Evidence of AS3MTd2d3-Associated Variants within 10q24.32-33 in the Genetic Risk of Major Affective Disorders.

Molecular Neuropsychiatry Pub Date : 2017-02-01 Epub Date: 2016-12-14 DOI:10.1159/000452998
Lingyi Li, Hong Chang, Tao Peng, Ming Li, Xiao Xiao
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引用次数: 16

Abstract

Genome-wide association studies suggest that 10q24.32-33 is a risk region for schizophrenia (SCZ). Considering the substantial genetic overlap between SCZ and major affective disorders, we would like to investigate whether the 10q24.32-33 region confers risk of affective disorders. We chose three SCZ genome-wide significant SNPs (rs7914558, rs7085104, and rs11191580) in 10q24.32-33 and collected the statistical data from European and Asian populations to perform systematic meta-analyses, which finally included up to 26,413 cases with affective disorders and 24,849 controls. Meta-analyses showed that all SNPs were nominally associated with major affective disorders. Considering the a priori evidence that these SNPs were associated with the expression of AS3MTd2d3 isoform in the human brain, our data confirms the potential involvement of AS3MTd2d3 in the genetic risk of major affective disorders.

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10q24.32-33内as3mtd2d3相关变异与主要情感障碍遗传风险的证据
全基因组关联研究表明,10q24.32-33是精神分裂症(SCZ)的危险区域。考虑到SCZ与主要情感性障碍之间存在大量的遗传重叠,我们想研究10q24.32-33区域是否具有情感性障碍的风险。我们在10q24.32-33中选择了三个SCZ全基因组显著snp (rs7914558、rs7085104和rs11191580),并收集了欧洲和亚洲人群的统计数据进行系统荟萃分析,最终包括多达26,413例情感性障碍患者和24,849例对照。荟萃分析显示,所有snp在名义上都与主要情感障碍有关。考虑到这些snp与AS3MTd2d3亚型在人脑中的表达相关的先验证据,我们的数据证实了AS3MTd2d3可能参与主要情感障碍的遗传风险。
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