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Single Nucleotide Polymorphism in the Promoter of the Human Interleukin-13 Gene Is Associated with Asthma in Malaysian Adults

机译:人类白细胞介素13基因启动子中的单核苷酸多态性与马来西亚成年人哮喘相关。

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摘要

Asthma susceptibility genes are mapped to a region on human chromosome 5q31-q33, which contains a cluster of proinflammatory cytokine genes such as interleukin-13 (IL-13), which is associated with asthma. This study investigated the allele frequencies of two single nucleotide polymorphisms (SNPs) (−1111C>T and 4257C>A) in the IL-13 gene between asthmatics and healthy volunteers as well as the relationship between these SNPs and IL-13 production. DNA extracted from buffy coat of asthmatic and control subjects was genotyped using the PCR-RFLP method. Amount of IL-13 produced by mitogen-stimulated peripheral blood leucocytes PBLs (PBLs) was determined by ELISA. The frequencies of the −1111C and 4257G wild-type alleles were 0.52 and 0.55 in asthmatics and were 0.67 and 0.56 in controls. A significant (P < 0.05) association was found between genotype and allele frequencies of SNP at position −1111C>T between asthmatic and control groups (OR, 1.810; 95% CI = 1.184 to 2.767; P < 0.05). The mitogen-stimulated PBLs from asthmatics produced higher amounts of IL-13 production (P < 0.001). The 4257GA heterozygous and 4257AA homozygous mutant alleles were associated with higher IL-13 production in asthmatics (P < 0.05). Our results show that the −1111T mutant allele are associated with asthma and the 4257A mutant alleles are associated with elevated IL-13 production.
机译:哮喘易感基因定位于人类染色体5q31-q33上的一个区域,该区域包含与哮喘相关的促炎细胞因子基因簇,例如白介素13(IL-13)。这项研究调查了哮喘患者和健康志愿者之间IL-13基因中两个单核苷酸多态性(SNP)(-1111C> T和4257C> A)的等位基因频率,以及这些SNP与IL-13产生的关系。使用PCR-RFLP方法对从哮喘和对照组受试者的血沉棕黄层中提取的DNA进行基因分型。通过ELISA确定由有丝分裂原刺激的外周血白细胞PBL(PBL)产生的IL-13的量。在哮喘患者中,-1111C和4257G野生型等位基因的频率分别为0.52和0.55,在对照组中分别为0.67和0.56。哮喘组与对照组之间在-1111C> T位点的SNP基因型与等位基因频率之间存在显着相关性(P <0.05)(OR,1.810; 95%CI = 1.184至2.767; P <0.05)。哮喘患者中有丝分裂原刺激的PBL产生更高的IL-13产生量(P <0.001)。在哮喘患者中,4257GA杂合和4257AA纯合突变等位基因与更高的IL-13产生相关(P <0.05)。我们的结果表明,-1111T突变等位基因与哮喘相关,而4257A突变等位基因与IL-13产生升高相关。

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