Relationship between airway inflammation, hyperresponsiveness, and obstruction in asthma

被引:172
作者
Woodruff, PG
Khashayar, R
Lazarus, SC
Janson, S
Avila, P
Boushey, HA
Segal, M
Fahy, JV
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Sch Nursing, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Biostat, San Francisco, CA 94143 USA
关键词
asthma; airway obstruction; eosinophils; neutrophils;
D O I
10.1067/mai.2001.119411
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Although the role of eosinophils in airway inflammation in chronic asthma has been extensively studied, a role for neutrophils has not been well characterized. Furthermore, prior studies have not systematically sought or controlled for factors that might confound the relationship between cellular markers of inflammation and physiologic measures of airway function. Objective: The purpose of this study was to determine whether eosinophilic and neutrophilic inflammation independently contribute to abnormalities of airway function in asthma. Methods: Multivariate analysis of data collected during screening and enrollment of 205 asthmatic adults for clinical trials was conducted to examine the relationships between cellular inflammation in induced sputum and FEV1 and methacholine responsiveness (PC20) while confounding factors were controlled for. Results: We found that age, sex, ethnicity, and use of inhaled corticosteroids were important confounding factors of the relationship between cellular inflammation and airway function. When these factors were controlled for, multivariate analysis showed that eosinophil percentage in induced sputum is independently associated with lower FEV1 and lower PC20 (P =.005 and P =.005, respectively). In the same models, increased sputum neutrophil percentage is independently associated with lower FEV1 (P =.038) but not with PC20 (P =.49). Conclusions: These results suggest that both eosinophilic inflammation and neutrophilic inflammation independently contribute to abnormalities of FEV1 in asthma. Therapies directed specifically at control of neutrophilic inflammation might be useful in improving airway caliber in patients with chronic asthma.
引用
收藏
页码:753 / 758
页数:6
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