Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Mass; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass; Harvard Medical School, Boston, Mass.
Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Mass.
J Allergy Clin Immunol. 2018 Jun;141(6):2037-2047.e10. doi: 10.1016/j.jaci.2018.04.010. Epub 2018 Apr 28.
Eosinophilic airway inflammation in patients with chronic obstructive pulmonary disease (COPD) is associated with exacerbations and responsivity to steroids, suggesting potential shared mechanisms with eosinophilic asthma. However, there is no consistent blood eosinophil count that has been used to define the increased exacerbation risk.
We sought to investigate blood eosinophil counts associated with exacerbation risk in patients with COPD.
Blood eosinophil counts and exacerbation risk were analyzed in patients with moderate-to-severe COPD by using 2 independent studies of former and current smokers with longitudinal data. The Genetic Epidemiology of COPD (COPDGene) study was analyzed for discovery (n = 1,553), and the Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) study was analyzed for validation (n = 1,895). A subset of the ECLIPSE study subjects were used to assess the stability of blood eosinophil counts over time.
COPD exacerbation risk increased with higher eosinophil counts. An eosinophil count threshold of 300 cells/μL or greater showed adjusted incidence rate ratios for exacerbations of 1.32 in the COPDGene study (95% CI, 1.10-1.63). The cutoff of 300 cells/μL or greater was validated for prospective risk of exacerbation in the ECLIPSE study, with adjusted incidence rate ratios of 1.22 (95% CI, 1.06-1.41) using 3-year follow-up data. Stratified analysis confirmed that the increased exacerbation risk associated with an eosinophil count of 300 cells/μL or greater was driven by subjects with a history of frequent exacerbations in both the COPDGene and ECLIPSE studies.
Patients with moderate-to-severe COPD and blood eosinophil counts of 300 cells/μL or greater had an increased risk exacerbations in the COPDGene study, which was prospectively validated in the ECLIPSE study.
慢性阻塞性肺疾病(COPD)患者的嗜酸性气道炎症与加重和对类固醇的反应性有关,这表明与嗜酸性哮喘有潜在的共同机制。然而,目前尚无一致的血嗜酸性粒细胞计数用于定义增加的加重风险。
我们旨在研究与 COPD 患者加重风险相关的血嗜酸性粒细胞计数。
利用具有纵向数据的两项独立的既往吸烟者和现吸烟者的研究,分析了中重度 COPD 患者的血嗜酸性粒细胞计数与加重风险的关系。COPDGene 研究用于发现分析(n=1553),ECLIPSE 研究(Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints)用于验证分析(n=1895)。ECLIPSE 研究的一个子研究用于评估血嗜酸性粒细胞计数随时间的稳定性。
随着嗜酸性粒细胞计数的升高,COPD 加重风险增加。COPDGene 研究中,嗜酸性粒细胞计数阈值为 300 个/μL 或更高时,调整后的加重发生率比为 1.32(95%CI,1.10-1.63)。在 ECLIPSE 研究中,300 个/μL 或更高的截定点验证了未来加重的风险,使用 3 年随访数据,调整后的发生率比为 1.22(95%CI,1.06-1.41)。分层分析证实,在 COPDGene 和 ECLIPSE 研究中,嗜酸性粒细胞计数为 300 个/μL 或更高与频繁加重史的患者相关,与增加的加重风险有关。
COPDGene 研究中,中重度 COPD 患者的血嗜酸性粒细胞计数为 300 个/μL 或更高时,发生加重的风险增加,这一结果在 ECLIPSE 研究中得到了前瞻性验证。