Characteristics of inflammatory phenotypes in patients with chronic obstructive pulmonary disease: a cross-sectional study

Author:

Wen XiangORCID,Deng Zhishan,Peng Jieqi,Yang Huajing,Wu FanORCID,Dai Cuiqiong,Zheng Youlan,Zhao Ningning,Wang ZihuiORCID,Xiao Shan,Xu Jianwu,Lu Lifei,Wu Xiaohui,Zhou Kunning,Dai Jianwei,Li Bing,Ran PixinORCID,Zhou YuminORCID

Abstract

BackgroundThe relationship between airway inflammation in chronic obstructive pulmonary disease (COPD) and clinical characteristics remains unclear. This study aimed to investigate the airway inflammatory phenotypes in COPD and their association with clinical characteristics.Methods895 patients with COPD were recruited from Guangdong Province, China in this study. Each patient underwent questionnaire interviews, spirometry testing, CT scans and induced sputum examination. Classification of airway inflammation phenotypes was based on sputum inflammatory cell counts. Covariance analysis was applied to assess associations with airway inflammation phenotypes.ResultsIn this study, we found that neutrophilic phenotype (NP, 58.0%) was the most common airway inflammation phenotype in patients with COPD, followed by mixed granulocytic phenotype (MGP, 32.6%), eosinophilic phenotype (EP, 5.4%) and paucigranulocytic phenotype (PP, 4.0%). Compared with NP patients, those with MGP exhibited more frequent chronic respiratory symptoms, and a higher proportion of individuals classified under Global Initiative for Chronic Obstructive Lung Disease stages 3 and 4. After adjusting for confounding factors, MGP patients had lower lung function, and more severe emphysema and air trapping. On the contrary, patients with PP had the best pulmonary function and less emphysema and air trapping.ConclusionsNP was the most common airway inflammation phenotype in patients with COPD. Patients with MGP had more respiratory symptoms, greater loss of lung function, and more severe emphysema and gas trapping compared with those with NP. Meanwhile, PP may be a phenotype of mild damage to lung structure in patients with COPD.

Funder

National Natural Science Foundation of China

the National Key Research and Development Program

Foundation of Guangzhou National Laboratory

the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program

Publisher

BMJ

Subject

Pulmonary and Respiratory Medicine

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