Impact of race on asthma treatment failures in the asthma clinical research network
- PMID: 21885625
- PMCID: PMC3361331
- DOI: 10.1164/rccm.201103-0514OC
Impact of race on asthma treatment failures in the asthma clinical research network
Abstract
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 10 ACRN trials (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 African Americans (19.7%; n = 46) experienced a 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.
Figures
Comment in
-
Long-acting β-agonists and asthma: the saga continues.Am J Respir Crit Care Med. 2011 Dec 1;184(11):1220-1. doi: 10.1164/rccm.201109-1683ED. Am J Respir Crit Care Med. 2011. PMID: 22162879 No abstract available.
References
-
- Centers for Disease Control and Prevention (CDC) Asthma prevalence and control characteristics by race/ethnicity—United States 2002. MMWR 2004;53:145–148
-
- Ford JG, Mccaffrey L. Understanding disparities in asthma outcomes among African Americans. Clin Chest Med 2006;27:423–430 - PubMed
-
- Nelson HS, Weiss ST, Bleecker ER, Yancey SW, Dorinsky PM. The Salmeterol Multicenter Asthma Research Trial. A comparison of usual pharmacotherapy for asthma or usual pharmacotherapy plus salmeterol. Chest 2006;129:15–26 - PubMed
-
- Martinez FD. Safety of long-acting beta-agonists: an urgent need to clear the air. N Engl J Med 2005;353:2637–2639 - PubMed
-
- Drazen JM, Israel E, Boushey HA, Chinchilli VM, Fahy JV, Fish JE, Lazarus SC, Lemanske RF, Martin RJ, Peters SP, et al. Comparison of regularly scheduled with as-needed use of albuterol in mild asthma. N Engl J Med 1996;335:841–847 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- U10 HL074227/HL/NHLBI NIH HHS/United States
- 5 U10 HL051810/HL/NHLBI NIH HHS/United States
- 5 U10 HL051845/HL/NHLBI NIH HHS/United States
- U10 HL051843/HL/NHLBI NIH HHS/United States
- 5 U10 HL051823/HL/NHLBI NIH HHS/United States
- 5 U10 HL051834/HL/NHLBI NIH HHS/United States
- U10 HL74227/HL/NHLBI NIH HHS/United States
- 5 U10 HL056443/HL/NHLBI NIH HHS/United States
- U10 HL051823/HL/NHLBI NIH HHS/United States
- U10 HL056443/HL/NHLBI NIH HHS/United States
- 5 U10 HL051843/HL/NHLBI NIH HHS/United States
- U10 HL051831/HL/NHLBI NIH HHS/United States
- U10 HL051845/HL/NHLBI NIH HHS/United States
- 5 U10 HL051831/HL/NHLBI NIH HHS/United States
- U10 HL051834/HL/NHLBI NIH HHS/United States
