首页> 外文OA文献 >A Preliminary study on the association of single Nucleotide Polymorphisms of interleukin 4 (IL4) , Il13, Il4 Receptor ALPHA (IL4Rα) & Toll-Like Receptor 4 (TLR4) Genes with Asthma in Indian Adults\ud IL13\ud , IL4 receptor \ud alpha (\ud IL4Rα\ud ) & Toll-like receptor 4 (\ud TLR4\ud ) genes with \ud asthma in Indian adults
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A Preliminary study on the association of single Nucleotide Polymorphisms of interleukin 4 (IL4) , Il13, Il4 Receptor ALPHA (IL4Rα) & Toll-Like Receptor 4 (TLR4) Genes with Asthma in Indian Adults\ud IL13\ud , IL4 receptor \ud alpha (\ud IL4Rα\ud ) & Toll-like receptor 4 (\ud TLR4\ud ) genes with \ud asthma in Indian adults

机译:印度成年人哮喘白细胞介素4(IL4),Il13,Il4受体ALPHA(IL4Rα)和Toll样受体4(TLR4)基因单核苷酸多态性的初步研究\ ud IL13 \ ud ,IL4受体\ ud 字母(\ ud IL4Rα\ ud )和Toll样受体4(\ ud TLR4 \ ud )具有\ ud的基因 印度成人哮喘

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摘要

Background & objectives: Interleukin 4 (IL4) and IL13 genes are believed to be responsible for inflammation of the airways in asthmatics. These share a common receptor component called IL4Rα which is another potentially important candidate gene linked to asthma phenotypes. Another gene Toll-like receptor 4 (TLR4) might affect the incidence or progression of asthma through the expression of proinflammatory genes. Several single nucleotide polymorphisms (SNPs) in IL4, IL13, IL4Rα and TLR4 have been reported to be linked to asthma or related phenotypes in several ethnic populations using linkage studies and association studies. However, the results have not been consistent. We investigated five SNPs (C-589T and C-33T of IL4, G+2044A of IL13, A+1902G of IL4Rα, and A+896G of TLR4) in patients with adult onset asthma to evaluate their role in manifestation and severity of asthma.\udMethods: Adult (>18 yr of age) patients with asthma (n=100) and healthy controls (n=50) were included in the study. Genotyping was performed using sequenom MassARRAY technology.\udResults: The mutant alleles of the C-589T and C-33T SNPs in the promoter region of IL4 were present in 4 per cent patients with asthma but absent from the control group suggesting that the variations in IL4 may contribute to asthma occurrence. The SNPs of other genes were seen in both controls and patients.\udInterpretation & conclusions: The results suggest the possible association between the genetic distribution of C-589T and C-33T SNPs of IL4 with asthma in Indian adults.
机译:背景与目的:白介素4(IL4)和IL13基因被认为与哮喘患者的气道炎症有关。它们共享一个共同的受体成分,称为IL4Rα,它是与哮喘表型相关的另一个潜在的重要候选基因。另一个基因Toll样受体4(TLR4)可能通过促炎基因的表达影响哮喘的发生或发展。据报道,通过连锁研究和关联研究,IL4,IL13,IL4Rα和TLR4中的几个单核苷酸多态性(SNP)与哮喘或相关表型相关。但是,结果并不一致。我们调查了成年哮喘患者中的五个SNP(IL4的C-589T和C-33T,IL13的G + 2044A,IL4Rα的A + 1902G和TLR4的A + 896G)以评估其在哮喘表现和严重程度中的作用方法:成人(> 18岁)哮喘(n = 100)和健康对照(n = 50)患者纳入研究。 \ ud结果:4%的哮喘患者中存在IL4启动子区域C-589T和C-33T SNP的突变等位基因,但对照组中没有,这表明IL4可能导致哮喘的发生。对照和患者均见到其他基因的SNP。\ ud解释与结论:结果表明,IL4的C-589T和C-33T SNP的遗传分布与印度成年人哮喘之间可能存在关联。

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