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哮喘中联合治疗对气道嗜酸性炎症的潜在掩盖作用。

Potential masking of airway eosinophilic inflammation by combination therapy in asthma.

机构信息

Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Center for Health Promotion, Samsung Medical Center, Seoul, Korea.

出版信息

Allergy Asthma Immunol Res. 2014 Mar;6(2):175-8. doi: 10.4168/aair.2014.6.2.175. Epub 2013 Nov 5.

Abstract

PURPOSE

Long-acting β2 agonists (LABA) may mask ongoing bronchial inflammation, leaving asthmatic patients at greater risk of severe complications. The aim of this study was to compare the effect of combination therapy using low-dose inhaled corticosteroids (ICS) plus LABA on airway inflammation in asthma to the effect of medium-dose ICS alone.

METHODS

Twenty-four patients with asthma not controlled by low-dose (400 µg per day) budesonide alone were enrolled in this prospective crossover study. Patients were randomized into 2 treatment phases: one receiving medium-dose (800 µg per day) budesonide (ICS phase), and the other receiving a combination therapy of low-dose budesonide/formoterol (360 µg/9 µg per day) delivered by a single inhaler (LABA phase). Each treatment phase lasted for 6 week, after which patients were crossed over. Asthma symptoms, lung function, and airway inflammation were compared between the 2 phases.

RESULTS

Twenty-three patients completed the study; adequate sputum samples were collected from 17 patients. Asthma symptoms and lung function remained similar between the 2 phases. However, the mean sputum eosinophil percentage was higher in the LABA phase than in the ICS phase (5.07±3.82% vs. 1.02±1.70%; P<0.01). Sputum eosinophilia (≥3%) was more frequently observed in the LABA phase than in the ICS phase (six vs. two).

CONCLUSION

Addition of LABA may mask airway eosinophilic inflammation in asthmatic patients whose symptoms are not controlled with low-dose ICS.

摘要

目的

长效β2 激动剂(LABA)可能掩盖持续存在的支气管炎症,使哮喘患者面临更大的严重并发症风险。本研究旨在比较低剂量吸入皮质激素(ICS)加 LABA 联合治疗对哮喘患者气道炎症的影响与中剂量 ICS 单独治疗的效果。

方法

24 例哮喘患者在单独使用低剂量(400μg/天)布地奈德不能控制的情况下,参与了这项前瞻性交叉研究。患者被随机分为 2 个治疗阶段:一个接受中剂量(800μg/天)布地奈德(ICS 阶段),另一个接受低剂量布地奈德/福莫特罗(360μg/9μg/天)联合治疗,由单一吸入器给药(LABA 阶段)。每个治疗阶段持续 6 周,然后患者交叉。比较两个阶段的哮喘症状、肺功能和气道炎症。

结果

23 例患者完成了研究;17 例患者采集了足够的痰液样本。两个阶段的哮喘症状和肺功能保持相似。然而,LABA 阶段的平均痰嗜酸性粒细胞百分比高于 ICS 阶段(5.07±3.82%对 1.02±1.70%;P<0.01)。LABA 阶段痰嗜酸性粒细胞增多(≥3%)比 ICS 阶段更常见(六例 vs. 两例)。

结论

在低剂量 ICS 不能控制症状的哮喘患者中,加用 LABA 可能掩盖气道嗜酸性粒细胞炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e628/3936048/4c24a431ba8a/aair-6-175-g001.jpg

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