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Title: Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12
Authors: Jackson, Victoria E.
Ntalla, Ioanna
Brightling, Chris E.
Sayers, I.
Morris, R.
Whincup, P.
Casas, J-P.
Amuzu, A.
Choi, M.
Dale, C.
Kumari, M.
Engmann, J.
Kalsheker, N.
Chappell, S.
Guetta-Baranes, T.
McKeever, T. M.
Tavendale, C. N. A.
Palmer, R.
Holloway, J. W.
Sayer, A. A.
Dennison, E. M.
Cooper, C.
Bafadhel, M.
Barker, Bethan
Bolton, C. E.
John, M. E.
Parker, S. G.
Moffat, M. F.
Wardlaw, A. J.
Connolly, M. J.
Porteous, D. J.
Smith, B. H.
Padmanabhan, S.
Hocking, L.
Stirrups, K. E.
Deloukas, P.
Strachan, D. P.
Hall, I. P.
Tobin, Martin D.
Wain, Louise V.
Taylor, Louise V.
First Published: 25-Feb-2016
Publisher: BMJ Publishing Group with British Thoracic Society (BTS)
Citation: Thorax, 2016;71:501-509
Abstract: Background Several regions of the genome have shown to be associated with COPD in genome-wide association studies of common variants. Objective To determine rare and potentially functional single nucleotide polymorphisms (SNPs) associated with the risk of COPD and severity of airflow limitation. Methods 3226 current or former smokers of European ancestry with lung function measures indicative of Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2 COPD or worse were genotyped using an exome array. An analysis of risk of COPD was carried out using ever smoking controls (n=4784). Associations with %predicted FEV1 were tested in cases. We followed-up signals of interest (p<10−5) in independent samples from a subset of the UK Biobank population and also undertook a more powerful discovery study by meta-analysing the exome array data and UK Biobank data for variants represented on both arrays. Results Among the associated variants were two in regions previously unreported for COPD; a low frequency non-synonymous SNP in MOCS3 (rs7269297, pdiscovery=3.08×10−6, preplication=0.019) and a rare SNP in IFIT3, which emerged in the meta-analysis (rs140549288, pmeta=8.56×10−6). In the meta-analysis of % predicted FEV1 in cases, the strongest association was shown for a splice variant in a previously unreported region, SERPINA12 (rs140198372, pmeta=5.72×10−6). We also confirmed previously reported associations with COPD risk at MMP12, HHIP, GPR126 and CHRNA5. No associations in novel regions reached a stringent exome-wide significance threshold (p<3.7×10−7). Conclusions This study identified several associations with the risk of COPD and severity of airflow limitation, including novel regions MOCS3, IFIT3 and SERPINA12, which warrant further study.
DOI Link: 10.1136/thoraxjnl-2015-207876
ISSN: 0040-6376
eISSN: 1468-3296
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © 2016, the authors. Licensee: BMJ. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See:
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation
Published Articles, Dept. of Health Sciences

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