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首页> 外文期刊>The journal of asthma >ADAM33 gene polymorphisms associate with asthma susceptibility and severity in East China han population
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ADAM33 gene polymorphisms associate with asthma susceptibility and severity in East China han population

机译:华东地区汉族人群ADAM33基因多态性与哮喘易感性和严重性相关

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摘要

Objective. Multiple genetic and environmental factors impact the pathogenesis of asthma. ADAM33 (a disintegrin and metalloproteinase domain 33) represents a novel susceptibility gene for asthma in several diverse populations. The aim of this study was to determine whether single nucleotide polymorphisms (SNPs) of the ADAM33 gene associate with asthma susceptibility and severity in the Chinese Han population. Methods. A total of 224 subjects were enrolled, including 74 normal controls and 150 asthmatic patients. The asthmatic enrollees were further categorized into high- or low-severity groups according to the percentage of forced expiratory volume in 1 second of predicted value, symptoms, nighttime awakening, requirement for short-acting β2-agonist, and interference with normal activities. Six SNPs (F + 1, ST + 4, S1, S2, T1, and T2) in ADAM33 were genotyped using the polymerase chain restriction fragment length polymorphism method. Results. Three SNPs (F + 1, T1, and T2) of ADAM33 were found to have significant associations with asthma in the study population (p = .0058-.0067). The allele frequencies of two SNPs (F + 1, T1) in both the low- and high-severity groups were significantly different from the allele frequency in the control group. The allelic frequency of the T2 SNP was significantly different from that of the control group only in the high-severity group (p = .0081). Haplotype analysis demonstrated that the frequency of 7575G, 12433T, and 12462C (GTC haplotype) is higher in healthy controls than amongst asthma patients (78.4% vs. 61.8%, p = .0004). Conclusions. Polymorphisms of the ADAM33 gene associate with asthma susceptibility in the east China Han population, and the genetic association is stronger in high-severity asthmatics.
机译:目的。多种遗传和环境因素影响哮喘的发病机理。 ADAM33(整合素和金属蛋白酶结构域33)代表了几个不同人群中哮喘的新型易感基因。这项研究的目的是确定ADAM33基因的单核苷酸多态性(SNPs)是否与中国汉族人群的哮喘易感性和严重程度有关。方法。共有224名受试者入组,包括74名正常对照和150名哮喘患者。根据1秒内预测值的强迫呼气量百分比,症状,夜间醒来,对短效β2-激动剂的需求以及对正常活动的干扰,将哮喘入选者进一步分为高严重度组或低严重度组。使用聚合酶链限制片段长度多态性方法对ADAM33中的六个SNP(F + 1,ST + 4,S1,S2,T1和T2)进行基因分型。结果。在研究人群中,发现ADAM33的三个SNP(F + 1,T1和T2)与哮喘有显着关联(p = .0058-.0067)。在低和高严重度组中,两个SNP(F + 1,T1)的等位基因频率与对照组的等位基因频率显着不同。仅在高严重度组中,T2 SNP的等位基因频率与对照组显着不同(p = .0081)。单倍型分析表明,健康对照者7575G,12433T和12462C(GTC单倍型)的发生率高于哮喘患者(78.4%对61.8%,p = .0004)。结论。在华东地区汉族人群中,ADAM33基因的多态性与哮喘易感性有关,而在高严重度哮喘患者中,遗传关联更强。

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