Exome array analysis identifies a common Variant in IL27 associated with chronic obstructive pulmonary disease

Brian D. Hobbs, Margaret M. Parker, Han Chen, Taotao Lao, Megan Hardin, Dandi Qiao, Iwona Hawrylkiewicz, Pawel Sliwinski, Jae Joon Yim, Woo Jin Kim, Deog Kyeom Kim, Peter J. Castaldi, Craig P. Hersh, Jarrett Morrow, Bartolome R. Celli, Victor M. Pinto-Plata, Gerald J. Criner, Nathaniel Marchetti, Raphael Bueno, Alvar AgustiBarry J. Make, James D. Crapo, Peter M. Calverley, Claudio F. Donner, David A. Lomas, Emiel F.M. Wouters, Jorgen Vestbo, Peter D. Pare, Robert D. Levy, Stephen I. Rennard, Xiaobo Zhou, Nan M. Laird, Xihong Lin, Terri H. Beaty, Edwin K. Silverman, Michael H. Cho

Research output: Contribution to journalArticlepeer-review

42 Scopus citations


Rationale: Chronic obstructive pulmonary disease (COPD) susceptibility is in part related to genetic variants. Most genetic studies have been focused on genome-wide common variants without a specific focus on coding variants, but common and rare coding variants may also affect COPD susceptibility. Objectives: To identify coding variants associated with COPD. Methods: Wetested nonsynonymous, splice, and stop variants derived from the Illumina HumanExome array for association with COPD in five study populations enriched for COPD.Weevaluated single variants with aminor allele frequency greater than 0.5% using logistic regression. Resultswere combined using a fixed effectsmeta-Analysis.We replicated novel single-variant associations in three additional COPD cohorts. Measurements and Main Results: We included 6,004 control subjects and 6,161 COPD cases across five cohorts for analysis. Our top result was rs16969968 (P = 1.7310214) in CHRNA5, a locus previously associated with COPD susceptibility and nicotine dependence. Additional top results were found in AGER,MMP3, and SERPINA1. A nonsynonymous variant, rs181206, in IL27 (P = 4.73 1026) was just below the level of exome-wide significance but attained exome-wide significance (P = 5.731028) when combined with results from other cohorts. Gene expression datasets revealed an association of rs181206 and the surrounding locus with expression of multiple genes; several were differentially expressed in COPD lung tissue, including TUFM. Conclusions: In an exome array analysis of COPD, we identified nonsynonymous variants at previously described loci and a novel exome-wide significant variant in IL27. This variant is at a locus previously described in genome-wide associations with diabetes, inflammatory bowel disease, and obesity and appears to affect genespotentially related to COPD pathogenesis.

Original languageEnglish (US)
Pages (from-to)48-57
Number of pages10
JournalAmerican Journal of Respiratory and Critical Care Medicine
Issue number1
StatePublished - Jul 1 2016
Externally publishedYes


  • Chronic Obstructive Pulmonary Disease
  • Exome
  • Genetics
  • IL-27

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine


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