BACKGROUND:Chronic obstructive pulmonary disease (COPD) is a heterogeneous disorder encompassing different phenotypes with different responses to treatment. The present 1-year, two-center hospital-based study investigated whether the plasma immunoglobulin E (IgE) level and/or eosinophil cell count could be used as biomarkers to stratify patients with COPD according to predicted responses to inhaled corticosteroids (ICS)-based therapy. METHODS:A hospital-data based cohort study of COPD patients treated at two territory hospital centers was conducted for 1 year. Allergic biomarkers, including blood eosinophil counts and IgE levels, were assessed at baseline. Lung function parameters, including forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and the COPD Assessment Test (CAT), were also evaluated. The frequencies of acute exacerbation (AE) and pneumonia were also measured. Eosinophilia and a high IgE level were defined as >3% and 173 IU/mL, respectively. RESULTS:A total of 304 patients were included. Among patients with eosinophilia and high IgE levels, ICS-based therapy was associated with significant improvements in FEV1, FVC, and CAT scores, compared with bronchodilator (BD) therapy (P≤0.042). ICS-based therapy was also associated with a significantly lower incidence of AE vs BD-based therapy (11.7% vs 24.1%; P<0.008). Among patients with only eosinophilia, ICS-based therapy yielded significantly better CAT score results vs BD-based treatment (7 vs 13; P=0.032). A receiver operating characteristic curve analysis found that the combination of a high plasma IgE level and eosinophilia most sensitively and specifically identified patients who would benefit from the addition of ICS to BD therapy. CONCLUSION:Our findings support the use of blood eosinophil cell counts plus IgE levels as predictive biomarkers of the ICS response in certain patients with COPD. Both biomarkers could potentially be used to stratify COPD patients regarding ICS-based therapy.

译文

背景:慢性阻塞性肺疾病(COPD)是一种异质性疾病,涵盖了不同的表型,对治疗的反应也不同。这项基于医院的为期1年,基于两个中心的研究调查了血浆免疫球蛋白E(IgE)水平和/或嗜酸性粒细胞计数是否可以用作根据对吸入性糖皮质激素(ICS)的预期反应对COPD患者进行分层的生物标志物-基础疗法。
方法:一项基于医院数据的队列研究,在两个地区的医院中心对COPD患者进行了为期一年的研究。在基线时评估了过敏生物标志物,包括血液嗜酸性粒细胞计数和IgE水平。还评估了肺功能参数,包括1秒内的强制呼气量(FEV1),强制肺活量(FVC)和COPD评估测试(CAT)。还测量了急性加重(AE)和肺炎的频率。嗜酸性粒细胞增多和高IgE水平分别定义为> 3%和173 IU / mL。
结果:共纳入304例患者。在嗜酸性粒细胞增多和高IgE水平的患者中,与支气管扩张剂(BD)治疗相比,基于ICS的治疗与FEV1,FVC和CAT评分的显着改善相关(P≤0.042)。与基于BD的治疗相比,基于ICS的治疗还与AE的发生率显着降低有关(11.7%对24.1%; P <0.008)。在仅有嗜酸性粒细胞增多症的患者中,基于ICS的疗法与基于BD的疗法相比,CAT评分结果明显更好(7 vs 13; P = 0.032)。接收器工作特征曲线分析发现,血浆IgE高水平和嗜酸性粒细胞增多的结合最敏感,最明确地确定了将从BD治疗中增加ICS受益的患者。
结论:我们的发现支持在某些COPD患者中使用血液嗜酸性粒细胞计数加上IgE水平作为ICS反应的预测生物标志物。两种生物标志物都可能用于对基于ICS疗法的COPD患者进行分层。

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