E. Oelsner, Benjamin M. Smith, Jennifer N. Nguyen, A. Manichaikul, E. Hoffman, E. Ampleford, Latchezar Dimitrov, Xiuquing Guo, K. Taylor, E. Bleecker, Xignan Li, D. Meyers, S. Peters, S. Rich, J. Rotter, R. G. Barr, V. Ortega
{"title":"最新摘要-计算机断层扫描(CT)上COPD遗传风险评分与肺部结构之间的相关性:SPIROMICS","authors":"E. Oelsner, Benjamin M. Smith, Jennifer N. Nguyen, A. Manichaikul, E. Hoffman, E. Ampleford, Latchezar Dimitrov, Xiuquing Guo, K. Taylor, E. Bleecker, Xignan Li, D. Meyers, S. Peters, S. Rich, J. Rotter, R. G. Barr, V. Ortega","doi":"10.1183/13993003.CONGRESS-2018.OA2187","DOIUrl":null,"url":null,"abstract":"Background: The extent to which genetic risk of COPD is mediated by variation in lung structure remains unknown. Aims: To determine whether a recently developed genetic risk score for lung function (GRS; Wain LV et al, Nat Genet 2017; 49(3):416-425) is associated with CT lung structure. Methods: In SPIROMICS, a cohort of COPD subjects and at-risk smokers (≥20 pack-years), a weighted GRS was calculated from 83 of 95 single nucleotide polymorphisms genotyped or imputed across 3 race/ethnic groups. Post-bronchodilator spirometry and CT scan measures (via Apollo/VIDA) of lung density, spatially-matched airway dimensions, and small airway counts (generations 6-9) were evaluated in models adjusted for age, age-squared, sex, height, BMI, principal components, smoking status, pack-years, CT model and voxel size. Results: Among 2,579 participants (average age 63 years, 53% male, 76% non-Hispanic White, 18% African-American, 6% Asian, 37% current smokers, median 44 pack-years, 63% with COPD), higher GRS was associated with lower FEV1 and FEV1/FVC, and the highest GRS quintile was associated with doubling of risk for moderate-to-severe COPD (p Conclusions: Variation in lung structure, whether developmental or acquired, is an important mediator of the genetic risk factors underlying COPD.","PeriodicalId":12709,"journal":{"name":"Genes and Environment","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2018-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Late Breaking Abstract - Associations between a COPD genetic risk score and lung structure on computed tomography (CT): SPIROMICS\",\"authors\":\"E. Oelsner, Benjamin M. Smith, Jennifer N. Nguyen, A. Manichaikul, E. Hoffman, E. Ampleford, Latchezar Dimitrov, Xiuquing Guo, K. Taylor, E. Bleecker, Xignan Li, D. Meyers, S. Peters, S. Rich, J. Rotter, R. G. Barr, V. Ortega\",\"doi\":\"10.1183/13993003.CONGRESS-2018.OA2187\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: The extent to which genetic risk of COPD is mediated by variation in lung structure remains unknown. Aims: To determine whether a recently developed genetic risk score for lung function (GRS; Wain LV et al, Nat Genet 2017; 49(3):416-425) is associated with CT lung structure. Methods: In SPIROMICS, a cohort of COPD subjects and at-risk smokers (≥20 pack-years), a weighted GRS was calculated from 83 of 95 single nucleotide polymorphisms genotyped or imputed across 3 race/ethnic groups. Post-bronchodilator spirometry and CT scan measures (via Apollo/VIDA) of lung density, spatially-matched airway dimensions, and small airway counts (generations 6-9) were evaluated in models adjusted for age, age-squared, sex, height, BMI, principal components, smoking status, pack-years, CT model and voxel size. Results: Among 2,579 participants (average age 63 years, 53% male, 76% non-Hispanic White, 18% African-American, 6% Asian, 37% current smokers, median 44 pack-years, 63% with COPD), higher GRS was associated with lower FEV1 and FEV1/FVC, and the highest GRS quintile was associated with doubling of risk for moderate-to-severe COPD (p Conclusions: Variation in lung structure, whether developmental or acquired, is an important mediator of the genetic risk factors underlying COPD.\",\"PeriodicalId\":12709,\"journal\":{\"name\":\"Genes and Environment\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2018-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genes and Environment\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1183/13993003.CONGRESS-2018.OA2187\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes and Environment","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1183/13993003.CONGRESS-2018.OA2187","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Late Breaking Abstract - Associations between a COPD genetic risk score and lung structure on computed tomography (CT): SPIROMICS
Background: The extent to which genetic risk of COPD is mediated by variation in lung structure remains unknown. Aims: To determine whether a recently developed genetic risk score for lung function (GRS; Wain LV et al, Nat Genet 2017; 49(3):416-425) is associated with CT lung structure. Methods: In SPIROMICS, a cohort of COPD subjects and at-risk smokers (≥20 pack-years), a weighted GRS was calculated from 83 of 95 single nucleotide polymorphisms genotyped or imputed across 3 race/ethnic groups. Post-bronchodilator spirometry and CT scan measures (via Apollo/VIDA) of lung density, spatially-matched airway dimensions, and small airway counts (generations 6-9) were evaluated in models adjusted for age, age-squared, sex, height, BMI, principal components, smoking status, pack-years, CT model and voxel size. Results: Among 2,579 participants (average age 63 years, 53% male, 76% non-Hispanic White, 18% African-American, 6% Asian, 37% current smokers, median 44 pack-years, 63% with COPD), higher GRS was associated with lower FEV1 and FEV1/FVC, and the highest GRS quintile was associated with doubling of risk for moderate-to-severe COPD (p Conclusions: Variation in lung structure, whether developmental or acquired, is an important mediator of the genetic risk factors underlying COPD.
期刊介绍:
Genes and Environment is an open access, peer-reviewed journal that aims to accelerate communications among global scientists working in the field of genes and environment. The journal publishes articles across a broad range of topics including environmental mutagenesis and carcinogenesis, environmental genomics and epigenetics, molecular epidemiology, genetic toxicology and regulatory sciences.
Topics published in the journal include, but are not limited to, mutagenesis and anti-mutagenesis in bacteria; genotoxicity in mammalian somatic cells; genotoxicity in germ cells; replication and repair; DNA damage; metabolic activation and inactivation; water and air pollution; ROS, NO and photoactivation; pharmaceuticals and anticancer agents; radiation; endocrine disrupters; indirect mutagenesis; threshold; new techniques for environmental mutagenesis studies; DNA methylation (enzymatic); structure activity relationship; chemoprevention of cancer; regulatory science. Genetic toxicology including risk evaluation for human health, validation studies on testing methods and subjects of guidelines for regulation of chemicals are also within its scope.