Guan Wei-Jie, Gao Yong-Hua, Xu Gang, Li Hui-Min, Yuan Jing-Jing, Zheng Jin-Ping, Chen Rong-Chang, Zhong Nan-Shan
1 State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Disease, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China ; 2 Department of Respiratory and Critical Care Medicine, First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China ; 3 Guangzhou First People's Hospital, Guangzhou 510120, China.
J Thorac Dis. 2016 Jan;8(1):14-23. doi: 10.3978/j.issn.2072-1439.2016.01.05.
Bronchial dilation testing is an important tool to assess airway reversibility in adults with bronchiectasis. This study aims to investigate the association of bronchodilator response (BDR) and clinical parameters in bronchiectasis, and the utility of BDR to indicate lung function decline and risks of bronchiectasis exacerbations (BEs).
We recruited 129 patients with clinically stable bronchiectasis. Baseline measurements included assessment of sputum inflammation and matrix metalloproteinase-8 and -9, sputum bacterial culture, spirometry, bronchial dilation test (for baseline FEV1 less than 80% predicted only) and chest high-resolution computed tomography (HRCT). Bronchiectasis patients were followed-up for 1 year to determine the incidence of BEs and lung function trajectories. Significant BDR was defined as FEV1 improvement from pre-dose value by at least 200 mL and 12%. Clinical trial registry No.: NCT01761214; URL: www.clinicaltrials.gov.
BDR was negatively correlated with baseline FEV1 percentage predicted, but not blood or sputum eosinophil count. Significant BDR was not associated with greater proportion of never-smokers, poorer past history, greater HRCT scores, poorer diffusing capacity or increased sputum matrix metalloproteinases (all P>0.05). There was a trend towards higher bronchiectasis severity index (BSI) and greater proportion of patients with Pseudomonas aeruginosa isolation or infection. Significant BDR at baseline was linked to poorer spirometry, but not more rapid lung function decline, throughout follow-up. Patients with significant BDR demonstrated non-significantly lower risks of experiencing the first BEs than those without (P=0.09 for log-rank test).
Significant BDR is associated with poorer lung function compared with non-significant BDR. Whether BDR predicts future risks of BEs needs to be tested in a larger cohort.
支气管扩张试验是评估成人支气管扩张症气道可逆性的重要工具。本研究旨在探讨支气管扩张剂反应(BDR)与支气管扩张症临床参数之间的关联,以及BDR在提示肺功能下降和支气管扩张症加重(BE)风险方面的作用。
我们招募了129例临床稳定的支气管扩张症患者。基线测量包括痰液炎症及基质金属蛋白酶-8和-9评估、痰液细菌培养、肺功能测定、支气管扩张试验(仅适用于基线第一秒用力呼气容积(FEV1)低于预测值80%的患者)以及胸部高分辨率计算机断层扫描(HRCT)。对支气管扩张症患者进行为期1年的随访,以确定BE的发生率和肺功能轨迹。显著BDR定义为FEV1较给药前值改善至少200 mL且提高12%。临床试验注册号:NCT01761214;网址:www.clinicaltrials.gov。
BDR与预测的基线FEV1百分比呈负相关,但与血液或痰液嗜酸性粒细胞计数无关。显著BDR与从不吸烟者比例更高、既往病史较差、HRCT评分更高、弥散功能较差或痰液基质金属蛋白酶增加均无关联(所有P>0.05)。支气管扩张症严重程度指数(BSI)有升高趋势,铜绿假单胞菌分离或感染的患者比例更高。基线时显著BDR与较差的肺功能测定结果相关,但在整个随访期间与肺功能下降更快无关。有显著BDR的患者发生首次BE的风险略低于无显著BDR的患者(对数秩检验P=0.09)。
与非显著BDR相比,显著BDR与较差的肺功能相关。BDR是否能预测未来BE的风险需要在更大的队列中进行检验。