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Association of Dysanapsis With Chronic Obstructive Pulmonary Disease Among Older Adults.
Smith, Benjamin M; Kirby, Miranda; Hoffman, Eric A; Kronmal, Richard A; Aaron, Shawn D; Allen, Norrina B; Bertoni, Alain; Coxson, Harvey O; Cooper, Chris; Couper, David J; Criner, Gerard; Dransfield, Mark T; Han, MeiLan K; Hansel, Nadia N; Jacobs, David R; Kaufman, Joel D; Lin, Ching-Long; Manichaikul, Ani; Martinez, Fernando J; Michos, Erin D; Oelsner, Elizabeth C; Paine, Robert; Watson, Karol E; Benedetti, Andrea; Tan, Wan C; Bourbeau, Jean; Woodruff, Prescott G; Barr, R Graham.
Affiliation
  • Smith BM; Department of Medicine, Columbia University Medical Center, New York, New York.
  • Kirby M; Department of Medicine, McGill University, Montreal, Quebec, Canada.
  • Hoffman EA; Department of Physics, Ryerson University, Toronto, Ontario, Canada.
  • Kronmal RA; Department of Radiology, University of Iowa, Iowa City.
  • Aaron SD; Department of Biomedical Engineering, University of Iowa, Iowa City.
  • Allen NB; Department of Internal Medicine, University of Iowa, Iowa City.
  • Bertoni A; Department of Biostatistics, University of Washington, Seattle.
  • Coxson HO; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Cooper C; Department of Medicine, Northwestern University, Chicago, Illinois.
  • Couper DJ; Department of Medicine, Wake Forest University, Winston-Salem, North Carolina.
  • Criner G; Department of Radiology, University of British Columbia, Vancouver, Canada.
  • Dransfield MT; Department of Medicine, University of California, Los Angeles.
  • Han MK; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill.
  • Hansel NN; Department of Medicine, Temple University, Philadelphia, Pennsylvania.
  • Jacobs DR; Department of Medicine, University of Alabama at Birmingham, Birmingham.
  • Kaufman JD; Department of Medicine, University of Michigan, Ann Arbor.
  • Lin CL; Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
  • Manichaikul A; Division of Epidemiology and Community Health School of Public Health, University of Minnesota, Minneapolis.
  • Martinez FJ; Department of Epidemiology, University of Washington, Seattle.
  • Michos ED; Department of Environmental and Occupational Health Sciences, University of Washington, Seattle.
  • Oelsner EC; Department of Mechanical Engineering, University of Iowa, Iowa City.
  • Paine R; Department of Public Health Sciences, University of Virginia, Charlottesville.
  • Watson KE; Department of Medicine, Cornell University, New York, New York.
  • Benedetti A; Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
  • Tan WC; Department of Medicine, Columbia University Medical Center, New York, New York.
  • Bourbeau J; Department of Medicine, University of Utah, Salt Lake City.
  • Woodruff PG; Department of Medicine, University of California, Los Angeles.
  • Barr RG; Department of Medicine, McGill University, Montreal, Quebec, Canada.
JAMA ; 323(22): 2268-2280, 2020 06 09.
Article in En | MEDLINE | ID: mdl-32515814
ABSTRACT
Importance Smoking is a major risk factor for chronic obstructive pulmonary disease (COPD), yet much of COPD risk remains unexplained.

Objective:

To determine whether dysanapsis, a mismatch of airway tree caliber to lung size, assessed by computed tomography (CT), is associated with incident COPD among older adults and lung function decline in COPD. Design, Setting, and

Participants:

A retrospective cohort study of 2 community-based samples the Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study, which involved 2531 participants (6 US sites, 2010-2018) and the Canadian Cohort of Obstructive Lung Disease (CanCOLD), which involved 1272 participants (9 Canadian sites, 2010-2018), and a case-control study of COPD the Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS), which involved 2726 participants (12 US sites, 2011-2016). Exposures Dysanapsis was quantified on CT as the geometric mean of airway lumen diameters measured at 19 standard anatomic locations divided by the cube root of lung volume (airway to lung ratio). Main Outcomes and

Measures:

Primary outcome was COPD defined by postbronchodilator ratio of forced expired volume in the first second to vital capacity (FEV1FVC) less than 0.70 with respiratory symptoms. Secondary outcome was longitudinal lung function. All analyses were adjusted for demographics and standard COPD risk factors (primary and secondhand tobacco smoke exposures, occupational and environmental pollutants, and asthma).

Results:

In the MESA Lung sample (mean [SD] age, 69 years [9 years]; 1334 women [52.7%]), 237 of 2531 participants (9.4%) had prevalent COPD, the mean (SD) airway to lung ratio was 0.033 (0.004), and the mean (SD) FEV1 decline was -33 mL/y (31 mL/y). Of 2294 MESA Lung participants without prevalent COPD, 98 (4.3%) had incident COPD at a median of 6.2 years. Compared with participants in the highest quartile of airway to lung ratio, those in the lowest had a significantly higher COPD incidence (9.8 vs 1.2 cases per 1000 person-years; rate ratio [RR], 8.12; 95% CI, 3.81 to 17.27; rate difference, 8.6 cases per 1000 person-years; 95% CI, 7.1 to 9.2; P < .001) but no significant difference in FEV1 decline (-31 vs -33 mL/y; difference, 2 mL/y; 95% CI, -2 to 5; P = .30). Among CanCOLD participants (mean [SD] age, 67 years [10 years]; 564 women [44.3%]), 113 of 752 (15.0%) had incident COPD at a median of 3.1 years and the mean (SD) FEV1 decline was -36 mL/y (75 mL/y). The COPD incidence in the lowest airway to lung quartile was significantly higher than in the highest quartile (80.6 vs 24.2 cases per 1000 person-years; RR, 3.33; 95% CI, 1.89 to 5.85; rate difference, 56.4 cases per 1000 person-years; 95% CI, 38.0 to 66.8; P<.001), but the FEV1 decline did not differ significantly (-34 vs -36 mL/y; difference, 1 mL/y; 95% CI, -15 to 16; P=.97). Among 1206 SPIROMICS participants (mean [SD] age, 65 years [8 years]; 542 women [44.9%]) with COPD who were followed up for a median 2.1 years, those in the lowest airway to lung ratio quartile had a mean FEV1 decline of -37 mL/y (15 mL/y), which did not differ significantly from the decline in MESA Lung participants (P = .98), whereas those in highest quartile had significantly faster decline than participants in MESA Lung (-55 mL/y [16 mL/y ]; difference, -17 mL/y; 95% CI, -32 to -3; P = .004). Conclusions and Relevance Among older adults, dysanapsis was significantly associated with COPD, with lower airway tree caliber relative to lung size associated with greater COPD risk. Dysanapsis appears to be a risk factor associated with COPD.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vital Capacity / Forced Expiratory Volume / Pulmonary Disease, Chronic Obstructive / Lung Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male Language: En Journal: JAMA Year: 2020 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vital Capacity / Forced Expiratory Volume / Pulmonary Disease, Chronic Obstructive / Lung Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male Language: En Journal: JAMA Year: 2020 Type: Article