@article {1675391,
	title = {The Association Between Lung Hyperinflation and Coronary Artery Disease in Smokers},
	journal = {Chest},
	volume = {160},
	number = {3},
	year = {2021},
	month = {2021 Sep},
	pages = {858-871},
	abstract = {BACKGROUND: Smokers manifest varied phenotypes of pulmonary impairment.

RESEARCH QUESTION: Which pulmonary phenotypes are associated with coronary artery disease (CAD) in smokers?

STUDY DESIGN AND METHODS: We analyzed data from the University of Pittsburgh COPD Specialized Center for Clinically Oriented Research (SCCOR) cohort (n~= 481) and the Genetic Epidemiology of COPD (COPDGene) cohort (n~= 2,580). Participants were current and former smokers with \> 10 pack-years of tobacco exposure. Data from the two cohorts were analyzed separately because of methodologic differences. Lung hyperinflation was assessed by plethysmography in the SCCOR cohort and by inspiratory and expiratory CT scan lung volumes in the COPDGene cohort. Subclinical CAD was assessed as the coronary artery calcium score, whereas clinical CAD was defined as a self-reported history of CAD or myocardial infarction (MI). Analyses were performed in all smokers and then repeated in those with airflow obstruction (FEV1 to FVC ratio,~\< 0.70).

RESULTS: Pulmonary phenotypes, including airflow limitation, emphysema, lung hyperinflation, diffusion capacity, and radiographic measures of airway remodeling, showed weak to moderate correlations (r~\< 0.7) with each other. In multivariate models adjusted for pulmonary phenotypes and CAD risk factors, lung hyperinflation was the only phenotype associated with calcium score, history of clinical CAD, or history of MI (per 0.2 higher expiratory and inspiratory CT scan lung volume; coronary calcium: OR, 1.2; 95\%~CI, 1.1-1.5; P~= .02; clinical CAD: OR, 1.6; 95\%~CI, 1.1-2.3; P~= .01; and MI in COPDGene: OR, 1.7; 95\%~CI, 1.0-2.8; P~= .05). FEV1 and emphysema were associated with increased risk of CAD (P~\< .05) in models adjusted for CAD risk factors; however, these associations were attenuated on adjusting for lung hyperinflation. Results were the same in those with airflow obstruction and were present in both cohorts.

INTERPRETATION: Lung hyperinflation is associated strongly with clinical and subclinical CAD in smokers, including those with airflow obstruction. After lung hyperinflation was accounted for, FEV1 and emphysema no longer were associated with CAD. Subsequent studies should consider measuring lung hyperinflation and examining its mechanistic role in CAD in current and former smokers.},
	keywords = {Airway Obstruction, Airway Remodeling, Asymptomatic Diseases, Biological Variation, Population, Coronary Artery Disease, Coronary Vessels, Female, Humans, Lung, Male, Middle Aged, Organ Size, Plethysmography, Pulmonary Emphysema, Respiratory Function Tests, Risk Factors, Smoking, Tomography, X-Ray Computed, United States},
	issn = {1931-3543},
	doi = {10.1016/j.chest.2021.04.066},
	author = {Chandra, Divay and Gupta, Aman and Kinney, Gregory L and Fuhrman, Carl R and Leader, Joseph K and Diaz, Alejandro A and Bon, Jessica and Barr, R Graham and Washko, George and Budoff, Matthew and Hokanson, John and Sciurba, Frank C}
}