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Factors predicting inhaled corticosteroid responsiveness in African American patients with asthma - 07/08/11

Doi : 10.1016/j.jaci.2010.08.002 
Wendy Gould, MD a, , Edward L. Peterson, PhD b, , Gloria Karungi, MBChB, MS c, Amanda Zoratti, BA c, John Gaggin, BSN c, Ghazwan Toma, MD, MPH c, Shiqing Yan, MD c, Albert M. Levin, PhD b, James J. Yang, PhD b, Karen Wells, BS b, Mingqun Wang, MS c, Robert R. Burke, MD, MS a, Kenneth Beckman, PhD d, Danijela Popadic, BS e, Susan J. Land, PhD e, Rajesh Kumar, MD f, Max A. Seibold, PhD g, David E. Lanfear, MD, MS a, c, Esteban G. Burchard, MD, MPH h, i, L. Keoki Williams, MD, MPH a, b,
a Department of Internal Medicine, Henry Ford Health System, Detroit, Mich 
b Department of Biostatistics and Research Epidemiology, Henry Ford Health System, Detroit, Mich 
c Center for Health Services Research, Henry Ford Health System, Detroit, Mich 
d Biomedical Genomics Center, University of Minnesota, Minneapolis, Minn 
e Applied Genomics Technology Center, Wayne State University, Detroit, Mich 
f Children’s Memorial Hospital, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Ill 
g Department of Medicine, National Jewish Health, Denver, Colo 
h Department of Medicine, University of California San Francisco, San Francisco General Hospital, San Francisco, Calif 
i Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, Calif 

Reprint requests: L. Keoki Williams, MD, MPH, Center for Health Services Research, Henry Ford Health System, 1 Ford Place, 3A, Detroit, MI 48202.

Abstract

Background

African American patients disproportionately experience uncontrolled asthma. Treatment with an inhaled corticosteroid (ICS) is considered first-line therapy for persistent asthma.

Objective

We sought to determine the degree to which African American patients respond to ICS medication and whether the level of response is influenced by other factors, including genetic ancestry.

Methods

Patients aged 12 to 56 years who received care from a large health system in southeast Michigan and who resided in Detroit were recruited to participate if they had a diagnosis of asthma. Patients were treated with 6 weeks of inhaled beclomethasone dipropionate, and pulmonary function was remeasured after treatment. Ancestry was determined by genotyping ancestry-informative markers. The main outcome measure was ICS responsiveness defined as the change in prebronchodilator FEV1 over the 6-week course of treatment.

Results

Among 147 participating African American patients with asthma, average improvement in FEV1 after 6 weeks of ICS treatment was 11.6%. The mean proportion of African ancestry in this group was 78.4%. The degree of baseline bronchodilator reversibility was the only factor consistently associated with ICS responsiveness, as measured by both an improvement in FEV1 and patient-reported asthma control (P = .001 and P = .021, respectively). The proportion of African ancestry was not significantly associated with ICS responsiveness.

Conclusions

Although baseline pulmonary function parameters appear to be associated with the likelihood to respond to ICS treatment, the proportion of genetic African ancestry does not. This study suggests that genetic ancestry might not contribute to differences in ICS controller response among African American patients with asthma.

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Key words : Inhaled corticosteroids, asthma, race-ethnicity, continental population groups, ancestry, urban health

Abbreviation used : ACT, ICS, SAPPHIRE


Plan


 Supported by grants from the Fund for Henry Ford Hospital; the American Asthma Foundation; the National Institute of Allergy and Infectious Diseases (AI79139, AI61774); the National Heart, Lung, and Blood Institute (HL79055); and the National Institute of Diabetes and Digestive and Kidney Diseases (DK64695), National Institutes of Health (L. K. W.). E. G. B. receives support from the National Institutes of Health (HL078885, HL088133, ES015794), the Robert Wood Johnson Foundation Amos Medical Faculty Development Program, and the Flight Attendant Medical Research Institute (FAMRI). R. K. receives support from the National Institutes of Health (K23HL093023-01).
 Disclosure of potential conflict of interest: E. L. Peterson receives research support from the National Institutes of Health (NIH). R. Kumar receives research support from the NIH, is a member of the American Thoracic Society, and is president of the Illinois Society of Allergy & Immunology. The rest of the authors have declared that they have no conflict of interest.


© 2010  American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 126 - N° 6

P. 1131-1138 - décembre 2010 Retour au numéro
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