Comparing Pruning and Thresholding with Continuous Shrinkage Polygenic Score Methods in a Large Sample of Ancestrally Diverse Adolescents from the ABCD Study®.

IF 2.6 4区 医学 Q2 BEHAVIORAL SCIENCES
Behavior Genetics Pub Date : 2023-05-01 Epub Date: 2023-04-05 DOI:10.1007/s10519-023-10139-w
Jonathan Ahern, Wesley Thompson, Chun Chieh Fan, Robert Loughnan
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引用次数: 0

Abstract

Using individuals' genetic data researchers can generate Polygenic Scores (PS) that are able to predict risk for diseases, variability in different behaviors as well as anthropomorphic measures. This is achieved by leveraging models learned from previously published large Genome-Wide Association Studies (GWASs) associating locations in the genome with a phenotype of interest. Previous GWASs have predominantly been performed in European ancestry individuals. This is of concern as PS generated in samples with a different ancestry to the original training GWAS have been shown to have lower performance and limited portability, and many efforts are now underway to collect genetic databases on individuals of diverse ancestries. In this study, we compare multiple methods of generating PS, including pruning and thresholding and Bayesian continuous shrinkage models, to determine which of them is best able to overcome these limitations. To do this we use the ABCD Study, a longitudinal cohort with deep phenotyping on individuals of diverse ancestry. We generate PS for anthropometric and psychiatric phenotypes using previously published GWAS summary statistics and examine their performance in three subsamples of ABCD: African ancestry individuals (n = 811), European ancestry Individuals (n = 6703), and admixed ancestry individuals (n = 3664). We find that the single ancestry continuous shrinkage method, PRScs (CS), and the multi ancestry meta method, PRScsx Meta (CSx Meta), show the best performance across ancestries and phenotypes.

Abstract Image

在ABCD研究®的大量祖先多样化青少年样本中,将修剪和阈值与连续收缩多基因评分方法进行比较。
利用个人的遗传数据,研究人员可以生成多基因评分(PS),该评分能够预测疾病风险、不同行为的可变性以及拟人化指标。这是通过利用从先前发表的大型全基因组关联研究(GWAS)中获得的模型来实现的,该研究将基因组中的位置与感兴趣的表型相关联。以前的GWAS主要在欧洲血统的个体中进行。这令人担忧,因为在与原始训练GWAS具有不同祖先的样本中生成的PS已被证明具有较低的性能和有限的可移植性,并且目前正在进行许多努力来收集不同祖先个体的基因数据库。在这项研究中,我们比较了生成PS的多种方法,包括修剪和阈值以及贝叶斯连续收缩模型,以确定其中哪种方法最能克服这些限制。为此,我们使用ABCD研究,这是一个对不同祖先的个体进行深入表型分析的纵向队列。我们使用先前发表的GWAS汇总统计数据生成了人体测量和精神表型的PS,并检查了它们在ABCD的三个子样本中的表现:非洲血统个体(n = 811),欧洲血统的个人(n = 6703)和混合祖先个体(n = 3664)。我们发现,单祖先连续收缩方法PRScs(CS)和多祖先元方法PRScsx-meta(CSx-meta)在祖先和表型方面表现出最好的性能。
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来源期刊
Behavior Genetics
Behavior Genetics 生物-行为科学
CiteScore
4.90
自引率
7.70%
发文量
30
审稿时长
6-12 weeks
期刊介绍: Behavior Genetics - the leading journal concerned with the genetic analysis of complex traits - is published in cooperation with the Behavior Genetics Association. This timely journal disseminates the most current original research on the inheritance and evolution of behavioral characteristics in man and other species. Contributions from eminent international researchers focus on both the application of various genetic perspectives to the study of behavioral characteristics and the influence of behavioral differences on the genetic structure of populations.
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