Zhao Fuxin, Bai Jian, Chen Wei, Xue Anquan, Li Chaohua, Yan Zhonghui, Chen Hui, Lu Fan, Hu Yongwu, Qu Jia, Zeng Changqing, Zhou Xiangtian
School of Optometry and Ophthalmology and Eye Hospital, Wenzhou Medical College, Wenzhou, Zhejiang, China.
Mol Vis. 2010 Oct 2;16:1920-7.
BH3-like motif containing, cell death inducer (BLID) and LOC399959 are two genes associated with the single nucleotide polymorphism (SNP) rs577948, which is a susceptibility locus for high myopia in Japanese subjects. The purpose of this study was to determine if BLID and LOC399959 are associated with high myopia in Chinese Han subjects.
High myopia subjects (n=476) had a spherical refractive error of less than -6.00 D in at least one eye and/or an axial length greater than 26 mm. Genomic DNA was extracted and genotyped from peripheral blood leukocytes of high myopes and controls (n=275). Using a case-control association study of candidate regions, linkage disequilibrium blocks for 19 tag SNPs (tSNPs), including rs577948, harbored within and surrounding the BLID and LOC399959 genes were analyzed on a MassArray platform using iPlex chemistry. Each of the tSNPs had an r(2)>0.8 and minor allele frequency >10% in the Chinese Han population. Haplotype association analysis was performed on Haploview 4.1 using Chi-square (χ(2)) tests.
None of the 19 tSNPs were statistically associated with high myopia.
While rs577948 may be associated with high myopia in Japanese subjects, it and the other tSNPs near the BLID and LOC399959 genes are not susceptibility loci for high myopia in the Chinese Han population. Thus, associations of SNPs with high myopia as determined by Genome-Wide Association Study (GWAS) may be restricted to certain ethnic or genetically distinct populations. Without systematic replication in other populations, the results of GWAS associations should be interpreted with great caution.
含BH3样基序的细胞死亡诱导因子(BLID)和LOC399959是与单核苷酸多态性(SNP)rs577948相关的两个基因,rs577948是日本人群中高度近视的一个易感位点。本研究的目的是确定BLID和LOC399959是否与中国汉族人群的高度近视相关。
高度近视受试者(n = 476)至少一只眼睛的球镜屈光不正小于-6.00 D和/或眼轴长度大于26 mm。从高度近视者和对照者(n = 275)的外周血白细胞中提取基因组DNA并进行基因分型。使用候选区域的病例对照关联研究,在MassArray平台上采用iPlex化学方法分析了BLID和LOC399959基因内部及周围包含rs577948在内的19个标签SNP(tSNP)的连锁不平衡块。每个tSNP在中国汉族人群中的r²>0.8且次要等位基因频率>10%。使用卡方(χ²)检验在Haploview 4.1上进行单倍型关联分析。
19个tSNP均与高度近视无统计学关联。
虽然rs577948可能与日本人群的高度近视相关,但它以及BLID和LOC399959基因附近的其他tSNP并非中国汉族人群高度近视的易感位点。因此,全基因组关联研究(GWAS)确定的SNP与高度近视的关联可能仅限于某些种族或基因不同的人群。在其他人群中没有进行系统重复验证的情况下,GWAS关联研究的结果应谨慎解读。