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. 2010 Sep 23;363(13):1211-1221.
doi: 10.1056/NEJMoa0906312.

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

Miriam F Moffatt #  1 , Ivo G Gut #  1 , Florence Demenais #  1 , David P Strachan  1 , Emmanuelle Bouzigon  1 , Simon Heath  1 , Erika von Mutius  1 , Martin Farrall  1 , Mark Lathrop  1 , William O C M Cookson  1 ; GABRIEL Consortium
Collaborators, Affiliations

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

Miriam F Moffatt et al. N Engl J Med. .

Abstract

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.)

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Figures

Figure 1
Figure 1. Manhattan Plot of Study Results
The results of genomewide association testing are shown for all subjects. The horizontal line indicates the stringent genomewide significance threshold (P≤7.2×10−8). Gene names are provided for loci at this level of significance and are also provided for loci at the less stringent threshold of P≤5×10−7 used by the Wellcome Trust Case-Control Consortium.
Figure 2
Figure 2. Forest Plots of Odds Ratios for Markers with Genomewide Association with Asthma According to Study Subgroup
The odds ratios and 95% confidence intervals for six loci show independent effects on asthma risk. For the calculation of these odds ratios, alternate alleles were designated as risk alleles. In order to include the subjects from our original genome screen, rs3771166 was imputed for subjects from the MRCA-UKC and MAGICS panels. Sample size is indicated by the size of the square at the center of each confidence interval. For a list of the complete names of each study or study group, see the Supplementary Appendix.
Figure 2
Figure 2. Forest Plots of Odds Ratios for Markers with Genomewide Association with Asthma According to Study Subgroup
The odds ratios and 95% confidence intervals for six loci show independent effects on asthma risk. For the calculation of these odds ratios, alternate alleles were designated as risk alleles. In order to include the subjects from our original genome screen, rs3771166 was imputed for subjects from the MRCA-UKC and MAGICS panels. Sample size is indicated by the size of the square at the center of each confidence interval. For a list of the complete names of each study or study group, see the Supplementary Appendix.
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