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ME-Bayes SL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups.

Jin JinJianan ZhanJingning ZhangRuzhang ZhaoJared Oâ ConnellYunxuan Jiangnull nullSteven BuyskeChristopher R GignouxChristopher HaimanEimear E KennyCharles KooperbergKari NorthBertram L KoelschGenevieve L WojcikHaoyu ZhangNilanjan Chatterjee
Published in: bioRxiv : the preprint server for biology (2023)
Polygenic risk scores (PRS) are now showing promising predictive performance on a wide variety of complex traits and diseases, but there exists a substantial performance gap across different populations. We propose ME-Bayes SL, a method for ancestry-specific polygenic prediction that borrows information in the summary statistics from genome-wide association studies (GWAS) across multiple ancestry groups. ME-Bayes SL conducts Bayesian hierarchical modeling under a multivariate spike-and-slab model for effect-size distribution and incorporates an ensemble learning step to combine information across different tuning parameter settings and ancestry groups. In our simulation studies and data analyses of 16 traits across four distinct studies, totaling 5.7 million participants with a substantial ancestral diversity, ME-Bayes SL shows promising performance compared to alternatives. The method, for example, has an average gain in prediction R 2 across 11 continuous traits of 40.2% and 49.3% compared to PRS- CSx and CT-SLEB, respectively, in the African Ancestry population. The best-performing method, however, varies by GWAS sample size, target ancestry, underlying trait architecture, and the choice of reference samples for LD estimation, and thus ultimately, a combination of methods may be needed to generate the most robust PRS across diverse populations.
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