Multiethnic polygenic risk scores improve risk prediction in diverse populations.

Genet Epidemiol
Authors
Keywords
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.

Year of Publication
2017
Journal
Genet Epidemiol
Volume
41
Issue
8
Pages
811-823
Date Published
2017 12
ISSN
1098-2272
DOI
10.1002/gepi.22083
PubMed ID
29110330
PubMed Central ID
PMC5726434
Links
Grant list
MC_QA137853 / Medical Research Council / United Kingdom
R01 GM105857 / GM / NIGMS NIH HHS / United States