Courtenay Monique D, Cade William, Schwartz Stephen G, Kovach Jaclyn L, Agarwal Anita, Wang Gaofeng, Haines Jonathan L, Pericak-Vance Margaret A, Scott Wiliam K
Human Genetics and Genomics, University of Miami Miller School Medicine, 1501 NW 10th Ave, Miami, FL, 33136, United States.
John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10 Ave, BRB-314 (M860), Miami, Florida, 33136, United States.
Invest Ophthalmol Vis Sci. 2014 Jul 11;55(8):4873-9. doi: 10.1167/iovs.14-14494.
Purpose:Age-Related Macular Degeneration (AMD) is the leading cause of irreversible visual loss in developed countries. Its etiology includes genetic and environmental factors. Although VEGFA variants are associated with AMD, the joint action of variants within the VEGF pathway and their interaction with non-genetic factors has not been investigated. Methods:Affymetrix 6.0 chipsets were used to genotype 668,238 SNPs in 1,207 AMD cases and 686 controls. Environmental exposures were collected by questionnaire. A set-based test was conducted using the chi-square statistic at each SNP derived from Kraft's 2df joint test. Pathway and gene-based test statistics were calculated as the mean of all independent SNP statistics. Phenotype labels were permuted 10,000 times to generate an empirical p-value. Results: While a main effect of the VEGF pathway was not identified, the pathway was associated with neovascular AMD in women when accounting for birth control pill (BCP) use (P= 0.017). Analysis of VEGF's subpathways found that SNPs in the Proliferation subpathway were associated with neovascular AMD (P=0.029) when accounting for BCP use. Nominally significant genes within this subpathway were also observed. Stratification by BCP use revealed novel significant genetic effects in women who had taken BCPs. Conclusions: These results illustrate that some AMD genetic risk factors may only be revealed when considering complex relationships among risk factors. This shows the utility of exploring pathways of previously associated genes to find novel effects. It also demonstrates the importance of incorporating environmental exposures in tests of genetic association at the SNP, gene, or pathway level.
年龄相关性黄斑变性(AMD)是发达国家不可逆视力丧失的主要原因。其病因包括遗传和环境因素。虽然VEGFA变异与AMD相关,但VEGF通路内变异的联合作用及其与非遗传因素的相互作用尚未得到研究。方法:使用Affymetrix 6.0芯片组对1207例AMD患者和686例对照中的668,238个单核苷酸多态性(SNP)进行基因分型。通过问卷调查收集环境暴露情况。使用基于Kraft的2自由度联合检验在每个SNP处的卡方统计量进行基于集合的检验。通路和基于基因的检验统计量计算为所有独立SNP统计量的平均值。对表型标签进行10,000次置换以生成经验p值。结果:虽然未发现VEGF通路的主要效应,但在考虑避孕药(BCP)使用情况时,该通路与女性新生血管性AMD相关(P = 0.017)。对VEGF子通路的分析发现,在考虑BCP使用情况时,增殖子通路中的SNP与新生血管性AMD相关(P = 0.029)。在该子通路中也观察到名义上显著的基因。按BCP使用情况分层显示,服用BCP的女性有新的显著遗传效应。结论:这些结果表明,一些AMD遗传风险因素可能只有在考虑风险因素之间的复杂关系时才会显现出来。这表明探索先前相关基因的通路以发现新效应的实用性。它还证明了在SNP、基因或通路水平的遗传关联测试中纳入环境暴露的重要性。