Comparing spirometry, impulse oscillometry with computed tomography for assessing small airway dysfunction in subjects with and without chronic obstructive pulmonary disease.

IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM BMC Pulmonary Medicine Pub Date : 2025-01-28 DOI:10.1186/s12890-025-03507-1
Suyin Huang, Fan Wu, Zhishan Deng, Jieqi Peng, Cuiqiong Dai, Lifei Lu, Kunning Zhou, Xiaohui Wu, Qi Wan, Gaoying Tang, Shengtang Chen, Changli Yang, Yongqing Huang, Shuqing Yu, Pixin Ran, Yumin Zhou
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Abstract

Background: 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.

Methods: We collected baseline data from the Early COPD (ECOPD) study. CT-defined SAD was defined as parametric response mapping quantifying SAD (PRMfSAD) ≥ 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.

Results: 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 (FEV1/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 (FEV1/FVC: adjusted difference = 3.9%, 95% CI: 1.9 to 5.8%, p < 0.001), less emphysema (inspiratory LAA- 950: adjusted difference=-2.1%, 95% CI:-3.1% to -1.1%, P < 0.001; PRMEmph: 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.

Conclusions: 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.

Clinical trial number: Not applicable.

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比较肺活量测定法、脉冲振荡测量法和计算机断层扫描法对有和无慢性阻塞性肺疾病受试者小气道功能障碍的评估。
背景:肺活量测定法、脉冲振荡测定法(IOS)和组织学检测小气道功能障碍(SAD)的一致性研究仍然很少。考虑到肺部组织病理学的侵袭性,我们的目的是将肺活量测定法和IOS与胸部计算机断层扫描(CT)检测SAD进行比较,并评估这三种技术评估的SAD受试者的临床特征。方法:我们收集早期COPD (ECOPD)研究的基线数据。ct定义的SAD定义为量化SAD的参数反应映射(PRMfSAD)≥15%。肺活量测定定义的SAD定义为最大呼气中流量(MMEF)、用力呼气流量50% (FEF50)和用力呼气流量75% (FEF75)低于预测的65%至少两项。ios定义的SAD定义为外周气道阻力R5 ~ R20 > 0.07 kPa/L/s。应用Kappa系数评价肺活量测定法、IOS和CT诊断SAD的一致性。采用Spearman相关分析评估三种技术测量的小气道功能参数之间的相关性。结果:2055名受试者纳入最终分析。肺活量测定法与CT在SAD评估中的一致性较低(Kappa = 0.126, 95%可信区间[CI]: 0.106 ~ 0.146, p1 /FVC:调整差值=-10.7%,95% CI:- 13.5% ~ -7.8%, p1 /FVC:调整差值= 3.9%,95% CI: 1.9 ~ 5.8%, p - 950:调整差值=-2.1%,95% CI:-3.1% ~ -1.1%, p Emph:调整差值=-2.3%,95% CI:- 3.2% ~ -1.4%, p结论:肺活量测定法与CT、IOS与CT、肺活量测定法、IOS与CT评估SAD的一致性较低。临床试验号:不适用。
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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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