A large-scale, consortium-based genomewide association study of asthma.

TitleA large-scale, consortium-based genomewide association study of asthma.
Publication TypeJournal Article
Year of Publication2010
AuthorsMoffatt, MF, Gut, IG, Demenais, F, Strachan, DP, Bouzigon, E, Heath, S, von Mutius, E, Farrall, M, Lathrop, M, Cookson, WOCM
Corporate AuthorsGABRIEL Consortium
JournalN Engl J Med
Date Published2010 Sep 23
KeywordsAdolescent, Age of Onset, Asthma, Case-Control Studies, Child, Chromosomes, Human, Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, HLA-DR Antigens, Humans, Hypersensitivity, Immunoglobulin E, Logistic Models, Male, Occupational Diseases, Odds Ratio, Polymorphism, Single Nucleotide, Th2 Cells

BACKGROUND: Susceptibility to asthma is influenced by genes and environment; implicated genes may indicate pathways for therapeutic intervention. Genetic risk factors may be useful in identifying subtypes of asthma and determining whether intermediate phenotypes, such as elevation of the total serum IgE level, are causally linked to disease.

METHODS: We carried out a genomewide association study by genotyping 10,365 persons with physician-diagnosed asthma and 16,110 unaffected persons, all of whom were matched for ancestry. We used random-effects pooled analysis to test for association in the overall study population and in subgroups of subjects with childhood-onset asthma (defined as asthma developing before 16 years of age), later-onset asthma, severe asthma, and occupational asthma.

RESULTS: We observed associations of genomewide significance between asthma and the following single-nucleotide polymorphisms: rs3771166 on chromosome 2, implicating IL1RL1/IL18R1 (P=3×10(−9)); rs9273349 on chromosome 6, implicating HLA-DQ (P=7×10(−14)); rs1342326 on chromosome 9, flanking IL33 (P=9×10(−10)); rs744910 on chromosome 15 in SMAD3 (P=4×10(−9)); and rs2284033 on chromosome 22 in IL2RB (P=1.1×10(−8)). Association with the ORMDL3/GSDMB locus on chromosome 17q21 was specific to childhood-onset disease (rs2305480, P=6×10(−23)). Only HLA-DR showed a significant genomewide association with the total serum IgE concentration, and loci strongly associated with IgE levels were not associated with asthma.

CONCLUSIONS: Asthma is genetically heterogeneous. A few common alleles are associated with disease risk at all ages. Implicated genes suggest a role for communication of epithelial damage to the adaptive immune system and activation of airway inflammation. Variants at the ORMDL3/GSDMB locus are associated only with childhood-onset disease. Elevation of total serum IgE levels has a minor role in the development of asthma. (Funded by the European Commission and others.)

Alternate JournalN. Engl. J. Med.
PubMed ID20860503
PubMed Central IDPMC4260321
Grant List059168 / / Wellcome Trust / United Kingdom
068545/Z/02 / / Wellcome Trust / United Kingdom
076113 / / Wellcome Trust / United Kingdom
077959 / / Wellcome Trust / United Kingdom
084703 / / Wellcome Trust / United Kingdom
5P30 ES07048 / ES / NIEHS NIH HHS / United States
G0000934 / / Medical Research Council / United Kingdom
G0401540 / / Medical Research Council / United Kingdom
G0501942 / / Medical Research Council / United Kingdom
G0800649 / / Medical Research Council / United Kingdom
G0902125 / / Medical Research Council / United Kingdom
G9815508 / / Medical Research Council / United Kingdom
MC_QA137934 / / Medical Research Council / United Kingdom
R01 HL62633-01 / HL / NHLBI NIH HHS / United States
WT084703MA / / Wellcome Trust / United Kingdom
/ / Canadian Institutes of Health Research / Canada