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Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

机译:全基因组屈光散光的联合研究揭示了具有球形等效屈光不正的遗传共决定:CREAM联盟

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摘要

To identify genetic variants associated with refractive astigmatism in the general population, meta-analyses of genome-wide association studies were performed for: White Europeans aged at least 25 years (20 cohorts, N = 31,968); Asian subjects aged at least 25 years (7 cohorts, N = 9,295); White Europeans aged <25 years (4 cohorts, N = 5,640); and all independent individuals from the above three samples combined with a sample of Chinese subjects aged <25 years (N = 45,931). Participants were classified as cases with refractive astigmatism if the average cylinder power in their two eyes was at least 1.00 diopter and as controls otherwise. Genome-wide association analysis was carried out for each cohort separately using logistic regression. Meta-analysis was conducted using a fixed effects model. In the older European group the most strongly associated marker was downstream of the neurexin-1 (NRXN1) gene (rs1401327, P = 3.92E−8). No other region reached genome-wide significance, and association signals were lower for the younger European group and Asian group. In the meta-analysis of all cohorts, no marker reached genome-wide significance: The most strongly associated regions were, NRXN1 (rs1401327, P = 2.93E−07), TOX (rs7823467, P = 3.47E−07) and LINC00340 (rs12212674, P = 1.49E−06). For 34 markers identified in prior GWAS for spherical equivalent refractive error, the beta coefficients for genotype versus spherical equivalent, and genotype versus refractive astigmatism, were highly correlated (r = −0.59, P = 2.10E−04). This work revealed no consistent or strong genetic signals for refractive astigmatism; however, the TOX gene region previously identified in GWAS for spherical equivalent refractive error was the second most strongly associated region. Analysis of additional markers provided evidence supporting widespread genetic co-susceptibility for spherical and astigmatic refractive errors.Electronic supplementary materialThe online version of this article (doi:10.1007/s00439-014-1500-y) contains supplementary material, which is available to authorized users.
机译:为了确定普通人群中与屈光散光有关的遗传变异,对以下人群进行了全基因组关联研究的荟萃分析:年龄至少25岁的白人欧洲人(20个队列,N = 31,968);年龄至少25岁的亚洲受试者(7组,N = 9,295);年龄小于25岁的欧洲白人(4组,N = 5,640);以及以上三个样本中的所有独立个体,以及年龄在25岁以下的中国受试者的样本(N = 45931)。如果参与者的两只眼睛的平均柱面度至少为1.00屈光度,则将其分类为屈光散光,否则为对照组。使用逻辑回归分别对每个队列进行全基因组关联分析。使用固定效应模型进行荟萃分析。在较年长的欧洲人群中,最紧密相关的标记是神经毒素-1(NRXN1)基因的下游(rs1401327,P = 3.92E-8)。没有其他区域达到全基因组范围的重要意义,年轻的欧洲组和亚洲组的关联信号较低。在所有队列的荟萃分析中,没有标记物达到全基因组范围的意义:最紧密相关的区域是NRXN1(rs1401327,P = 2.93E-07),TOX(rs7823467,P = 3.47E-07)和LINC00340( rs12212674,P = 1.49E-06)。对于先前的GWAS中为球面等效屈光不正确定的34个标记,基因型与球面等效以及基因型与屈光散光的β系数高度相关(r = -0.59,P = 2.10E-0)。这项工作没有发现屈光散光的一致或强烈的遗传信号。然而,先前在GWAS中为球面等效屈光不正确定的TOX基因区域是第二个最紧密相关的区域。对其他标记物的分析提供了支持广泛的遗传共感性的球面和散光屈光不正的证据。电子补充材料本文的在线版本(doi:10.1007 / s00439-014-1500-y)包含补充材料,授权用户可以使用。 。

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