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An Association Study Between Genetic Polymorphisms in Functional Regions of Five Genes and the Risk of Schizophrenia

机译:五个基因功能区遗传多态性与精神分裂症风险的相关性研究

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Schizophrenia is a severe mental disorder that is likely to be strongly determined by genetic factors. To identify markers of disks, large homolog 2 (DLG2), FAT atypical cadherin 3 (FAT3), kinectin1 (KTN1), deleted in colorectal carcinoma (DCC), and glycogen synthase kinase-3 beta (GSK3 beta) that contribute to the genetic susceptibility to schizophrenia, we systematically screened for polymorphisms in the functional regions of these genes. A total of 22 functional single-nucleotide polymorphisms (SNPs) in 940 Chinese subjects were genotyped using SNaPshot. The results first suggested that the allelic and genotypic frequencies of the DCC polymorphism rs2229080 were nominally associated with schizophrenia. The patients were significantly less likely to be CC homozygous (P = 0.005, odds ratio [OR] = 0.635, 95 % confidence interval [95 % CI] = 0.462-0.873), and the schizophrenia subjects exhibited lower frequency of the C allele (P = 0.024, OR = 0.811, 95 % CI = 0.676-0.972). Regarding GSK3 beta, there was a significant difference in genotype distribution of rs3755557 between schizophrenia and healthy control subjects (P = 0.009). The patients exhibited a significantly lower frequency of the T allele of rs3755557 (P = 0.002, OR = 0.654, 95 % CI = 0.498-0.860). Our results point to the polymorphisms of DCC and GSK3 beta as contributors to the genetic basis of individual differences in the susceptibility to schizophrenia.
机译:精神分裂症是一种严重的精神障碍,很可能由遗传因素强烈决定。要识别磁盘标记,大同系物2(DLG2),FAT非典型钙黏着蛋白3(FAT3),kinectin1(KTN1)(在结直肠癌(DCC)中删除)和糖原合酶激酶3 beta(GSK3 beta)有助于遗传对精神分裂症的易感性,我们系统地筛选了这些基因功能区域的多态性。使用SNaPshot对940名中国受试者的22个功能性单核苷酸多态性(SNP)进行基因分型。结果首先表明,DCC多态性rs2229080的等位基因和基因型频率与精神分裂症相关。患者出现CC纯合子的可能性显着降低(P = 0.005,优势比[OR] = 0.635,95%置信区间[95%CI] = 0.462-0.873),精神分裂症患者的C等位基因频率较低( P = 0.024,OR = 0.811,95%CI = 0.676-0.972)。关于GSK3 beta,精神分裂症患者与健康对照组的rs3755557基因型分布存在显着差异(P = 0.009)。患者显示出rs3755557的T等位基因的频率明显降低(P = 0.002,OR = 0.654,95%CI = 0.498-0.860)。我们的结果指出,DCC和GSK3 beta的多态性是导致精神分裂症易感性个体差异的遗传基础的原因。

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