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1. Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function

Author

Yang, T. (Tianzhong), Jackson, V. E. (Victoria E.), Smith, A. V. (Albert V.), Chen, H. (Han), Bartz, T. M. (Traci M.), Sitlani, C. M. (Colleen M.), Psaty, B. M. (Bruce M.), Gharib, S. A. (Sina A.), O’Connor, G. T. (George T.), Dupuis, J. (Josée), Xu, J. (Jiayi), Lohman, K. (Kurt), Liu, Y. (Yongmei), Kritchevsky, S. B. (Stephen B.), Cassano, P. A. (Patricia A.), Flexeder, C. (Claudia), Gieger, C. (Christian), Karrasch, S. (Stefan), Peters, A. (Annette), Schulz, H. (Holger), Harris, S. E. (Sarah E.), Starr, J. M. (John M.), Deary, I. J. (Ian J.), Manichaikul, A. (Ani), Oelsner, E. C. (Elizabeth C.), Barr, R. G. (R. G.), Taylor, K. D. (Kent D.), Rich, S. S. (Stephen S.), Bonten, T. N. (Tobias N.), Mook-Kanamori, D. O. (Dennis O.), Noordam, R. (Raymond), Li-Gao, R. (Ruifang), Jarvelin, M.-R. (Marjo-Riitta), Wielscher, M. (Matthias), Terzikhan, N. (Natalie), Lahousse, L. (Lies), Brusselle, G. (Guy), Weiss, S. (Stefan), Ewert, R. (Ralf), Gläser, S. (Sven), Homuth, G. (Georg), Shrine, N. (Nick), Hall, I. P. (Ian P.), Tobin, M. (Martin), London, S. J. (Stephanie J.), Wei, P. (Peng), Morrison, A. C. (Alanna C.), Yang, T. (Tianzhong), Jackson, V. E. (Victoria E.), Smith, A. V. (Albert V.), Chen, H. (Han), Bartz, T. M. (Traci M.), Sitlani, C. M. (Colleen M.), Psaty, B. M. (Bruce M.), Gharib, S. A. (Sina A.), O’Connor, G. T. (George T.), Dupuis, J. (Josée), Xu, J. (Jiayi), Lohman, K. (Kurt), Liu, Y. (Yongmei), Kritchevsky, S. B. (Stephen B.), Cassano, P. A. (Patricia A.), Flexeder, C. (Claudia), Gieger, C. (Christian), Karrasch, S. (Stefan), Peters, A. (Annette), Schulz, H. (Holger), Harris, S. E. (Sarah E.), Starr, J. M. (John M.), Deary, I. J. (Ian J.), Manichaikul, A. (Ani), Oelsner, E. C. (Elizabeth C.), Barr, R. G. (R. G.), Taylor, K. D. (Kent D.), Rich, S. S. (Stephen S.), Bonten, T. N. (Tobias N.), Mook-Kanamori, D. O. (Dennis O.), Noordam, R. (Raymond), Li-Gao, R. (Ruifang), Jarvelin, M.-R. (Marjo-Riitta), Wielscher, M. (Matthias), Terzikhan, N. (Natalie), Lahousse, L. (Lies), Brusselle, G. (Guy), Weiss, S. (Stefan), Ewert, R. (Ralf), Gläser, S. (Sven), Homuth, G. (Georg), Shrine, N. (Nick), Hall, I. P. (Ian P.), Tobin, M. (Martin), London, S. J. (Stephanie J.), Wei, P. (Peng), and Morrison, A. C. (Alanna C.)

Abstract

Genome-wide association studies have identified numerous common genetic variants associated with spirometric measures of pulmonary function, including forced expiratory volume in one second (FEV₁), forced vital capacity, and their ratio. However, variants with lower minor allele frequencies are less explored. We conducted a large-scale gene-smoking interaction meta-analysis on exonic rare and low-frequency variants involving 44,429 individuals of European ancestry in the discovery stage and sought replication in the UK BiLEVE study with 45,133 European ancestry samples and UK Biobank study with 59,478 samples. We leveraged data on cigarette smoking, the major environmental risk factor for reduced lung function, by testing gene-by-smoking interaction effects only and simultaneously testing the genetic main effects and interaction effects. The most statistically significant signal that replicated was a previously reported low-frequency signal in GPR126, distinct from common variant associations in this gene. Although only nominal replication was obtained for a top rare variant signal rs142935352 in one of the two studies, interaction and joint tests for current smoking and PDE3B were significantly associated with FEV₁. This study investigates the utility of assessing gene-by-smoking interactions and underscores their effects on potential pulmonary function.

