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DiscoDivas: Leveraging genetic-ancestry continuum information to interpolate PRS for admixed populations
Yunfeng Ruan1, Rohan Bhukar1, Aniruddh Patel2
1Program in Medical and Population, Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, MA, USA; Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.
None:
Genome-wide association study (GWAS) summary statistics for training and individual-level cohorts for fine-tuning are essential for constructing predictive polygenic risk score (PRS) models. However, the relatively low representation of admixed populations in both GWAS summary statistics and individual-level datasets hinders the development of PRSs and equitable clinical translation for admixed populations. Prior work indicates that the most informative PRS model for a genetically homogeneous sample varies linearly in an ancestry continuum space. Guided by these observations, we introduce a genetic-distance-assisted PRS combination pipeline for diverse genetic ancestries (DiscoDivas) to interpolate a harmonized PRS for diverse, especially admixed, genetic ancestries. DiscoDivas leverages multiple PRS models fine-tuned within existing samples, which are mostly of single ancestry, and genetic distance. It provides a new approach to generate genetic-ancestry-specific PRSs when a suitably matched individual-level fine-tuning cohort is unavailable or underpowered. DiscoDivas treats genetic ancestry as a continuous variable and does not require shifting across different models when calculating PRSs for different ancestries. We generated PRSs with DiscoDivas and the current conventional method, i.e., fine-tuning multiple GWAS PRSs using the matched or similar genetic-ancestry samples. DiscoDivas generated a harmonized PRS, performing comparable to or better than the conventional approach, with the greatest advantage exhibited in admixed individuals.
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