...
首页> 外文期刊>Molecular vision >Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
【24h】

Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population

机译:BLID和LOC399959作为中国汉族人群高度近视的候选基因的评估

获取原文

摘要

Purpose: BH3-like motif containing, celldeath inducer (BLID) and LOC399959 are two genesassociated 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 LOC399959are associated with high myopia in Chinese Han subjects. Methods: High myopia subjects (n=476)had a spherical refractive error of less than ?6.00 D in at least oneeye and/or an axial length greater than 26 mm. Genomic DNA wasextracted and genotyped from peripheral blood leukocytes of high myopesand controls (n=275). Using a case-control association study ofcandidate regions, linkage disequilibrium blocks for 19 tag SNPs(tSNPs), including rs577948, harbored within and surrounding the BLIDand LOC399959 genes were analyzed on a MassArray platform usingiPlex chemistry. Each of the tSNPs had an r20.8 andminor allele frequency 10% in the Chinese Han population. Haplotypeassociation analysis was performed on Haploview 4.1 using Chi-square (χ2)tests. Results: None of the 19 tSNPs werestatistically associated with high myopia. Conclusions: While rs577948 may beassociated with high myopia in Japanese subjects, it and the othertSNPs near the BLID and LOC399959 genes are notsusceptibility loci for high myopia in the Chinese Han population.Thus, associations of SNPs with high myopia as determined byGenome-Wide Association Study (GWAS) may be restricted to certainethnic or genetically distinct populations. Without systematicreplication in other populations, the results of GWAS associationsshould be interpreted with great caution.
机译:目的:含有BH3样基序的细胞死亡诱导物(BLID)和LOC399959是与单核苷酸多态性(SNP)rs577948相关的两个基因,该基因是日本受试者高度近视的易感性位点。本研究的目的是确定BLID是否LOC399959和LOC399959与中国汉族人群高度近视有关。方法:高度近视的受试者(n = 476)在至少一只眼中的球面屈光误差小于6.00 D,并且/或者眼轴长度大于26 mm。从高近视者和对照组(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研究,在BLIDand LOC399959基因内部和周围隐藏的19个标签SNPs(tSNPs),包括rs577948的连锁不平衡嵌段,使用iPlex化学方法在MassArray平台上进行了分析。在中国汉族人群中,每个tSNP的r2> 0.8,次要等位基因频率> 10%。使用卡方检验(χ2)对Haploview 4.1进行了单倍型关联分析。结果:19个tSNP均无统计学意义与高度近视相关。结论:尽管rs577948可能与日本受试者的高度近视有关,但它与BLID和LOC399959基因附近的othertSNP并不是中国汉族人群高度近视的易感基因位点。因此,根据全基因组关联研究确定,SNP与高度近视的关联(GWAS)可能仅限于某些种族或遗传上不同的人群。在没有其他人群的系统复制的情况下,应非常谨慎地解释GWAS协会的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号