Research Center, CHU Sainte-Justine, Montreal, QC, Canada.
Mediators Inflamm. 2011;2011:301695. doi: 10.1155/2011/301695. Epub 2011 Aug 24.
Short-acting b2-adrenergic receptor agonists are commonly used bronchodilators for symptom relief in asthmatics. The aim of this study was to test whether genetic variants in PDE4D gene, a key regulator of b2-adrenoceptor-induced cAMP turnover in airway smooth muscle cells, affect the response to short-acting b2-agonists. Bronchodilator responsiveness was assessed in 133 asthmatic children by % change in baseline forced expiratory volume in one second (FEV(1)) after administration of albuterol. The analyses were performed in patients with airway obstruction (FEV(1)/FVC ratio below 90%, n = 93). FEV(1) % change adjusted for baseline FEV(1) values was significantly different between genotypes of rs1544791 G/A polymorphism (P = 0.006) and -1345 C/T (rs1504982) promoter variation (P = 0.03). The association remained significant with inclusion of age, sex, atopy, and controller medication into multivariate model (P = 0.004 and P = 0.02, resp.). Our work identifies new genetic variants implicated in modulation of asthma treatment, one of them (rs1544791) previously associated with asthma phenotype.
短效β2-肾上腺素受体激动剂是治疗哮喘患者症状的常用支气管扩张剂。本研究旨在测试 PDE4D 基因(气道平滑肌细胞中β2-肾上腺素受体诱导的 cAMP 转化的关键调节剂)的遗传变异是否影响对短效β2-激动剂的反应。通过测定沙丁胺醇给药后基础 1 秒用力呼气量(FEV1)的百分比变化,评估 133 名哮喘儿童的支气管扩张剂反应性。在气道阻塞患者(FEV1/FVC 比值低于 90%,n=93)中进行分析。rs1544791 G/A 多态性(P=0.006)和-1345 C/T(rs1504982)启动子变异(P=0.03)的基因型之间,调整基础 FEV1 值后的 FEV1%变化差异具有统计学意义。将年龄、性别、特应性和控制药物纳入多变量模型后,相关性仍然显著(P=0.004 和 P=0.02)。我们的工作确定了新的遗传变异与哮喘治疗的调节有关,其中一个(rs1544791)先前与哮喘表型有关。