呼出气一氧化氮
哮喘
横断面研究
呼出气冷凝液
表型
炎症
痰
内科学
医学
临床意义
肺活量测定
免疫学
病理
化学
基因
肺结核
生物化学
作者
Yu Han,Xin Zhang,Ji Wang,Gang Wang,Brian G. Oliver,Hong Ping Zhang,De Ying Kang,Gang Wang,Zhixin Qiu,Wei Min Li,Gang Wang
标识
DOI:10.1016/j.jaip.2020.07.048
摘要
Background Asthma is a heterogeneous disease with multiple phenotypes; however, the relevance of phenotype overlap remains largely unexplored. Objective To examine the relationship between phenotype overlap and clinical and inflammatory profiles of asthma. Methods In this cross-sectional study, adult participants with stable asthma (n = 522) underwent multidimensional assessments. The 10 most common phenotypes of asthma were defined and then classified into those commonly associated with Type (T) 2 or non-T2 inflammation. Furthermore, phenotype overlap scores (POS), representing the cumulative concomitant phenotypes, were used to analyze its association with clinical and inflammatory asthmatic profiles. Results Among the 522 participants, 73.4% (n = 383) had phenotype overlap, and mixed T2 and non-T2 inflammation coexisted in 47.5% (n = 248). T2 POS was positively associated with eosinophils, IgE, and fractional exhaled nitric oxide (FeNO), and negatively with Asthma Quality of Life Questionnaire (AQLQ), sputum neutrophils, IL-17A, IL-8, and TNF-α. Non-T2 POS was positively associated with Asthma Control Questionnaire, neutrophils and sputum IL-8, and negatively with AQLQ, forced expiratory volume in 1 s, blood eosinophils, IgE, and FeNO (all P Conclusions Phenotype overlap is extremely common in asthmatic patients and significantly associated with clinical and inflammatory profiles. Patients with phenotypes associated with mixed T2 and non-T2 inflammation might be unresponsive to medications owing to increased non-T2 inflammation. Multidimensional asthma assessment identifies clinically relevant phenotype overlap.
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