Wake Forest School of Medicine, Winston-Salem, NC, USA.
Weill Cornell Medical College of Cornell University, New York, NY, USA.
Lancet Respir Med. 2017 Dec;5(12):956-967. doi: 10.1016/S2213-2600(17)30432-0. Epub 2017 Nov 13.
Increased concentrations of eosinophils in blood and sputum in chronic obstructive pulmonary disease (COPD) have been associated with increased frequency of exacerbations, reduced lung function, and corticosteroid responsiveness. We aimed to assess whether high eosinophil concentrations in either sputum or blood are associated with a severe COPD phenotype, including greater exacerbation frequency, and whether blood eosinophils are predictive of sputum eosinophils.
We did a multicentre observational study analysing comprehensive baseline data from SPIROMICS in patients with COPD aged 40-80 years who had a smoking history of at least 20 pack-years, recruited from six clinical sites and additional subsites in the USA between Nov 12, 2010, and April 21, 2015. Inclusion criteria for this analysis were SPIROMICS baseline visit data with complete blood cell counts and, in a subset, acceptable sputum counts. We stratified patients on the basis of blood and sputum eosinophil concentrations and compared their demographic characteristics, as well as results from questionnaires, clinical assessments, and quantitative CT (QCT). We also analysed whether blood eosinophil concentrations reliably predicted sputum eosinophil concentrations. This study is registered with ClinicalTrials.gov (NCT01969344).
Of the 2737 patients recruited to SPIROMICS, 2499 patients were smokers and had available blood counts, and so were stratified by mean blood eosinophil count: 1262 patients with low (<200 cells per μL) and 1237 with high (≥200 cells per μL) blood eosinophil counts. 827 patients were eligible for stratification by mean sputum eosinophil percentage: 656 with low (<1·25%) and 171 with high (≥1·25%) sputum eosinophil percentages. The high sputum eosinophil group had significantly lower median FEV percentage predicted than the low sputum eosinophil group both before (65·7% [IQR 51·8-81·3] vs 75·7% [59·3-90·2], p<0·0001) and after (77·3% [63·1-88·5] vs 82·9% [67·8-95·9], p=0·001) bronchodilation. QCT density measures for emphysema and air trapping were significantly higher in the high sputum eosinophil group than the low sputum eosinophil group. Exacerbations requiring corticosteroids treatment were more common in the high versus low sputum eosinophil group (p=0·002). FEV percentage predicted was significantly different between low and high blood eosinophil groups, but differences were less than those observed between the sputum groups. The high blood eosinophil group had slightly increased airway wall thickness (0·02 mm difference, p=0·032), higher St George Respiratory Questionnaire symptom scores (p=0·037), and increased wheezing (p=0·018), but no evidence of an association with COPD exacerbations (p=0·35) or the other indices of COPD severity, such as emphysema measured by CT density, COPD assessment test scores, Body-mass index, airflow Obstruction, Dyspnea, and Exercise index, or Global Initiative for Chronic Obstructive Lung Disease stage. Blood eosinophil counts showed a weak but significant association with sputum eosinophil counts (receiver operating characteristic area under the curve of 0·64, p<0·0001), but with a high false-discovery rate of 72%.
In a large, well characterised cohort of former and current smoking patients with a broad range of COPD severity, high concentrations of sputum eosinophils were a better biomarker than high concentrations of blood eosinophils to identify a patient subgroup with more severe disease, more frequent exacerbations, and increased emphysema by QCT. Blood eosinophils alone were not a reliable biomarker for COPD severity or exacerbations, or for sputum eosinophils. Clinical trials targeting eosinophilic inflammation in COPD should consider assessing sputum eosinophils.
National Institutes of Health, and National Heart, Lung, and Blood Institute.
慢性阻塞性肺疾病(COPD)患者血液和痰中的嗜酸性粒细胞浓度增加与加重频率增加、肺功能降低和皮质类固醇反应性相关。我们旨在评估血液或痰中嗜酸性粒细胞浓度升高是否与 COPD 严重程度表型相关,包括加重频率更高,以及血液嗜酸性粒细胞是否可预测痰嗜酸性粒细胞。
我们进行了一项多中心观察性研究,分析了 SPIROMICS 中年龄在 40-80 岁、吸烟史至少 20 包年的 COPD 患者的综合基线数据,这些患者来自美国的 6 个临床地点和另外的亚地点,招募时间为 2010 年 11 月 12 日至 2015 年 4 月 21 日。本分析的纳入标准为 SPIROMICS 基线访视数据,包括全血细胞计数,以及亚组患者的可接受痰计数。我们根据血液和痰嗜酸性粒细胞浓度对患者进行分层,并比较了他们的人口统计学特征,以及问卷调查、临床评估和定量 CT(QCT)的结果。我们还分析了血液嗜酸性粒细胞浓度是否能可靠地预测痰嗜酸性粒细胞浓度。这项研究在 ClinicalTrials.gov 注册(NCT01969344)。
在 SPIROMICS 招募的 2737 名患者中,2499 名患者为吸烟者,且有血液计数资料,因此根据平均血液嗜酸性粒细胞计数进行分层:1262 名患者血液嗜酸性粒细胞计数低(<200 个/μL),1237 名患者血液嗜酸性粒细胞计数高(≥200 个/μL)。827 名患者符合平均痰嗜酸性粒细胞百分比分层标准:656 名患者痰嗜酸性粒细胞百分比低(<1.25%),171 名患者痰嗜酸性粒细胞百分比高(≥1.25%)。高痰嗜酸性粒细胞组的中位 FEV%预计值明显低于低痰嗜酸性粒细胞组,无论是在支气管扩张治疗前(65.7%[IQR 51.8-81.3]比 75.7%[59.3-90.2],p<0.0001)还是在支气管扩张治疗后(77.3%[63.1-88.5]比 82.9%[67.8-95.9],p=0.001)。QCT 肺气肿和空气潴留的密度测量值在高痰嗜酸性粒细胞组明显高于低痰嗜酸性粒细胞组。高痰嗜酸性粒细胞组比低痰嗜酸性粒细胞组更常见需要皮质类固醇治疗的加重(p=0.002)。FEV%预计值在低血嗜酸性粒细胞组和高血嗜酸性粒细胞组之间有显著差异,但差异小于痰组之间的差异。高血嗜酸性粒细胞组气道壁厚度略有增加(0.02 毫米差异,p=0.032),圣乔治呼吸问卷症状评分较高(p=0.037),喘息更多(p=0.018),但与 COPD 加重(p=0.35)或其他 COPD 严重程度指标,如 CT 密度测量的肺气肿、COPD 评估测试评分、体重指数、气流阻塞、呼吸困难和运动指数,或全球慢性阻塞性肺疾病阶段均无关联。血液嗜酸性粒细胞计数与痰嗜酸性粒细胞计数呈弱但显著相关(受试者工作特征曲线下面积为 0.64,p<0.0001),但假阳性率高达 72%。
在一个由以前和现在吸烟的患者组成的大型、特征明确的队列中,嗜酸性粒细胞的浓度范围广泛,血液和痰中嗜酸性粒细胞浓度升高均比血液嗜酸性粒细胞浓度升高更能识别疾病严重程度较高、加重频率更高、QCT 肺气肿程度更高的患者亚组。单独的血液嗜酸性粒细胞计数不是 COPD 严重程度或加重的可靠生物标志物,也不是痰嗜酸性粒细胞的生物标志物。针对 COPD 炎症的临床试验应考虑评估痰嗜酸性粒细胞。
美国国立卫生研究院和美国国家心肺血液研究所。