One-year progression of CT emphysema subtypes predict lung function decline: SPIROMICS
RATIONALE: Intermediate endpoints that predict lung function decline are needed to improve the efficiency of clinical trials in chronic obstructive pulmonary disease (COPD). OBJECTIVES: To test if one-year progression of quantitative computed tomography (QCT) measures predicts subsequent FEV₁ decline. METHODS: SPIROMICS recruited individuals with ≥ 20 pack-years smoking history with or without COPD and nonsmoking controls who underwent four annual and a later fifth visit. We analyzed chest CT scans at visits one and two for machine-learned CT emphysema subtypes (combined bronchitic-apical emphysema [CBaE], diffuse emphysema) and standard QCT measures of emphysema (percent emphysema-950HU, 15th percentile HU, volume-adjusted lung density), airways, functional small airways, hyperinflation, parenchymal texture and vasculature. Linear mixed-effects models evaluated associations between one-year QCT measure changes and FEV₁ decline from visits two through five, adjusting for demographics, site, enrollment group, baseline QCT value, and time-varying anthropometrics and smoking. MEASUREMENTS AND MAIN RESULTS: Among 880 participants (43% mild/moderate COPD, 17% severe COPD, 29% smoking controls, 11% nonsmoking controls), FEV₁ declined -30.4mL/year (95% CI: -34.5, -26.3). A standard deviation (SD) one-year increase in CBaE and diffuse emphysema predicted an accelerated decline in FEV1 of - 4.2 mL/year (95% CI: -8.3, -0.2) and -6.2 mL/year (95% CI: -10.7, -1.8), respectively. Changes in standard QCT emphysema measures also predicted change in FEV1 decline, but only CBaE and diffuse emphysema remained independently predictive of accelerated FEV1 decline when all were considered together. CONCLUSIONS: One-year progression of CT emphysema subtypes predicted accelerated FEV₁ decline, supporting their potential use as intermediate endpoints in COPD trials.
Authors
- Elsa D. Angelini (ORCID: https://orcid.org/0000-0002-1602-300X)
- Jeffrey L. Curtis (ORCID: https://orcid.org/0000-0001-5191-4847)
- Emilia A. Hermann (ORCID: https://orcid.org/0000-0003-3428-0728)
- Robert Paine (ORCID: https://orcid.org/0000-0002-4511-4437)
- Andrew F. Laine (ORCID: https://orcid.org/0000-0003-3797-0628)
- Alejandro Comellas
- Yifei Sun
- Prescott Woodruff
- MeiLan K. Han (ORCID: https://orcid.org/0000-0002-9095-4419)
- Victor Ortega
- Igor Barjaktarevic
- Eric A Hoffman
- Nadia N Hansel
- Fernando J Martinez
- Wassim Labaki
- Benjamin Smith
- Gerard Criner
- David A Lynch
- J Michael Wells
- Jessica Bon
- David Couper
- Christopher B Cooper
- Jerry A Krishnan
- R Graham Barr
Institutions
- Télécom Paris (FR)
- University of Iowa (US)
- Johns Hopkins University (US)
- University of California, Los Angeles (US)
- University of California, San Francisco (US)
- Cornell University (US)
- Columbia University Irving Medical Center (US)
- Johns Hopkins Medicine (US)
- National Jewish Health (US)
- University of Alabama at Birmingham (US)
- University of Illinois Chicago (US)
- University of Chicago (US)
- Pulmonary and Allergy Associates (US)
- Mayo Clinic in Arizona (US)
- Institut Polytechnique de Paris (FR)
- Mayo Clinic in Florida (US)
- Department of Health (ZA)
- Weill Cornell Medical College in Qatar (QA)
- Pulmonary and Critical Care Associates (US)
- University of San Francisco (US)
- University of Missouri (US)
- Columbia University (US)
- Temple University (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- American Journal of Respiratory and Critical Care Medicine
- Published
- 2026-09-25
- DOI
- https://doi.org/10.1093/ajrccm/aamag497
- Primary Topic
- Chronic Obstructive Pulmonary Disease (COPD) Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00