Queensland Institute of Medical Research, Brisbane, Australia.
Invest Ophthalmol Vis Sci. 2012 Oct 11;53(11):7131-6. doi: 10.1167/iovs.12-10489.
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 × 10(-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.
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.
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 × 10(-8). The SNP with strongest association was rs2444240 (P = 3.658 × 10(-7)), which is 31 kb upstream to the TRIM29 gene.
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.
角膜曲率(CC)的不规则性与各种眼部疾病高度相关,如圆锥角膜和近视。该样本发现全基因组显著(5×10(-8))命中的能力有限,但具有良好的复制能力。因此,尝试测试最近在亚洲人群中发现与 CC 相关的 FRAP1 和 PDGFRA 基因中的等位基因是否也会影响北欧血统的澳大利亚人的 CC。还报告了澳大利亚人 CC 的初始全基因组关联研究(GWAS)的结果。
对来自澳大利亚的 1788 对双胞胎及其家庭以及来自西澳大利亚州出生队列的 1013 个人进行了全基因组关联研究。在单独进行个体分析和质量控制后,对每个队列的结果进行了荟萃分析。
荟萃分析显示 rs2114039 与角膜曲率之间存在显著的关联(P=0.0045)。先前在亚洲人群中发现 PDGFRA 附近的 SNP rs2114039 与角膜曲率有关。在我们的澳大利亚样本中未发现 FRAP1 基因座的任何 SNP 与 rs2114039 相关。没有 SNP 超过全基因组显著性阈值 5×10(-8)。关联最强的 SNP 是 rs2444240(P=3.658×10(-7)),它位于 TRIM29 基因上游 31kb。
本研究证实了 PDGFRA 基因在澳大利亚人群中决定角膜曲率方面的重要作用,同时还强调了 TRIM29 基因座与 CC 的潜在关联。