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Effect of differing doses of inhaled budesonide on markers ofairway inflammation in patients with mild asthma

机译:布地奈德不同剂量吸入对标志物的影响轻度哮喘患者的气道炎症

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摘要

BACKGROUND—It is desirable to prescribe the minimal effective dose of inhaled steroids to control asthma. To ensure that inflammation is suppressed whilst using the lowest possible dose, a sensitive and specific method for assessing airway inflammation is needed.
METHODS—The usefulness of exhaled nitric oxide (NO), sputum eosinophils, and methacholine airway responsiveness (PC20) for monitoring airway inflammatory changes following four weeks of treatment with an inhaled corticosteroid (budesonide via Turbohaler) were compared. Mild stable steroid naive asthmatic subjects were randomised into two double blind, placebo controlled studies. The first was a parallel group study involving three groups receiving either 100 µg/day budesonide (n = 8), 400 µg/day budesonide (n = 7), or a matched placebo (n = 6). The second was a crossover study involving 10 subjects randomised to receive 1600 µg budesonide or placebo. The groups were matched with respect to age, PC20, baseline FEV1 (% predicted), exhaled NO, and sputum eosinophilia.
RESULTS—There were significant improvements in FEV1 following 400 µg and 1600 µg budesonide (11.3% and 6.5%, respectively, p<0.05). Thiswas accompanied by significant reductions in eosinophil numbers ininduced sputum (0.7 and 0.9 fold, p<0.05). However, levels of exhaledNO were reduced following each budesonide dose while PC20was improved only with 1600 µg budesonide. These results suggestthat exhaled NO and PC20 may not reflect the control of airway inflammation as accurately as the number of eosinophils insputum. There were dose dependent changes in exhaled NO, sputum eosinophils, and PC20 to inhaled budesonide but a plateauresponse of exhaled NO was found at a dose of 400 µg daily.
CONCLUSION—Monitoringthe number of eosinophils in induced sputum may be the most accurateguide to establish the minimum dose of inhaled steroids needed tocontrol inflammation. This, however, requires further studies involvinga larger number of patients.

机译:背景技术期望开出吸入类固醇的最小有效剂量以控制哮喘。为确保在使用最低剂量的情况下抑制炎症,需要一种灵敏且特定的评估气道炎症的方法。
方法-呼出气一氧化氮(NO),痰嗜酸性粒细胞和乙酰甲胆碱气道反应性(PC20比较了用吸入皮质类固醇(通过Turbohaler的布地奈德)治疗4周后监测气道炎症的变化。轻度稳定的类固醇初治哮喘受试者被随机分为两个双盲,安慰剂对照研究。第一项是平行组研究,涉及三个小组,分别接受100μg/天的布地奈德(n = 8),400μg/天的布地奈德(n = 7)或匹配的安慰剂(n = 6)。第二项是一项交叉研究,涉及10名随机接受1600 µg布地奈德或安慰剂的受试者。这些组在年龄,PC20,基线FEV1(预测的百分比),呼出NO和痰嗜酸性粒细胞增多方面是匹配的。
结果—布地奈德400μg和1600μg后FEV1有显着改善(11.3%和6.5%分别为p <0.05)。这个伴随着嗜酸性粒细胞数量的显着减少诱导痰(0.7和0.9倍,p <0.05)。但是,呼气水平每次布地奈德剂量后,NO均降低,而PC20仅使用1600 µg布地奈德即可改善。这些结果表明呼出的NO和PC20可能不如嗜酸性粒细胞数量准确反映出对气道炎症的控制痰。呼出的一氧化氮,痰中的嗜酸性粒细胞和PC20与布地奈德相比有剂量依赖性变化,但处于平稳状态每天400 µg的剂量发现呼出NO的反应。
结论—监测诱导痰中嗜酸性粒细胞的数量可能是最准确的指南确定所需的最小吸入类固醇剂量控制炎症。但是,这需要进一步的研究,包括更多的患者。

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