학술논문

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
Document Type
article
Author
Dana B HancockMaría Soler ArtigasSina A GharibAmanda HenryAni ManichaikulAdaikalavan RamasamyDaan W LothMedea ImbodenBeate KochWendy L McArdleAlbert V SmithJoanna SmolonskaAkshay SoodWenbo TangJemma B WilkGuangju ZhaiJing Hua ZhaoHugues AschardKristin M BurkartIvan CurjuricMark EijgelsheimPaul ElliottXiangjun GuTamara B HarrisChrister JansonGeorg HomuthPirro G HysiJason Z LiuLaura R LoehrKurt LohmanRuth J F LoosAlisa K ManningKristin D MarcianteMa'en ObeidatDirkje S PostmaMelinda C AldrichGuy G BrusselleTing-hsu ChenGudny EiriksdottirNora FranceschiniJoachim HeinrichJerome I RotterCisca WijmengaO Dale WilliamsAmy R BentleyAlbert HofmanCathy C LaurieThomas LumleyAlanna C MorrisonBonnie R JoubertFernando RivadeneiraDavid J CouperStephen B KritchevskyYongmei LiuMatthias WjstLouise V WainJudith M VonkAndré G UitterlindenThierry RochatStephen S RichBruce M PsatyGeorge T O'ConnorKari E NorthDaniel B MirelBernd MeibohmLenore J LaunerKay-Tee KhawAnna-Liisa HartikainenChristopher J HammondSven GläserJonathan MarchiniPeter KraftNicholas J WarehamHenry VölzkeBruno H C StrickerTimothy D SpectorNicole M Probst-HenschDeborah JarvisMarjo-Riitta JarvelinSusan R HeckbertVilmundur GudnasonH Marike BoezenR Graham BarrPatricia A CassanoDavid P StrachanMyriam FornageIan P HallJosée DupuisMartin D TobinStephanie J London
Source
PLoS Genetics, Vol 8, Iss 12, p e1003098 (2012)
Subject
Genetics
QH426-470
Language
English
ISSN
1553-7390
1553-7404
Abstract
Genome-wide association studies have identified numerous genetic loci for spirometic measures of pulmonary function, forced expiratory volume in one second (FEV(1)), and its ratio to forced vital capacity (FEV(1)/FVC). Given that cigarette smoking adversely affects pulmonary function, we conducted genome-wide joint meta-analyses (JMA) of single nucleotide polymorphism (SNP) and SNP-by-smoking (ever-smoking or pack-years) associations on FEV(1) and FEV(1)/FVC across 19 studies (total N = 50,047). We identified three novel loci not previously associated with pulmonary function. SNPs in or near DNER (smallest P(JMA = )5.00×10(-11)), HLA-DQB1 and HLA-DQA2 (smallest P(JMA = )4.35×10(-9)), and KCNJ2 and SOX9 (smallest P(JMA = )1.28×10(-8)) were associated with FEV(1)/FVC or FEV(1) in meta-analysis models including SNP main effects, smoking main effects, and SNP-by-smoking (ever-smoking or pack-years) interaction. The HLA region has been widely implicated for autoimmune and lung phenotypes, unlike the other novel loci, which have not been widely implicated. We evaluated DNER, KCNJ2, and SOX9 and found them to be expressed in human lung tissue. DNER and SOX9 further showed evidence of differential expression in human airway epithelium in smokers compared to non-smokers. Our findings demonstrated that joint testing of SNP and SNP-by-environment interaction identified novel loci associated with complex traits that are missed when considering only the genetic main effects.