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气道白细胞介素-1β与全身炎症作为哮喘和慢性阻塞性肺疾病未来急性加重风险的预测指标

Airway IL-1β and Systemic Inflammation as Predictors of Future Exacerbation Risk in Asthma and COPD.

作者信息

Fu Juan-Juan, McDonald Vanessa M, Baines Katherine J, Gibson Peter G

机构信息

Respiratory Group, Department of Integrated Traditional Chinese and Western Medicine, West China Hospital, Sichuan University, Sichuan, China; Priority Research Centre for Asthma and Respiratory Diseases, Newcastle, NSW, Australia.

Priority Research Centre for Asthma and Respiratory Diseases, Newcastle, NSW, Australia; School of Nursing and Midwifery, Faculty of Health, University of Newcastle, Newcastle, NSW, Australia.

出版信息

Chest. 2015 Sep;148(3):618-629. doi: 10.1378/chest.14-2337.

Abstract

BACKGROUND

The innate inflammatory pathways involved in the frequent exacerbator phenotypes of asthma and COPD are not well understood. This study aimed to investigate airway innate immune activation and systemic inflammation as predictors of exacerbations in asthma and COPD.

METHODS

In this prospective cohort study, baseline airway IL-1β, serum C-reactive protein, and IL-6 were assessed in 152 participants with stable asthma (n = 63) or COPD (n = 89) and were related to exacerbations over the following 12 months. Clinical characteristics and inflammatory biomarkers were compared between the frequent (two or more exacerbations in the follow-up) and infrequent exacerbators. The frequent exacerbation phenotype and exacerbation frequency were analyzed with multivariable modeling. The relationships among airway inflammation, systemic inflammation, and future exacerbations were examined using path analysis.

RESULTS

Ninety-four participants experienced a total of 201 exacerbations, and 36.4% had two or more exacerbations. Serum IL-6 and sputum gene expression of IL-1β at baseline were higher in the frequent exacerbators with COPD. Significant pathways initiated by previous exacerbations were identified as occurring through activation of the IL-1β-systemic inflammatory axis leading to future exacerbations in COPD. Systemic inflammation was also associated with increased exacerbation risk in asthma.

CONCLUSIONS

Airway IL-1β and systemic inflammation are associated with frequent exacerbations and may mediate a vicious cycle between previous and future exacerbations in COPD. Treatment strategies aimed at attenuating these inflammatory pathways to reduce COPD exacerbations deserve further investigation.

摘要

背景

哮喘和慢性阻塞性肺疾病(COPD)频繁加重型患者所涉及的先天性炎症途径尚未完全明确。本研究旨在调查气道先天性免疫激活和全身炎症作为哮喘和COPD加重的预测因素。

方法

在这项前瞻性队列研究中,对152例稳定期哮喘患者(n = 63)或COPD患者(n = 89)的基线气道白细胞介素-1β(IL-1β)、血清C反应蛋白和IL-6进行了评估,并将其与接下来12个月内的病情加重情况相关联。比较了频繁加重者(随访期间发作两次或更多次)和不频繁加重者之间的临床特征和炎症生物标志物。采用多变量模型分析频繁加重型表型和加重频率。使用路径分析研究气道炎症、全身炎症与未来病情加重之间的关系。

结果

94名参与者共经历了201次病情加重,其中36.4%的人发作两次或更多次。COPD频繁加重者基线时血清IL-6和痰液中IL-1β的基因表达较高。先前加重引发的重要途径被确定为通过激活IL-1β-全身炎症轴导致COPD未来病情加重。全身炎症也与哮喘加重风险增加有关。

结论

气道IL-1β和全身炎症与频繁加重有关,可能介导COPD既往和未来加重之间的恶性循环。旨在减轻这些炎症途径以减少COPD加重的治疗策略值得进一步研究。

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