Sputum neutrophil counts are associated with more severe asthma phenotypes using cluster analysis

被引:544
作者
Moore, Wendy C. [1 ,2 ]
Hastie, Annette T. [1 ,2 ]
Li, Xingnan [1 ,2 ]
Li, Huashi [1 ,2 ]
Busse, William W. [3 ]
Jarjour, Nizar N. [3 ]
Wenzel, Sally E. [4 ]
Peters, Stephen P. [1 ,2 ]
Meyers, Deborah A. [1 ,2 ]
Bleecker, Eugene R. [1 ,2 ]
机构
[1] Wake Forest Sch Med, Ctr Genom & Personalized Med Res, Winston Salem, NC 27157 USA
[2] Sect Pulm Crit Care Allergy & Immunol Dis, Winston Salem, NC USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Allergy Pulm & Crit Care Div, Madison, WI 53706 USA
[4] Univ Pittsburgh, Sch Med Pulm Allergy & Crit Care Med, Bethesda, MD USA
[5] NHLBI, Severe Asthma Res Program, Bethesda, MD 20892 USA
关键词
Severe Asthma Research Program; severe asthma; sputum; eosinophils; neutrophils; phenotype; cluster analysis; AIRWAY INFLAMMATION; EOSINOPHIL COUNTS; DOUBLE-BLIND; CLARITHROMYCIN; EXACERBATIONS; PREVENTION; TRIAL;
D O I
10.1016/j.jaci.2013.10.011
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
Background: Clinical cluster analysis from the Severe Asthma Research Program (SARP) identified 5 asthma subphenotypes that represent the severity spectrum of early-onset allergic asthma, late-onset severe asthma, and severe asthma with chronic obstructive pulmonary disease characteristics. Analysis of induced sputum from a subset of SARP subjects showed 4 sputum inflammatory cellular patterns. Subjects with concurrent increases in eosinophil (>= 2%) and neutrophil (>= 40%) percentages had characteristics of very severe asthma. Objective: To better understand interactions between inflammation and clinical subphenotypes, we integrated inflammatory cellular measures and clinical variables in a new cluster analysis. Methods: Participants in SARP who underwent sputum induction at 3 clinical sites were included in this analysis (n = 423). Fifteen variables, including clinical characteristics and blood and sputum inflammatory cell assessments, were selected using factor analysis for unsupervised cluster analysis. Results: Four phenotypic clusters were identified. Cluster A (n = 132) and B (n = 127) subjects had mild-to-moderate early-onset allergic asthma with paucigranulocytic or eosinophilic sputum inflammatory cell patterns. In contrast, these inflammatory patterns were present in only 7% of cluster C (n = 117) and D (n = 47) subjects who had moderate-to-severe asthma with frequent health care use despite treatment with high doses of inhaled or oral corticosteroids and, in cluster D, reduced lung function. The majority of these subjects (>83%) had sputum neutrophilia either alone or with concurrent sputum eosinophilia. Baseline lung function and sputum neutrophil percentages were the most important variables determining cluster assignment. Conclusion: This multivariate approach identified 4 asthma subphenotypes representing the severity spectrum from mild-to-moderate allergic asthma with minimal or eosinophil-predominant sputum inflammation to moderate-to-severe asthma with neutrophil-predominant or mixed granulocytic inflammation.
引用
收藏
页码:1557 / +
页数:12
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