Woolcock Institute of Medical Research, PO Box M77, Missenden Rd, Glebe NSW 2050, Australia; University of Sydney, Darlington, Australia; Cooperative Research Centre for Asthma and Airways, Glebe, Australia.
Respir Physiol Neurobiol. 2013 Oct 1;189(1):106-11. doi: 10.1016/j.resp.2013.07.009. Epub 2013 Jul 19.
Airway hyperresponsiveness (AHR) occurs in both asthma and COPD. In older people with asthma, AHR is associated with increased acinar ventilation heterogeneity, but it is unknown if this association exists in COPD. Thirty one COPD and 19 age-matched asthmatic subjects had measures of spirometry, lung volumes, exhaled nitric oxide, ventilation heterogeneity, and methacholine challenge. Indices of acinar (Sacin) and conducting (Scond) airway ventilation heterogeneity were calculated from the multiple breath nitrogen washout. Predictors of AHR were then determined. In COPD, AHR was predicted by lower Sacin and lower FVC (model r(2)=0.35, p=0.001). In asthma, AHR was predicted by higher Sacin and higher residual volume (model r(2)=0.62, p<0.001). These findings suggest that airway responsiveness in COPD and asthma is determined by underlying disease-specific processes, rather than a common pattern of physiological abnormality.
气道高反应性(AHR)既存在于哮喘中,也存在于 COPD 中。在患有哮喘的老年人中,AHR 与腺泡通气异质性增加有关,但在 COPD 中是否存在这种相关性尚不清楚。31 例 COPD 患者和 19 例年龄匹配的哮喘患者进行了肺量计测量、肺容积测量、呼出气一氧化氮测量、通气异质性测量和乙酰甲胆碱挑战。从多次呼吸氮冲洗中计算出腺泡(Sacin)和传导(Scond)气道通气异质性指数。然后确定 AHR 的预测因素。在 COPD 中,AHR 由较低的 Sacin 和较低的 FVC 预测(模型 r(2)=0.35,p=0.001)。在哮喘中,AHR 由较高的 Sacin 和较高的残气量预测(模型 r(2)=0.62,p<0.001)。这些发现表明,COPD 和哮喘中的气道反应性是由特定疾病的潜在过程决定的,而不是由常见的生理异常模式决定的。