Published
2021

2. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

Author

Shrine, N. (Nick), Guyatt, A. L. (Anna L.), Erzurumluoglu, A. M. (A. Mesut), Jackson, V. E. (Victoria E.), Hobbs, B. D. (Brian D.), Melbourne, C. A. (Carl A.), Batini, C. (Chiara), Fawcett, K. A. (Katherine A.), Song, K. (Kijoung), Sakornsakolpat, P. (Phuwanat), Li, X. (Xingnan), Boxall, R. (Ruth), Reeve, N. F. (Nicola F.), Obeidat, M. (Ma'en), Zhao, J. H. (Jing Hua), Wielscher, M. (Matthias), Weiss, S. (Stefan), Kentistou, K. A. (Katherine A.), Cook, J. P. (James P.), Sun, B. B. (Benjamin B.), Zhou, J. (Jian), Hui, J. (Jennie), Karrasch, S. (Stefan), Imboden, M. (Medea), Harris, S. E. (Sarah E.), Marten, J. (Jonathan), Enroth, S. (Stefan), Kerr, S. M. (Shona M.), Surakka, I. (Ida), Vitart, V. (Veronique), Lehtimäki, T. (Terho), Allen, R. J. (Richard J.), Bakke, P. S. (Per S.), Beaty, T. H. (Terri H.), Bleecker, E. R. (Eugene R.), Bosse, Y. (Yohan), Brandsma, C.-A. (Corry-Anke), Chen, Z. (Zhengming), Crapo, J. D. (James D.), Danesh, J. (John), DeMeo, D. L. (Dawn L.), Dudbridge, F. (Frank), Ewert, R. (Ralf), Gieger, C. (Christian), Gulsvik, A. (Amund), Hansell, A. L. (Anna L.), Hao, K. (Ke), Hoffman, J. D. (Joshua D.), Hokanson, J. E. (John E.), Homuth, G. (Georg), Joshi, P. K. (Peter K.), Joubert, P. (Philippe), Langenberg, C. (Claudia), Li, X. (Xuan), Li, L. (Liming), Lin, K. (Kuang), Lind, L. (Lars), Locantore, N. (Nicholas), Luan, J. (Jian'an), Mahajan, A. (Anubha), Maranville, J. C. (Joseph C.), Murray, A. (Alison), Nickle, D. C. (David C.), Packer, R. (Richard), Parker, M. M. (Margaret M.), Paynton, M. L. (Megan L.), Porteous, D. J. (David J.), Prokopenko, D. (Dmitry), Qiao, D. (Dandi), Rawal, R. (Rajesh), Runz, H. (Heiko), Sayers, I. (Ian), Sin, D. D. (Don D.), Smith, B. H. (Blair H.), Artigas, M. S. (Maria Soler), Sparrow, D. (David), Tal-Singer, R. (Ruth), Timmers, P. R. (Paul R. H. J.), Van den Berge, M. (Maarten), Whittaker, J. C. (John C.), Woodruff, P. G. (Prescott G.), Verges-Armstrong, L. M. (Laura M.), Troyanskaya, O. G. (Olga G.), Raitakari, O. T. (Olli T.), Kähönen, M. (Mika), Polasek, O. (Ozren), Gyllensten, U. (Ulf), Rudan, I. (Igor), Deary, I. J. (Ian J.), Probst-Hensch, N. M. (Nicole M.), Schulz, H. (Holger), James, A. L. (Alan L.), Wilson, J. F. (James F.), Stubbe, B. (Beate), Zeggini, E. (Eleftheria), Järvelin, M.