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Association between Functional Small Airway Disease and FEV1 Decline in Chronic Obstructive Pulmonary Disease.
Bhatt, Surya P; Soler, Xavier; Wang, Xin; Murray, Susan; Anzueto, Antonio R; Beaty, Terri H; Boriek, Aladin M; Casaburi, Richard; Criner, Gerard J; Diaz, Alejandro A; Dransfield, Mark T; Curran-Everett, Douglas; Galbán, Craig J; Hoffman, Eric A; Hogg, James C; Kazerooni, Ella A; Kim, Victor; Kinney, Gregory L; Lagstein, Amir; Lynch, David A; Make, Barry J; Martinez, Fernando J; Ramsdell, Joe W; Reddy, Rishindra; Ross, Brian D; Rossiter, Harry B; Steiner, Robert M; Strand, Matthew J; van Beek, Edwin J R; Wan, Emily S; Washko, George R; Wells, J Michael; Wendt, Chris H; Wise, Robert A; Silverman, Edwin K; Crapo, James D; Bowler, Russell P; Han, MeiLan K.
Afiliação
  • Bhatt SP; 1 Division of Pulmonary, Allergy and Critical Care Medicine, and.
  • Soler X; 2 UAB Lung Health Center, University of Alabama at Birmingham, Birmingham, Alabama.
  • Wang X; 3 Division of Pulmonary, Critical Care and Sleep Medicine, University of California San Diego, San Diego, California.
  • Murray S; 4 School of Public Health.
  • Anzueto AR; 4 School of Public Health.
  • Beaty TH; 5 Division of Pulmonary and Critical Care Medicine, University of Texas Health Science Center at San Antonio, and South Texas Veterans Health Care System, San Antonio, Texas.
  • Boriek AM; 6 Department of Epidemiology, School of Public Health, and.
  • Casaburi R; 7 Pulmonary, Critical Care and Sleep Medicine, Baylor College of Medicine, Houston, Texas.
  • Criner GJ; 8 Division of Pulmonary and Critical Care Physiology and Medicine, and Rehabilitation Clinical Trials Center Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California.
  • Diaz AA; 9 Pulmonary and Critical Care Medicine, and.
  • Dransfield MT; 10 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Curran-Everett D; 1 Division of Pulmonary, Allergy and Critical Care Medicine, and.
  • Galbán CJ; 2 UAB Lung Health Center, University of Alabama at Birmingham, Birmingham, Alabama.
  • Hoffman EA; 11 Department of Biostatistics and Bioinformatics.
  • Hogg JC; 12 Department of Biostatistics and Informatics, and.
  • Kazerooni EA; 13 Department of Radiology, Center for Molecular Imaging.
  • Kim V; 14 Department of Radiology.
  • Kinney GL; 15 Department of Medicine, and.
  • Lagstein A; 16 Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa.
  • Lynch DA; 17 Department of Pathology and Laboratory Medicine, University of British Columbia, and James Hogg Research Centre, St. Paul's Hospital, Vancouver, Canada.
  • Make BJ; 18 Department of Radiology.
  • Martinez FJ; 9 Pulmonary and Critical Care Medicine, and.
  • Ramsdell JW; 19 Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Denver, Colorado.
  • Reddy R; 20 Department of Pathology.
  • Ross BD; 21 Department of Radiology, and.
  • Rossiter HB; 22 Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, Colorado.
  • Steiner RM; 23 Division of Pulmonary & Critical Care Medicine, and.
  • Strand MJ; 3 Division of Pulmonary, Critical Care and Sleep Medicine, University of California San Diego, San Diego, California.
  • van Beek EJ; 24 Division of Thoracic Surgery, University of Michigan, Ann Arbor, Michigan.
  • Wan ES; 13 Department of Radiology, Center for Molecular Imaging.
  • Washko GR; 8 Division of Pulmonary and Critical Care Physiology and Medicine, and Rehabilitation Clinical Trials Center Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California.
  • Wells JM; 25 Department of Radiology, Temple University Hospital, Philadelphia, Pennsylvania.
  • Wendt CH; 11 Department of Biostatistics and Bioinformatics.
  • Wise RA; 12 Department of Biostatistics and Informatics, and.
  • Silverman EK; 26 Clinical Research Imaging Centre, University of Edinburgh, Edinburgh, United Kingdom.
  • Crapo JD; 27 Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; and.
  • Bowler RP; 10 Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Han MK; 1 Division of Pulmonary, Allergy and Critical Care Medicine, and.
Am J Respir Crit Care Med ; 194(2): 178-84, 2016 07 15.
Article em En | MEDLINE | ID: mdl-26808615
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Respiratório / Doença Pulmonar Obstrutiva Crônica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Respiratório / Doença Pulmonar Obstrutiva Crônica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article