Chinedu O Ejike1, Han Woo1, Panagis Galiatsatos1, Laura M Paulin2, Jerry A Krishnan3, Christopher B Cooper4,5, David J Couper6, Richard E Kanner7, Russell P Bowler8, Eric A Hoffman9, Alejandro P Comellas9, Gerard J Criner10, R Graham Barr11, Fernando J Martinez12, MeiLan K Han13, Carlos H Martinez14, Victor E Ortega15, Trisha M Parekh16, Stephanie A Christenson17, Neeta Thakur17, Aaron Baugh17, Daniel C Belz1, Sarath Raju1, Amanda J Gassett18, Joel D Kaufman18, Nirupama Putcha1, Nadia N Hansel1. 1. Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland. 2. Section of Pulmonary and Critical Care, Dartmouth-Hitchcock Medical Center, Geisel School of Medicine, Hanover, New Hampshire. 3. Division of Pulmonary, Critical Care, Sleep, and Allergy, University of Illinois, Chicago, Illinois. 4. Department of Medicine and. 5. Department of Physiology, University of California, Los Angeles, School of Medicine, Los Angeles, California. 6. Department of Biostatistics, University of North Carolina, Chapel Hill, North Carolina. 7. Division of Pulmonary and Critical Care, University of Utah School of Medicine, Salt Lake City, Utah. 8. Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, Colorado. 9. Division of Pulmonary, Critical Care and Occupational Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa. 10. Division of Pulmonary and Critical Care, Temple University Hospital, Philadelphia, Pennsylvania. 11. Division of Pulmonary, Allergy and Critical Care Medicine, Presbyterian Hospital, Columbia University Medical Center, New York, New York. 12. Department of Internal Medicine, Weill Cornell Medical College, New York, New York. 13. Division of Pulmonary and Critical Care Medicine, University of Michigan Health System, Ann Arbor, Michigan. 14. Division of Pulmonary and Critical Care, Oaklawn Hospital, Marshall, Michigan. 15. Center for Genomics and Personalized Medicine Research, Wake Forest University, Winston-Salem, North Carolina. 16. Division of Pulmonary, Allergy and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Alabama. 17. Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, San Francisco, California; and. 18. Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington.
Abstract
Rationale: Black adults have worse health outcomes compared with white adults in certain chronic diseases, including chronic obstructive pulmonary disease (COPD). Objectives: To determine to what degree disadvantage by individual and neighborhood socioeconomic status (SES) may contribute to racial disparities in COPD outcomes. Methods: Individual and neighborhood-scale sociodemographic characteristics were determined in 2,649 current or former adult smokers with and without COPD at recruitment into SPIROMICS (Subpopulations and Intermediate Outcome Measures in COPD Study). We assessed whether racial differences in symptom, functional, and imaging outcomes (St. George's Respiratory Questionnaire, COPD Assessment Test score, modified Medical Research Council dyspnea scale, 6-minute-walk test distance, and computed tomography [CT] scan metrics) and severe exacerbation risk were explained by individual or neighborhood SES. Using generalized linear mixed model regression, we compared respiratory outcomes by race, adjusting for confounders and individual-level and neighborhood-level descriptors of SES both separately and sequentially.Measurements and Main Results: After adjusting for COPD risk factors, Black participants had significantly worse respiratory symptoms and quality of life (modified Medical Research Council scale, COPD Assessment Test, and St. George's Respiratory Questionnaire), higher risk of severe exacerbations and higher percentage of emphysema, thicker airways (internal perimeter of 10 mm), and more air trapping on CT metrics compared with white participants. In addition, the association between Black race and respiratory outcomes was attenuated but remained statistically significant after adjusting for individual-level SES, which explained up to 12-35% of racial disparities. Further adjustment showed that neighborhood-level SES explained another 26-54% of the racial disparities in respiratory outcomes. Even after accounting for both individual and neighborhood SES factors, Black individuals continued to have increased severe exacerbation risk and persistently worse CT outcomes (emphysema, air trapping, and airway wall thickness).Conclusions: Disadvantages by individual- and neighborhood-level SES each partly explain disparities in respiratory outcomes between Black individuals and white individuals. Strategies to narrow the gap in SES disadvantages may help to reduce race-related health disparities in COPD; however, further work is needed to identify additional risk factors contributing to persistent disparities.
Rationale: Black adults have worse health outcomes compared with white adults in certain chronic diseases, including chronic obstructive pulmonary disease (COPD). Objectives: To determine to what degree disadvantage by individual and neighborhood socioeconomic status (SES) may contribute to racial disparities in COPD outcomes. Methods: Individual and neighborhood-scale sociodemographic characteristics were determined in 2,649 current or former adult smokers with and without COPD at recruitment into SPIROMICS (Subpopulations and Intermediate Outcome Measures in COPD Study). We assessed whether racial differences in symptom, functional, and imaging outcomes (St. George's Respiratory Questionnaire, COPD Assessment Test score, modified Medical Research Council dyspnea scale, 6-minute-walk test distance, and computed tomography [CT] scan metrics) and severe exacerbation risk were explained by individual or neighborhood SES. Using generalized linear mixed model regression, we compared respiratory outcomes by race, adjusting for confounders and individual-level and neighborhood-level descriptors of SES both separately and sequentially.Measurements and Main Results: After adjusting for COPD risk factors, Black participants had significantly worse respiratory symptoms and quality of life (modified Medical Research Council scale, COPD Assessment Test, and St. George's Respiratory Questionnaire), higher risk of severe exacerbations and higher percentage of emphysema, thicker airways (internal perimeter of 10 mm), and more air trapping on CT metrics compared with white participants. In addition, the association between Black race and respiratory outcomes was attenuated but remained statistically significant after adjusting for individual-level SES, which explained up to 12-35% of racial disparities. Further adjustment showed that neighborhood-level SES explained another 26-54% of the racial disparities in respiratory outcomes. Even after accounting for both individual and neighborhood SES factors, Black individuals continued to have increased severe exacerbation risk and persistently worse CT outcomes (emphysema, air trapping, and airway wall thickness).Conclusions: Disadvantages by individual- and neighborhood-level SES each partly explain disparities in respiratory outcomes between Black individuals and white individuals. Strategies to narrow the gap in SES disadvantages may help to reduce race-related health disparities in COPD; however, further work is needed to identify additional risk factors contributing to persistent disparities.
Entities:
Keywords:
COPD; neighborhood disadvantage; racial disparities; socioeconomic status
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