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首页> 外文期刊>Allergy & Rhinology >Association of IL13R alpha 1 +1398A/G polymorphism in a North Indian population with asthma: A case-control study
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Association of IL13R alpha 1 +1398A/G polymorphism in a North Indian population with asthma: A case-control study

机译:北印度人群哮喘中IL13R alpha 1 + 1398A / G多态性的关联:病例对照研究

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Background: Interleukin 13 (IL13) is directly involved in the secretion of total serum immunoglobulin E (IgE), which plays a major role in the asthma pathogenesis. Objective: One of the polymorphic receptor of IL13 is IL13Rα1, which after binding to IL13, initiates signal transduction that results in mucin secretion, airway hyperreactivity, fibrosis, and chitinase up-regulation, which increases asthma risk. Methods: In the present study, the role of IL13Rα1 +1398A/G gene polymorphisms in asthma was detected with a total of 964 individuals, including 483 healthy controls and 481 asthma patients from a North Indian population using polymerase chain reaction-restriction fragment length polymorphism method. Results: Statistical analysis revealed that the mutant allele (G) is predominant in asthma patients (42.7%) than the controls (38.2%), which shows an increased risk toward asthma with odds ratio = 1.21, 95% confidence interval (1.00‐1.45), χ2 = 4.10 and p = 0.043. Furthermore, the phenotypic characteristics also reveal a significant association with the disease (p Conclusions: This is the first study conducted in India and +1398A/G polymorphism in noncoding region of IL13Rα1 confer risk toward asthma in the studied population.
机译:背景:白介素13(IL13)直接参与总血清免疫球蛋白E(IgE)的分泌,在哮喘的发病机理中起主要作用。目的:IL13Rα1是IL13的一种多态性受体,与IL13结合后,会启动信号转导,导致粘蛋白分泌,气道高反应性,纤维化和几丁质酶上调,从而增加哮喘风险。方法:在本研究中,使用聚合酶链反应-限制性片段长度多态性技术检测了总共964例个体中的IL13Rα1+ 1398A / G基因多态性在哮喘中的作用,包括483名健康对照者和481名来自北印度人口的哮喘患者方法。结果:统计分析表明,哮喘患者中突变等位基因(G)比对照组(38.2%)占优势(42.7%),这显示患哮喘的风险增加,优势比= 1.21,95%置信区间(1.00-1.45) ),χ 2 = 4.10,p = 0.043。此外,表型特征还显示出与该疾病的显着相关性(p结论:这是在印度进行的第一项研究,IL13Rα1非编码区的+ 1398A / G多态性使研究人群罹患哮喘的风险增加。

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