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Reversible Airflow Obstruction Predicts Future Chronic Obstructive Pulmonary Disease Development in the SPIROMICS Cohort: An Observational Cohort Study.
Buhr, Russell G; Barjaktarevic, Igor Z; Quibrera, P Miguel; Bateman, Lori A; Bleecker, Eugene R; Couper, David J; Curtis, Jeffrey L; Dolezal, Brett A; Han, MeiLan K; Hansel, Nadia N; Krishnan, Jerry A; Martinez, Fernando J; McKleroy, William; Paine, Robert; Rennard, Stephen I; Tashkin, Donald P; Woodruff, Prescott G; Kanner, Richard E; Cooper, Christopher B.
Afiliação
  • Buhr RG; Division of Pulmonary and Critical Care Medicine, and.
  • Barjaktarevic IZ; Center for the Study of Healthcare Innovation, Implementation, and Policy, Health Services Research and Development, Greater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California.
  • Quibrera PM; Division of Pulmonary and Critical Care Medicine, and.
  • Bateman LA; Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
  • Bleecker ER; Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
  • Couper DJ; Division of Genetics, Genomics, and Precision Medicine, University of Arizona, Tucson, Arizona.
  • Curtis JL; Collaborative Studies Coordinating Center, Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina.
  • Dolezal BA; Division of Pulmonary and Critical Care Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan.
  • Han MK; Medical Service, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, Michigan.
  • Hansel NN; Division of Pulmonary and Critical Care Medicine, and.
  • Krishnan JA; Division of Pulmonary and Critical Care Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan.
  • Martinez FJ; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • McKleroy W; Breathe Chicago Center, Division of Pulmonary and Critical Care Medicine, University of Illinois at Chicago College of Medicine, Chicago, Illinois.
  • Paine R; Division of Pulmonary and Critical Care Medicine, Columbia University College of Physicians and Surgeons, New York, New York.
  • Rennard SI; Division of Pulmonary and Critical Care Medicine, University of California, San Francisco, California.
  • Tashkin DP; Division of Respiratory, Critical Care, and Occupational Medicine, University of Utah School of Medicine, Salt Lake City, Utah.
  • Woodruff PG; Veterans Affairs Salt Lake City Healthcare System, Salt Lake City, Utah; and.
  • Kanner RE; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska.
  • Cooper CB; Division of Pulmonary and Critical Care Medicine, and.
Am J Respir Crit Care Med ; 206(5): 554-562, 2022 09 01.
Article em En | MEDLINE | ID: mdl-35549640
ABSTRACT
Rationale Chronic obstructive pulmonary disease (COPD) is defined by fixed spirometric ratio, FEV1/FVC < 0.70 after inhaled bronchodilators. However, the implications of variable obstruction (VO), in which the prebronchodilator FEV1/FVC ratio is less than 0.70 but increases to 0.70 or more after inhaled bronchodilators, have not been determined.

Objectives:

We explored differences in physiology, exacerbations, and health status in participants with VO compared with reference participants without obstruction.

Methods:

Data from the SPIROMICS (Subpopulations and Intermediate Outcome Measures in COPD Study) cohort were obtained. Participants with VO were compared with reference participants without obstruction. Measurements and Main

Results:

We assessed differences in baseline radiographic emphysema and small airway disease at study entry, baseline, and change in lung function by spirometry, functional capacity by 6-minute walk, health status using standard questionnaires, exacerbation rates, and progression to COPD between the two groups. All models were adjusted for participant characteristics, asthma history, and tobacco exposure. We assessed 175 participants with VO and 603 reference participants without obstruction. Participants with VO had 6.2 times the hazard of future development of COPD controlling for other factors (95% confidence interval, 4.6-8.3; P < 0.001). Compared with reference participants, the VO group had significantly lower baseline pre- and post-bronchodilator (BD) FEV1, and greater decline over time in post-BD FEV1, and pre- and post-BD FVC. There were no significant differences in exacerbations between groups.

Conclusions:

Significant risk for future COPD development exists for those with pre- but not post-BD airflow obstruction. These findings support consideration of expanding spirometric criteria defining COPD to include pre-BD obstruction. Clinical trial registered with www.clinicaltrials.gov (NCT01969344).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Doença Pulmonar Obstrutiva Crônica / Obstrução das Vias Respiratórias Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Doença Pulmonar Obstrutiva Crônica / Obstrução das Vias Respiratórias Idioma: En Ano de publicação: 2022 Tipo de documento: Article