Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.

Journal: Nature Communications
Published:
Abstract

We assess performance and limitations of polygenic risk scores (PRSs) for multiple blood pressure (BP) phenotypes in diverse population groups. We compare "clumping-and-thresholding" (PRSice2) and LD-based (LDPred2) methods to construct PRSs from each of multiple GWAS, as well as multi-PRS approaches that sum PRSs with and without weights, including PRS-CSx. We use datasets from the MGB Biobank, TOPMed study, UK biobank, and from All of Us to train, assess, and validate PRSs in groups defined by self-reported race/ethnic background (Asian, Black, Hispanic/Latino, and White). For both SBP and DBP, the PRS-CSx based PRS, constructed as a weighted sum of PRSs developed from multiple independent GWAS, perform best across all race/ethnic backgrounds. Stratified analysis in All of Us shows that PRSs are better predictive of BP in females compared to males, individuals without obesity, and middle-aged (40-60 years) compared to older and younger individuals.

Authors
Nuzulul Kurniansyah, Matthew Goodman, Alyna Khan, Jiongming Wang, Elena Feofanova, Joshua Bis, Kerri Wiggins, Jennifer Huffman, Tanika Kelly, Tali Elfassy, Xiuqing Guo, Walter Palmas, Henry Lin, Shih-jen Hwang, Yan Gao, Kendra Young, Gregory Kinney, Jennifer Smith, Bing Yu, Simin Liu, Sylvia Wassertheil Smoller, Joann Manson, Xiaofeng Zhu, Yii-der Chen, I-te Lee, C Gu, Donald Lloyd Jones, Sebastian Zöllner, Myriam Fornage, Charles Kooperberg, Adolfo Correa, Bruce Psaty, Donna Arnett, Carmen Isasi, Stephen Rich, Robert Kaplan, Susan Redline, Braxton Mitchell, Nora Franceschini, Daniel Levy, Jerome Rotter, Alanna Morrison, Tamar Sofer