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COPD 患者长期停用吸入性皮质类固醇后气道炎症。

Airway inflammation in COPD after long-term withdrawal of inhaled corticosteroids.

机构信息

Dept of Pulmonology, Leiden University Medical Center, Leiden, the Netherlands

Dept of Pulmonary Medicine, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.

出版信息

Eur Respir J. 2017 Jan 3;49(1). doi: 10.1183/13993003.00839-2016. Print 2017 Jan.

Abstract

Long-term treatment with inhaled corticosteroids (ICS) might attenuate lung function decline and decrease airway inflammation in a subset of patients with chronic obstructive pulmonary disease (COPD), and discontinuing ICS treatment could result in further lung function decline. We hypothesised that airway inflammation increases after ICS withdrawal following long-term ICS treatment in COPD.In the GLUCOLD-1 study (GL1), 114 patients with moderate-severe COPD were randomised to 6-month or 30-month treatment with fluticasone propionate (500 µg twice daily), 30-month treatment with fluticasone/salmeterol (500/50 µg twice daily) or placebo. During the 5-year follow-up study (GL2), patients were followed prospectively while being treated by their physician. Bronchial biopsies and induced sputum were collected at baseline, at 30 months (end of GL1) and at 7.5 years (end of GL2) to assess inflammatory cell counts. Data were analysed using linear mixed-effects models.In patients using ICS during GL1 and using ICS 0-50% of the time during GL2 (n=61/85), there were significant increases in GL2 bronchial CD3 (fold change per year calculated as GL2 minus GL1 2.68, 95% CI 1.87-3.84), CD4 (1.91, 95% CI 1.33-2.75) and CD8 cells (1.71, 95% CI 1.15-2.53), and mast cells (1.91, 95% CI 1.36-2.68). The sputum total cell counts increased significantly in GL2 (1.90, 95% CI 1.42-2.54), as did counts of macrophages (2.10, 95% CI 1.55-2.86), neutrophils (1.92, 95% CI 1.39-2.65) and lymphocytes (2.01, 95% CI 1.46-2.78).ICS discontinuation increases airway inflammation in patients with moderate-severe COPD, suggesting that the anti-inflammatory effects of ICS in COPD are not maintained after ICS discontinuation.

摘要

长期使用吸入性皮质类固醇(ICS)可能会减轻慢性阻塞性肺疾病(COPD)患者的肺功能下降,并减少气道炎症,而停止 ICS 治疗可能会导致进一步的肺功能下降。我们假设在 COPD 患者长期使用 ICS 后停药,气道炎症会增加。

在 GLUCOLD-1 研究(GL1)中,114 名中重度 COPD 患者被随机分为 6 个月或 30 个月接受丙酸氟替卡松(500μg,每日 2 次)治疗、30 个月接受氟替卡松/沙美特罗(500/50μg,每日 2 次)治疗或安慰剂治疗。在 5 年随访研究(GL2)中,患者在接受医生治疗的同时前瞻性地进行随访。在基线、30 个月(GL1 结束时)和 7.5 年(GL2 结束时)收集支气管活检和诱导痰样,以评估炎症细胞计数。数据采用线性混合效应模型进行分析。

在 GL1 期间使用 ICS 且在 GL2 期间使用 ICS 0-50%时间的患者(n=61/85),GL2 支气管 CD3(每年计算的 GL2 减去 GL1 的倍数变化为 2.68,95%CI 1.87-3.84)、CD4(1.91,95%CI 1.33-2.75)和 CD8 细胞(1.71,95%CI 1.15-2.53)以及肥大细胞(1.91,95%CI 1.36-2.68)均显著增加。GL2 中的痰液总细胞计数显著增加(1.90,95%CI 1.42-2.54),巨噬细胞(2.10,95%CI 1.55-2.86)、中性粒细胞(1.92,95%CI 1.39-2.65)和淋巴细胞(2.01,95%CI 1.46-2.78)的计数也增加。

ICS 停药会增加中重度 COPD 患者的气道炎症,提示 COPD 患者中 ICS 的抗炎作用在停药后无法维持。

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