Integrated Medical Science Department, CE Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.
Mol Psychiatry. 2012 Dec;17(12):1194-205. doi: 10.1038/mp.2011.183. Epub 2012 Jan 31.
Investigating and understanding gene-environment interaction (G × E) in a neurodevelopmentally and biologically plausible manner is a major challenge for schizophrenia research. Hypoxia during neurodevelopment is one of several environmental factors related to the risk of schizophrenia, and links between schizophrenia candidate genes and hypoxia regulation or vascular expression have been proposed. Given the availability of a wealth of complex genetic information on schizophrenia in the literature without knowledge on the connections to environmental factors, we now systematically collected genes from candidate studies (using SzGene), genome-wide association studies (GWAS) and copy number variation (CNV) analyses, and then applied four criteria to test for a (theoretical) link to ischemia-hypoxia and/or vascular factors. In all, 55% of the schizophrenia candidate genes (n=42 genes) met the criteria for a link to ischemia-hypoxia and/or vascular factors. Genes associated with schizophrenia showed a significant, threefold enrichment among genes that were derived from microarray studies of the ischemia-hypoxia response (IHR) in the brain. Thus, the finding of a considerable match between genes associated with the risk of schizophrenia and IHR and/or vascular factors is reproducible. An additional survey of genes identified by GWAS and CNV analyses suggested novel genes that match the criteria. Findings for interactions between specific variants of genes proposed to be IHR and/or vascular factors with obstetric complications in patients with schizophrenia have been reported in the literature. Therefore, the extended gene set defined here may form a reasonable and evidence-based starting point for hypothesis-based testing of G × E interactions in clinical genetic and translational neuroscience studies.
以神经发育和生物学合理的方式研究基因-环境相互作用(G×E)是精神分裂症研究的主要挑战。神经发育过程中的缺氧是与精神分裂症风险相关的几个环境因素之一,并且已经提出了精神分裂症候选基因与缺氧调节或血管表达之间的联系。鉴于文献中存在大量关于精神分裂症的复杂遗传信息,但缺乏与环境因素的关联知识,我们现在系统地从候选研究(使用 SzGene)、全基因组关联研究(GWAS)和拷贝数变异(CNV)分析中收集基因,然后应用四项标准来测试与缺血缺氧和/或血管因素的(理论)联系。总的来说,精神分裂症候选基因的 55%(n=42 个基因)符合与缺血缺氧和/或血管因素有关的标准。与精神分裂症相关的基因在大脑缺血缺氧反应(IHR)的基因芯片研究中表现出显著的三倍富集。因此,与精神分裂症风险相关的基因与 IHR 和/或血管因素之间存在相当匹配的发现是可重复的。对 GWAS 和 CNV 分析确定的基因的进一步调查表明,有一些新的基因符合标准。文献中报道了与精神分裂症患者产科并发症相关的特定基因变体与 IHR 和/或血管因素之间相互作用的发现。因此,这里定义的扩展基因集可能为临床遗传和转化神经科学研究中基于假设的 G×E 相互作用测试提供合理且基于证据的起点。