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教育对遗传变异与屈光不正之间的关联有影响:五项新加坡研究的荟萃分析。

Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies.

机构信息

Saw Swee Hock School of Public Health.

出版信息

Hum Mol Genet. 2014 Jan 15;23(2):546-54. doi: 10.1093/hmg/ddt431. Epub 2013 Sep 6.

Abstract

Refractive error is a complex ocular trait governed by both genetic and environmental factors and possibly their interplay. Thus far, data on the interaction between genetic variants and environmental risk factors for refractive errors are largely lacking. By using findings from recent genome-wide association studies, we investigated whether the main environmental factor, education, modifies the effect of 40 single nucleotide polymorphisms on refractive error among 8461 adults from five studies including ethnic Chinese, Malay and Indian residents of Singapore. Three genetic loci SHISA6-DNAH9, GJD2 and ZMAT4-SFRP1 exhibited a strong association with myopic refractive error in individuals with higher secondary or university education (SHISA6-DNAH9: rs2969180 A allele, β = -0.33 D, P = 3.6 × 10(-6); GJD2: rs524952 A allele, β = -0.31 D, P = 1.68 × 10(-5); ZMAT4-SFRP1: rs2137277 A allele, β = -0.47 D, P = 1.68 × 10(-4)), whereas the association at these loci was non-significant or of borderline significance in those with lower secondary education or below (P for interaction: 3.82 × 10(-3)-4.78 × 10(-4)). The evidence for interaction was strengthened when combining the genetic effects of these three loci (P for interaction = 4.40 × 10(-8)), and significant interactions with education were also observed for axial length and myopia. Our study shows that low level of education may attenuate the effect of risk alleles on myopia. These findings further underline the role of gene-environment interactions in the pathophysiology of myopia.

摘要

屈光不正(refractive error)是一种由遗传和环境因素共同控制的复杂眼部特征,这些因素可能相互作用。迄今为止,有关遗传变异与屈光不正环境风险因素之间相互作用的数据还很缺乏。本研究利用全基因组关联研究(genome-wide association studies)的结果,调查了主要环境因素(教育)是否会改变 40 个单核苷酸多态性(single nucleotide polymorphisms)对来自包括新加坡华族、马来族和印度族居民在内的 5 项研究中的 8461 名成年人屈光不正的影响。在接受过中学或大学以上教育的个体中,3 个遗传位点 SHISA6-DNAH9、GJD2 和 ZMAT4-SFRP1 与近视性屈光不正存在强烈关联(SHISA6-DNAH9:rs2969180 A 等位基因,β=-0.33 D,P=3.6×10(-6);GJD2:rs524952 A 等位基因,β=-0.31 D,P=1.68×10(-5);ZMAT4-SFRP1:rs2137277 A 等位基因,β=-0.47 D,P=1.68×10(-4)),而在接受中学以下教育的个体中,这些位点的关联则不显著或具有边缘显著性(P 交互作用=3.82×10(-3)-4.78×10(-4))。当结合这三个位点的遗传效应时,交互作用的证据得到了加强(P 交互作用=4.40×10(-8)),并且在眼轴长度和近视方面也观察到与教育的显著交互作用。本研究表明,低教育水平可能会减弱风险等位基因对近视的影响。这些发现进一步强调了基因-环境相互作用在近视发病机制中的作用。

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