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Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach

机译:分析精神分裂症的单核苷酸多态性:荟萃分析方法

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Background: Schizophrenia is a severe mental disorder affecting >21 million people worldwide. Some genetic studies reported that single nucleotide polymorphism (SNP) involving variant rs1344706 from the ZNF804A gene in human beings is associated with the risk of schizophrenia in several populations. Similar results tend to conflict with other reports in literature, indicating that no true significant association exists between rs1344706 and schizophrenia. We seek to determine the level of association of this SNP with schizophrenia in the Asian population using more recent genome-wide association study (GWAS) datasets. Methods: Applying a computational approach with inclusion of more recent GWAS datasets, we conducted a meta-analysis to examine the level of association of SNP rs1344706 and the risk of schizophrenia disorder among the Asian population constituting Chinese, Indonesians, Japanese, Kazakhs and Singaporeans. For a total of 21 genetic studies, including a total of 28,842 cases and 35,630 controls, regression analysis, publication bias, Cochran’s Q and I 2 tests were performed. The DerSimonian and Laird random-effects model was used to assess the association of the genetic variant to schizophrenia. Leave-one-out sensitivity analysis was also conducted to determine the influence of each study on the final outcome of the association study. Results: Our summarized analysis for Asian population revealed a pooled odds ratio of 1.06, 95% confidence interval of 1.01–1.11 and two-tailed P -value of 0.0228. Our test for heterogeneity showed the presence of large heterogeneity ( I 2=53.44%, P =0.00207) and Egger’s regression test ( P =0.8763) and Begg’s test ( P =0.8347), indicating no presence of publication bias among our selected studies. In our sensitivity analysis, 10 different studies comprising of ~50% of the entire study had an impact on our final results as each leave-one-out test became insignificant. Our result suggests that genetic variant rs1344706 might be associated with the development of schizophrenia in Asians.
机译:背景:精神分裂症是一种严重的精神障碍,全世界范围内有2100万人受到影响。一些遗传学研究报道,人类中涉及ZNF804A基因变异rs1344706的单核苷酸多态性(SNP)与若干人群的精神分裂症风险有关。类似的结果倾向于与文献中的其他报告相抵触,表明rs1344706与精神分裂症之间不存在真正的显着关联。我们试图确定使用较新的全基因组关联研究(GWAS)数据集在亚洲人口中此SNP与精神分裂症的关联水平。方法:采用包括最近的GWAS数据集在内的计算方法,我们进行了荟萃分析,以研究SNP rs1344706的关联水平和精神分裂症患病风险,该疾病构成了中国人,印度尼西亚人,日本人,哈萨克人和新加坡人的亚洲人群。总共进行了21项遗传研究,包括28,842例病例和35,630例对照,进行了回归分析,发表偏倚,Cochran Q和I 2 测试。 DerSimonian和Laird随机效应模型用于评估遗传变异与精神分裂症的关联。还进行了留一法敏感性分析,以确定每项研究对关联研究最终结果的影响。结果:我们对亚洲人群的汇总分析显示,混合比值比为1.06,95%置信区间为1.01-1.11,两尾P值为0.0228。我们的异质性测试显示存在较大的异质性(I 2 = 53.44%,P = 0.00207)和Egger回归测试(P = 0.8763)和Begg检验(P = 0.8347),表明不存在异质性在我们选择的研究中发表偏见。在我们的敏感性分析中,约占整个研究的50%的10项不同研究对我们的最终结果产生了影响,因为每次留一法测试都变得无关紧要。我们的结果表明,遗传变异rs1344706可能与亚洲人精神分裂症的发生有关。

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