Pharmacogenetic differences in response to albuterol between Puerto Ricans and Mexicans with asthma

被引:181
作者
Choudhry, S
Ung, N
Avila, PC
Ziv, E
Nazario, S
Casal, J
Torres, A
Gorman, JD
Salari, K
Rodriguez-Santana, JR
Toscano, M
Sylvia, JS
Alioto, M
Castro, RA
Salazar, M
Gomez, I
Fagan, JK
Salas, J
Clark, S
Lilly, C
Matallana, H
Selman, M
Chapela, R
Sheppard, D
Weiss, ST
Ford, JG
Boushey, HA
Drazen, JM
Rodriguez-Cintron, W
Silverman, EK
Burchard, EG [1 ]
机构
[1] Univ Calif San Francisco, San Francisco, CA 94143 USA
[2] San Francisco Gen Hosp, Lung Biol Ctr, San Francisco, CA 94110 USA
[3] Univ Puerto Rico, Sch Med, San Juan Vet Adm Med Ctr, San Juan, PR 00936 USA
[4] Pediat Pulm Program San Juan, San Juan, PR USA
[5] Brigham & Womens Hosp, Boston, MA 02115 USA
[6] Harlem Hosp Med Ctr, Harlem Lung Ctr, New York, NY USA
[7] Columbia Univ, New York, NY USA
[8] Inst Nacl Enfermedades Resp, Mexico City, DF, Mexico
关键词
asthma genetics; beta(2)-adrenergic receptor gene; Latinos; pharmacogenetic;
D O I
10.1164/rccm.200409-1286OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: In the United States, Puerto Ricans and Mexicans have the highest and lowest asthma prevalence, morbidity, and mortality, respectively. Ethnic-specific differences in the response to drug treatment may contribute to differences in disease outcomes. Genetic variants at the beta(2)-adrenergic receptor (beta(2)AR) may modify asthma severity and albuterol responsiveness. We tested the association of beta(2)AR genotypes with asthma severity and bronchodilator response to albuterol in Puerto Ricans and Mexicans with asthma. Methods: We used both family-based and cross-sectional tests of association with 8 beta(2)AR single nucleotide polymorphisms in 684 Puerto Rican and Mexican families. Regression analyses were used to determine the interaction between genotype, asthma severity, and bronchodilator drug responsiveness. Results: Among Puerto Ricans with asthma, the arginine (Arg) 16 allele was associated with greater bronchodilator response using both family-based and cross-sectional tests (p = 0.00001-0.01). We found a strong interaction of baseline FEV1 with the Arg16Glycine (Gly) polymorphism in predicting bronchodilator response. Among Puerto Ricans with asthma with baseline FEV1 < 80% of predicted, but not in those with FEV1 > 80%, there was a very strong association between the Arg16 genotype and greater bronchodilator responsiveness. No association was observed between Arg16Gly genotypes and drug responsiveness among Mexicans with asthma. Conclusions: Ethnic-specific pharmacogenetic differences exist between Arg16Gly genotypes, asthma severity, and bronchodilator response in Puerto Ricans and Mexicans with asthma. These findings underscore the need for additional research on racial/ethnic differences in asthma morbidity and drug responsiveness.
引用
收藏
页码:563 / 570
页数:8
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