Using the Genetic Architecture of Substance Use Disorders to Advance Gene Identification and Understanding of Pathways of Risk

利用药物滥用疾病的遗传结构来推进基因识别和对风险途径的理解

• 批准号: 10201550
• 负责人: DANIELLE M DICK
• 金额: $ 55.49万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-07-01 至 2022-01-18
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10201550
• 关键词: Adolescence; Affect; Age; Alcohols; Area; Behavioral; Bioinformatics; Biological; Complex; Consumption; Data; Data Set; Detection; Development; Environment; Environmental Risk Factor; Foundations; Genes; Genetic; Genetic Risk; Genetic Techniques; Genetic Variation; Genomics; Goals; Health; Human; Individual; Intervention; Lead; Maps; Mediating; Mental disorders; Meta-Analysis; Methods; Multivariate Analysis; National Longitudinal Survey of Adolescent to Adult Health; Opiate Addiction; Outcome; Pathway interactions; Phenotype; Prevention; Process; Psychiatry; Risk; Running; Sample Size; Sampling; Signal Transduction; Structure; Substance Use Disorder; Techniques; Testing; Translating; Twin Multiple Birth; Variant; addiction; alcohol use disorder; behavioral phenotyping; clinical Diagnosis; emerging adulthood; gene discovery; genetic architecture; genetic association; genetic variant; genome wide association study; genome-wide; high risk; improved; insight; longitudinal dataset; marijuana use disorder; novel; opioid use disorder; personalized medicine; polygenic risk score; population based; racial and ethnic; sex; substance use; substance use treatment; trait

Project Summary This project has two complementary goals: (1) to advance discovery of genes involved in substance use disorders using new multivariate genomic techniques, and (2) to characterize the risk associated with identified variants in diverse longitudinal samples in order to understand the spectrum of phenotypes associated with identified variants, across development, and in conjunction with the environment. Each of these areas represents critical steps in using genetic data to improve prevention, intervention, and treatment for substance use disorders (SUDs), and will lay the foundation as we move into an era of personalized medicine. Human gene identification efforts for substance use disorders lag behind other areas of psychiatry, in part due to constrained sample sizes of available SUD cases. However, recent meta-analyses of substance-related phenotypes such as age of initiation, consumption and problems, reveal significant genetic correlations across substance use outcomes, as well as with numerous other psychiatric and behavioral traits. These findings map onto twin data demonstrating significant genetic correlations across substance use disorders and other externalizing traits. This project will (Aim 1) apply new multivariate genetic methods to capitalize on genetic sharing between substance use phenotypes and related traits in order to boost power to detect common variants associated with substance use outcomes, and to characterize the latent pathways by which genetic variants operate. Bioinformatic characterization of these identified genetic variants will provide insight into underlying biological risk pathways, and phenotypic characterization of resultant polygenic risk scores will help us understand how risk unfolds across development and in conjunction with the environment. We will apply results from the multivariate analyses to two complementary longitudinal datasets, consisting of a population-based and high-risk sample, in order to (Aim 2a) map the behavioral phenotypes associated with the genetic risk scores identified in Aim 1 across adolescence and emerging adulthood; (Aim 2b) test for pathways of risk specific to sex and racial/ethnic background; and (Aim 2c) test for moderation of genetic risk by key environmental factors. Jointly, these analyses will advance our understanding of how genetic variation contributes to risk for substance use disorders.

项目摘要 该项目有两个互补的目标：（1）促进发现参与基因， 使用新的多元基因组技术的物质使用障碍，和（2）表征 与不同纵向样本中识别的变异相关的风险，以了解 与已鉴定变体相关的表型谱，跨越发育， 与环境的结合。这些领域中的每一个都代表了利用遗传学的关键步骤。 改善物质使用障碍（SUD）预防、干预和治疗的数据， 并将为我们进入个性化医疗时代奠定基础。人类基因 物质使用障碍的识别工作落后于精神病学的其他领域， 由于可用SUD病例的样本量有限。然而，最近的荟萃分析， 物质相关的表型，如开始的年龄，消费和问题，揭示 物质使用结果之间的显着遗传相关性，以及与许多其他 精神和行为特征这些发现映射到双胞胎数据上， 物质使用障碍和其他外在特征之间的遗传相关性。这个项目 将（目标1）应用新的多元遗传方法，利用遗传共享之间 物质使用表型和相关性状，以提高检测常见变异的能力 与物质使用结果相关，并描述潜在的途径， 遗传变异的作用。这些鉴定的遗传变体的生物信息学表征将 深入了解潜在的生物风险途径，以及 由此产生的多基因风险评分将帮助我们了解风险如何在发育过程中展开， 与环境结合。我们将多变量分析的结果应用于两个 补充纵向数据集，包括基于人口的高风险样本， 目的2a：绘制与遗传风险评分相关的行为表型 在目标1中确定的青春期和成年初显期;（目标2b）测试 性别和种族/族裔背景特有的风险;以及（目标2c）检测遗传风险的适度性 关键的环境因素。这些分析将共同促进我们对如何 遗传变异会增加药物使用障碍的风险。