Department of Respiratory Diseases, Hvidovre Hospital, Copenhagen, Denmark.
Clin Exp Allergy. 2010 Apr;40(4):576-81. doi: 10.1111/j.1365-2222.2010.03447.x. Epub 2010 Feb 1.
Excessive airway narrowing in response to broncho-active stimuli is a predictor for severe exacerbations in asthma. Leukotriene receptor antagonists (LTRAs) have complementary properties to inhaled corticosteroids (ICS) on asthma control.
The LTRA montelukast may provide an additional protection against excessive airway narrowing. We tested the add-on effects of montelukast on the maximal response plateau and PD(20) to inhaled methacholine in asthmatics on a stable dose of ICS.
Thirty-one patients with allergic asthma [14M/17F, 19-50 years, forced expiratory volume in 1 s (FEV(1)) >70% pred., PD(20) <3.9 micromol methacholine], with a twice documented response plateau to methacholine, were randomized in a double-blind (montelukast 10 mg or matching placebo once daily), 12-week parallel study. Bronchoprovocation tests with methacholine (0.03-256 micromol or > or =40% decline in FEV(1)) were repeated every 4 weeks and after wash-out. The main study objectives were changes from baseline in maximal FEV(1) decline at the response plateau (i.e. >2 post-dose FEV(1) values within 5%) and PD(20) to methacholine after 12 weeks' treatment.
Neither treatment affected baseline FEV(1) (P=0.62). Compared with placebo, montelukast significantly decreased the maximal response plateau to methacholine (mean difference 9.4%; 95% confidence interval 3.9-15.7; P<0.005), improved the FEV(1) decline (mean change in FEV(1) decline was 2.1% [montelukast] and -0.8% [placebo], respectively, P<0.05), and increased PD(20) methacholine (mean change in PD(20) of 5.3 [montelukast] and 1.4 [placebo] doubling doses, respectively, P<0.001).
Add-on montelukast to ICS has disease-modifying effects in adults with persistent asthma, and hence reduces the risk of excessive airway narrowing (NCT 00913328).
过度的气道狭窄对支气管活性刺激的反应是哮喘严重恶化的预测因子。白三烯受体拮抗剂(LTRAs)在哮喘控制方面与吸入皮质类固醇(ICS)具有互补作用。
LTRA 孟鲁司特可能对过度气道狭窄提供额外的保护。我们在接受稳定剂量 ICS 的哮喘患者中测试了孟鲁司特对吸入乙酰甲胆碱最大反应平台和 PD(20)的附加作用。
31 例过敏性哮喘患者[14M/17F,19-50 岁,1 秒用力呼气量(FEV(1))>70%预测值,PD(20)<3.9 微摩尔乙酰甲胆碱],两次记录到乙酰甲胆碱反应平台,随机分为双盲(孟鲁司特 10 mg 或匹配安慰剂每日一次),12 周平行研究。每 4 周重复一次乙酰甲胆碱支气管激发试验(0.03-256 微摩尔或 FEV(1)下降>或=40%),并在洗脱后重复。主要研究目的是从基线开始,在乙酰甲胆碱的最大 FEV(1)下降(即 5%内的 2 个后剂量 FEV(1)值)和 PD(20)在 12 周治疗后变化。
与安慰剂相比,孟鲁司特显著降低了乙酰甲胆碱的最大反应平台(平均差异 9.4%;95%置信区间 3.9-15.7;P<0.005),改善了 FEV(1)下降(孟鲁司特的 FEV(1)下降的平均变化为 2.1%,而安慰剂的变化为-0.8%,P<0.05),并增加了 PD(20)乙酰甲胆碱(孟鲁司特的 PD(20)变化为 5.3 倍,而安慰剂的变化为 1.4 倍,分别为 P<0.001)。
ICS 联合孟鲁司特治疗成人持续性哮喘具有疾病修饰作用,因此降低了过度气道狭窄的风险(NCT 00913328)。