Population Structure of Hispanics in the United States: The Multi-Ethnic Study of Atherosclerosis

Ani Manichaikul(University of Virginia), Walter Palmas(Columbia University), Carlos J. Rodríguez(Wake Forest University), Carmen Peralta(San Francisco VA Medical Center), Jasmin Divers(Wake Forest University), Xiuqing Guo(Cedars-Sinai Medical Center), Wei‐Min Chen(University of Virginia), Quenna Wong(University of Washington), Kayleen Williams(University of Washington), Kathleen F. Kerr(University of Washington), Kent D. Taylor(Cedars-Sinai Medical Center), Michael Y. Tsai(University of Minnesota), Mark O. Goodarzi(Cedars-Sinai Medical Center), Michèle M. Sale(University of Virginia), Ana V. Diez–Roux(Michigan United), Stephen S. Rich(University of Virginia), Jerome I. Rotter(Cedars-Sinai Medical Center), