Chromosome 17: association of a large inversion polymorphism with corticosteroid response in asthma

被引:33
作者
Tantisira, Kelan G. [1 ,2 ,3 ,4 ]
Lazarus, Ross [1 ,3 ,4 ]
Litonjua, Augusto A. [1 ,2 ,3 ,4 ]
Klanderman, Barbara [1 ,3 ,4 ]
Weiss, Scott T. [1 ,3 ,4 ]
机构
[1] Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Div Pulm, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Ctr Genom Med, Dept Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
关键词
asthma; corticosteroid; CRHR1; inversion; MAPT; pharmacogenetics; tau haplotype;
D O I
10.1097/FPC.0b013e3282fe6ebf
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A 900-kb inversion exists within a large region of conserved linkage disequilibrium (LD) on chromosome 17. CRHR1 is located within the inversion region and associated with inhaled corticosteroid response in asthma. We hypothesized that CRHR1 variants are in LD with the inversion, supporting a potential role for natural selection in the genetic response to corticosteroids. We genotyped six single nucleotide polymorphisms (SNPs) spanning chromosome 17: 40,410,565-42,372,240, including four SNPs defining inversion status. Similar allele frequencies and strong LD were noted between the inversion and a CRHR1 SNP previously associated with lung function response to inhaled corticosteroids. Each inversion-defining SNP was strongly associated with inhaled corticosteroid response in adult asthma (P values 0.002-0.005). The CRHR1 response to inhaled corticosteroids may thus be explained by natural selection resulting from inversion status or by long-range LD with another gene. Additional pharmacogenetic investigations into regions of chromosomal diversity, including copy number variation and inversions, are warranted.
引用
收藏
页码:733 / 737
页数:5
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