Department of Genetics, University of Madras, Dr. ALM PG Institute of Basic Medical Sciences, Taramani Campus, Chennai 600 113, India.
Centre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, Australia.
Schizophr Res. 2018 Sep;199:189-194. doi: 10.1016/j.schres.2018.03.028. Epub 2018 Mar 26.
Schizophrenia is a complex psychiatric disorder involving multiple genes each contributing a small risk. Genome-wide association studies (GWASs) have identified hundreds of risk loci for schizophrenia including miR-137, a miRNA shown to be involved in neuronal development. Several genes regulated by miR-137 were also reported as top risk genes associated with schizophrenia and has been hypothesised that the dysregulation of miR-137 and its target could be involved in the aetiology of schizophrenia. Here, we replicated the four European GWAS hits, miR-137-rs1625579 and three of its validated target gene loci SNPs (ZNF804a-rs1344706, CACNA1C-rs4765905 and TCF4-rs9960767) by genotyping in 2074 samples (schizophrenia cases-1005; controls-1069) from South Indian Population. In this study, only the CACNA1C rs4765905 showed a significant association (OR=1.24, p=0.006). Three SNPs (rs1625579, rs1344706 and rs4765905) showed a consistent direction of effect with previous studies and the polygenic risk score constructed using the weighted sum of these three SNPs showed a significant association with Schizophrenia in this population (OR=3.78, p=0.005). Further, we carried out meta-analysis combining our results with the Psychiatric Genomics Consortium (PGC2) data and observed a considerable increase in GWAS significance.
精神分裂症是一种复杂的精神疾病,涉及多个基因,每个基因都贡献了一小部分风险。全基因组关联研究(GWAS)已经确定了数百个与精神分裂症相关的风险位点,包括 miR-137,一种被证明参与神经元发育的 miRNA。几个受 miR-137 调节的基因也被报道为与精神分裂症相关的顶级风险基因,并且假设 miR-137 及其靶标的失调可能与精神分裂症的发病机制有关。在这里,我们通过对来自印度南部人群的 2074 个样本(精神分裂症病例 1005 个;对照组 1069 个)进行基因分型,复制了四个欧洲 GWAS 发现的结果,包括 miR-137-rs1625579 及其三个已验证的靶基因位点 SNPs(ZNF804a-rs1344706、CACNA1C-rs4765905 和 TCF4-rs9960767)。在这项研究中,只有 CACNA1C rs4765905 显示出显著的相关性(OR=1.24,p=0.006)。三个 SNP(rs1625579、rs1344706 和 rs4765905)与之前的研究显示出一致的效应方向,并且使用这三个 SNP 的加权总和构建的多基因风险评分显示出与该人群中精神分裂症的显著相关性(OR=3.78,p=0.005)。此外,我们结合 Psychiatric Genomics Consortium(PGC2)的数据进行了荟萃分析,观察到 GWAS 显著性有了相当大的提高。