Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma

被引:21
作者
Dahlin, Amber [1 ,2 ]
Litonjua, Augusto [1 ,2 ,3 ]
Lima, John J. [4 ]
Tamari, Mayumi [5 ]
Kubo, Michiaki [5 ]
Irvin, Charles G. [6 ]
Peters, Stephen P. [7 ]
Tantisira, Kelan G. [1 ,2 ,3 ]
机构
[1] Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Brigham & Womens Hosp, Div Pulm & Crit Care Med, Boston, MA 02115 USA
[4] Nemours Childrens Clin, Jacksonville, FL USA
[5] RIKEN, Ctr Integrat Med Sci, Yokohama, Kanagawa, Japan
[6] Univ Vermont, Burlington, VT USA
[7] Wake Forest Sch Med, Winston Salem, NC USA
基金
美国国家卫生研究院;
关键词
LEUKOTRIENE RECEPTOR ANTAGONISTS; PERSISTENT ASTHMA; INHALED CORTICOSTEROIDS; CHILDHOOD ASTHMA; KOREAN CHILDREN; TRIAL; POLYMORPHISMS; PATHWAY; RESPONSIVENESS; HETEROGENEITY;
D O I
10.1371/journal.pone.0129385
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Genome-wide association study (GWAS) is a powerful tool to identify novel pharmacogenetic single nucleotide polymorphisms (SNPs). Leukotriene receptor antagonists (LTRAs) are a major class of asthma medications, and genetic factors contribute to variable responses to these drugs. We used GWAS to identify novel SNPs associated with the response to the LTRA, montelukast, in asthmatics. Methods Using genome-wide genotype and phenotypic data available from American Lung Association - Asthma Clinical Research Center (ALA-ACRC) cohorts, we evaluated 8-week change in FEV1 related to montelukast administration in a discovery population of 133 asthmatics. The top 200 SNPs from the discovery GWAS were then tested in 184 additional samples from two independent cohorts. Results Twenty-eight SNP associations from the discovery GWAS were replicated. Of these, rs6475448 achieved genome-wide significance (combined P = 1.97 x 10(-09)), and subjects from all four studies who were homozygous for rs6475448 showed increased Delta FEV1 from baseline in response to montelukast. Conclusions Through GWAS, we identified a novel pharmacogenomic locus related to improved montelukast response in asthmatics.
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页数:9
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共 41 条
[21]  
Liptak, 1958, MAGYAR TUD AKAD MAT, V3, P171
[22]   Activation of platelets in bronchial asthma [J].
Moritani, C ;
Ishioka, S ;
Haruta, Y ;
Kambe, M ;
Yamakido, M .
CHEST, 1998, 113 (02) :452-458
[23]   Pharmacogenetics of asthma controller treatment [J].
Mougey, E. B. ;
Chen, C. ;
Tantisira, K. G. ;
Blake, K. V. ;
Peters, S. P. ;
Wise, R. A. ;
Weiss, S. T. ;
Lima, J. J. .
PHARMACOGENOMICS JOURNAL, 2013, 13 (03) :242-250
[24]   Absorption of montelukast is transporter mediated: a common variant of OATP2B1 is associated with reduced plasma concentrations and poor response [J].
Mougey, Edward B. ;
Feng, Hua ;
Castro, Mario ;
Irvin, Charles G. ;
Lima, John J. .
PHARMACOGENETICS AND GENOMICS, 2009, 19 (02) :129-138
[25]   Efficacy of zileuton controlled-release tablets administered twice daily in the treatment of moderate persistent asthma: a 3-month randomized controlled study [J].
Nelson, Harold ;
Kemp, James ;
Berger, William ;
Corren, Jonathon ;
Casale, Thomas ;
Dube, Louise ;
Walton-Bowen, Karen ;
LaVallee, Nicole ;
Stepanians, Miganush .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2007, 99 (02) :178-184
[26]   Update on Recent Advances in the Management of Aspirin Exacerbated Respiratory Disease [J].
Palikhe, Nami Shrestha ;
Kim, Joo-Hee ;
Park, Hae-Sim .
YONSEI MEDICAL JOURNAL, 2009, 50 (06) :744-750
[27]  
Park HW, 2014, J ALLERGY CLIN IMMUN
[28]  
Peters SP, 2007, NEW ENGL J MED, V356, P2027
[29]   MLLT3 regulates early human erythroid and megakaryocytic cell fate [J].
Pina, Cristina ;
May, Gillian ;
Soneji, Shamit ;
Hong, Dengli ;
Enver, Tariq .
CELL STEM CELL, 2008, 2 (03) :264-273
[30]   PLINK: A tool set for whole-genome association and population-based linkage analyses [J].
Purcell, Shaun ;
Neale, Benjamin ;
Todd-Brown, Kathe ;
Thomas, Lori ;
Ferreira, Manuel A. R. ;
Bender, David ;
Maller, Julian ;
Sklar, Pamela ;
de Bakker, Paul I. W. ;
Daly, Mark J. ;
Sham, Pak C. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (03) :559-575