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ADRB2 Gene Polymorphisms and Salbutamol Responsiveness in Serbian Children with Asthma

机译:塞尔维亚哮喘儿童的ADRB2基因多态性和沙丁胺醇反应性

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摘要

Inhaled β2 adrenergic receptor (β2-AR) agonists are the mainstay of asthma therapy. The β2-AR protein is encoded by the ADRB2 gene and variants within this gene can have significant consequences for modulating the response to asthma therapy. This cross-sectional study performed at the University Children’s Hospital in Belgrade, included 54 children with asthma. The subjects were genotyped for ADRB2 +46A>G (Arg16Gly, rs1042713) and +79C>G (Gln27Glu, rs 1042714) polymorphisms and the association with asthma severity and response to inhaled salbutamol was examined. In Serbian asthmatic children, allele +46A was detected with a frequency of 41.7% and allele +79G was detected with a frequency of 23.1%. Allele +46G was found to be associated with a better response to inhaled salbutamol (p <0.05) and with mild form of asthma (p <0.05). Polymorphism ADRB2 +46A>G may be a determinant of asthma severity and response to salbutamol in children with asthma. We did not find any association of +79C>G polymorphisms with the asthma severity and bronchodilator response to inhaled salbutamol. The results of this study can be potentially useful for personalization of asthma treatment.
机译:吸入的β2肾上腺素能受体(β2-AR)激动剂是哮喘治疗的主要手段。 β2-AR蛋白由ADRB2基因编码,该基因中的变体可能对调节对哮喘治疗的反应具有重大影响。在贝尔格莱德的大学儿童医院进行的这项横断面研究包括了54名患有哮喘的儿童。对受试者进行ADRB2 + 46A> G(Arg16Gly,rs1042713)和+ 79C> G(Gln27Glu,rs1042714)多态性的基因分型,并检查其与哮喘严重程度和吸入沙丁胺醇反应的相关性。在塞尔维亚哮喘儿童中,等位基因+ 46A的频率为41.7%,等位基因+ 79G的频率为23.1%。发现等位基因+ 46G与吸入沙丁胺醇的更好反应有关(p <0.05)和轻度哮喘(p <0.05)。 ADRB2 + 46A> G多态性可能是哮喘患儿哮喘严重程度和对沙丁胺醇反应的决定因素。我们没有发现+ 79C> G多态性与哮喘严重程度和支气管扩张剂对吸入沙丁胺醇的反应有关。这项研究的结果可能对个性化哮喘治疗有用。

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