Your browser doesn't support javascript.
loading
Forced Expiratory Flow at 25%-75% Links COPD Physiology to Emphysema and Disease Severity in the SPIROMICS Cohort.
Ronish, Bonnie E; Couper, David J; Barjaktarevic, Igor Z; Cooper, Christopher B; Kanner, Richard E; Pirozzi, Cheryl S; Kim, Victor; Wells, James M; Han, MeiLan K; Woodruff, Prescott G; Ortega, Victor E; Peters, Stephen P; Hoffman, Eric A; Buhr, Russell G; Dolezal, Brett A; Tashkin, Donald P; Liou, Theodore G; Bateman, Lori A; Schroeder, Joyce D; Martinez, Fernando J; Barr, R Graham; Hansel, Nadia N; Comellas, Alejandro P; Rennard, Stephen I; Arjomandi, Mehrdad; Paine Iii, Robert.
Afiliação
  • Ronish BE; Division of Respiratory, Critical Care and Occupational Pulmonary Medicine, University of Utah, Salt Lake City, Utah, United States.
  • Couper DJ; Department of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Cooper CB; Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
  • Kanner RE; Department of Physiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
  • Pirozzi CS; Division of Respiratory, Critical Care and Occupational Pulmonary Medicine, University of Utah, Salt Lake City, Utah, United States.
  • Kim V; Division of Respiratory, Critical Care and Occupational Pulmonary Medicine, University of Utah, Salt Lake City, Utah, United States.
  • Wells JM; Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine, Temple University Hospital, Philadelphia, Pennsylvania, United States.
  • Han MK; Division of Pulmonary, Allergy, and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States.
  • Woodruff PG; Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, Michigan, United States.
  • Ortega VE; Department of Medicine, University of California San Francisco, San Francisco, California, United States.
  • Peters SP; Division of Internal Medicine, Wake Forest School of Medicine, Winston Salem, North Carolina, United States.
  • Hoffman EA; Division of Internal Medicine, Wake Forest University Health Sciences, Winston-Salem, North Carolina, United States.
  • Buhr RG; Department of Radiology, Division of Physiologic Imaging, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States.
  • Dolezal BA; Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
  • Tashkin DP; Center for the Study of Healthcare Innovation, Implementation, and Policy, VA Health Services Research and Development, Greater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California, United States.
  • Liou TG; Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
  • Bateman LA; Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States.
  • Schroeder JD; Division of Respiratory, Critical Care and Occupational Pulmonary Medicine, University of Utah, Salt Lake City, Utah, United States.
  • Martinez FJ; Department of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Barr RG; Division of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utah, United States.
  • Hansel NN; Division of Pulmonary and Critical Care, Weill Cornell Medicine, New York, New York, United States.
  • Comellas AP; Department of Internal Medicine, Columbia University, New York, New York, United States.
  • Rennard SI; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
  • Arjomandi M; Department of Internal Medicine, Division of Pulmonary, Critical Care and Occupational Medicine, University of Iowa, Iowa City, Iowa, United States.
  • Paine Iii R; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States.
Chronic Obstr Pulm Dis ; 9(2): 111-121, 2022 Apr 29.
Article em En | MEDLINE | ID: mdl-35114743
ABSTRACT

BACKGROUND:

Forced expiratory volume in 1 second (FEV1) is central to the diagnosis of chronic obstructive pulmonary disease (COPD) but is imprecise in classifying disease burden. We examined the potential of the maximal mid-expiratory flow rate (forced expiratory flow rate between 25% and 75% [FEF25%-75%]) as an additional tool for characterizing pathophysiology in COPD.

OBJECTIVE:

To determine whether FEF25%-75% helps predict clinical and radiographic abnormalities in COPD. STUDY DESIGN AND

METHODS:

The SubPopulations and InteRediate Outcome Measures In COPD Study (SPIROMICS) enrolled a prospective cohort of 2978 nonsmokers and ever-smokers, with and without COPD, to identify phenotypes and intermediate markers of disease progression. We used baseline data from 2771 ever-smokers from the SPIROMICS cohort to identify associations between percent predicted FEF25%-75% (%predFEF25%-75%) and both clinical markers and computed tomography (CT) findings of smoking-related lung disease.

RESULTS:

Lower %predFEF25-75% was associated with more severe disease, manifested radiographically by increased functional small airways disease, emphysema (most notably with homogeneous distribution), CT-measured residual volume, total lung capacity (TLC), and airway wall thickness, and clinically by increased symptoms, decreased 6-minute walk distance, and increased bronchodilator responsiveness (BDR). A lower %predFEF25-75% remained significantly associated with increased emphysema, functional small airways disease, TLC, and BDR after adjustment for FEV1 or forced vital capacity (FVC).

INTERPRETATION:

The %predFEF25-75% provides additional information about disease manifestation beyond FEV1. These associations may reflect loss of elastic recoil and air trapping from emphysema and intrinsic small airways disease. Thus, %predFEF25-75% helps link the anatomic pathology and deranged physiology of COPD.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Chronic Obstr Pulm Dis Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Chronic Obstr Pulm Dis Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos