Lee D K C, Jackson C M, Bates C E, Lipworth B J
Asthma and Allergy Research Group, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, UK.
Thorax. 2004 Aug;59(8):662-7. doi: 10.1136/thx.2003.019059.
The development of tolerance following the use of long acting beta(2) agonists in asthmatic patients with either the homozygous arginine (Arg-16) or glycine (Gly-16) genotypes is poorly documented, especially in relation to the acute reliever response to salbutamol in constricted airways. A study was undertaken to evaluate the Arg-16 and Gly-16 genotypes for the acute salbutamol response following methacholine bronchial challenge between the first and last doses of formoterol (FM) and salmeterol (SM) combination inhalers.
Parallel groups of 10 matched homozygous Arg-16 and 10 homozygous Gly-16 patients completed a randomised, double blind, double dummy, crossover study. Following a 1 week washout period, patients received treatment for 2 weeks with either inhaled budesonide (BUD) 200 micro g + FM 6 micro g (two puffs twice daily) or inhaled fluticasone propionate (FP) 250 micro g + SM 50 micro g (one puff twice daily). After washouts and randomised treatments (1 hour after the first and last inhalation) a methacholine challenge was performed followed by salbutamol 200 micro g, with recovery over 30 minutes (the primary outcome).
Washout values for forced expiratory volume in 1 second (FEV(1)), methacholine hyperreactivity, and salbutamol recovery were similar for both treatments and genotypes. Pre-challenge FEV(1) values for both genotypes did not differ significantly between the first and last doses of each treatment. Salbutamol recovery as mean (SE) area under the 30 minute time-response curve was significantly delayed (p<0.05) equally in both genotype and treatment groups. There were no differences in salbutamol recovery in either genotype or treatment group.
Acute salbutamol recovery in methacholine constricted airways was significantly delayed to a similar degree in both genotypes due to cross tolerance induced by FM or SM.
对于患有纯合精氨酸(Arg - 16)或甘氨酸(Gly - 16)基因型的哮喘患者,使用长效β₂受体激动剂后耐受性的发展情况鲜有文献记载,尤其是在狭窄气道中对沙丁胺醇的急性缓解反应方面。开展了一项研究,以评估在福莫特罗(FM)和沙美特罗(SM)联合吸入器的首剂和末剂之间进行乙酰甲胆碱支气管激发试验后,Arg - 16和Gly - 16基因型对沙丁胺醇急性反应的情况。
10名匹配的纯合Arg - 16患者和10名纯合Gly - 16患者组成平行组,完成了一项随机、双盲、双模拟、交叉研究。在为期1周的洗脱期后,患者接受2周的治疗,治疗方案为吸入布地奈德(BUD)200μg + FM 6μg(每日两次,每次两喷)或吸入丙酸氟替卡松(FP)250μg + SM 50μg(每日两次,每次一喷)。在洗脱期和随机治疗后(首次和末次吸入后1小时),进行乙酰甲胆碱激发试验,随后给予200μg沙丁胺醇,观察30分钟内的恢复情况(主要结局)。
两种治疗方法和两种基因型的一秒用力呼气容积(FEV₁)、乙酰甲胆碱高反应性和沙丁胺醇恢复的洗脱值相似。每种治疗的首剂和末剂之间,两种基因型的激发前FEV₁值无显著差异。在基因型和治疗组中,沙丁胺醇在30分钟时间 - 反应曲线下的平均(SE)面积恢复均显著延迟(p < 0.05)。基因型组或治疗组中沙丁胺醇恢复情况均无差异。
由于FM或SM诱导的交叉耐受性,两种基因型在乙酰甲胆碱诱发狭窄的气道中,沙丁胺醇的急性恢复均显著延迟至相似程度。