Derivation and validation of a pre-bronchodilator FEV1/FVC threshold for point-of-care diagnosis triage of COPD in primary care: a multi-cohort population-based study
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Updated: Aug 21, 2026

Phase-Resolved Functional Lung MRI for Pulmonary Ventilation and Perfusion (V/Q) Assessment
Published on: August 9, 2024
Jisong Yan1,2, Yinqi Ding3, Minghui Shi1,4
1National Center for Respiratory Medicine, State Key Laboratory of Respiratory Health and Multimorbidity, National Clinical Research Center for Respiratory Diseases, Institute of Respiratory Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, Beijing, PR China.
Background:
Post-bronchodilator (BD) spirometry is underused in primary care settings, limiting COPD diagnosis. This study aimed to derive and validate pre-BD thresholds that safely rule in COPD and enable immediate diagnosis.
Methods:
We derived pre-BD FEV1/FVC thresholds using a nationally representative derivation dataset (CPHS, n = 6360 with pre-BD ratio <0.7), with cross-sectional external validation in the China Kadoorie Biobank (CKB, n = 1890) and longitudinal validation in a national screening cohort (NSC, n = 7620 with 1-year follow-up). The optimal threshold was selected based on positive predictive value (PPV) for post-BD FEV1/FVC <0.7. One-year longitudinal follow-up assessed diagnostic stability and prognostic value.
Findings:
A pre-BD threshold of 0.56 was identified, yielding a PPV of 0.953 (95% CI, 0.939-0.965) in derivation set and 0.919 (95% CI, 0.875-0.940) in the CKB validation set. In subgroups with higher prior probability (male, age >60 years, smoking, and with respiratory symptoms), the PPV was further increased. At one-year follow-up in the NSC, 86.9% of participants with baseline pre-BD <0.56 still met the post-BD COPD criteria. Patients below 0.56 had significantly higher risks of acute exacerbation (OR, 3.34; 95% CI, 2.55-4.37) and respiratory hospitalization (OR, 3.42; 95% CI, 2.65-4.42). An alternative threshold of 0.62 gave a PPV of 0.891 (95% CI, 0.866-0.913) in CKB and allowed 33.8%-49.0% of participants across cohorts to bypass post-BD testing.
Interpretation:
A pre-BD FEV1/FVC threshold of 0.56 effectively "rules-in" COPD in primary care and identifies patients with poor prognosis. The alternative threshold of 0.62 offers a practical option to further reduce post-BD testing while maintaining an acceptable PPV. Both thresholds facilitate pragmatic triage and early diagnosis without routine post-BD testing.
Funding:
This work was funded by National High Level Hospital Clinical Research Funding (2025-NHLHCRF-JBGS-B-WZ-18), Noncommunicable Chronic Diseases-National Science and Technology Major Project (2023ZD0506003, 2023ZD0506306, 2023ZD0510101, 2023ZD0510100), Social Development Project of Yunnan Province (202403AC100006) and Beijing Nova Program (20250484849).
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