Multiancestry Study of Gene-Lifestyle Interactions for Cardiovascular Traits in 610 475 Individuals From 124 Cohorts: Design and Rationale.

D C Rao, Yun J Sung, Thomas W Winkler, Karen Schwander, Ingrid Borecki, L Adrienne Cupples, W James Gauderman, Kenneth Rice, Patricia B Munroe, Bruce M Psaty
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引用次数: 52

Abstract

Background— Several consortia have pursued genome-wide association studies for identifying novel genetic loci for blood pressure, lipids, hypertension, etc. They demonstrated the power of collaborative research through meta-analysis of study-specific results. Methods and Results— The Gene-Lifestyle Interactions Working Group was formed to facilitate the first large, concerted, multiancestry study to systematically evaluate gene–lifestyle interactions. In stage 1, genome-wide interaction analysis is performed in 53 cohorts with a total of 149 684 individuals from multiple ancestries. In stage 2 involving an additional 71 cohorts with 460 791 individuals from multiple ancestries, focused analysis is performed for a subset of the most promising variants from stage 1. In all, the study involves up to 610 475 individuals. Current focus is on cardiovascular traits including blood pressure and lipids, and lifestyle factors including smoking, alcohol, education (as a surrogate for socioeconomic status), physical activity, psychosocial variables, and sleep. The total sample sizes vary among projects because of missing data. Large-scale gene–lifestyle or more generally gene–environment interaction (G×E) meta-analysis studies can be cumbersome and challenging. This article describes the design and some of the approaches pursued in the interaction projects. Conclusions— The Gene-Lifestyle Interactions Working Group provides an excellent framework for understanding the lifestyle context of genetic effects and to identify novel trait loci through analysis of interactions. An important and novel feature of our study is that the gene–lifestyle interaction (G×E) results may improve our knowledge about the underlying mechanisms for novel and already known trait loci.

Abstract Image

Abstract Image

来自124个队列的610 475个个体的心血管特征的基因-生活方式相互作用的多祖先研究:设计和原理。
背景:一些联合体已经开始进行全基因组关联研究,以确定血压、血脂、高血压等的新基因位点。他们通过对特定研究结果的荟萃分析展示了合作研究的力量。方法和结果:基因-生活方式相互作用工作组的成立是为了促进第一个大型的、协调的、多祖先的研究,以系统地评估基因-生活方式相互作用。在第一阶段,对53个队列进行了全基因组相互作用分析,共有来自多个祖先的149684个个体。在第二阶段,涉及另外71个队列,来自多个祖先的460791个个体,对第一阶段最有希望的变体子集进行了重点分析。总的来说,这项研究涉及了多达610 475人。目前的重点是心血管特征,包括血压和血脂,以及生活方式因素,包括吸烟、饮酒、教育(代替社会经济地位)、体育活动、社会心理变量和睡眠。由于缺少数据,各个项目的总样本量各不相同。大规模的基因-生活方式或更普遍的基因-环境相互作用(G×E)荟萃分析研究可能是繁琐和具有挑战性的。本文描述了交互项目中的设计和一些方法。结论:基因-生活方式相互作用工作组为理解遗传效应的生活方式背景和通过相互作用分析识别新的性状位点提供了一个很好的框架。我们研究的一个重要和新颖的特点是,基因-生活方式相互作用(G×E)的结果可能会提高我们对新的和已知的性状位点的潜在机制的认识。
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来源期刊
Circulation: Cardiovascular Genetics
Circulation: Cardiovascular Genetics CARDIAC & CARDIOVASCULAR SYSTEMS-GENETICS & HEREDITY
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Circulation: Genomic and Precision Medicine considers all types of original research articles, including studies conducted in human subjects, laboratory animals, in vitro, and in silico. Articles may include investigations of: clinical genetics as applied to the diagnosis and management of monogenic or oligogenic cardiovascular disorders; the molecular basis of complex cardiovascular disorders, including genome-wide association studies, exome and genome sequencing-based association studies, coding variant association studies, genetic linkage studies, epigenomics, transcriptomics, proteomics, metabolomics, and metagenomics; integration of electronic health record data or patient-generated data with any of the aforementioned approaches, including phenome-wide association studies, or with environmental or lifestyle factors; pharmacogenomics; regulation of gene expression; gene therapy and therapeutic genomic editing; systems biology approaches to the diagnosis and management of cardiovascular disorders; novel methods to perform any of the aforementioned studies; and novel applications of precision medicine. Above all, we seek studies with relevance to human cardiovascular biology and disease.
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