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多民族多基因风险评分可改善不同人群的风险预测。

Multiethnic polygenic risk scores improve risk prediction in diverse populations.

作者信息

Márquez-Luna Carla, Loh Po-Ru, Price Alkes L

机构信息

Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, United States of America.

Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, United States of America.

出版信息

Genet Epidemiol. 2017 Dec;41(8):811-823. doi: 10.1002/gepi.22083. Epub 2017 Nov 7.

DOI:10.1002/gepi.22083
PMID:29110330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5726434/
Abstract

Methods for genetic risk prediction have been widely investigated in recent years. However, most available training data involves European samples, and it is currently unclear how to accurately predict disease risk in other populations. Previous studies have used either training data from European samples in large sample size or training data from the target population in small sample size, but not both. Here, we introduce a multiethnic polygenic risk score that combines training data from European samples and training data from the target population. We applied this approach to predict type 2 diabetes (T2D) in a Latino cohort using both publicly available European summary statistics in large sample size (N = 40k) and Latino training data in small sample size (N = 8k). Here, we attained a >70% relative improvement in prediction accuracy (from R = 0.027 to 0.047) compared to methods that use only one source of training data, consistent with large relative improvements in simulations. We observed a systematically lower load of T2D risk alleles in Latino individuals with more European ancestry, which could be explained by polygenic selection in ancestral European and/or Native American populations. We predict T2D in a South Asian UK Biobank cohort using European (N = 40k) and South Asian (N = 16k) training data and attained a >70% relative improvement in prediction accuracy, and application to predict height in an African UK Biobank cohort using European (N = 113k) and African (N = 2k) training data attained a 30% relative improvement. Our work reduces the gap in polygenic risk prediction accuracy between European and non-European target populations.

摘要

近年来,遗传风险预测方法得到了广泛研究。然而,大多数现有的训练数据都涉及欧洲样本,目前尚不清楚如何准确预测其他人群的疾病风险。以往的研究要么使用大样本量的欧洲样本训练数据,要么使用小样本量的目标人群训练数据,但没有同时使用两者。在此,我们引入了一种多民族多基因风险评分,它结合了欧洲样本的训练数据和目标人群的训练数据。我们将这种方法应用于一个拉丁裔队列中2型糖尿病(T2D)的预测,使用了大样本量(N = 40k)的公开可用欧洲汇总统计数据和小样本量(N = 8k)的拉丁裔训练数据。在此,与仅使用一种训练数据来源的方法相比,我们在预测准确性上实现了超过70%的相对提升(从R = 0.027提高到0.047),这与模拟中的大幅相对提升一致。我们观察到欧洲血统较多的拉丁裔个体中T2D风险等位基因的负荷系统性较低,这可以用欧洲祖先和/或美洲原住民群体中的多基因选择来解释。我们使用欧洲(N = 40k)和南亚(N = 16k)训练数据在一个英国生物银行南亚队列中预测T2D,并在预测准确性上实现了超过70%的相对提升,而在一个英国生物银行非洲队列中使用欧洲(N = 113k)和非洲(N = 2k)训练数据预测身高则实现了30%的相对提升。我们的工作缩小了欧洲和非欧洲目标人群在多基因风险预测准确性方面的差距。

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本文引用的文献

1
Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data.胜者之咒校正和可变阈值法可提高基于全基因组关联研究汇总水平数据的多基因风险建模性能。
PLoS Genet. 2016 Dec 30;12(12):e1006493. doi: 10.1371/journal.pgen.1006493. eCollection 2016 Dec.
2
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).新的NHGRI-EBI已发表全基因组关联研究目录(GWAS目录)。
Nucleic Acids Res. 2017 Jan 4;45(D1):D896-D901. doi: 10.1093/nar/gkw1133. Epub 2016 Nov 29.
3
Population Structure of UK Biobank and Ancient Eurasians Reveals Adaptation at Genes Influencing Blood Pressure.
Comparison of polygenic risk scores for type 2 diabetes developed from different ancestry groups.
不同血统群体开发的2型糖尿病多基因风险评分的比较。
NPJ Metab Health Dis. 2025 May 3;3(1):17. doi: 10.1038/s44324-025-00059-0.
4
Genomic risk prediction for type 2 diabetes in Australian individuals aged 70 years and older.澳大利亚70岁及以上人群2型糖尿病的基因组风险预测。
Diabetes Obes Metab. 2025 Sep;27(9):5259-5268. doi: 10.1111/dom.16579. Epub 2025 Jul 2.
5
Unsupervised Ensemble Learning for Efficient Integration of Pre-trained Polygenic Risk Scores.用于高效整合预训练多基因风险评分的无监督集成学习
Res Sq. 2025 Apr 1:rs.3.rs-5976048. doi: 10.21203/rs.3.rs-5976048/v1.
6
Sequencing and health data resource of children of African ancestry.非洲裔儿童的测序与健康数据资源。
medRxiv. 2025 Mar 26:2025.03.22.25324419. doi: 10.1101/2025.03.22.25324419.
7
Update on the genetics of allergic diseases.过敏性疾病遗传学的最新进展。
J Allergy Clin Immunol. 2025 Jun;155(6):1738-1752. doi: 10.1016/j.jaci.2025.03.012. Epub 2025 Mar 24.
8
Cardiac Repair and Regeneration via Advanced Technology: Narrative Literature Review.通过先进技术实现心脏修复与再生:叙述性文献综述
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9
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Commun Med (Lond). 2025 Feb 22;5(1):47. doi: 10.1038/s43856-025-00750-9.
10
Polygenic prediction for underrepresented populations through transfer learning by utilizing genetic similarity shared with European populations.通过利用与欧洲人群共享的遗传相似性,借助迁移学习对代表性不足的人群进行多基因预测。
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英国生物银行与古代欧亚人群的人口结构揭示了影响血压基因的适应性变化。
Am J Hum Genet. 2016 Nov 3;99(5):1130-1139. doi: 10.1016/j.ajhg.2016.09.014. Epub 2016 Oct 20.
4
Genomics is failing on diversity.基因组学在多样性方面表现不佳。
Nature. 2016 Oct 13;538(7624):161-164. doi: 10.1038/538161a.
5
Using Genetic Distance to Infer the Accuracy of Genomic Prediction.利用遗传距离推断基因组预测的准确性。
PLoS Genet. 2016 Sep 2;12(9):e1006288. doi: 10.1371/journal.pgen.1006288. eCollection 2016 Sep.
6
Transethnic Genetic-Correlation Estimates from Summary Statistics.基于汇总统计数据的跨种族遗传相关性估计
Am J Hum Genet. 2016 Jul 7;99(1):76-88. doi: 10.1016/j.ajhg.2016.05.001. Epub 2016 Jun 16.
7
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Genome Res. 2016 Jul;26(7):969-79. doi: 10.1101/gr.201996.115. Epub 2016 Jun 14.
8
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10
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