Version 2 2020-05-15, 13:36Version 2 2020-05-15, 13:36
Version 1 2020-05-15, 13:36Version 1 2020-05-15, 13:36
conference contribution
posted on 2020-05-15, 13:36authored byN Shrine, MS Artigas, MA Portelli, MD Tobin, IP Hall, CE Brightling, LV Wain, I Sayers
<p>The genetic architecture of asthma to date has been described by the discovery of around 20 loci from genome-wide association studies (GWAS), primarily with cases covering mild-to-moderate asthma. We hypothesised that moderate-to-severe asthma, which is currently difficult to treat, may have a specific genetic architecture, however there have not been large GWAS of moderate-to-severe asthma.</p><p>Accordingly, we selected 5,135 European ancestry moderate-severe asthma cases (British Thoracic Society criteria 3 or above) and 25,675 controls free from lung disease, allergic rhinitis and atopic dermatitis, from UK Biobank and the Genetics of Asthma Severity & Phenotypes (GASP) cohort (cases only). We tested 33,771,858 SNPs and indels genome-wide (imputation against combined UK10K and 1000 genomes phase 3 panels) for association with moderate-severe asthma.</p><p>We identified 23 independent signals associated with moderate-to-severe asthma (<i>P</i> < 5×10<sup>-8</sup>), including novels signals in or near <i>GATA3, RIC1, ZNF652, RPAP3 and MUC5AC,</i> highlighting regions that harbour variants that effect gene expression or genes that play a role in respiratory disease and immune response. Previously described asthma loci where replicated including signals in or near <i>D2HGDH, CD247, HLA-DQB1, HLA-DQA1, TSLP/WDR36, IL1RL1/IL18R1, CLEC16A, GATA3, IL33, SMAD3, SLC22A5/IL13, C11orf30, ZBTB10, IKZF3-ORMDL3 and IKZF4.</i></p><p>This largest GWAS of moderate-severe asthma to date and highlights novel loci that may provide new biological insights relevant to treatment of severe asthma.</p>
History
Citation
GENETIC EPIDEMIOLOGY, 2017, 41 (7), pp. 694-694 (1)
Author affiliation
/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Infection, Immunity and Inflammation
Source
Annual Meeting of the International-Genetic-Epidemiology-Society (IGES), Queens Coll, Cambridge, ENGLAND