Spahn Joseph D, Covar Ronina A, Jain Neal, Gleason Melanie, Shimamoto Reed, Szefler Stanley J, Gelfand Erwin W
Division of Clinical Pharmacology, Department of Pediatrics, National Jewish Medical and Research Center, University of Colorado Health Sciences Center, Denver 80206, USA.
Ann Allergy Asthma Immunol. 2006 Apr;96(4):541-9. doi: 10.1016/S1081-1206(10)63548-X.
Montelukast is a widely used controller agent in childhood asthma. It is modestly effective in reducing symptoms, decreasing the need for rescue albuterol, and improving forced expiratory volume in 1 second (FEV1).
To determine whether montelukast therapy improves peripheral airway obstruction as measured by lung volumes, air trapping, airway resistance (Raw), and specific conductance (Sgaw).
Twenty-one children aged 9 to 18 years with mild-to-moderate asthma were randomized into a double-blind, placebo-controlled study to receive montelukast (5 or 10 mg) or matching placebo daily for 8 weeks. Symptoms and albuterol use were recorded twice daily, and exhaled nitric oxide measurement, forced oscillometry, spirometry, and body box plethysmography (before and after beta-agonist use) were performed at randomization and at 2, 4, 6, and 8 weeks. Circulating eosinophil counts and serum eosinophil cationic protein (ECP) levels were obtained at randomization and at 8 weeks.
Montelukast-treated patients had lower residual volume (P = .05), residual volume-total lung capacity ratio (P = .04), Raw (P = .02), Sgaw (P = .03), and serum ECP levels (P = .02) at 8 weeks compared with those treated with placebo. There was a trend toward reduced daytime and nighttime albuterol use, although the difference did not reach statistical significance. There were no significant differences in FEV1, FEV1-forced vital capacity ratio, exhaled nitric oxide levels, or daytime and nighttime symptom scores between the 2 groups.
Montelukast therapy was associated with less air trapping, hyperinflation, and Raw and better Sgaw compared with placebo. Lower serum ECP levels, a surrogate measure of airway inflammation, were associated with improvements in lung function.
孟鲁司特是儿童哮喘中广泛使用的控制药物。它在减轻症状、减少急救沙丁胺醇的使用以及提高一秒用力呼气量(FEV1)方面有一定疗效。
确定孟鲁司特治疗是否能改善通过肺容积、气体潴留、气道阻力(Raw)和比传导率(Sgaw)测量的外周气道阻塞情况。
将21名9至18岁的轻至中度哮喘儿童随机分为一项双盲、安慰剂对照研究,接受孟鲁司特(5或10毫克)或匹配的安慰剂,每日一次,共8周。每天记录症状和沙丁胺醇的使用情况,并在随机分组时以及第2、4、6和8周进行呼出一氧化氮测量、强迫振荡法、肺量计检查和体箱体积描记法(使用β受体激动剂前后)。在随机分组时和第8周获取循环嗜酸性粒细胞计数和血清嗜酸性粒细胞阳离子蛋白(ECP)水平。
与接受安慰剂治疗的患者相比,接受孟鲁司特治疗的患者在第8周时残气量(P = 0.05)、残气量与肺总量之比(P = 0.04)、Raw(P = 0.02)、Sgaw(P = 0.03)和血清ECP水平(P = 0.02)较低。白天和夜间沙丁胺醇的使用有减少趋势,尽管差异未达到统计学意义。两组之间在FEV1、FEV1与用力肺活量之比、呼出一氧化氮水平或白天和夜间症状评分方面没有显著差异。
与安慰剂相比,孟鲁司特治疗与更少的气体潴留、肺过度充气和Raw以及更好的Sgaw相关。较低的血清ECP水平(气道炎症的替代指标)与肺功能改善相关。