Department of Oncology, Haematology and Respiratory Diseases, University of Modena and Reggio Emilia, Italy.
Allergy. 2010 Apr;65(4):474-81. doi: 10.1111/j.1398-9995.2009.02167.x. Epub 2009 Oct 1.
Asthma and chronic obstructive pulmonary disease (COPD) are chronic respiratory diseases involving an interaction between genetic and environmental factors. Interleukin-13 (IL13) has been suggested to have a role in both asthma and COPD. We investigated whether single nucleotide polymorphisms (SNPs) in the IL13 pathway may contribute to the susceptibility and severity of asthma and COPD in adults.
Twelve SNPs in IL13 pathway genes -IL4, IL13, IL4RA, IL13RA1, IL13RA2 and STAT6- were genotyped in subjects with asthma (n = 299) and in subjects with COPD or healthy smokers (n = 992). Genetic association was evaluated using genotype and allele models for asthma severity, atopy phenotypes and COPD susceptibility. Linear regression was used to determine the effects of polymorphism on baseline lung function (FEV(1), FEV(1)/FVC).
In asthmatics, three IL13 SNPs - rs1881457(-1512), rs1800925(-1111) and rs20541(R130Q) - were associated with atopy risk. One SNP in IL4RA1 [rs1805010(I75V)] was associated with asthma severity, and several IL13 SNPs showed borderline significance. IL13 SNPs rs1881457(-1512) and rs1800925(-1111) were associated with better FEV(1) and FEV(1)/FVC in asthmatics. IL13 SNPs rs2066960(intron 1), rs20541(R130Q) and rs1295685(exon 4) were associated with COPD risk and lower baseline lung function in the recessive model. In females, but not in males, rs2250747 of the IL13RA1 gene was associated with COPD and lower FEV(1).
These data suggest that IL13 SNPs (promoter and coding region) and, to a lesser extent, IL4RA SNPs may contribute to atopy and asthma. We also provide tentative evidence that IL13 SNPs in the coding region may be of significance in COPD susceptibility.
哮喘和慢性阻塞性肺疾病(COPD)是涉及遗传和环境因素相互作用的慢性呼吸道疾病。白细胞介素-13(IL13)被认为在哮喘和 COPD 中均有作用。我们研究了白细胞介素 13 通路中的单核苷酸多态性(SNP)是否可能导致成年人哮喘和 COPD 的易感性和严重程度。
对哮喘患者(n=299)和 COPD 或健康吸烟者(n=992)的 IL13 通路基因-IL4、IL13、IL4RA、IL13RA1、IL13RA2 和 STAT6 中的 12 个 SNP 进行基因分型。采用基因型和等位基因模型评估哮喘严重程度、过敏表型和 COPD 易感性的遗传相关性。线性回归用于确定多态性对基线肺功能(FEV1、FEV1/FVC)的影响。
在哮喘患者中,三个 IL13 SNP(rs1881457(-1512)、rs1800925(-1111)和 rs20541(R130Q))与过敏风险相关。IL4RA1 中的一个 SNP [rs1805010(I75V)]与哮喘严重程度相关,几个 IL13 SNP 具有边缘意义。IL13 SNPs rs1881457(-1512)和 rs1800925(-1111)与哮喘患者的 FEV1 和 FEV1/FVC 更好相关。IL13 SNPs rs2066960(内含子 1)、rs20541(R130Q)和 rs1295685(外显子 4)与 COPD 风险和隐性模型中的基线肺功能降低相关。在女性中,但不在男性中,IL13RA1 基因的 rs2250747 与 COPD 和 FEV1 降低相关。
这些数据表明,IL13 SNP(启动子和编码区)以及在较小程度上,IL4RA SNP 可能导致过敏和哮喘。我们还提供了初步证据,表明编码区中的 IL13 SNP 可能与 COPD 的易感性有关。