Krefting Research Centre, University of Gothenburg, BOX 424, SE 40530 Göteborg, Sweden.
Clin Transl Allergy. 2011 Oct 31;1(1):12. doi: 10.1186/2045-7022-1-12.
Inhaled glucocorticoids are efficient in protecting against asthma exacerbations, but methods to compare their efficacy vs systemic effects have only been attempted in larger multi-centre studies. The aim of the current study was therefore to directly compare the effects of two separate inhaled glucocorticoids, mometasone and budesonide, to compare the effects on the early and late asthmatic responses to inhaled allergen in patients with mild allergic asthma, and sputum eosinophils, and to relate the clinical positive effects to any systemic effects observed.
Twelve patients with documented early and late asthmatic responses (EAR and LAR) to inhaled allergen at a screening visit were randomized in a double-blind fashion to treatment with mometasone (200 μg × 2 or 400 μg × 2), budesonide (400 μg × 2) or placebo in a double-blind crossover fashion for a period of seven days. Challenge with the total allergen dose causing both an EAR and LAR was given on the last day of treatment taken in the morning. Lung function was assessed using FEV1, and systemic glucocorticoid activity was quantified using 24 h urinary cortisol.
Mometasone and budesonide attenuate both EAR and LAR to allergen to a similar degree. No significant dose-related effects on the lung function parameters were observed. Both treatments reduced the relative amount of sputum eosinophils (%) after allergen. At the dose of 800 μg daily, mometasone reduced 24 h urinary cortisol by approximately 35%. Both drugs were well tolerated.
Mometasone and budesonide are equieffective in reducing early and late asthmatic responses induced by inhaled allergen challenge. Mometasone 800 μg given for seven days partially affects the HPA axis.
吸入性糖皮质激素在预防哮喘恶化方面非常有效,但比较其疗效和全身作用的方法仅在较大的多中心研究中进行过尝试。因此,本研究的目的是直接比较两种不同的吸入性糖皮质激素(莫米松和布地奈德)对轻度过敏性哮喘患者吸入变应原后早期和晚期哮喘反应的影响,并比较其对痰中嗜酸性粒细胞的影响,将临床疗效与观察到的任何全身作用相关联。
12 例在筛选就诊时已确诊有吸入性变应原引起的早发和迟发哮喘反应(EAR 和 LAR)的患者,以双盲方式随机分为莫米松(200μg×2 或 400μg×2)、布地奈德(400μg×2)或安慰剂组,以双盲交叉方式治疗 7 天。在最后一天的治疗期间,在早上给予引起 EAR 和 LAR 的总过敏原剂量进行挑战。使用 FEV1 评估肺功能,使用 24 小时尿皮质醇定量检测全身糖皮质激素活性。
莫米松和布地奈德均可相似程度地减轻 EAR 和 LAR 对变应原的反应。未观察到与剂量相关的肺功能参数的显著影响。两种治疗均减少了变应原后痰中嗜酸性粒细胞的相对量(%)。莫米松 800μg 日剂量可使 24 小时尿皮质醇降低约 35%。两种药物均耐受良好。
莫米松和布地奈德在减轻吸入性变应原激发引起的 EAR 和 LAR 方面等效。莫米松 7 天给药 800μg 部分影响 HPA 轴。