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首页> 外文期刊>Respiratory medicine >Montelukast and bronchial inflammation in asthma: a randomised, double-blind placebo-controlled trial.
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Montelukast and bronchial inflammation in asthma: a randomised, double-blind placebo-controlled trial.

机译:孟鲁司特和哮喘支气管炎症:一项随机,双盲安慰剂对照试验。

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BACKGROUND: Examination of bronchoalveolar lavage, induced sputum, and peripheral blood indicate that cysteinyl leukotriene receptor blockers decrease inflammatory cells in asthma but these do not examine airway tissue per se. OBJECTIVES: Our objective was to determine the effect of montelukast, a leukotriene receptor antagonist, on airway tissue inflammatory cells by direct bronchoscopic examination of the bronchial mucosa. METHODS: Adult subjects with mild asthma (pre-bronchodilator FEV(1)> or =70% predicted; PC(20) of < or =4 mg/mL) were given 10mg/day oral montelukast (N=38) or placebo (N=37) for 6 weeks. Bronchial mucosal eosinophils and mast cells were identified and counted. RESULTS: Change from baseline in numbers of biopsy EG2+ ("activated") eosinophils was the primary endpoint; numbers of total (chromotrope 2R+) eosinophils and (tryptase+) mast cells were secondary. Unexpectedly, there were many patients with zero EG2+ eosinophils at baseline. There was a within-group decrease in EG2+ cells, from 13.54 cells/mm (at baseline) to 0.79 cells/mm at 6 weeks in the montelukast group (LS mean change; 95% confidence interval=-13.59 [-25.45, -1.74]cells/mm; P<0.05), a change not observed in the placebo group (-1.17 [-13.26, 10.91]cells/mm; NS). The zero-inflated Poisson statistical model demonstrated that montelukast significantly reduced post-treatment EG2+ cells by 80% compared with placebo (95% CI [70.6-86.8%]; P<0.0001). The data for total eosinophils showed similar changes. The reduction in mast cell numbers was 12% (95% CI [7.9, 16.0]; P<0.0001). CONCLUSION: Direct examination of airway tissue confirms that montelukast decreases the number of eosinophils and mast cells in asthma.
机译:背景:检查支气管肺泡灌洗液,诱导的痰​​液和外周血表明,半胱氨酰白三烯受体阻滞剂可减少哮喘中的炎性细胞,但它们本身并未检查气道组织。目的:我们的目的是通过直接支气管镜检查支气管粘膜来确定白三烯受体拮抗剂孟鲁司特对气道组织炎症细胞的作用。方法:成年轻度哮喘患者(支气管扩张剂前FEV(1)>或= 70%预测; PC(20)<或= 4 mg / mL)每天口服孟鲁司特10mg(N = 38)或安慰剂( N = 37),持续6周。鉴定和计数支气管粘膜嗜酸性粒细胞和肥大细胞。结果:活检EG2 +(“活化”)嗜酸性粒细胞的数量与基线相比变化是主要终点。总数(嗜铬2R +)嗜酸性粒细胞和(胰蛋白酶+)肥大细胞数量次之。出乎意料的是,基线时有许多患者的EG2 +嗜酸性粒细胞为零。孟鲁司特组EG2 +细胞在组内下降,从第6周的13.54个细胞/毫米(基线)下降到0.79个细胞/毫米(LS均值变化; 95%置信区间= -13.59 [-25.45,-1.74 Δs/ mm; P <0.05),在安慰剂组中未观察到变化(-1.17 [-13.26,10.91] cells / mm; NS)。零膨胀的Poisson统计模型表明,与安慰剂相比,孟鲁司特显着降低了治疗后EG2 +细胞80%(95%CI [70.6-86.8%]; P <0.0001)。总嗜酸性粒细胞的数据显示相似的变化。肥大细胞数量减少了12%(95%CI [7.9,16.0]; P <0.0001)。结论:直接检查气道组织证实孟鲁司特减少了哮喘患者嗜酸性粒细胞和肥大细胞的数量。

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