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Genetic Variants near PDGFRA Are Associated with Corneal Curvature in Australians

机译:PDGFRA附近的遗传变异与澳大利亚人的角膜曲率相关

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Purpose.: Irregularity in the corneal curvature (CC) is highly associated with various eye disorders such as keratoconus and myopia. The sample had limited power to find genomewide significant (5 ?? 10a??8) hits but good power for replication. Thus, an attempt was made to test whether alleles in the FRAP1 and PDGFRA genes, recently found to be associated with CC in Asian populations, also influence CC in Australians of North European ancestry. Results of initial genomewide association studies (GWAS) for CC in Australians were also reported. Methods.: Two population-based cohorts of 1788 Australian twins and their families, as well as 1013 individuals from a birth cohort from Western Australia, were genotyped using genomewide arrays. Following separate individual analysis and quality control, the results from each cohort underwent meta-analysis. Results.: Meta-analysis revealed significant replication of association between rs2114039 and corneal curvature (P = 0.0045). The SNP rs2114039 near PDGFRA has been previously implicated in Asians. No SNP at the FRAP1 locus was found to be associated in our Australian samples. No SNP surpassed the genomewide significance threshold of 5 ?? 10a??8. The SNP with strongest association was rs2444240 (P = 3.658 ?? 10a??7), which is 31 kb upstream to the TRIM29 gene. Conclusions.: A significant role of the PDGFRA gene in determining corneal curvature in the Australian population was confirmed in this study, also highlighting the putative association of the TRIM29 locus with CC.
机译:目的:角膜曲率(CC)的不规则性与各种眼部疾病(例如圆锥角膜和近视)高度相关。该样品具有有限的能力来发现全基因组范围内的重要片段(5 ?? 10a ?? 8),但具有很好的复制能力。因此,尝试测试最近发现与亚洲人群的CC相关的FRAP1和PDGFRA基因中的等位基因是否也影响北欧北欧人的CC。还报道了澳大利亚人对CC的初步全基因组关联研究(GWAS)的结果。方法:使用全基因组阵列对两个基于人口的队列,分别是1788个澳大利亚双胞胎及其家人,以及来自西澳大利亚州一个出生队列的1013个个体进行基因分型。在分别进行单独的分析和质量控制后,每个队列的结果均进行了荟萃分析。结果:荟萃分析显示rs2114039与角膜曲率之间的关联显着复制(P = 0.0045)。 PDGFRA附近的SNP rs2114039以前曾与亚洲人有关。在我们的澳大利亚样本中,未发现FRAP1基因座上的SNP。没有SNP超过全基因组显着性阈值5 ?? 10a ?? 8。关联最强的SNP是rs2444240(P = 3.658 ?? 10a ?? 7),在TRIM29基因上游31 kb。结论:这项研究证实了PDGFRA基因在确定澳大利亚人群角膜曲率中的重要作用,也强调了TRIM29基因座与CC的假定联系。

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