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Asthma: Gln27glu And Arg16gly Polymorphisms Of The Beta2-adrenergic Receptor Gene As Risk Factors

机译:哮喘:β2-肾上腺素能受体基因的Gln27glu和Arg16gly多态性为危险因素

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摘要

Background: Asthma is caused by both environmental and genetic factors. The ADRB2 gene, which encodes the beta 2-adrenergic receptor, is one of the most extensively studied genes with respect to asthma prevalence and severity. The Arg16Gly (+46A > G) and Gln27Glu (+79C > G) polymorphisms in the ADRB2 gene cause changes in the amino acids flanking the receptor ligand site, altering the response to bronchodilators and the risk of asthma through complex pathways. The ADRB2 polymorphisms affect beta-adrenergic bronchodilator action and are a tool to identify at-risk populations.Objective: To determine the frequency of these two polymorphisms in allergic asthma patients and healthy subjects and to correlate these data with the occurrence and severity of asthma.Methods: Eighty-eight allergic asthma patients and 141 healthy subjects were included in this study. The ADRB2 polymorphisms were analyzed using the amplification-refractory mutation system - polymerase chain reaction (ARMS-PCR) technique. The statistical analysis was performed with the SPSS 21.0 software using the Fisher's Exact and χ2 tests.Results: The ADRB2 polymorphisms were associated with asthma occurrence. The Arg16Arg, Gln27Gln and Gln27Glu genotypes were risk factors; the odds ratios were 6.782 (CI = 3.07 to 16.03), 2.120 (CI = 1.22 to 3.71) and 8.096 (CI = 3.90 to 17.77), respectively. For the Gly16Gly and Glu27Glu genotypes, the odds ratios were 0.312 (CI = 0.17 to 0.56) and 0.084 (CI = 0.04 to 0.17), respectively. The haplotype analysis showed that there were associations between the following groups: Arg16Arg-Gln27Gln (OR = 5.108, CI = 1.82 to 16.37), Gly16Gly-Glu27Glu (OR = 2.816, CI = 1.25 to 6.54), Arg16Gly-Gln27Glu (OR = 0.048, CI = 0.01 to 0.14) and Gly16Gly-Gln27Glu (OR = 0.1036, CI = 0.02 to 0.39). The polymorphism Gln27Glu was associated with asthma severity, as the Gln27Gln genotype was a risk factor for severe asthma (OR = 2.798, CI = 1.099 to 6.674) and the Gln27Glu genotype was a protective factor for mild (OR = 3.063, CI = 1.037 to 9.041) and severe (OR = 0.182, CI = 0.048 to 0.691) asthma.Conclusions: The Arg16Gly and Gln27Glu polymorphisms in the ADRB2 gene are associated with asthma presence and severity. © 2014 de Paiva et al.; licensee BioMed Central Ltd.
机译:背景:哮喘是由环境和遗传因素引起的。编码β2-肾上腺素能受体的ADRB2基因是关于哮喘患病率和严重程度研究最广泛的基因之一。 ADRB2基因中的Arg16Gly(+ 46A> G)和Gln27Glu(+ 79C> G)多态性导致受体配体位点侧翼的氨基酸发生变化,从而改变了对支气管扩张药的反应以及通过复杂途径发生哮喘的风险。 ADRB2基因多态性影响β-肾上腺素支气管扩张剂的作用,是识别高危人群的工具。目的:确定过敏性哮喘患者和健康受试者中这两种基因多态性的发生频率,并将这些数据与哮喘的发生和严重程度相关联。方法:本研究纳入了88名过敏性哮喘患者和141名健康受试者。使用扩增-难治突变系统-聚合酶链反应(ARMS-PCR)技术分析ADRB2多态性。采用SPSS 21.0软件通过Fisher精确检验和χ2检验进行统计分析。结果:ADRB2基因多态性与哮喘的发生有关。 Arg16Arg,Gln27Gln和Gln27Glu基因型是危险因素。比值比分别为6.782(CI = 3.07至16.03),2.120(CI = 1.22至3.71)和8.096(CI = 3.90至17.77)。对于Gly16Gly和Glu27Glu基因型,优势比分别为0.312(CI = 0.17至0.56)和0.084(CI = 0.04至0.17)。单倍型分析表明以下组之间存在关联:Arg16Arg-Gln27Gln(OR = 5.108,CI = 1.82至16.37),Gly16Gly-Glu27Glu(OR = 2.816,CI = 1.25至6.54),Arg16Gly-Gln27Glu(OR = 0.048) ,CI = 0.01至0.14)和Gly16Gly-Gln27Glu(OR = 0.1036,CI = 0.02至0.39)。 Gln27Glu多态性与哮喘严重程度相关,因为Gln27Gln基因型是重度哮喘的危险因素(OR = 2.798,CI = 1.099至6.674),而Gln27Glu基因型是轻度保护性因素(OR = 3.063,CI = 1.037至1.037)。结论:ADRB2基因中的Arg16Gly和Gln27Glu多态性与哮喘的存在和严重程度有关。9.041)和严重(OR = 0.182,CI = 0.048至0.691)哮喘。 ©2014 de Paiva等;被许可人BioMed Central Ltd.

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