Pharmacogenetics of asthma

被引:15
作者
Pascual, Rodolfo M. [1 ]
Bleecker, Eugene R. [1 ]
机构
[1] Wake Forest Univ Hlth Sci, Ctr Genom & Personalized Med Res, Winston Salem, NC 27157 USA
关键词
GLUCOCORTICOID-RECEPTOR GENE; IMPROVED LUNG-FUNCTION; BETA(2)-ADRENERGIC RECEPTOR; BETA-2-ADRENERGIC RECEPTOR; POLYMORPHISMS; SALMETEROL; GENOTYPE; AGONIST; MONTELUKAST; ASSOCIATION;
D O I
10.1016/j.coph.2010.05.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Current asthma treatments are effective for most but not all patients. Asthma is classified as a complex genetic disease with its pathogenesis and expression (severity) determined by the interaction of many genes and environmental factors. Asthma is characterized by its heterogeneity in terms of its clinical and inflammatory phenotypes and their responses to therapy. This disease heterogeneity likely has played a role in variable results from clinical trials that evaluate specific inhibitors of inflammatory mediators ('biologics') in asthma. Moreover, although existing treatments are effective and safe in most asthma patients they may be less effective or potentially harmful in others. In addition, if an individual with asthma is less responsive to standard therapies such as corticosteroids because of specific pharmacogenetic interactions then that patient with asthma will be classified as having more severe or difficult-to-treat asthma. Pharmacogenetic approaches hold the promise of matching individualized treatments to specific genotypes in a way that minimizes side effects while improving therapeutic outcomes.
引用
收藏
页码:226 / 235
页数:10
相关论文
共 48 条
[1]   Molecular mechanisms of corticosteroid resistance [J].
Adcock, Ian M. ;
Barnes, Peter J. .
CHEST, 2008, 134 (02) :394-401
[2]   Epigenetic regulation of airway inflammation [J].
Adcock, Ian M. ;
Tsaprouni, Loukia ;
Bhavsar, Pankaj ;
Ito, Kazuhiro .
CURRENT OPINION IN IMMUNOLOGY, 2007, 19 (06) :694-700
[3]   Glucocorticoid resistance in inflammatory diseases [J].
Barnes, Peter J. ;
Adcock, Ion M. .
LANCET, 2009, 373 (9678) :1905-1917
[4]   Effect of ADRB2 polymorphisms on response to longacting β2-agonist therapy:: a pharmacogenetic analysis of two randomised studies [J].
Bleecker, Eugene R. ;
Postma, Dirkje S. ;
Lawrance, Rachael M. ;
Meyers, Deborah A. ;
Ambrose, Helen J. ;
Goldman, Mitch .
LANCET, 2007, 370 (9605) :2118-2125
[5]   Salmeterol response is not affected by β2-adrenergic receptor genotype in subjects with persistent asthma [J].
Bleecker, Eugene R. ;
Yancey, Steven W. ;
Baitinger, Leslie A. ;
Edwards, Lisa D. ;
Klotsman, Michael ;
Anderson, Wayne H. ;
Dorinsky, Paul M. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 118 (04) :809-816
[6]  
Bleecker ER, 2010, AM J RESP CRIT CARE, V181, P676, DOI [10.1164/rccm.200809-1511OC, 10.1164/200809-1511OC]
[7]   Maternal intake of vitamin D during pregnancy and risk of recurrent wheeze in children at 3 y of age [J].
Camargo, Carlos A., Jr. ;
Rifas-Shiman, Sheryl L. ;
Litonjua, Augusto A. ;
Rich-Edwards, Janet W. ;
Weiss, Scott T. ;
Gold, Diane R. ;
Kleinman, Ken ;
Gillman, Matthew W. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2007, 85 (03) :788-795
[8]   SEREVENT NATIONWIDE SURVEILLANCE STUDY - COMPARISON OF SALMETEROL WITH SALBUTAMOL IN ASTHMATIC-PATIENTS WHO REQUIRE REGULAR BRONCHODILATOR TREATMENT [J].
CASTLE, W ;
FULLER, R ;
HALL, J ;
PALMER, J .
BRITISH MEDICAL JOURNAL, 1993, 306 (6884) :1034-1037
[9]  
CRANE J, 1989, LANCET, V1, P917
[10]   Comparison of regularly scheduled with as-needed use of albuterol in mild asthma [J].
Drazen, JM ;
Israel, E ;
Boushey, HA ;
Chinchilli, VM ;
Fahy, JV ;
Fish, JE ;
Lazarus, SC ;
Lemanske, RF ;
Martin, RJ ;
Peters, SP ;
Sorkness, C ;
Szefler, SJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (12) :841-847