,其基于潜在的遗传危险因素,并与多种焦虑症,重度抑郁症和神经质病共有。我们对它们进行了两个阶段的实验,其中在阶段I(N = 3 76)中筛选了所有候选遗传标记的关联性,并在阶段2(N = 752)中测试了其阳性结果的复制性。我们分析了来自四个GABA受体基因:GABRA2,GABRA3,GABRA6和GABRG2的26个单核苷酸多态性(SNP)的数据。结果:在第1阶段基因分型的26个SNP中,我们在GABRA3中鉴定出两个在第2阶段中达到阈值(P <=。1)的标记物。这两个标记物的表型关联在第2阶段中没有复制。结论:这些发现表明,GABRA2,GABRA3,GABRA6和GABRG2基因的共同变异在焦虑谱障碍的责任中不发挥主要作用。

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