Jie Zhijun, Hu Zhilin, Bai Chunxue, Jin Meiling
Department of Respiratory Medicine, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, PR China.
J Asthma. 2011 Dec;48(10):979-85. doi: 10.3109/02770903.2011.624233. Epub 2011 Oct 31.
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.
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.
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).
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.
多种遗传和环境因素影响哮喘的发病机制。ADAM33(一种去整合素和金属蛋白酶结构域33)在多个不同人群中是一种新发现的哮喘易感基因。本研究的目的是确定ADAM33基因的单核苷酸多态性(SNP)是否与中国汉族人群的哮喘易感性和严重程度相关。
共纳入224名受试者,包括74名正常对照者和150名哮喘患者。根据一秒用力呼气容积占预计值的百分比、症状、夜间觉醒情况、短效β2激动剂的使用需求以及对正常活动的影响,将哮喘患者进一步分为高严重程度组或低严重程度组。采用聚合酶链反应-限制性片段长度多态性方法对ADAM33基因中的6个SNP(F + 1、ST + 4、S1、S2、T1和T2)进行基因分型。
在研究人群中发现ADAM33基因的3个SNP(F + 1、T1和T2)与哮喘有显著相关性(p = 0.0058 - 0.0067)。低严重程度组和高严重程度组中两个SNP(F + 1、T1)的等位基因频率与对照组的等位基因频率均有显著差异。T2 SNP的等位基因频率仅在高严重程度组中与对照组有显著差异(p = 0.0081)。单倍型分析表明,健康对照组中7575G、12433T和12462C(GTC单倍型)的频率高于哮喘患者(78.4%对61.8%,p = 0.0004)。
ADAM33基因多态性与中国华东汉族人群的哮喘易感性相关,且在高严重程度哮喘患者中遗传关联更强。