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An immunogenetic analysis of nucleotide-binding oligomerization domain-1 (NOD1) variation in asthma.

机译:哮喘患者核苷酸结合寡聚域-1(NOD1)变异的免疫遗传学分析。

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摘要

Asthma is a chronic inflammatory disease affecting approximately 7.2 percent of adults residing in the United States. The greatest burden of hospitalization and mortality is mainly observed in ethnic minority populations, thus making asthma one of the leading health disparities in the United States. Many years of research have attributed asthma susceptibility to genetic predisposition; yet, disease etiology remains unknown. In this study, genetic polymorphisms in the nucleotide-binding oligomerization domain-1 (NOD1) gene were investigated for their association with asthma onset and propagation. NOD1, which codes for an intracellular microbial pattern recognition receptor, is thought to be involved in the pathogenesis of asthma. In a case-control study design, single nucleotide polymorphisms (SNPs) in the regulatory and structural domains of NOD1 were genotyped and analyzed for their association with asthma in an African American population. The results from this study suggest that SNPs rs2075818, rs5743336, and rs2907748 are associated with asthma and highlight gene-environmental interactions as a major contributor to asthma prevalence. This study begins to unravel the relationship of innate immune responses, inflammation, and asthma.
机译:哮喘是一种慢性炎性疾病,影响了居住在美国的大约7.2%的成年人。住院和死亡的最大负担主要在少数民族人群中观察到,因此使哮喘成为美国主要的健康差距之一。多年的研究将哮喘易感性归因于遗传易感性。然而,疾病病因仍然未知。在这项研究中,研究了核苷酸结合寡聚域-1(NOD1)基因的遗传多态性与哮喘发作和传播的关系。 NOD1编码细胞内微生物模式识别受体,被认为与哮喘的发病机理有关。在病例对照研究设计中,对NOD1调控和结构域中的单核苷酸多态性(SNP)进行了基因分型,并分析了它们与非裔美国人人群中哮喘的相关性。这项研究的结果表明,SNP rs2075818,rs5743336和rs2907748与哮喘有关,并强调基因与环境的相互作用是哮喘患病率的主要因素。这项研究开始揭示先天免疫反应,炎症和哮喘的关系。

著录项

  • 作者

    Jackson, Chazeman S.;

  • 作者单位

    Howard University.;

  • 授予单位 Howard University.;
  • 学科 Biology Genetics.;Health Sciences Immunology.;Health Sciences Epidemiology.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 109 p.
  • 总页数 109
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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