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Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology.
Wang, Ying; Kanai, Masahiro; Tan, Taotao; Kamariza, Mireille; Tsuo, Kristin; Yuan, Kai; Zhou, Wei; Okada, Yukinori; Huang, Hailiang; Turley, Patrick; Atkinson, Elizabeth G; Martin, Alicia R.
Affiliation
  • Wang Y; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Kanai M; Stanley Center for Psychiatric Research and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Tan T; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Kamariza M; Stanley Center for Psychiatric Research and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Tsuo K; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
  • Yuan K; Department of Statistical Genetics, Osaka University Graduate School of Medicine, Suita, Japan.
  • Zhou W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Okada Y; Society of Fellows, Harvard University, Cambridge, MA 02138, USA.
  • Huang H; Stanley Center for Psychiatric Research and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Turley P; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Atkinson EG; Stanley Center for Psychiatric Research and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Martin AR; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
Cell Genom ; 3(10): 100408, 2023 Oct 11.
Article in En | MEDLINE | ID: mdl-37868036
ABSTRACT
Polygenic risk scores (PRSs) developed from multi-ancestry genome-wide association studies (GWASs), PRSmulti, hold promise for improving PRS accuracy and generalizability across populations. To establish best practices for leveraging the increasing diversity of genomic studies, we investigated how various factors affect the performance of PRSmulti compared with PRSs constructed from single-ancestry GWASs (PRSsingle). Through extensive simulations and empirical analyses, we showed that PRSmulti overall outperformed PRSsingle in understudied populations, except when the understudied population represented a small proportion of the multi-ancestry GWAS. Furthermore, integrating PRSs based on local ancestry-informed GWASs and large-scale, European-based PRSs improved predictive performance in understudied African populations, especially for less polygenic traits with large-effect ancestry-enriched variants. Our work highlights the importance of diversifying genomic studies to achieve equitable PRS performance across ancestral populations and provides guidance for developing PRSs from multiple studies.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Genom Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Genom Year: 2023 Document type: Article