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Association of ADAM33 gene polymorphisms with adult-onset asthma and its severity in an Indian adult population

机译:在印度成人人群中,ADAM33基因多态性与成人哮喘及其严重程度的关系

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摘要

ADAM33, a member of the ADAM (a disintegrin and metalloprotease) gene family, is an asthma susceptibility gene originally identified by positional cloning. In the present study, we investigated the possible association of five single-nucleotide polymorphisms (SNPs) in the ADAM33 (rs511898, rs528557, rs44707, rs597980 and rs2787094) with adult-onset asthma in an Indian population. The study included 175 patients with mild intermittent (n = 44), mild persistent (n = 108) or moderate persistent (n = 23) subgroups of asthma, and 253 nonasthmatic control individuals. SNPs were genotyped with the help of restriction fragment length polymorphism polymerase chain reaction (RFLP-PCR) method, and data were analysed using chi-square test and logistic regression model. Bonferroni’s correction for multiple comparisons was applied for each hypothesis. Genotypes and allele frequencies of SNPs rs511898 and rs528557 were significantly associated with adult-onset asthma (P = 0.010-0.001). A significant association of the homozygous mutant genotype and mutant alleles of SNPs rs2787094, rs44707 and rs597980 with the asthma was also observed (P = 0.020-0.001). A positive association between asthma and haplotypes AGCCT, GGCCT, AGACT, GCAGT, GGACT, ACCCC and AGACC were also found (P = 0.036-0.001, OR = 2.07–8.49). Haplotypes AGCGT, GCAGC, ACAGC, ACAGT, GGAGC and GGCGT appear to protect against asthma (P = 0.013-0.0001, OR = 0.34–0.10). Our data suggest that ADAM33 gene polymorphisms serve as genetic risk factors for asthma in Indian adult population.
机译:ADAM33是ADAM(一种整合素和金属蛋白酶)基因家族的成员,是一种哮喘易感基因,最初是通过位置克隆来鉴定的。在本研究中,我们调查了印度人群中ADAM33(rs511898,rs528557,rs44707,rs597980和rs2787094)中的五个单核苷酸多态性(SNP)与成人哮喘的可能关联。该研究包括175例轻度间歇性(n = 44),轻度持续性(n = 108)或中度持续性(n = 23)哮喘亚组的患者和253名非哮喘对照组。利用限制性片段长度多态性聚合酶链反应(RFLP-PCR)方法对SNPs进行基因分型,并使用卡方检验和逻辑回归模型分析数据。每个假设均适用Bonferroni对多个比较的修正。 rs511898和rs528557 SNP的基因型和等位基因频率与成年哮喘显着相关(P = 0.010- <0.001)。还观察到SNP rs2787094,rs44707和rs597980的纯合突变基因型和突变等位基因与哮喘有显着相关性(P = 0.020- <0.001)。哮喘与单体型AGCCT,GGCCT,AGACT,GCAGT,GGACT,ACCCC和AGACC之间也呈正相关(P = 0.036- <0.001,OR = 2.07–8.49)。单倍型AGCGT,GCAGC,ACAGC,ACAGT,GGAGC和GGCGT似乎可以预防哮喘(P = 0.013- <0.0001,OR = 0.34-0.10)。我们的数据表明,ADAM33基因多态性可作为印度成年人口哮喘的遗传危险因素。

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  • 来源
    《Journal of Genetics》 |2011年第2期|p.265-273|共9页
  • 作者单位

    Department of Pediatrics, Chhtrapati Shahuji Maharaj Medical University, Chowk, Lucknow 226 003, India;

    Department of Pediatrics, Chhtrapati Shahuji Maharaj Medical University, Chowk, Lucknow 226 003, India;

    Department of Pulmonary Medicine, Chhtrapati Shahuji Maharaj Medical University, Chowk, Lucknow 226 003, India;

    Department of Pathology, Chhtrapati Shahuji Maharaj Medical University, Chowk, Lucknow 226 003, India;

    Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, 208 016, India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    polymorphisms; asthma; severity; haplotypes; linkage disequilibrium;

    机译:多态性;哮喘;严重度;单倍型;连锁不平衡;

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