The pharmacogenetics and pharmacogenomics of asthma therapy

被引:44
作者
Tse, S. M. [1 ]
Tantisira, K.
Weiss, S. T.
机构
[1] Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
asthma; pharmacogenetics; treatment response; LEUKOTRIENE RECEPTOR ANTAGONIST; ALOX5 PROMOTER GENOTYPE; IMPROVED LUNG-FUNCTION; BETA(2)-ADRENERGIC RECEPTOR; CLINICAL-RESPONSE; BETA-2-ADRENERGIC RECEPTOR; INHALED CORTICOSTEROIDS; TRANSCRIPTION FACTOR; CHILDHOOD ASTHMA; BETA(2) AGONIST;
D O I
10.1038/tpj.2011.46
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Despite the availability of several classes of asthma medications and their overall effectiveness, a significant portion of patients fail to respond to these therapeutic agents. Evidence suggests that genetic factors may partly mediate the heterogeneity in asthma treatment response. This review discusses important findings in asthma pharmacogenetic and pharmacogenomic studies conducted to date, examines limitations of these studies and, finally, proposes future research directions in this field. The focus will be on the three major classes of asthma medications: beta-adrenergic receptor agonists, inhaled corticosteroids and leukotriene modifiers. Although many studies are limited by small sample sizes and replication of the findings is needed, several candidate genes have been identified. High-throughput technologies are also allowing for large-scale genetic investigations. Thus, the future is promising for a personalized treatment of asthma, which will improve therapeutic outcomes, minimize side effects and lead to a more cost-effective care. The Pharmacogenomics Journal (2011) 11, 383-392; doi:10.1038/tpj.2011.46; published online 11 October 2011
引用
收藏
页码:383 / 392
页数:10
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