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首页> 外文期刊>Pharmacogenetics and genomics >Association between TAAR6 polymorphisms and airway responsiveness to inhaled corticosteroids in asthmatic patients
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Association between TAAR6 polymorphisms and airway responsiveness to inhaled corticosteroids in asthmatic patients

机译:TAAR6基因多态性与哮喘患者吸入皮质类固醇的气道反应性之间的关系

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摘要

Background Genetic polymorphisms may be responsible for the wide variation in response to inhaled corticosteroids in asthmatic patients. We had previously reported that one polymorphism rs7772821, located on the 3 '-UTR of trace amine-associated receptor 6 (TAAR6), is significantly associated with percentile changes in the forced expiratory volume in 1 s (% increment FEV1) after inhaled corticosteroid treatment in asthmatics using a genome-wide association study. The aim of the present study was to validate the association between 15 single-nucleotide polymorphisms (SNPs) on the TAAR6 and airway responsiveness to inhaled corticosteroids in the asthmatics. Methods The % increment FEV1 induced by 4 weeks' treatment with inhaled fluticasone propionate (1000 mu g daily) was measured in 246 asthmatics. The 15 SNPs of TAAR6 were genotyped using a TaqMan assay. An association analysis between % increment FEV1 and TAAR6 polymorphisms was carried out using a linear regression model controlling for age, sex, smoking status, presence of atopy, and baseline FEV1 as covariates. Results Among the 15 SNPs and seven haplotypes of TAAR6, rs7772821 (T > G) on the 3 '-UTR showed the strongest correlation with inhaled corticosteroid-induced % increment FEV1 (P-corr=0.002 in the codominant model, P-corr=0.03 in the dominant model, P-corr=0.01 in the recessive model). The % increment FEV1 of the rs7772821T > G minor homozygotes (60.77%) was higher than that of patients harboring either the rs7772821 T/G or T/T genotypes (21.32 and 31.60%, respectively). Conclusion The TAAR6 rs7772821 polymorphism may be one of the important genetic factors for predicting the response to treatment with inhaled corticosteroids in asthmatics.
机译:背景遗传多态性可能是导致哮喘患者吸入皮质类固醇激素反应差异很大的原因。我们之前曾报道过,一种多态性rs7772821位于痕量胺相关受体6(TAAR6)的3'-UTR上,与吸入皮质类固醇治疗后1秒内强迫呼气量的百分位变化显着相关(FEV1递增百分比)使用全基因组关联研究进行哮喘治疗本研究的目的是验证TAAR6上的15个单核苷酸多态性(SNP)与哮喘患者吸入皮质类固醇的气道反应性之间的关联。方法测定246例哮喘患者吸入丙酸氟替卡松(每天1000微克)4周后诱导的FEV1增加百分比。使用TaqMan分析对TAAR6的15个SNP进行基因分型。使用线性回归模型(控制年龄,性别,吸烟状况,特应性疾病的存在和基线FEV1作为协变量)对%FFE1增加和TAAR6多态性之间的关联性进行分析。结果TAAR6的15个SNP和7个单倍型中,3'-UTR上的rs7772821(T> G)与吸入糖皮质激素引起的%FEV1增高最强相关(在共显性模型中,P-corr = 0.002,P-corr =在优势模型中为0.03,在隐性模型中为P-corr = 0.01)。 rs7772821T> G次要纯合子的FEV1的增量百分比(60.77%)高于具有rs7772821 T / G或T / T基因型的患者(分别为21.32和31.60%)。结论TAAR6基因rs7772821位点的多态性可能是预测哮喘患者吸入皮质类固醇激素治疗反应的重要遗传因素之一。

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