-R. (Marjo-Riitta), Wareham, N. (Nick), Silverman, E. K. (Edwin K.), Hayward, C. (Caroline), Morris, A. P. (Andrew P.), Butterworth, A. S. (Adam S.), Scott, R. A. (Robert A.), Walters, R. G. (Robin G.), Meyers, D. A. (Deborah A.), Cho, M. H. (Michael H.), Strachan, D. P. (David P.), Hall, I. P. (Ian P.), Tobin, M. D. (Martin D.), Wain, L. V. (Louise, V), Shrine, N. (Nick), Guyatt, A. L. (Anna L.), Erzurumluoglu, A. M. (A. Mesut), Jackson, V. E. (Victoria E.), Hobbs, B. D. (Brian D.), Melbourne, C. A. (Carl A.), Batini, C. (Chiara), Fawcett, K. A. (Katherine A.), Song, K. (Kijoung), Sakornsakolpat, P. (Phuwanat), Li, X. (Xingnan), Boxall, R. (Ruth), Reeve, N. F. (Nicola F.), Obeidat, M. (Ma'en), Zhao, J. H. (Jing Hua), Wielscher, M. (Matthias), Weiss, S. (Stefan), Kentistou, K. A. (Katherine A.), Cook, J. P. (James P.), Sun, B. B. (Benjamin B.), Zhou, J. (Jian), Hui, J. (Jennie), Karrasch, S. (Stefan), Imboden, M. (Medea), Harris, S. E. (Sarah E.), Marten, J. (Jonathan), Enroth, S. (Stefan), Kerr, S. M. (Shona M.), Surakka, I. (Ida), Vitart, V. (Veronique), Lehtimäki, T. (Terho), Allen, R. J. (Richard J.), Bakke, P. S. (Per S.), Beaty, T. H. (Terri H.), Bleecker, E. R. (Eugene R.), Bosse, Y. (Yohan), Brandsma, C.-A. (Corry-Anke), Chen, Z. (Zhengming), Crapo, J. D. (James D.), Danesh, J. (John), DeMeo, D. L. (Dawn L.), Dudbridge, F. (Frank), Ewert, R. (Ralf), Gieger, C. (Christian), Gulsvik, A. (Amund), Hansell, A. L. (Anna L.), Hao, K. (Ke), Hoffman, J. D. (Joshua D.), Hokanson, J. E. (John E.), Homuth, G. (Georg), Joshi, P. K. (Peter K.), Joubert, P. (Philippe), Langenberg, C. (Claudia), Li, X. (Xuan), Li, L. (Liming), Lin, K. (Kuang), Lind, L. (Lars), Locantore, N. (Nicholas), Luan, J. (Jian'an), Mahajan, A. (Anubha), Maranville, J. C. (Joseph C.), Murray, A. (Alison), Nickle, D. C. (David C.), Packer, R. (Richard), Parker, M. M. (Margaret M.), Paynton, M. L. (Megan L.), Porteous, D. J. (David J.), Prokopenko, D. (Dmitry), Qiao, D. (Dandi), Rawal, R. (Rajesh), Runz, H. (Heiko), Sayers, I. (Ian), Sin, D. D. (Don D.), Smith, B. H. (Blair H.), Artigas, M. S. (Maria Soler), Sparrow, D. (David), Tal-Singer, R. (Ruth), Timmers, P. R. (Paul R. H. J.), Van den Berge, M. (Maarten), Whittaker, J. C. (John C.), Woodruff, P. G. (Prescott G.), Verges-Armstrong, L. M. (Laura M.), Troyanskaya, O. G. (Olga G.), Raitakari, O. T. (Olli T.), Kähönen, M. (Mika), Polasek, O. (Ozren), Gyllensten, U. (Ulf), Rudan, I. (Igor), Deary, I. J. (Ian J.), Probst-Hensch, N. M. (Nicole M.), Schulz, H. (Holger), James, A. L. (Alan L.), Wilson, J. F. (James F.), Stubbe, B. (Beate), Zeggini, E. (Eleftheria), Järvelin, M.-R. (Marjo-Riitta), Wareham, N. (Nick), Silverman, E. K. (Edwin K.), Hayward, C. (Caroline), Morris, A. P. (Andrew P.), Butterworth, A. S. (Adam S.), Scott, R. A. (Robert A.), Walters, R. G. (Robin G.), Meyers, D. A. (Deborah A.), Cho, M. H. (Michael H.), Strachan, D. P. (David P.), Hall, I. P. (Ian P.), Tobin, M. D. (Martin D.), and Wain, L. V. (Louise, V)

