Walsh C J, Zaihra T, Benedetti A, Fugère C, Olivenstein R, Lemière C, Hamid Q, Martin J G
Department of Medicine, Institute of Medical Sciences, Keenan Centre for Biomedical Research, Li Ka Shing Knowledge institute, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.
Department of Mathematics, SUNY-Brockport, Brockport, NY, USA.
Clin Exp Allergy. 2016 Oct;46(10):1291-302. doi: 10.1111/cea.12762. Epub 2016 Jun 27.
Airway inflammatory phenotyping is increasingly applied to subjects with asthma. However, its relationship to clinical outcomes in difficult asthma is incompletely elucidated.
The goal of our study was to determine the relationship between exacerbation rates and phenotypes of difficult asthma based on the longitudinal measures of sputum eosinophils and neutrophils.
Subjects in the longitudinal observational study from two tertiary care centres that completed 1 year of observation and provided at least three sputum samples were classified by inflammatory phenotypes using previously established thresholds. Kaplan-Meier curves and univariable and multivariable Cox proportional hazard models were used to determine the association between inflammatory phenotypes and exacerbation rate.
During the study, 115 exacerbations occurred in 73 severe asthmatic subjects. Subjects with the persistently eosinophilic phenotype had a significantly shorter time to first exacerbation and greater risk of exacerbation over a 1-year period than those with the non-eosinophilic phenotype based on the univariable and multivariable Cox proportional hazard model (hazard ratio [HR], 3.24; 95% confidence interval [CI], 1.35-7.72; adjusted HR, 3.90; 95% CI, 1.34-11.36). No significant differences in time to first exacerbation or exacerbation risk over a 1-year period were observed among the neutrophilic phenotypes.
The persistent eosinophilic phenotype is associated with increased exacerbation risk compared with the non-eosinophilic phenotype in severe asthma. No differences in time to first exacerbation or exacerbation risk over a 1-year period were detected among neutrophilic phenotypes.
气道炎症表型分析越来越多地应用于哮喘患者。然而,其与难治性哮喘临床结局的关系尚未完全阐明。
我们研究的目的是基于痰液嗜酸性粒细胞和中性粒细胞的纵向测量结果,确定难治性哮喘的急性加重率与表型之间的关系。
来自两个三级医疗中心的纵向观察性研究中的受试者,完成了1年的观察并提供了至少三份痰液样本,使用先前确定的阈值按炎症表型进行分类。采用Kaplan-Meier曲线以及单变量和多变量Cox比例风险模型来确定炎症表型与急性加重率之间的关联。
在研究期间,73名重度哮喘患者发生了115次急性加重。基于单变量和多变量Cox比例风险模型,持续性嗜酸性粒细胞表型的受试者首次急性加重的时间明显短于非嗜酸性粒细胞表型的受试者,且在1年期间急性加重的风险更高(风险比[HR],3.24;95%置信区间[CI],1.35 - 7.72;调整后HR,3.90;95%CI,1.34 - 11.36)。在中性粒细胞表型之间,未观察到首次急性加重时间或1年期间急性加重风险的显著差异。
与非嗜酸性粒细胞表型相比,重度哮喘中持续性嗜酸性粒细胞表型与急性加重风险增加相关。在中性粒细胞表型之间,未检测到首次急性加重时间或1年期间急性加重风险的差异。