Chang Lü-Hua, Li Ming, Luo Xiong-Jian, Liu Xing-Yan, Yin Li-De, Yang Shun-Ying, Diao Hong-Bo, Su Bing, Pu Xing-Fu
The First Affiliated Hospital of Kunming Medical College, Kunming 650032, China.
Dongwuxue Yanjiu. 2011 Oct;32(5):504-8. doi: 10.3724/SP.J.1141.2011.05504.
Previous research on gene expression analysis and association tests have suggested that RELN is a risk gene for schizophrenia in world populations. Based on the reported down-regulation of RELN in schizophrenia patients compared with normal subjects, we speculated that variants in the RELN promoter region may confer risk for schizophrenia. In this study, we investigated the associations of three SNPs in the promoter region of RELN with schizophrenia in a case-control sample from southwestern China (940 cases and 1 369 controls). The results suggested that none of the SNPs showed significant associations in our sample, indicating the risk variants for schizophrenia in RELN may not be located in the promoter region. We also performed meta-analysis by combining our data with previously reported data on the Chinese population with a total sample size of 2 843 individuals, and the result remained non-significant. Collectively, our results suggested variants in the RELN promoter may not harbor risk SNPs associated with schizophrenia in the Chinese population.
先前关于基因表达分析和关联测试的研究表明,RELN是全球人群中精神分裂症的一个风险基因。基于报道,与正常受试者相比,精神分裂症患者中RELN表达下调,我们推测RELN启动子区域的变异可能赋予精神分裂症风险。在本研究中,我们在中国西南部的一个病例对照样本(940例病例和1369例对照)中研究了RELN启动子区域的三个单核苷酸多态性(SNP)与精神分裂症的关联。结果表明,在我们的样本中,没有一个SNP显示出显著关联,这表明RELN中精神分裂症的风险变异可能不在启动子区域。我们还通过将我们的数据与先前报道的中国人群数据合并进行荟萃分析,总样本量为2843人,结果仍然不显著。总体而言,我们的结果表明,RELN启动子中的变异可能不包含与中国人群精神分裂症相关的风险单核苷酸多态性。