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首页> 外文期刊>Biological psychiatry >Association of COL25A1 with comorbid antisocial personality disorder and substance dependence
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Association of COL25A1 with comorbid antisocial personality disorder and substance dependence

机译:COL25A1与合并性反社会人格障碍和物质依赖的关联

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摘要

Background: Antisocial personality disorder (ASPD) is a psychiatric disorder characterized by a long-term pattern of manipulating, exploiting, or violating the rights of others. Methods: Subjects ascertained for genetic studies of substance dependence (SD) and diagnosed with ASPD and comorbid SD were included in a two-stage genetic association study. In the discovery stage, 627 single nucleotide polymorphisms (SNPs) located in 179 candidate genes for addiction were analyzed in a case-control cohort and family-based cohort. The significant findings were replicated in an independent case-control cohort. Results: One SNP, rs13134663, in the collagen XXV alpha 1 gene (COL25A1) was significantly associated with ASPD in both African Americans and European Americans (smallest p values were.0002 and.0004, respectively). There was also evidence of association with the same SNP in independent samples of African American and European American cases and control subjects (p =.035 and.033, respectively). Analysis of the combined set of case-control subjects yielded an allelic p value of 9 × 10 -6 with odds ratio (95% confidence interval) of 1.3 (1.16, 1.47) (smallest p = 1 × 10 -7; Bonferroni threshold p =.00012). Conclusions: The COL25A1 gene, located at chromosome 4q25, encodes the collagen-like Alzheimer amyloid plaque component precursor, a type II transmembrane protein specifically expressed in neurons; it co-localizes with amyloid β in senile plaques in Alzheimer disease brains. This SNP maps to the transcription factor binding site and is conserved in 17 vertebrates, including mice and rats. Our findings suggest that COL25A1 may be associated with ASPD, especially in the context of SD.
机译:背景:反社会人格障碍(ASPD)是一种精神病性疾病,其特征是长期操纵,剥削或侵犯他人权利的模式。方法:确定为药物依赖性(SD)遗传研究并诊断为ASPD和合并症SD的受试者包括在两阶段遗传关联研究中。在发现阶段,在病例对照队列和基于家庭的队列中分析了179个成瘾候选基因中的627个单核苷酸多态性(SNP)。重大发现被复制到一个独立的病例对照队列中。结果:在非洲裔美国人和欧洲裔美国人中,胶原蛋白XXV alpha 1基因(COL25A1)中的一个SNP rs13134663与ASPD显着相关(最小p值分别为.0002和.0004)。在非裔美国人和欧洲人的病例以及对照受试者的独立样本中,也有证据表明同一SNP具有相关性(分别为p = .035和.033)。对病例对照受试者组合的分析得出等位基因p值为9×10 -6,比值比(95%置信区间)为1.3(1.16,1.47)(最小p = 1×10 -7; Bonferroni阈值p = .00012)。结论:位于染色体4q25的COL25A1基因编码胶原蛋白样的阿尔茨海默氏淀粉样斑块成分前体,是一种在神经元中特异性表达的II型跨膜蛋白。它与阿尔茨海默氏病大脑中老年斑中的淀粉样蛋白β共同定位。该SNP映射到转录因子结合位点,并且在包括小鼠和大鼠在内的17个脊椎动物中被保守。我们的发现表明,COL25A1可能与ASPD相关,尤其是在SD的情况下。

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