4.2 Article

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

期刊

PHARMACOGENETICS AND GENOMICS
卷 18, 期 8, 页码 733-737

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/FPC.0b013e3282fe6ebf

关键词

asthma; corticosteroid; CRHR1; inversion; MAPT; pharmacogenetics; tau haplotype

资金

  1. NCRR NIH HHS [M01 RR003186, M01 RR 00079, M01 RR 03186, M01 RR000079] Funding Source: Medline
  2. NHGRI NIH HHS [K23 HG003983, K23 HG003983-03, K23 HG 3983] Funding Source: Medline
  3. NHLBI NIH HHS [N01HR16045, U10 HL051843, U10 HL051834, HR 16052, N01 HR 16044, N01HR16048, HR 16046, U01 HL065899, P01 HL 083069, HR 16049, U01 HL 51831, HR 16051, U01 HL 65899, U01 HL 51845, N01HR16047, N01HR16050, P01 HL083069, U01 HL 51834, N01HR16044, N01HR16051, U10 HL051845-07, HR 16045, U01 HL 51843, U01 HL065899-01, N01HR16052, U01 HL 51510, HR 16047, U10 HL051831, N01HR16049, HR 16050, HR 16048, P01 HL083069-01A1, U10 HL051845, N01HR16046, N01 HR 16049] Funding Source: Medline

向作者/读者索取更多资源

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.

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