Rationale: Quantifying functional small airways disease (fSAD) requires additional expiratory computed tomography (CT) scan, limiting clinical applicability. Artificial intelligence (AI) could enable fSAD quantification from chest CT scan at total lung capacity (TLC) alone (fSAD).
Objectives: To evaluate an AI model for estimating fSAD, compare it with dual-volume parametric response mapping fSAD (fSAD), and assess its clinical associations and repeatability in chronic obstructive pulmonary disease (COPD).
Methods: We analyzed 2513 participants from the SubPopulations and InteRmediate Outcome Measures in COPD Study (SPIROMICS). Using a randomly sampled subset ( = 1055), we developed a generative model to produce virtual expiratory CTs for estimating fSAD in the remaining 1458 SPIROMICS participants. We compared fSAD with dual volume, parametric response mapping fSAD. We investigated univariate and multivariable associations of fSAD with FEV, FEV/FVC, six-minute walk distance (6MWD), St. George's Respiratory Questionnaire (SGRQ), and FEV decline. The results were validated in a subset ( = 458) from COPDGene study. Multivariable models were adjusted for age, race, sex, BMI, baseline FEV, smoking pack years, smoking status, and percent emphysema.
Measurements And Main Results: Inspiratory fSAD showed a strong correlation with fSAD in both SPIROMICS (Pearson's R = 0.895) and COPDGene (R = 0.897) cohorts. Higher fSAD levels were significantly associated with lower lung function, including lower postbronchodilator FEV (L) and FEV/FVC ratio, and poorer quality of life reflected by higher total SGRQ scores, independent of percent CT emphysema. In SPIROMICS, individuals with higher fSAD experienced an annual decline in FEV of 1.156 mL (relative decrease; 95% CI: 0.613, 1.699; < 0.001) per year for every 1% increase in fSAD. The rate of decline in COPDGene was slightly lower at 0.866 mL / year (relative decrease; 95% CI: 0.345, 1.386; < 0.001) for percent increase in fSAD. Inspiratory fSAD demonstrated greater consistency between repeated measurements with a higher intraclass correlation coefficient (ICC) of 0.99 (95% CI: 0.98, 0.99) compared to fSAD [ICC: 0.83 (95% CI: 0.76, 0.88)].
Conclusions: Small airways disease can be reliably assessed from a single inspiratory CT scan using generative AI, eliminating the need for an additional expiratory CT scan. fSAD estimation from inspiratory CT correlates strongly with fSAD, demonstrates a significant association with FEV decline, and offers greater repeatability.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1164/rccm.202409-1847OC | DOI Listing |
Am J Respir Crit Care Med
March 2025
University of Iowa, Radiology and Biomedical Engineering, Iowa City, Iowa, United States;
Rationale: Quantifying functional small airways disease (fSAD) requires additional expiratory computed tomography (CT) scan, limiting clinical applicability. Artificial intelligence (AI) could enable fSAD quantification from chest CT scan at total lung capacity (TLC) alone (fSAD).
Objectives: To evaluate an AI model for estimating fSAD, compare it with dual-volume parametric response mapping fSAD (fSAD), and assess its clinical associations and repeatability in chronic obstructive pulmonary disease (COPD).
Med Biol Eng Comput
February 2025
College of Medicine and Biological Information Engineering, Northeastern University, Shenyang, China.
Chronic obstructive pulmonary disease (COPD) is a highly heterogeneous disease with various phenotypes. Registered inspiratory and expiratory CT images can generate the parametric response map (PRM) that characterizes phenotypes' spatial distribution and proportions. However, increased radiation dosage, scan time, quality control, and patient cooperation requirements limit the utility of PRM.
View Article and Find Full Text PDFBMC Pulm Med
January 2025
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.
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.
Eur Radiol
January 2025
Department of Diagnostic and Interventional Radiology, University Hospital of Heidelberg, Heidelberg, Germany.
Objectives: We hypothesized that semiquantitative visual scoring of lung MRI is suitable for GOLD-grade specific characterization of parenchymal and airway disease in COPD and that MRI scores correlate with quantitative CT (QCT) and pulmonary function test (PFT) parameters.
Methods: Five hundred ninety-eight subjects from the COSYCONET study (median age = 67 (60-72)) at risk for COPD or with GOLD1-4 underwent PFT, same-day paired inspiratory/expiratory CT, and structural and contrast-enhanced MRI. QCT assessed total lung volume (TLV), emphysema, and air trapping by parametric response mapping (PRM, PRM) and airway disease by wall percentage (WP).
Ann Am Thorac Soc
November 2024
UCSF, Division of Pulmonary and Critical Care Medicine, Department of Medicine and CVRI, San Francisco, California, United States.
Among tobacco-exposed persons with preserved spirometry (TEPS), we previously demonstrated that different lung volume indices, specifically elevated total lung capacity (TLC) versus elevated ratio of functional residual capacity-to-TLC (FRC/TLC), identify different lung disease characteristics in the COPDGene cohort. Determine differential disease characteristics and trajectories associated with the lung volume indices among TEPS in the SPIROMICS cohort. We categorized TEPS (n=814) by tertiles (low, intermediate, high) of TLC or residual volume-to-TLC (RV/TLC) derived from baseline CT images, and then examined clinical and spirometric disease trajectories in mutually exclusive categories of participants with high TLC without high RV/TLC ([TLC]) versus high RV/TLC without high TLC ([RV/TLC]).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!