Miyake Masahiro, Yamashiro Kenji, Nakanishi Hideo, Nakata Isao, Akagi-Kurashige Yumiko, Tsujikawa Akitaka, Moriyama Muka, Ohno-Matsui Kyoko, Mochizuki Manabu, Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahisa
Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mol Vis. 2012;18:2726-35. Epub 2012 Nov 17.
The objective of this study was to investigate whether genetic variations in the paired box 6 (PAX6) gene are associated with high myopia in Japanese subjects.
A total of 1,307 unrelated Japanese patients with high myopia (axial length ≥26 mm in both eyes) and two independent control groups were evaluated (333 cataract patients without high myopia and 923 age-matched healthy Japanese individuals). We genotyped three tag single-nucleotide polymorphisms (SNPs) in PAX6: rs2071754, rs644242, and rs3026354. These SNPs provided 100% coverage of all phase II HapMap SNPs within the PAX6 region (minor allele frequency ≥0.10; r(2) threshold: 0.90). Chi-square tests for trend and multivariable logistic regression were conducted.
Genotype distributions in the three SNPs were in accordance with the Hardy-Weinberg equilibrium. After adjusting for age and sex, evaluation of cataract control showed a marginal association with high myopia in rs644242 (odds ratio [95% confidence interval]=0.69 [0.49-0.96], p=0.026), and a significant association was observed in healthy Japanese controls (0.79 [0.66-0.96], p=0.015). We pooled two control cohorts to evaluate the association. This analysis revealed a strong association between rs644242 and high myopia (0.78 [0.65-0.92], p=0.0045). The rs644242 A allele was a protective allele for development of high myopia. Subanalysis also revealed that rs644242 was significantly associated with extreme high myopia (0.78 [0.64-0.95], p=0.0165). The other two SNPs did not show a significant association with this condition.
The current study showed a significant association of PAX6 with high and extreme myopia in Japanese participants. The A allele of rs644242 is a protective allele.
本研究旨在调查配对盒6(PAX6)基因的遗传变异是否与日本人群中的高度近视相关。
共评估了1307名无亲缘关系的日本高度近视患者(双眼眼轴长度≥26mm)以及两个独立的对照组(333名无高度近视的白内障患者和923名年龄匹配的健康日本个体)。我们对PAX6基因中的三个标签单核苷酸多态性(SNP)进行了基因分型:rs2071754、rs644242和rs3026354。这些SNP对PAX6区域内所有II期国际人类基因组单体型图(HapMap)SNP提供了100%的覆盖(次要等位基因频率≥0.10;r²阈值:0.90)。进行了趋势卡方检验和多变量逻辑回归分析。
三个SNP的基因型分布符合哈迪-温伯格平衡。在调整年龄和性别后,对白内障对照组的评估显示rs644242与高度近视存在边缘关联(优势比[95%置信区间]=0.69[0.49 - 0.96],p = 0.026),在健康日本对照组中观察到显著关联(0.79[0.66 - 0.96],p = 0.015)。我们合并了两个对照组来评估这种关联。该分析揭示了rs644242与高度近视之间存在强关联(0.78[0.65 - 0.92],p = 0.0045)。rs644242的A等位基因是高度近视发展的保护等位基因。亚分析还显示rs644242与极端高度近视显著相关(0.78[0.64 - 0.95],p = 0.0165)。另外两个SNP与该疾病未显示出显著关联。
当前研究表明PAX6与日本参与者中的高度和极端近视存在显著关联。rs644242的A等位基因是保护等位基因。