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Abstract
Polygenic risk scores (PRS) have shown successes in clinics, but most PRS methods focus only on participants with distinct primary continental ancestry without accommodating recently-admixed individuals with mosaic continental ancestry backgrounds for different segments of their genomes. Here, we develop GAUDI, a novel penalized-regression-based method specifically designed for admixed individuals. GAUDI explicitly models ancestry-differential effects while borrowing information across segments with shared ancestry in admixed genomes. We demonstrate marked advantages of GAUDI over other methods through comprehensive simulation and real data analyses for traits with associated variants exhibiting ancestral-differential effects. Leveraging data from the Women’s Health Initiative study, we show that GAUDI improves PRS prediction of white blood cell count and C-reactive protein in African Americans by > 64% compared to alternative methods, and even outperforms PRS-CSx with large European GWAS for some scenarios. We believe GAUDI will be a valuable tool to mitigate disparities in PRS performance in admixed individuals.
Most polygenic risk score (PRS) methods focus only on individuals with distinct primary continental ancestry, without accommodating recently-admixed individuals. Here, the authors develop a novel penalized regression-based PRS method specifically designed for admixed individuals.
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1 University of North Carolina at Chapel Hill, Department of Biostatistics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000 0001 2248 3208)
2 University of Washington, Department of Biostatistics, Seattle, USA (GRID:grid.34477.33) (ISNI:0000 0001 2298 6657)
3 University of North Carolina at Chapel Hill, Department of Epidemiology, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000 0001 2248 3208)
4 Fred Hutchinson Cancer Center, Division of Public Health Sciences, Seattle, USA (GRID:grid.270240.3) (ISNI:0000 0001 2180 1622)
5 Rutgers University, Department of Genetics, New Brunswick, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796)
6 Rutgers University, Department of Statistics, New Brunswick, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796)
7 Vanderbilt University Medical Center, Vanderbilt Genetics Institute, Nashville, USA (GRID:grid.412807.8) (ISNI:0000 0004 1936 9916); Vanderbilt University Medical Center, Department of Biostatistics, Nashville, USA (GRID:grid.412807.8) (ISNI:0000 0004 1936 9916)
8 Johns Hopkins University, Department of Medicine, Baltimore, USA (GRID:grid.21107.35) (ISNI:0000 0001 2171 9311)
9 University of Washington, Department of Epidemiology, Seattle, USA (GRID:grid.34477.33) (ISNI:0000 0001 2298 6657)
10 and Cancer Center, Medical College of Wisconsin, Division of Biostatistics, Institute for Health and Equity, Milwaukee, USA (GRID:grid.30760.32) (ISNI:0000 0001 2111 8460)
11 Vanderbilt University Medical Center, Vanderbilt Genetics Institute, Nashville, USA (GRID:grid.412807.8) (ISNI:0000 0004 1936 9916); Vanderbilt University Medical Center, Division of Genetic Medicine, Department of Medicine, Nashville, USA (GRID:grid.412807.8) (ISNI:0000 0004 1936 9916)
12 University of North Carolina at Chapel Hill, Department of Genetics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000 0001 2248 3208)
13 University of North Carolina at Chapel Hill, Department of Biostatistics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000 0001 2248 3208); University of North Carolina at Chapel Hill, Department of Genetics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000 0001 2248 3208)