Huang Suyin, Wu Fan, Deng Zhishan, Peng Jieqi, Dai Cuiqiong, Lu Lifei, Zhou Kunning, Wu Xiaohui, Wan Qi, Tang Gaoying, Chen Shengtang, Yang Changli, Huang Yongqing, Yu Shuqing, Ran Pixin, Zhou Yumin
State Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease & National Center for Respiratory Medicine & Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.
Guangzhou National Laboratory, Guangzhou, 510000, China.
BMC Pulm Med. 2025 Jan 28;25(1):45. doi: 10.1186/s12890-025-03507-1.
Studies on consistency among spirometry, impulse oscillometry (IOS), and histology for detecting small airway dysfunction (SAD) remain scarce. Considering invasiveness of lung histopathology, we aimed to compare spirometry and IOS with chest computed tomography (CT) for SAD detection, and evaluate clinical characteristics of subjects with SAD assessed by these three techniques.
We collected baseline data from the Early COPD (ECOPD) study. CT-defined SAD was defined as parametric response mapping quantifying SAD (PRM) ≥ 15%. Spirometry-defined SAD was defined as at least two of maximal mid-expiratory flow (MMEF), forced expiratory flow 50% (FEF50), and forced expiratory flow 75% (FEF75) less than 65% of predicted. IOS-defined SAD was defined as peripheral airway resistance R5 - R20 > 0.07 kPa/L/s. The consistency of spirometry, IOS and CT for diagnosing SAD was assessed using Kappa coefficient. Correlations among the three techniques-measured small airway function parameters were assessed by Spearman correlation analysis.
2055 subjects were included in the final analysis. There was low agreement in SAD assessment between spirometry and CT (Kappa = 0.126, 95% confidence interval [CI]: 0.106 to 0.146, p < 0.001), between IOS and CT (Kappa = 0.266, 95% CI: 0.219 to 0.313, p < 0.001), as well as among spirometry, IOS, and CT (Kappa = 0.056, 95% CI: 0.029 to 0.082, p < 0.001). The correlation was moderate (|r|: 0.5 to 0.7, p < 0.05) between spirometry and CT-measured small airway function parameters, and weak (|r|< 0.4, p < 0.05) between IOS and CT-measured small airway function parameters. Only spirometry-defined SAD group had more lower lung function (FEV/FVC: adjusted difference=-10.7%, 95% CI: -13.5% to -7.8%, p < 0.001) and increased airway wall thickness (Pi 10: adjusted difference = 0.3 mm, 95% CI: 0 to 0.6 mm, p = 0.046) than only CT-defined SAD group. Only IOS-defined SAD group had better lung function (FEV/FVC: adjusted difference = 3.9%, 95% CI: 1.9 to 5.8%, p < 0.001), less emphysema (inspiratory LAA: adjusted difference=-2.1%, 95% CI:-3.1% to -1.1%, P < 0.001; PRM: adjusted difference=-2.3%, 95% CI: -3.2% to -1.4%, p < 0.001), and thicker airway wall (Pi 10: adjusted difference = 0.2 mm, 95% CI: 0.1 mm to 0.4 mm, p = 0.005) than only CT-defined SAD group.
There was low consistency in the assessment of SAD between spirometry and CT, between IOS and CT, as well as among spirometry, IOS, and CT.
Not applicable.
关于肺量计、脉冲振荡法(IOS)和组织学检测小气道功能障碍(SAD)之间一致性的研究仍然很少。考虑到肺组织病理学的侵入性,我们旨在比较肺量计和IOS与胸部计算机断层扫描(CT)在检测SAD方面的差异,并评估通过这三种技术评估的SAD患者的临床特征。
我们从早期慢性阻塞性肺疾病(ECOPD)研究中收集了基线数据。CT定义的SAD定义为参数反应映射量化SAD(PRM)≥15%。肺量计定义的SAD定义为最大呼气中期流量(MMEF)、用力呼气流量50%(FEF50)和用力呼气流量75%(FEF75)中至少两项低于预测值的65%。IOS定义的SAD定义为外周气道阻力R5 - R20>0.07 kPa/L/s。使用Kappa系数评估肺量计、IOS和CT诊断SAD的一致性。通过Spearman相关分析评估这三种技术测量的小气道功能参数之间的相关性。
2055名受试者纳入最终分析。肺量计与CT之间(Kappa = 0.126,95%置信区间[CI]:0.106至0.146,p < 0.001)、IOS与CT之间(Kappa = 0.266,95% CI:0.219至0.313,p < 0.001)以及肺量计、IOS和CT之间(Kappa = 0.056,95% CI:0.029至0.082,p < 0.001)在SAD评估方面的一致性较低。肺量计与CT测量的小气道功能参数之间的相关性为中等(|r|:0.5至0.7,p < 0.05),IOS与CT测量的小气道功能参数之间的相关性较弱(|r| < 0.4,p < 0.05)。仅肺量计定义的SAD组比仅CT定义的SAD组有更低的肺功能(FEV/FVC:调整差异=-10.7%,95% CI:-13.5%至-7.8%,p < 0.001)和增加的气道壁厚度(Pi 10:调整差异 = 0.3 mm,95% CI:0至0.6 mm,p = 0.046)。仅IOS定义的SAD组比仅CT定义的SAD组有更好的肺功能(FEV/FVC:调整差异 = 3.9%,95% CI:1.9至5.8%,p < 0.001)、更少的肺气肿(吸气性LAA:调整差异=-2.1%,95% CI:-3.1%至-1.1%,P < 0.001;PRM:调整差异=-2.3%,95% CI:-3.2%至-1.4%,p < 0.001)和更厚的气道壁(Pi 10:调整差异 = 0.2 mm,95% CI:0.1 mm至0.4 mm,p = 0.005)。
肺量计与CT之间、IOS与CT之间以及肺量计、IOS和CT之间在SAD评估方面的一致性较低。
不适用。