Modeling the longitudinal changes of ancestry diversity in the Million Veteran Program

Author:

Wendt Frank RORCID,Pathak Gita AORCID,Vahey Jacqueline,Qin Xuejun,Koller Dora,Cabrera-Mendoza Brenda,Haeny Angela,Harrington Kelly M,Rajeevan Nallakkandi,Duong Linh M,Levey Daniel FORCID,De Angelis Flavio,De Lillo Antonella,Bigdeli Tim B,Pyarajan Saiju,Gaziano J. Michael,Gelernter JoelORCID,Aslan Mihaela,Provenzale Dawn,Helmer Drew A.,Hauser Elizabeth R.,Polimanti RenatoORCID, ,

Abstract

AbstractThe Million Veteran Program (MVP) participants represent 100 years of US history, including significant social and demographic change over time. Our study assessed two aspects of the MVP: (i) longitudinal changes in population diversity and (ii) how these changes can be accounted for in genome-wide association studies (GWAS). The MVP was divided into five birth cohorts (N-range=123,888 [born from 1943-1947] to 136,699 [born from 1948-1953]). Groups of participants were defined by (i) HARE (harmonized ancestry and race/ethnicity) and (ii) a random-forest clustering approach using the 1000 Genomes Project and the Human Genome Diversity Project (1kGP+HGDP) reference panels (77 world populations representing six continental groups). In these groups, we performed GWASs of height, a trait potentially affected by population stratification. Birth cohorts demonstrate important trends in ancestry diversity over time. More recent HARE-assigned Europeans, Africans, and Hispanics had lower European ancestry proportions than older birth cohorts (0.010<Cohen’s d<0.259, p<7.80×10−4). Conversely, HARE-assigned East Asians showed an increase in European ancestry proportion over time. In GWAS of height using HARE assignments, genomic inflation due to population stratification was prevalent across all birth cohorts (linkage disequilibrium score regression intercept=1.08±0.042). The 1kGP+HGDP-based ancestry assignment significantly reduced the population stratification (mean intercept reduction=0.045±0.007, p<0.05) confounding in the GWAS statistics. This study provides a comprehensive characterization of ancestry diversity of the MVP cohort over time and highlights that more refined modeling of genetic diversity (e.g., the 1kGP+HGDP-based ancestry assignment) can more accurately capture the polygenic architecture of traits and diseases that could be affected by population stratification.

Publisher

Cold Spring Harbor Laboratory

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