TY - JOUR
T1 - Impact of race on asthma treatment failures in the Asthma Clinical Research Network
AU - Wechsler, Michael E.
AU - Castro, Mario
AU - Lehman, Erik
AU - Chinchilli, Vernon M.
AU - Sutherland, E. Rand
AU - Denlinger, Loren
AU - Lazarus, Stephen C.
AU - Peters, Stephen P.
AU - Israel, Elliot
AU - Martin, Richard J.
AU - Szefler, Stanley J.
AU - Cherniack, Reuben
AU - Lemanske, Robert F.
AU - Sorkness, Christine A.
AU - Jarjour, Nizar
AU - Craig, Tim
AU - Kunselman, Susan J.
AU - Boushey, Homer A.
AU - Fahy, John V.
AU - Kraft, Monica
AU - Wasserman, Steven
AU - Ramsdell, Joe
AU - Calhoun, William J.
AU - Ameredes, Bill
AU - Walter, Michael
AU - Bleecker, Eugene
AU - DiMango, Emily
AU - Pesola, Gene R.
AU - Smith, Robert
PY - 2011/12/1
Y1 - 2011/12/1
N2 - Rationale: Recent studies suggest that people with asthma of different racial backgrounds may respond differently to various therapies. Objectives: To use data from well-characterized participants in prior Asthma Clinical Research Network (ACRN) trials to determine whether racial differences affected asthma treatment failures. Methods: We analyzed baseline phenotypes and treatment failure rates (worsening asthma resulting in systemic corticosteroid use, hospitalization, emergency department visit, prolonged decrease in peak expiratory flow, increase in albuterol use, or safety concerns) in subjects participating in 10ACRNtrials (1993-2003). Self-declared race was reported in each trial and treatment failure rates were stratified by race. Measurements and Main Results: A total of 1,200 unique subjects (whites = 795 [66%]; African Americans = 233 [19%]; others = 172 [14%]; mean age = 32) were included in the analyses. At baseline, African Americans had fewer asthma symptoms (P < 0.001) and less average daily rescue inhaler use (P = 0.007) than whites. There were no differences in baseline FEV 1 (% predicted); asthma quality of life; bronchial hyperreactivity; or exhaled nitric oxide concentrations. A total of 147 treatment failures were observed; a significantly higher proportion of AfricanAmericans(19.7%;n=46) experienceda treatment failure compared with whites (12.7%; n = 101) (odds ratio = 1.7; 95% confidence interval, 1.2-2.5; P = 0.007). When stratified by treatment, African Americans receiving long-acting β-agonists were twice as likely as whites to experience a treatment failure (odds ratio = 2.1; 95% confidence interval, 1.3-3.6; P = 0.004), even when used with other controller therapies. Conclusions: Despite having fewer asthma symptoms and less rescue β-agonist use, African-Americans with asthma have more treatment failures compared with whites, especially when taking long-acting β-agonists.
AB - Rationale: Recent studies suggest that people with asthma of different racial backgrounds may respond differently to various therapies. Objectives: To use data from well-characterized participants in prior Asthma Clinical Research Network (ACRN) trials to determine whether racial differences affected asthma treatment failures. Methods: We analyzed baseline phenotypes and treatment failure rates (worsening asthma resulting in systemic corticosteroid use, hospitalization, emergency department visit, prolonged decrease in peak expiratory flow, increase in albuterol use, or safety concerns) in subjects participating in 10ACRNtrials (1993-2003). Self-declared race was reported in each trial and treatment failure rates were stratified by race. Measurements and Main Results: A total of 1,200 unique subjects (whites = 795 [66%]; African Americans = 233 [19%]; others = 172 [14%]; mean age = 32) were included in the analyses. At baseline, African Americans had fewer asthma symptoms (P < 0.001) and less average daily rescue inhaler use (P = 0.007) than whites. There were no differences in baseline FEV 1 (% predicted); asthma quality of life; bronchial hyperreactivity; or exhaled nitric oxide concentrations. A total of 147 treatment failures were observed; a significantly higher proportion of AfricanAmericans(19.7%;n=46) experienceda treatment failure compared with whites (12.7%; n = 101) (odds ratio = 1.7; 95% confidence interval, 1.2-2.5; P = 0.007). When stratified by treatment, African Americans receiving long-acting β-agonists were twice as likely as whites to experience a treatment failure (odds ratio = 2.1; 95% confidence interval, 1.3-3.6; P = 0.004), even when used with other controller therapies. Conclusions: Despite having fewer asthma symptoms and less rescue β-agonist use, African-Americans with asthma have more treatment failures compared with whites, especially when taking long-acting β-agonists.
KW - African Americans
KW - Asthma
KW - Long-acting β-agonist
KW - Race
KW - Treatment failure
UR - http://www.scopus.com/inward/record.url?scp=82555196052&partnerID=8YFLogxK
U2 - 10.1164/rccm.201103-0514OC
DO - 10.1164/rccm.201103-0514OC
M3 - Article
C2 - 21885625
AN - SCOPUS:82555196052
SN - 1073-449X
VL - 184
SP - 1247
EP - 1253
JO - American journal of respiratory and critical care medicine
JF - American journal of respiratory and critical care medicine
IS - 11
ER -