Zhang Ji, Yu Chang, Noonan Gertrude, Reiss Theodore F
Department of Clinical Biostatistics, Merck Research Laboratories, Rahway, New Jersey 07065, USA.
Clin Ther. 2002 Apr;24(4):574-82. doi: 10.1016/s0149-2918(02)85133-5.
Peak expiratory flow (PEF) is an important measure of airway functin in asthma. PEF variability (PEFvar) assessment is described in asthma treatment guidelines as another means of evaluating patient status and response to therapy.
The goal of this study was to determine the clinical effect of oral montelukast, a leukotriene receptor antagonist, on PEFvar in asthmatic patients and to assess the relationship of PEFvar with other clinical measures.
This was a retrospective analysis of data from a multicenter, randomized, double-blind, placebo-controlled, parallel-group study, details of which have been published previously. Eligible patients had chronic stable asthma, had a forced expiratory volume in 1 second (FEV1) that was 50% to 85% of the predicted value, used inhaled beta-agonists, had at least 15% improvement in absolute FEV1 after inhaled beta-agonist administration, and showed a minimal predefined level of daytime asthma symptoms. Treatment consisted of a 2-week, single-blind, placebo run-in period followed by a 12-week, double-blind treatment period (montelukast 10 mg or matching placebo once daily at bedtime).
Six hundred eighty-one patients (age range, 15-79 years) were randomized to treatment at 50 centers. Baseline PEFvar was 11.44% +/- 6.55% and 10.62% +/- 6.48% in the montelukast and placebo groups, respectively. PEFvar decreased 20.1% and 7.5% from baseline in the montelukast and placebo groups, respectively. The between-group difference was significant (P < 0.001). PEFvar had low correlation with other clinical measures.
Over 12 weeks of treatment, montelukast significantly reduced PEFvar compared with placebo, indicating improved asthma control. The relative reduction in PEFvar was similar in patients with different degrees of variability at baseline. PEFvar did not correlate highly with other outcome variables and may measure different aspects of the disease.
呼气峰值流速(PEF)是哮喘气道功能的一项重要指标。哮喘治疗指南中将PEF变异性(PEFvar)评估描述为评估患者病情及对治疗反应的另一种方法。
本研究的目的是确定白三烯受体拮抗剂口服孟鲁司特对哮喘患者PEFvar的临床疗效,并评估PEFvar与其他临床指标的关系。
这是一项对多中心、随机、双盲、安慰剂对照、平行组研究数据的回顾性分析,该研究的详细情况此前已发表。符合条件的患者患有慢性稳定型哮喘,其1秒用力呼气容积(FEV1)为预测值的50%至85%,使用吸入性β受体激动剂,吸入β受体激动剂后绝对FEV1至少改善15%,且白天哮喘症状显示出最低预定水平。治疗包括为期2周的单盲、安慰剂导入期,随后是为期12周的双盲治疗期(孟鲁司特10毫克或匹配的安慰剂,每晚睡前服用一次)。
681例患者(年龄范围15 - 79岁)在50个中心被随机分配接受治疗。孟鲁司特组和安慰剂组的基线PEFvar分别为11.44%±6.55%和10.62%±6.48%。孟鲁司特组和安慰剂组的PEFvar分别较基线下降了20.1%和7.5%。组间差异有统计学意义(P < 0.001)。PEFvar与其他临床指标的相关性较低。
在12周的治疗过程中,与安慰剂相比,孟鲁司特显著降低了PEFvar,表明哮喘控制得到改善。基线变异性不同程度的患者中,PEFvar的相对降低相似。PEFvar与其他结局变量的相关性不高,可能衡量了疾病的不同方面。