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Polymorphisms of the TCF4 Gene Are Associated With the Risk of Schizophrenia in the Han Chinese

机译:TCF4基因的多态性与汉族中精神分裂症的风险有关

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Schizophrenia (SCZ) is a complex and severe mental disorder with highly heritability (80%). Several large genome-wide association studies have identified that the transcription factor 4 (TCF4) polymorphisms were strongly associated with SCZ. Therefore, the present study was to replicate the potential relationships between the TCF4 polymorphisms and SCZ. Furthermore, the study also investigated whether other variants were associated with SCZ in the Han Chinese. We conducted a case-control study including 499 patients and 500 healthy controls. Five SNPs were successfully genotyped and evaluated the association with SCZ by using chi(2) test and genetic model analysis. We found that the genotype "AG" of rs9320010 and "GA" of rs7235757 decreased SCZ risk (OR = 0.70, 95% CI = 0.50-0.99, P = 0.041; OR = 0.69, 95% CI = 0.49-0.97, P = 0.034, respectively). In the genetic model analysis, we also observed that the allele "A" of rs9320010 and "G" of rs7235757 were inversely related with the risk of SCZ in the dominant model (OR = 0.72, 95% CI = 0.52-0.98, P = 0.039; OR = 0.69, 95% CI = 0.50-0.96, P = 0.025, respectively). Further interaction and stratification analysis suggested that rs1452787 was notably correlated with increased SCZ risk in males (OR = 2.77, 95% CI = 1.43-5.35, P = 0.002). Our study indicated that rs9320010, rs7235757, and rs1452787 were prominently associated with SCZ. Further studies are required to verify our findings and focus on determining the biological functions of the SNPs. (C) 2016 Wiley Periodicals, Inc.
机译:精神分裂症(SCZ)是一种复杂,严重的精神障碍,具有高度遗传(80%)。若干大型基因组关联研究已经确定转录因子4(TCF4)多态性与SCZ强烈相关。因此,本研究是复制TCF4多态性和SCZ之间的潜在关系。此外,研究还研究了汉族中的其他变体是否与SCZ相关联。我们进行了一个病例对照研究,包括499名患者和500例健康对照。通过使用CHI(2)试验和遗传模型分析,成功基因分型和评估了与SCZ的关联。我们发现RS9320010的基因型“AG”和RS7235757的“GA”降低了SCZ风险(或= 0.70,95%CI = 0.50-0.99,P = 0.041;或= 0.69,95%CI = 0.49-0.97,P = 0.034分别)。在遗传模型分析中,我们还观察到RS9320010的等位基因“A”为RS7235757的rs7235757与主导模型中SCZ的风险相反(或= 0.72,95%CI = 0.52-0.98,P = 0.039;或= 0.69,95%CI = 0.50-0.96,P = 0.025)。进一步的相互作用和分层分析表明,RS1452787的rs1452787与雄性的SCZ风险增加(或= 2.77,95%CI = 1.43-5.35,P = 0.002)。我们的研究表明,RS9320010,RS7235757和RS1452787突出与SCZ相关联。需要进一步的研究来验证我们的调查结果并专注于确定SNP的生物学功能。 (c)2016 Wiley期刊,Inc。

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