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Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies.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。
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2
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8
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2
Myopia: a review of current concepts, association with nonophthalmological conditions, and treatment strategy in children and adolescents.近视:儿童和青少年近视的当前概念、与非眼科疾病的关联及治疗策略综述
Clin Exp Pediatr. 2025 Aug;68(8):554-565. doi: 10.3345/cep.2025.00115. Epub 2025 Apr 1.
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The burden of refraction disorders in 204 countries and territories from 1990 to 2021: A systematic analysis from the global burden of disease 2021.1990年至2021年204个国家和地区屈光不正疾病负担:来自《2021年全球疾病负担》的系统分析
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Temporal Regulation of Myopia and Inflammation-Associated Pathways in the Interphotoreceptor Retinoid-Binding Protein Knockout Mouse Model.光感受器间类视黄醇结合蛋白基因敲除小鼠模型中近视和炎症相关通路的时间调控
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Education interacts with genetic variants near GJD2, RBFOX1, LAMA2, KCNQ5 and LRRC4C to confer susceptibility to myopia.教育与 GJD2、RBFOX1、LAMA2、KCNQ5 和 LRRC4C 附近的遗传变异相互作用,导致近视易感性。
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本文引用的文献

1
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.九个眼部轴长相关位点通过全基因组关联研究发现,包括与屈光不正共享的位点。
Am J Hum Genet. 2013 Aug 8;93(2):264-77. doi: 10.1016/j.ajhg.2013.06.016.
2
Prevalence of refractive errors in a multiethnic Asian population: the Singapore epidemiology of eye disease study.多民族亚洲人群屈光不正的患病率:新加坡眼病流行病学研究。
Invest Ophthalmol Vis Sci. 2013 Apr 9;54(4):2590-8. doi: 10.1167/iovs.13-11725.
3
Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.全基因组分析表明细胞外基质重塑、视觉循环和神经元发育在近视中起作用。
PLoS Genet. 2013;9(2):e1003299. doi: 10.1371/journal.pgen.1003299. Epub 2013 Feb 28.
4
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.全基因组多祖先队列荟萃分析确定了多个新的屈光不正和近视易感性位点。
Nat Genet. 2013 Mar;45(3):314-8. doi: 10.1038/ng.2554. Epub 2013 Feb 10.
5
What factors are associated with myopia in young adults? A survey study in Taiwan Military Conscripts.哪些因素与年轻人的近视有关?一项在台湾新兵中的调查研究。
Invest Ophthalmol Vis Sci. 2013 Feb 5;54(2):1026-33. doi: 10.1167/iovs.12-10480.
6
Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.视蛋白编码序列的变异导致伴近视和二色视的 X 连锁型 cones 功能障碍综合征。
Invest Ophthalmol Vis Sci. 2013 Feb 15;54(2):1361-9. doi: 10.1167/iovs.12-11156.
7
Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia.中国中高度近视患者15号染色体长臂1区4带标记物的相关性研究
Mol Vis. 2012;18:2633-46. Epub 2012 Oct 26.
8
Wnt antagonist SFRP1 functions as a secreted mediator of senescence.Wnt 拮抗剂 SFRP1 作为衰老的分泌介质发挥作用。
Mol Cell Biol. 2012 Nov;32(21):4388-99. doi: 10.1128/MCB.06023-11. Epub 2012 Aug 27.
9
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.染色体 1q41 上的遗传变异影响眼轴长度和高度近视。
PLoS Genet. 2012;8(6):e1002753. doi: 10.1371/journal.pgen.1002753. Epub 2012 Jun 7.
10
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium.大规模国际复制和荟萃分析研究证实 15q14 位点与近视有关。CREAM 联盟。
Hum Genet. 2012 Sep;131(9):1467-80. doi: 10.1007/s00439-012-1176-0. Epub 2012 Jun 5.

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.

DOI:10.1093/hmg/ddt431
PMID:24014484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3869359/
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。