Suppr超能文献

SPIROMICS COPD 队列中绝对血嗜酸性粒细胞计数低的临床意义。

Clinical Implications of Low Absolute Blood Eosinophil Count in the SPIROMICS COPD Cohort.

机构信息

Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University, Nashville, TN.

University of North Carolina, Chapel Hill, NC.

出版信息

Chest. 2023 Mar;163(3):515-528. doi: 10.1016/j.chest.2022.10.029. Epub 2022 Nov 4.

Abstract

BACKGROUND

The Global Initiative for Chronic Obstructive Lung Disease (GOLD) considers blood eosinophil counts < 100 cells/μL (BEC) in people with COPD to predict poor inhaled corticosteroid (ICS) responsiveness. However, the BEC phenotype is inadequately characterized, especially in advanced COPD.

RESEARCH QUESTION

Are there differences between GOLD group D patients with high BEC and those with low BEC regarding baseline characteristics and longitudinal outcomes?

STUDY DESIGN AND METHODS

We used multivariable mixed models and logistic regression to contrast clinical characteristics and outcomes of BEC vs BEC > 100 (BEC) in all subjects with COPD (n = 1,414) and GOLD group D subjects (n = 185) not receiving ICS.

RESULTS

We identified n = 485 with BEC (n = 61 GOLD group D) and n = 929 people with BEC (n = 124 GOLD group D). BEC status was stable at 6 weeks and approximately 52 weeks (intraclass correlations of 0.78 and 0.71, respectively). Compared with BEC, BEC comprised more women, with greater current smoking, and less frequent childhood asthma. Among all analyzed participants, the two BEC-defined subsets showed similar rates of lung function decline (mean slope, BEC vs BEC, -50 vs -39 mL/y; P = .140), exacerbations (0.40 vs 0.36/y; P = .098), subsequent ICS initiation (2.5% vs 4.4%; P = .071), and mortality (7.8% vs 8.4%; P = .715). However, in GOLD group D, people with BEC showed higher exacerbation rates within 365 days of enrollment (0.62 vs 0.33/y; P = .002) and total follow-up (1.16 vs 0.83/y; P = .014). They also had greater lung function decline (mean slope of -68 mL/y vs -23 mL/y; P = .036) and had greater emphysema at baseline (voxels < 950 Hounsfield units at total lung capacity of 7.46% vs 4.61%; P = .029).

INTERPRETATION

In non-ICS-treated GOLD group D COPD, people with BEC had more baseline emphysema, prospective exacerbations, and lung function decline. Our analysis has identified a particularly vulnerable subpopulation of people with COPD, suggesting the need for studies focused specifically on their therapeutic treatment.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov; No.: NCT01969344; URL: www.

CLINICALTRIALS

gov.

摘要

背景

全球慢性阻塞性肺疾病倡议(GOLD)认为,COPD 患者血液嗜酸性粒细胞计数 <100 个/μL(BEC)可预测吸入皮质类固醇(ICS)反应不佳。然而,BEC 表型的特征描述不足,尤其是在晚期 COPD 中。

研究问题

在未接受 ICS 治疗的所有 COPD 患者(n=1414)和 GOLD 组 D 患者(n=185)中,BEC 较高和较低的 GOLD 组 D 患者在基线特征和纵向结局方面是否存在差异?

研究设计和方法

我们使用多变量混合模型和逻辑回归来对比 BEC 与 BEC > 100(BEC)在所有 COPD 患者(n=1414)和未接受 ICS 治疗的 GOLD 组 D 患者(n=185)中的临床特征和结局。

