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Understanding the role of novel gene-environmental and gene-gene interactions in the pathogenesis of age related macular degeneration.

机译:了解新的基因-环境和基因-基因相互作用在年龄相关性黄斑变性的发病机理中的作用。

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摘要

The purpose of the study was to assess single nucleotide polymorphisms (SNPs) in NOS2 A, ESR1, ESR2 and MMP-2 genes that may affect the risk for age-related macular degeneration (AMD) and may interact with environmental factors such as estrogen exposure and smoking, thereby modifying their effect on AMD.;AMD is an ocular degenerative disease with known genetic and environmental factors. However, the disease risk genes identified so far account only for part of the genetic attributable risk and the role of new disease risk genes remain to be evaluated.;For non-genetic risk factors, the most extensively analyzed are smoking and estrogen exposure. Smoking increases the risk for development of AMD and estrogen exposure has a protective effect. Both of these factors have been linked to oxidative pathway activation and extracellular matrix homeostasis (ECM) through interactions with the NOS2A and metallomatrix proteinase (MMP) genes, respectively. In addition, estrogen exerts its activity through the estrogen receptors ERalpha and ERbeta.;We examined a Caucasian cohort of AMD cases and controls. Nine hundred and ninety-eight individuals (males and females) for the NOS2A gene and 777 females for both the ESR1/2 and MMP-2 genes were assessed.;We genotyped TagSNPs within these selected candidate gene regions using HapMap phase II or III. Multivariable logistic regression or generalized estimating equation (GEE) models containing SNP genotypes, age, sex, environmental factor and genotype/environmental interaction were constructed. In addition, because we previously reported interactions between the ARMS2 locus and estrogen exposure and smoking, we also analyzed interactions within ARMS2 locus.;We found that SNPs in NOS2A are associated with increased risk for AMD and might modulate the smoking effect on AMD. The synergistic interaction between NOS2A and smoking is independent of the ARMS2 locus.;No SNP in the MMP-2 gene was significantly associated with increased risk for AMD. We also detected no significant interactions with estrogen exposure or with the ARMS2 locus.;SNPs within the ESR1 gene are associated with an increased risk for developing AMD and the inverse association of AMD and HRT is dependent on SNP genotypes in ESR1 and ESR2 and independent of the ARMS2 locus.
机译:这项研究的目的是评估NOS2 A,ESR1,ESR2和MMP-2基因中的单核苷酸多态性(SNP),这些基因可能会影响与年龄相关的黄斑变性(AMD)的风险,并可能与诸如雌激素暴露的环境因素相互作用以及吸烟,从而改变了它们对AMD的影响。; AMD是一种具有已知遗传和环境因素的眼部退行性疾病。然而,迄今为止确定的疾病风险基因仅占遗传归因风险的一部分,新的疾病风险基因的作用仍有待评估。对于非遗传风险因素,分析最广泛的是吸烟和雌激素暴露。吸烟会增加患AMD的风险,而接触雌激素具有保护作用。这两个因素已分别通过与NOS2A和金属瘤胃蛋白酶(MMP)基因的相互作用与氧化途径激活和细胞外基质稳态(ECM)相关。此外,雌激素通过雌激素受体ERalpha和ERbeta发挥其活性。我们检查了一组AMD病例和对照组。评估了NOS2A基因的989位个体(男性和女性)和ESR1 / 2和MMP-2基因的777位女性。我们使用HapMap II期或III期在这些选定的候选基因区域内对TagSNP进行了基因分型。构建了包含SNP基因型,年龄,性别,环境因素和基因型/环境相互作用的多变量logistic回归或广义估计方程(GEE)模型。此外,由于我们先前报道了ARMS2基因座与雌激素暴露和吸烟之间的相互作用,因此我们还分析了ARMS2基因座内的相互作用。我们发现NOS2A中的SNP与AMD风险增加有关,并可能调节吸烟对AMD的影响。 NOS2A与吸烟之间的协同相互作用与ARMS2基因座无关。; MMP-2基因中没有SNP与AMD风险增加显着相关。我们也未发现与雌激素暴露或与ARMS2基因座发生显着相互作用。; ESR1基因内的SNP与罹患AMD的风险增加相关,而AMD与HRT的逆向依赖于ESR1和ESR2中的SNP基因型且与ARMS2轨迹。

著录项

  • 作者

    Ayala-Haedo, Juan A.;

  • 作者单位

    University of Miami.;

  • 授予单位 University of Miami.;
  • 学科 Ecology.;Genetics.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 129 p.
  • 总页数 129
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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