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首页> 外文期刊>The world journal of biological psychiatry: the official journal of the World Federation of Societies of Biological Psychiatry >Do obsessive-compulsive disorder and Tourette syndrome share a common susceptibility gene? An association study of the BDNF Val66Met polymorphism in the Chinese Han population
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Do obsessive-compulsive disorder and Tourette syndrome share a common susceptibility gene? An association study of the BDNF Val66Met polymorphism in the Chinese Han population

机译:强迫症和图雷特综合征是否有共同的易感基因?中国汉族人群BDNF Val66Met多态性的关联研究

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Objectives. We explored the association between the BDNF Val66Met polymorphism and susceptibility to both obsessive-compulsive disorder (OCD) and Tourette syndrome (TS) in the Chinese Han population. Methods. Genotyping for the BDNF Val66Met polymorphism was performed in 321 OCD patients and 426 healthy control subjects and case-control association study data were analysed. Additionally, we evaluated the genetic contribution of this variant in 331 TS patients (including 267 TS trios) and 519 controls using the transmission disequilibrium test (TDT) and case-control study. Results. A statistically significant difference was found in the genetic contribution of the BDNF Val66Met polymorphism between both the OCD ((2) = 7.50, P = 0.023 by genotype; (2) = 6.67, P = 0.01 by allele) and TS ((2) = 6.76, P = 0.03 by genotype; (2) = 4.27, P = 0.04 by allele), and control groups. TDT and GHRR analysis for TS trios also showed a significant transform disequilibrium of this polymorphism (TDT: (2) = 3.96, P = 0.05; HHRR: (2) = 4.33 P = 0.04; GHRR: (2) = 5.74, P = 0.02; (2) = 0.98, P = 0.37). There was also a significant gender trend between patients and controls in female cases for OCD and in male cases for TS. Conclusions. Our study supports the involvement of the BDNF Val66Met polymorphism as a common genetic susceptibility for OCD and TS in the Chinese Han population, showing specific gender trends.
机译:目标。我们探讨了BDNF Val66Met多态性与中国汉族人群对强迫症(OCD)和图雷特综合征(TS)的敏感性之间的关联。方法。在321名强迫症患者和426名健康对照者中进行了BDNF Val66Met多态性的基因分型,并分析了病例对照研究数据。此外,我们使用传播不平衡测试(TDT)和病例对照研究评估了该变体在331名TS患者(包括267名TS三重奏)和519名对照中的遗传贡献。结果。 BDNF Val66Met多态性在OCD((2)= 7.50,基因型P = 0.023;(2)= 6.67,P = 0.01基因等位基因)和TS((2) = 6.76,按基因型P = 0.03;(2)= 4.27,按等位基因P = 0.04)和对照组。 TS三重奏的TDT和GHRR分析也显示了该多态性的显着转换不平衡(TDT:(2)= 3.96,P = 0.05; HHRR:(2)= 4.33 P = 0.04; GHRR:(2)= 5.74,P = 0.02;(2)= 0.98,P = 0.37)。对于OCD的女性病例和对于TS的男性病例,患者和对照之间也存在显着的性别趋势。结论。我们的研究支持BDNF Val66Met多态性作为中国汉族人群OCD和TS的常见遗传易感性的参与,显示出特定的性别趋势。

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