Association between Functional Small Airway Disease and FEV1 Decline in Chronic Obstructive Pulmonary Disease

Surya P. Bhatt(University of Alabama at Birmingham), Xavier Soler(University of California System), Xin Wang, Susan Murray, Antonio Anzueto(The University of Texas at San Antonio Health Science Center), Terri H. Beaty(Faculty of Public Health), Aladin M. Boriek(Baylor College of Medicine), Richard Casaburi(The Lundquist Institute), Gerard J. Criner(Pulmonary and Critical Care Associates), Alejandro A. Díaz(Brigham and Women's Hospital), Mark T. Dransfield(University of Alabama at Birmingham), Douglas Curran‐Everett(Institute for Medical Informatics and Biostatistics), Craig J. Galbán, Eric A. Hoffman(University of Iowa), James C. Hogg(University of British Columbia), Ella A. Kazerooni, V. Kim(Pulmonary and Critical Care Associates), Gregory L. Kinney(Colorado School of Public Health), Amir Lagstein, David A. Lynch, Barry J. Make(National Jewish Health), Fernando J. Martínez(Pulmonary and Critical Care Associates), Joe Ramsdell(University of California System), Rishindra M. Reddy(University of Michigan), Brian D. Ross, Harry B. Rossiter(The Lundquist Institute), Robert M. Steiner(Temple University Hospital), Matthew Strand(Institute for Medical Informatics and Biostatistics), Edwin J.R. van Beek(University of Edinburgh), Emily S. Wan(Brigham and Women's Hospital), George R. Washko(Brigham and Women's Hospital), J. Michael Wells(University of Alabama at Birmingham), Chris H. Wendt(University of Minnesota), Robert A. Wise(Johns Hopkins University), Edwin K. Silverman(Brigham and Women's Hospital), James D. Crapo(National Jewish Health), Russell P. Bowler(National Jewish Health), MeiLan K. Han(Pulmonary and Critical Care Associates)
American Journal of Respiratory and Critical Care Medicine
January 25, 2016
Cited by 386Open Access
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Abstract

RATIONALE: The small conducting airways are the major site of airflow obstruction in chronic obstructive pulmonary disease and may precede emphysema development. OBJECTIVES: We hypothesized a novel computed tomography (CT) biomarker of small airway disease predicts FEV1 decline. METHODS: We analyzed 1,508 current and former smokers from COPDGene with linear regression to assess predictors of change in FEV1 (ml/yr) over 5 years. Separate models for subjects without and with airflow obstruction were generated using baseline clinical and physiologic predictors in addition to two novel CT metrics created by parametric response mapping (PRM), a technique pairing inspiratory and expiratory CT images to define emphysema (PRM(emph)) and functional small airways disease (PRM(fSAD)), a measure of nonemphysematous air trapping. MEASUREMENTS AND MAIN RESULTS: Mean (SD) rate of FEV1 decline in ml/yr for GOLD (Global Initiative for Chronic Obstructive Lung Disease) 0-4 was as follows: 41.8 (47.7), 53.8 (57.1), 45.6 (61.1), 31.6 (43.6), and 5.1 (35.8), respectively (trend test for grades 1-4; P < 0.001). In multivariable linear regression, for participants without airflow obstruction, PRM(fSAD) but not PRM(emph) was associated with FEV1 decline (P < 0.001). In GOLD 1-4 participants, both PRM(fSAD) and PRM(emph) were associated with FEV1 decline (P < 0.001 and P = 0.001, respectively). Based on the model, the proportional contribution of the two CT metrics to FEV1 decline, relative to each other, was 87% versus 13% and 68% versus 32% for PRM(fSAD) and PRM(emph) in GOLD 1/2 and 3/4, respectively. CONCLUSIONS: CT-assessed functional small airway disease and emphysema are associated with FEV1 decline, but the association with functional small airway disease has greatest importance in mild-to-moderate stage chronic obstructive pulmonary disease where the rate of FEV1 decline is the greatest. Clinical trial registered with www.clinicaltrials.gov (NCT 00608764).


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