Abstract

Reduced lung function predicts mortality and is key to the diagnosis of chronic obstructive pulmonary disease (COPD). In a genome-wide association study in 400,102 individuals of European ancestry, we define 279 lung function signals, 139 of which are new. In combination, these variants strongly predict COPD in independent populations. Furthermore, the combined effect of these variants showed generalizability across smokers and never smokers, and across ancestral groups. We highlight biological pathways, known and potential drug targets for COPD and, in phenome-wide association studies, autoimmune-related and other pleiotropic effects of lung function–associated variants. This new genetic evidence has potential to improve future preventive and therapeutic strategies for COPD.

Published
2019

3. Evidence for large-scale gene-by-smoking interaction effects on pulmonary function

Author

Aschard, H. (Hugues), Tobin, M. D. (Martin D), Hancock, D. B. (Dana B), Skurnik, D. (David), Sood, A. (Akshay), James, A. (Alan), Smith, A. V. (Albert Vernon), Manichaikul, A. W. (Ani W), Campbell, A. (Archie), Prins, B. P. (Bram P), Hayward, C. (Caroline), Loth, D. W. (Daan W), Porteous, D. J. (David J), Strachan, D. P. (David P), Zeggini, E. (Eleftheria), O’Connor, G. T. (George T), Brusselle, G. G. (Guy G), Boezen, H. M. (H Marike), Schulz, H. (Holger), Deary, I. J. (Ian J), Hall, I. P. (Ian P), Rudan, I. (Igor), Kaprio, J. (Jaakko), Wilson, J. F. (James F), Wilk, J. B. (Jemma B), Huffman, J. E. (Jennifer E), Zhao, J. H. (Jing Hua), de Jong, K. (Kim), Lyytikäinen, L.-P. (Leo-Pekka), Wain, L. V. (Louise V), Järvelin, M.-R. (Marjo-Riitta), Kähönen, M. (Mika), Fornage, M. (Myriam), Polasek, O. (Ozren), Cassano, P. A. (Patricia A), Barr, R. G. (R Graham), Rawal, R. (Rajesh), Harris, S. E. (Sarah E), Gharib, S. A. (Sina A), Enroth, S. (Stefan), Heckbert, S. R. (Susan R), Lehtimäki, T. (Terho), Gyllensten, U. (Ulf), Understanding Society Scientific Group, Jackson, V. E. (Victoria E), Gudnason, V. (Vilmundur), Tang, W. (Wenbo), Dupuis, J. (Josée), Artigas, M. S. (María Soler), Joshi, A. D. (Amit D), London, S. J. (Stephanie J), Kraft, P. (Peter), Groningen Research Institute for Asthma and COPD (GRIAC), and Life Course Epidemiology (LCE)

Subjects
RISK, Medicin och hälsovetenskap, Science & Technology, PREDICTION, 0104 Statistics, respiratory system, genetic risk score, Medical and Health Sciences, DISEASE, smoking, gene-environment interaction, respiratory tract diseases, LUNG-FUNCTION, OPPORTUNITIES, 1117 Public Health And Health Services, FEV1/FVC, EPIDEMIOLOGY, OBSTRUCTION, GENOME-WIDE ASSOCIATION, ENVIRONMENT INTERACTIONS, gene–environment interaction, Life Sciences & Biomedicine, Public, Environmental & Occupational Health
Abstract

Background: Smoking is the strongest environmental risk factor for reduced pulmonary function. The genetic component of various pulmonary traits has also been demonstrated, and at least 26 loci have been reproducibly associated with either FEV1 (forced expiratory volume in 1 second) or FEV1/FVC (FEV1/forced vital capacity). Although the main effects of smoking and genetic loci are well established, the question of potential gene-by-smoking interaction effect remains unanswered. The aim of the present study was to assess, using a genetic risk score approach, whether the effect of these 26 loci on pulmonary function is influenced by smoking. Methods: We evaluated the interaction between smoking exposure, considered as either ever vs never or pack-years, and a 26-single nucleotide polymorphisms (SNPs) genetic risk score in relation to FEV1 or FEV1/FVC in 50 047 participants of European ancestry from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) and SpiroMeta consortia. Results: We identified an interaction (βint = −0.036, 95% confidence interval, −0.040 to −0.032, P = 0.00057) between an unweighted 26 SNP genetic risk score and smoking status (ever/never) on the FEV1/FVC ratio. In interpreting this interaction, we showed that the genetic risk of falling below the FEV1/FVC threshold used to diagnose chronic obstructive pulmonary disease is higher among ever smokers than among never smokers. A replication analysis in two independent datasets, although not statistically significant, showed a similar trend in the interaction effect. Conclusions: This study highlights the benefit of using genetic risk scores for identifying interactions missed when studying individual SNPs and shows, for the first time, that persons with the highest genetic risk for low FEV1/FVC may be more susceptible to the deleterious effects of smoking.

Published
2017

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