Hurst John R, Perera Wayomi R, Wilkinson Tom M A, Donaldson Gavin C, Wedzicha Jadwiga A
F.R.C.P., Academic Unit of Respiratory Medicine, Royal Free and University College Medical School, Royal Free Hospital London NW3 2PF UK.
Am J Respir Crit Care Med. 2006 Jan 1;173(1):71-8. doi: 10.1164/rccm.200505-704OC. Epub 2005 Sep 22.
In addition to pulmonary involvement, stable chronic obstructive pulmonary disease (COPD) is associated with nasal and systemic inflammation. Although exacerbations of COPD are associated with increased pulmonary and systemic inflammation, determinants of the systemic response remain obscure, and nor is it known whether there is nasal involvement.
To investigate upper airway, lower airway, and systemic inflammation at exacerbation of COPD.
We sampled sputum, nasal wash, and serum from 41 exacerbations (East London cohort) for analysis of pathogenic microorganisms and inflammatory indices (sputum/nasal wash leukocytes, interleukin [IL]-6, IL-8, and myeloperoxidase; serum IL-6 and C-reactive protein). Values were compared with stable COPD.
Exacerbation of COPD is associated with greater nasal, sputum, and serum inflammation than the stable state. At exacerbation, inflammatory markers were highly correlated within nasal wash and serum (all r >/= 0.62, p < 0.001), but not sputum. The degree of upper airway inflammation correlated with the degree of lower airway inflammation (e.g., nasal wash/sputum myeloperoxidase; r = 0.50, p = 0.001). The degree of systemic inflammation correlated with the degree of lower airway inflammation (e.g., serum IL-6/sputum IL-8; r = 0.35, p = 0.026), and was greater in the presence of a sputum bacterial pathogen (29.0 g/dl C-reactive protein difference, p = 0.002). We did not find relationships between the upper airway and systemic compartments.
Exacerbation of COPD is associated with pan-airway inflammation; the systemic inflammatory response is proportional to that occurring in the lower airway and greater in the presence of a bacterial pathogen.
除了肺部受累外,稳定期慢性阻塞性肺疾病(COPD)还与鼻腔及全身炎症相关。虽然COPD急性加重与肺部及全身炎症增加有关,但全身反应的决定因素仍不清楚,鼻腔是否受累也不清楚。
研究COPD急性加重时上呼吸道、下呼吸道及全身炎症情况。
我们采集了41例急性加重期患者(东伦敦队列)的痰液、鼻腔灌洗液和血清,用于分析致病微生物和炎症指标(痰液/鼻腔灌洗液白细胞、白细胞介素[IL]-6、IL-8和髓过氧化物酶;血清IL-6和C反应蛋白)。将这些值与稳定期COPD患者进行比较。
COPD急性加重期的鼻腔、痰液和血清炎症比稳定期更严重。急性加重期时,炎症标志物在鼻腔灌洗液和血清中高度相关(所有r≥0.62,p<0.001),但在痰液中不相关。上呼吸道炎症程度与下呼吸道炎症程度相关(例如,鼻腔灌洗液/痰液髓过氧化物酶;r=0.50,p=0.001)。全身炎症程度与下呼吸道炎症程度相关(例如,血清IL-6/痰液IL-8;r=0.35,p=0.026),且在痰液中有细菌病原体时更严重(C反应蛋白差异为29.0mg/dl,p=0.002)。我们未发现上呼吸道和全身炎症之间的关联。
COPD急性加重与全气道炎症相关;全身炎症反应与下呼吸道炎症反应成比例,且在有细菌病原体时更严重。