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变应原激发后吸入布地奈德可减轻哮喘患者的迟发哮喘反应,并抑制与之相关的气道对乙酰甲胆碱反应性的增加。

Postallergen inhaled budesonide reduces late asthmatic response and inhibits the associated increase of airway responsiveness to methacholine in asthmatics.

作者信息

Paggiaro P L, Dente F L, Morelli M C, Bancalari L, Di Franco A, Giannini D, Vagaggini B, Bacci E, Fabbri L M, Giuntini C

机构信息

Second Institute of Internal Medicine, Pisa, Italy.

出版信息

Am J Respir Crit Care Med. 1994 Jun;149(6):1447-51. doi: 10.1164/ajrccm.149.6.8004297.

DOI:10.1164/ajrccm.149.6.8004297
PMID:8004297
Abstract

To determine whether inhaled budesonide given after allergen inhalation challenge inhibits the late asthmatic response (LAR) and/or the associated increase of airway responsiveness to methacholine, we performed a double-blind randomized cross-over study in 12 adult asthmatics (eight male, four female; mean age, 20.3 yr; range, 18 to 29 yr) sensitized to Dermatophagoides pteronyssinus (DP) previously shown to develop early and late asthmatic response to allergen challenge with DP. On different days each subject was randomized to receive budesonide 800 micrograms by Turbuhaler or placebo, given three times; (1) after allergen inhalation, after the onset of LAR, when FEV1 had fallen by > or = 15%; (2) 2 h later; (3) 4 h later. Airway responsiveness to methacholine was measured before allergen challenge at 8 to 10 h from allergen inhalation and 24 h after the allergen inhalation. Inhaled budesonide significantly reduced the LAR induced by allergen (maximal % fall in FEV1, delta FEV1%: -23 +/- 6% with budesonide versus -38 +/- 9% with placebo; p < 0.001) and inhibited the associated increase of airway responsiveness (geometric mean of PD20FEV1 methacholine: 0.047 mg after budesonide versus 0.033 mg after placebo at 8 to 10 h, p < 0.05; 0.119 mg after budesonide versus 0.062 mg after placebo at 24 h, p < 0.01). These results suggest that inhaled budesonide may not only prevent but also reduce the late asthmatic response induced by allergen and that it might also be considered in the treatment of exacerbation of asthma.

摘要

为了确定在变应原吸入激发试验后给予吸入性布地奈德是否能抑制迟发性哮喘反应(LAR)和/或气道对乙酰甲胆碱反应性的相关增加,我们对12名成年哮喘患者(8名男性,4名女性;平均年龄20.3岁;范围18至29岁)进行了一项双盲随机交叉研究,这些患者先前已被证明对户尘螨(DP)致敏,对DP变应原激发试验会出现早发性和迟发性哮喘反应。在不同的日子,每位受试者被随机分配接受通过都保吸入800微克布地奈德或安慰剂,分三次给予;(1)在变应原吸入后,LAR开始发作,FEV1下降≥15%时;(2)2小时后;(3)4小时后。在变应原激发试验前、变应原吸入后8至10小时以及变应原吸入后24小时测量气道对乙酰甲胆碱的反应性。吸入性布地奈德显著降低了变应原诱导的LAR(FEV1的最大下降百分比,ΔFEV1%:布地奈德组为-23±6%,安慰剂组为-38±9%;p<0.001),并抑制了气道反应性的相关增加(乙酰甲胆碱PD20FEV1的几何平均值:8至10小时时,布地奈德组为0.047毫克,安慰剂组为0.033毫克,p<0.05;24小时时,布地奈德组为0.119毫克,安慰剂组为0.062毫克,p<0.01)。这些结果表明,吸入性布地奈德不仅可以预防,还可以减轻变应原诱导的迟发性哮喘反应,并且在哮喘加重的治疗中也可能值得考虑使用。

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