Matheson Melanie C, Ellis Justine A, Raven Joan, Johns David P, Walters E Haydn, Abramson Michael J
Department of Epidemiology and Preventive Medicine, Monash University, Monash, VIC, Australia.
Centre for Molecular, Environmental, Genetic and Analytic Epidemiology, School of Population Health, The University of Melbourne, Level 2/723 Swanston Street, Carlton, VIC, 3053, Australia.
J Hum Genet. 2006;51(11):943. doi: 10.1007/s10038-006-0043-z. Epub 2006 Sep 1.
The beta(2)-adrenergic receptor (beta(2)AR) is a transmembrane protein expressed by airway smooth muscle cells. In vitro studies have shown that polymorphisms at amino acid positions 16 and 27 alter receptor function. The aim of this study was to examine the associations between the beta ( 2 ) AR polymorphisms and risks of asthma, chronic obstructive pulmonary disease (COPD) and respiratory symptoms in a sample of adults. Participants were part of a cross-sectional population-based study of risk factors for respiratory disease. A total of 1,090 Caucasian participants completed a detailed respiratory questionnaire, spirometry, methacholine challenge and measurement of gas transfer. Genotyping for beta ( 2 ) AR polymorphisms at positions 16 and 27 was performed using the tetra-primer amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) method. Haplotype frequencies for the two polymorphisms were estimated using the E-M algorithm. We found the Arg16 homozygotes had an increased risk of COPD (OR 5.13; 95% CI 1.40,18.8), asthma (2.44; 1.12,5.31) and symptoms of wheeze (1.84; 1.02,3.35). The Gln27 homozygotes had an increased risk of asthma (2.08; 1.05,4.13) and bronchial hyperreactivity (BHR) (1.92; 1.07,3.46). The Arg16/Gln27 haplotype was associated with asthma (1.63; 1.12,2.38) and COPD (2.91; 1.42,5.94). The Arg16/Gln27 beta(2)AR haplotype is important in COPD, asthma and BHR, and may be associated with more severe respiratory symptoms in middle-aged and older adults.
β2肾上腺素能受体(β2AR)是一种由气道平滑肌细胞表达的跨膜蛋白。体外研究表明,第16和27位氨基酸位置的多态性会改变受体功能。本研究的目的是在一组成年人样本中检验β2AR多态性与哮喘、慢性阻塞性肺疾病(COPD)风险及呼吸道症状之间的关联。参与者是一项基于人群的呼吸道疾病危险因素横断面研究的一部分。共有1090名白种人参与者完成了详细的呼吸道问卷、肺功能测定、乙酰甲胆碱激发试验和气体交换测量。使用四引物扩增阻滞突变系统-聚合酶链反应(ARMS-PCR)方法对第16和27位的β2AR多态性进行基因分型。使用期望最大化(E-M)算法估计这两种多态性的单倍型频率。我们发现,第16位精氨酸纯合子患COPD(比值比[OR] 5.13;95%置信区间[CI] 1.40, 18.8)、哮喘(2.44;1.12, 5.31)和喘息症状(1.84;1.02, 3.35)的风险增加。第27位谷氨酰胺纯合子患哮喘(2.08;1.05, 4.13)和支气管高反应性(BHR)(1.92;1.07, 3.46)的风险增加。第16位精氨酸/第27位谷氨酰胺单倍型与哮喘(1.63;1.12, 2.38)和COPD(2.91;1.42, 5.94)相关。第16位精氨酸/第27位谷氨酰胺β2AR单倍型在COPD、哮喘和BHR中具有重要意义,并且可能与中老年人群更严重的呼吸道症状相关。