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首页> 外文期刊>The Indian journal of medical research. >Haplotype analysis of ADAM33 polymorphisms in asthma: A pilot study
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Haplotype analysis of ADAM33 polymorphisms in asthma: A pilot study

机译:哮喘患者ADAM33多态性单倍型分析:试验研究

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Background & objectives: ADAM33 is implicated as a potentially strong candidate gene for asthma and bronchial hyper-responsiveness. Many polymorphisms of ADAM33 have been studied along with ADAM33 expression in various cells of the lungs. Haplotype analysis also showed association with asthma in different populations across the world. Therefore, the aim of this study was to perform a comprehensive screening of ADAM33 polymorphisms in adult patients with asthma.Methods: Thirty five polymorphisms of ADAM33 were genotyped in 55 patients with asthma and 53 controls. The association of single nucleotide polymorphisms (SNPs) and haplotypes with phenotypes of asthma was analysed.Results: The genotype, minor allele frequency, odds ratio and Hardy-Weinberg equilibrium did not show any significant difference among cases and controls. No association was found between SNPs of ADAM33 with the severity of asthma. Correlation analysis of ADAM33 SNPs to the phenotypes, based on clinical variables and allergen sensitization, did not show significant difference. Haplotype analysis showed that rs2280090 and rs2280091 were associated with asthma in the patient group. Interpretation & conclusions: Haplotype analysis showed an association of the two SNP variations with asthma. These SNPs lead to amino acid change and are prone to phosphorylation, which may affect expression levels and protein function of ADAM33 and asthma susceptibility.
机译:背景和目标:ADAM33涉及哮喘和支气管超响应性的潜在强烈候选基因。已经在肺部的各种细胞中研究了ADAM33的许多多态性。单倍型分析还显示出与世界各地不同人群的哮喘相关联。因此,本研究的目的是在成人哮喘患者中进行全面的筛选Adam33多态性。方法:55例哮喘和53例对照的55例患者基因分型三十五个多态性。分析了单核苷酸多态性(SNP)和单倍型与哮喘表型的关联。结果:基因型,次要等位基因频率,差异比和硬质 - Weinberg均衡未显示出病例和对照的任何显着差异。在ADAM33的SNP之间没有发现任何关联,严重程度的哮喘。基于临床变量和过敏原致敏的表型对表型的相关分析并没有显示出显着差异。单倍型分析表明,RS2280090和RS2280091与患者组中的哮喘相关。解释与结论:单倍型分析显示两种与哮喘的SNP变化的关联。这些SNP导致氨基酸变化,易于磷酸化,这可能影响ADAM33和哮喘易感性的表达水平和蛋白质功能。

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