Factors predicting inhaled corticosteroid responsiveness in African American patients with asthma

被引:32
作者
Gould, Wendy [2 ]
Peterson, Edward L. [3 ]
Karungi, Gloria [1 ]
Zoratti, Amanda [1 ]
Gaggin, John [1 ]
Toma, Ghazwan [1 ]
Yan, Shiqing [1 ]
Levin, Albert M. [3 ]
Yang, James J. [3 ]
Wells, Karen [3 ]
Wang, Mingqun [1 ]
Burke, Robert R. [2 ]
Beckman, Kenneth [4 ]
Popadic, Danijela [5 ]
Land, Susan J. [5 ]
Kumar, Rajesh [6 ]
Seibold, Max A. [7 ]
Lanfear, David E. [1 ,2 ]
Burchard, Esteban G. [8 ,9 ]
Williams, L. Keoki [1 ,2 ,3 ]
机构
[1] Henry Ford Hlth Syst, Ctr Hlth Serv Res, Detroit, MI 48202 USA
[2] Henry Ford Hlth Syst, Dept Internal Med, Detroit, MI 48202 USA
[3] Henry Ford Hlth Syst, Dept Biostat & Res Epidemiol, Detroit, MI 48202 USA
[4] Univ Minnesota, Biomed Genom Ctr, Minneapolis, MN USA
[5] Wayne State Univ, Appl Genom Technol Ctr, Detroit, MI USA
[6] Northwestern Univ, Childrens Mem Hosp, Dept Pediat, Feinberg Sch Med, Chicago, IL 60614 USA
[7] Natl Jewish Hlth, Dept Med, Denver, CO USA
[8] Univ Calif San Francisco, Dept Med, San Francisco Gen Hosp, San Francisco, CA USA
[9] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
Inhaled corticosteroids; asthma; race-ethnicity; continental population groups; ancestry; urban health; POPULATION-STRUCTURE; BRONCHODILATOR RESPONSIVENESS; RACIAL-DIFFERENCES; GENETIC-STRUCTURE; PUERTO-RICANS; UNITED-STATES; LUNG-FUNCTION; ADMIXTURE; CHILDREN; PHARMACOGENETICS;
D O I
10.1016/j.jaci.2010.08.002
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
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. (J Allergy Clin Immunol 2010;126:1131-8.)
引用
收藏
页码:1131 / 1138
页数:8
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