External validation of an IOS-derived model for airflow obstruction and COPD in a community-based cohort
Lifei Lu1, Jieqi Peng1,2, Si Li1
1State 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, China.
Abstract:
A model based on impulse oscillometry (IOS) predicting airflow limitation and chronic obstructive pulmonary disease (COPD) has been developed in hospital-based populations. However, its diagnostic performance in community-recruited cohorts and its potential complementary value when combined with commonly used questionnaire-based tools remain to be evaluated. To externally validate the IOS-derived model for airflow obstruction (AO) and COPD in a community-based cohort, and to assess whether combining it with the COPD Screening Questionnaire (COPD-SQ) improves diagnostic accuracy compared to either tool alone. This was a cross-sectional analysis of baseline data from the ongoing Early Chronic Obstructive Pulmonary Disease (ECOPD) prospective cohort study. Participants completed pre-bronchodilator IOS tests, pre- and post-bronchodilator spirometry tests. The previously developed IOS-derived model (incorporating age, sex, height, weight, and IOS parameters) was applied to this Chinese population cohort. The COPD-SQ (7 items) was also administered. We defined a pre-bronchodilator FEV1/FVC < 0.70 as airflow obstruction (AO) and a post-bronchodilator FEV1/FVC < 0.70 as COPD. Receiver operating characteristic (ROC) curves were used to evaluate the diagnostic performance of the IOS-derived model, COPD-SQ, and their combination for AO and COPD. Differences in area under the curve (AUC) were compared using DeLong's test. A total of 1858 participants with complete IOS parameters were analyzed. The IOS-derived model showed acceptable diagnostic accuracy for AO (AUC 0.826, 95% CI 0.808-0.844, sensitivity 67.4%, specificity 80.6%) and COPD (AUC 0.836, 95% CI 0.818-0.854, sensitivity 71.6%, specificity 78.1%) in this community-based cohort. The combination of the IOS-derived model and COPD-SQ demonstrated modestly higher diagnostic accuracy for AO (AUC 0.839 vs 0.826 for IOS-derived model or 0.784 for COPD-SQ, all P < 0.001) and COPD (AUC 0.851 vs 0.836 or 0.795, all P < 0.001) compared to either tool alone. In this community-recruited cohort with a relatively high prevalence of airflow limitation and COPD, the IOS-derived model exhibited good diagnostic performance and, when combined with the COPD-SQ, showed modestly improved accuracy for identifying AO and COPD compared to single-modality approaches. These findings support further evaluation of the model in unselected general populations and real-world primary care settings.
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