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.

译文

:速效b2-肾上腺素能受体激动剂通常用于支气管扩张药,以缓解哮喘患者的症状。这项研究的目的是测试PDE4D基因(b2-肾上腺素受体诱导的气道平滑肌细胞cAMP转换的关键调节剂)的遗传变异是否影响对短效b2-激动剂的反应。通过在服用沙丁胺醇后一秒钟内基线强迫呼气量的百分比变化(FEV(1))对133名哮喘儿童的支气管扩张剂反应性进行了评估。该分析是在气道阻塞患者中进行的(FEV(1)/ FVC比率低于90%,n = 93)。 rs1544791 G / A多态性(P = 0.006)和-1345 C / T(rs1504982)启动子变异的基因型之间,经基线FEV(1)值调整的FEV(1)%变化显着不同(P = 0.03)。在将年龄,性别,特应性疾病和控制药物纳入多变量模型后,这种关联仍然很显着(分别为P = 0.004和P = 0.02)。我们的工作确定了与哮喘治疗调节有关的新遗传变异,其中之一(rs1544791)以前与哮喘表型有关。

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