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本文引用的文献

1
Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.通过全基因组基因-环境相互作用分析揭示年龄相关性黄斑变性非吸烟者的遗传因素。
Ann Hum Genet. 2013 May;77(3):215-31. doi: 10.1111/ahg.12011.
2
Seven new loci associated with age-related macular degeneration.七个与年龄相关性黄斑变性相关的新基因座。
Nat Genet. 2013 Apr;45(4):433-9, 439e1-2. doi: 10.1038/ng.2578. Epub 2013 Mar 3.
3
Isoforms of secretory group two phospholipase A (sPLA2) in mouse ocular surface epithelia and lacrimal glands.小鼠眼表面上皮和泪腺中分泌型 II 组磷脂酶 A2(sPLA2)的同工型。
Invest Ophthalmol Vis Sci. 2012 May 14;53(6):2845-55. doi: 10.1167/iovs.11-8684.
4
Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.重新考虑使用单变量检验统计量作为合并检验的替代方法,用于具有罕见变异的序列数据的关联检验方法。
PLoS One. 2012;7(2):e30238. doi: 10.1371/journal.pone.0030238. Epub 2012 Feb 17.
5
Ginsenoside Rg1 attenuates lipopolysaccharide-induced inflammatory responses via the phospholipase C-γ1 signaling pathway in murine BV-2 microglial cells.人参皂苷 Rg1 通过磷脂酶 C-γ1 信号通路减轻脂多糖诱导的小鼠 BV-2 小胶质细胞炎症反应。
Curr Med Chem. 2012;19(5):770-9. doi: 10.2174/092986712798992066.
6
Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset.使用WTCCC克罗恩病数据集对七种通路分析算法的比较。
BMC Res Notes. 2011 Oct 7;4:386. doi: 10.1186/1756-0500-4-386.
7
Rare-variant association testing for sequencing data with the sequence kernel association test.基于序列核关联检验的测序数据罕见变异关联分析
Am J Hum Genet. 2011 Jul 15;89(1):82-93. doi: 10.1016/j.ajhg.2011.05.029. Epub 2011 Jul 7.
8
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.FRK/COL10A1 和 VEGFA 附近的常见变异与年龄相关性黄斑变性的晚期有关。
Hum Mol Genet. 2011 Sep 15;20(18):3699-709. doi: 10.1093/hmg/ddr270. Epub 2011 Jun 10.
9
sPLA2-IIa amplifies ocular surface inflammation in the experimental dry eye (DE) BALB/c mouse model.分泌型 PLA2-IIa 在实验性干眼 (DE) BALB/c 小鼠模型中加重眼表炎症。
Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4780-8. doi: 10.1167/iovs.10-6350.
10
c-Cbl inhibits angiogenesis and tumor growth by suppressing activation of PLCγ1.c-Cbl 通过抑制 PLCγ1 的激活来抑制血管生成和肿瘤生长。
Oncogene. 2011 May 12;30(19):2198-206. doi: 10.1038/onc.2010.597. Epub 2011 Jan 17.

基于集合的血管内皮生长因子(VEGF)通路单核苷酸多态性(SNP)与外源性雌激素之间相互作用的联合检验发现其与年龄相关性黄斑变性有关联。

Set-based joint test of interaction between SNPs in the VEGF pathway and exogenous estrogen finds association with age-related macular degeneration.

作者信息

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

机构信息

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.

出版信息

Invest Ophthalmol Vis Sci. 2014 Jul 11;55(8):4873-9. doi: 10.1167/iovs.14-14494.

DOI:10.1167/iovs.14-14494
PMID:25015356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4126792/
Abstract

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.

摘要

目的

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。