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首页> 外文期刊>The journal of asthma >Genetic variants of ADAM33 are associated with asthma susceptibility in the Punjabi population of Pakistan
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Genetic variants of ADAM33 are associated with asthma susceptibility in the Punjabi population of Pakistan

机译:ADAM33的遗传变异与巴基斯坦旁遮普邦的哮喘易感性有关

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Objective: A disintegrin and metalloproteinase 33 (ADAM33) gene has been considered as an asthma susceptibility gene due to its possible role in airway remodeling, abnormal cell proliferation, and differentiation. Association of this gene with asthma has been reported in several genetic studies on various populations. The current study aims to evaluate the association of ADAM33 gene polymorphisms with the risk of asthma in the Punjabi population of Pakistan. Method: A total of 101 asthma patients and 102 age-matched healthy controls from Lahore, a city in Punjab, were recruited. ADAM33 single nucleotide polymorphisms (SNPs) T+1[rs2280089], T2[rs2280090], T1[rs2280091], ST+5[rs597980], ST+4[rs44707], S2[rs528557], Q-1[rs612709], and F+1[rs511898] were genotyped in both patients and controls using single base extension and capillary electrophoresis-based genetic analyzer. The basic allelic and genotypic model was analyzed for association of the SNPs with asthma using SHEsis software. Haploview software was used to calculate pairwise linkage disequilibrium (LD) among six of the genotyped SNPs. Results: Of the 8 SNPs genotyped, only S2[rs528557] showed significant association with asthma (Allele p=0.0189, Genotype p=0.021). SNPs T+1[rs2280089], T2[rs2280090], T1[rs2280091], ST+4[rs44707], S2[rs528557], and Q-1[rs612709] were found to be in moderate to strong LD. The significantly higher frequency of haplotype AAGTCG in healthy controls suggests a protective effect against asthma risk in the studied population (p=0.0059). Conclusion: These findings suggest that genetic variants of ADAM33 gene may play important roles in asthma susceptibility in the Punjabi population of Pakistan.
机译:目的:整合素和金属蛋白酶33(ADAM33)基因因其可能在气道重塑,异常细胞增殖和分化中发挥作用而被认为是哮喘易感基因。该基因与哮喘的关联已在各种人群的多项遗传学研究中报道。当前的研究旨在评估ADAM33基因多态性与巴基斯坦旁遮普族人群哮喘风险的相关性。方法:招募了来自旁遮普邦拉合尔市的101名哮喘患者和102名年龄匹配的健康对照者。 ADAM33单核苷酸多态性(SNP)T + 1 [rs2280089],T2 [rs2280090],T1 [rs2280091],ST + 5 [rs597980],ST + 4 [rs44707],S2 [rs528557],Q-1 [rs612709],使用单碱基延伸和基于毛细管电泳的遗传分析仪对患者和对照中的F1和F + 1 [rs511898]进行基因分型。使用SHEsis软件分析了基本的等位基因和基因型模型,以分析SNP与哮喘的相关性。使用Haploview软件计算了六个基因型SNP之间的成对连锁不平衡(LD)。结果:在8个SNP基因型中,只有S2 [rs528557]与哮喘显着相关(等位基因p = 0.0189,基因型p = 0.021)。发现SNP T + 1 [rs2280089],T2 [rs2280090],T1 [rs2280091],ST + 4 [rs44707],S2 [rs528557]和Q-1 [rs612709]处于中等至强LD。在健康对照中,单倍型AAGTCG的频率明显较高,这表明在研究人群中有预防哮喘风险的保护作用(p = 0.0059)。结论:这些发现表明,ADAM33基因的遗传变异可能在巴基斯坦旁遮普邦的哮喘易感性中起重要作用。

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