结果

我们确定了 n=485 例 BEC(n=61 例 GOLD 组 D)和 n=929 例 BEC(n=124 例 GOLD 组 D)。BEC 状态在 6 周和大约 52 周时保持稳定(组内相关系数分别为 0.78 和 0.71)。与 BEC 相比,BEC 组中更多的女性,当前吸烟的频率更高,而儿童时期哮喘的频率更低。在所有分析的参与者中,两个 BEC 定义的亚组显示出相似的肺功能下降率(平均斜率,BEC 与 BEC,-50 与-39mL/y;P=0.140),急性加重(0.40 与 0.36/y;P=0.098),随后开始使用 ICS(2.5%与 4.4%;P=0.071)和死亡率(7.8%与 8.4%;P=0.715)。然而,在 GOLD 组 D 中,BEC 患者在入组后 365 天内急性加重发生率更高(0.62 与 0.33/y;P=0.002)和总随访期(1.16 与 0.83/y;P=0.014)。他们的肺功能下降也更明显(平均斜率为-68mL/y 与-23mL/y;P=0.036),并且基线时肺气肿更严重(全肺容量为 7.46%时<950 个 Hounsfield 单位的体积比为 4.61%;P=0.029)。

解释

在未接受 ICS 治疗的 GOLD 组 D COPD 患者中,BEC 患者的基线肺气肿更严重,未来急性加重的风险更高,肺功能下降更明显。我们的分析确定了 COPD 患者中一个特别脆弱的亚群,这表明需要专门针对他们的治疗进行研究。

临床试验注册

ClinicalTrials.gov;编号:NCT01969344;网址:www.clinicaltrials.gov。

临床试验

ClinicalTrials.gov。

相似文献

1
Clinical Implications of Low Absolute Blood Eosinophil Count in the SPIROMICS COPD Cohort.
Chest. 2023 Mar;163(3):515-528. doi: 10.1016/j.chest.2022.10.029. Epub 2022 Nov 4.
2
Association of sputum and blood eosinophil concentrations with clinical measures of COPD severity: an analysis of the SPIROMICS cohort.
Lancet Respir Med. 2017 Dec;5(12):956-967. doi: 10.1016/S2213-2600(17)30432-0. Epub 2017 Nov 13.
3
Association between COPD exacerbations and lung function decline during maintenance therapy.
Thorax. 2020 Sep;75(9):744-753. doi: 10.1136/thoraxjnl-2019-214457. Epub 2020 Jun 12.
4
Burden of illness in blood eosinophilic phenotype COPD patients in New Zealand.
Respir Investig. 2021 Jul;59(4):487-497. doi: 10.1016/j.resinv.2021.03.009. Epub 2021 May 14.
8
Inhaled corticosteroid use by exacerbations and eosinophils: a real-world COPD population.
Int J Chron Obstruct Pulmon Dis. 2019 Apr 16;14:853-861. doi: 10.2147/COPD.S189585. eCollection 2019.

本文引用的文献

1
High eosinophil counts predict decline in FEV: results from the CanCOLD study.
Eur Respir J. 2021 May 27;57(5). doi: 10.1183/13993003.00838-2020. Print 2021 May.
2
Triple Inhaled Therapy at Two Glucocorticoid Doses in Moderate-to-Very-Severe COPD.
N Engl J Med. 2020 Jul 2;383(1):35-48. doi: 10.1056/NEJMoa1916046. Epub 2020 Jun 24.
4
Eosinophils in chronic obstructive pulmonary disease: are they just another biomarker?
Curr Opin Pulm Med. 2020 Mar;26(2):169-174. doi: 10.1097/MCP.0000000000000660.
7
Inhaled corticosteroids, blood eosinophils, and FEV decline in patients with COPD in a large UK primary health care setting.
Int J Chron Obstruct Pulmon Dis. 2019 May 23;14:1063-1073. doi: 10.2147/COPD.S200919. eCollection 2019.
8
Low and High Blood Eosinophil Counts as Biomarkers in Hospitalized Acute Exacerbations of COPD.
Chest. 2019 Jul;156(1):92-100. doi: 10.1016/j.chest.2019.02.406. Epub 2019 Apr 9.
9
Blood eosinophil count as a prognostic biomarker in COPD.
Int J Chron Obstruct Pulmon Dis. 2018 Oct 31;13:3589-3596. doi: 10.2147/COPD.S179734. eCollection 2018.
10
Blood eosinophils and inhaled corticosteroids in patients with COPD: systematic review and meta-analysis.
Int J Chron Obstruct Pulmon Dis. 2018 Sep 6;13:2775-2784. doi: 10.2147/COPD.S175017. eCollection 2018.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验