4.8 Article

Genomewide Association between GLCCI1 and Response to Glucocorticoid Therapy in Asthma

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 365, Issue 13, Pages 1173-1183

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa0911353

Keywords

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Funding

  1. National Institutes of Health (NIH) [U01 HL65899, P01 HL083069, R01 HG003646, R01 HL092197, K23 HG3983]
  2. NIH Pharmacogenomics Research Network
  3. Ministry of Education, Culture, Sports, Science, and Technology in Japan
  4. National Heart, Lung, and Blood Institute (NHLBI) [U01 HL65899, P01 HL083069, U01 HL075419, R01 HL086601, T32 HL07427]
  5. NHLBI [U01 HL51510, U01 HL51834, U01 HL51831, U01 HL51845, U01 HL51843, M01 RR00079, M01 RR03186, N02-HL-6-4278]
  6. GlaxoSmithKline
  7. Grants-in-Aid for Scientific Research [23791204] Funding Source: KAKEN

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BACKGROUND The response to treatment for asthma is characterized by wide interindividual variability, with a significant number of patients who have no response. We hypothesized that a genomewide association study would reveal novel pharmacogenetic determinants of the response to inhaled glucocorticoids. METHODS We analyzed a small number of statistically powerful variants selected on the basis of a family-based screening algorithm from among 534,290 single-nucleotide polymorphisms (SNPs) to determine changes in lung function in response to inhaled glucocorticoids. A significant, replicated association was found, and we characterized its functional effects. RESULTS We identified a significant pharmacogenetic association at SNP rs37972, replicated in four independent populations totaling 935 persons (P = 0.0007), which maps to the glucocorticoid-induced transcript 1 gene (GLCCI1) and is in complete linkage disequilibrium (i.e., perfectly correlated) with rs37973. Both rs37972 and rs37973 are associated with decrements in GLCCI1 expression. In isolated cell systems, the rs37973 variant is associated with significantly decreased luciferase reporter activity. Pooled data from treatment trials indicate reduced lung function in response to inhaled glucocorticoids in subjects with the variant allele (P = 0.0007 for pooled data). Overall, the mean (+/- SE) increase in forced expiratory volume in 1 second in the treated subjects who were homozygous for the mutant rs37973 allele was only about one third of that seen in similarly treated subjects who were homozygous for the wild-type allele (3.2 +/- 1.6% vs. 9.4 +/- 1.1%), and their risk of a poor response was significantly higher (odds ratio, 2.36; 95% confidence interval, 1.27 to 4.41), with genotype accounting for about 6.6% of overall inhaled glucocorticoid response variability. CONCLUSIONS A functional GLCCI1 variant is associated with substantial decrements in the response to inhaled glucocorticoids in patients with asthma. (Funded by the National Institutes of Health and others; ClinicalTrials.gov number, NCT00000575.)

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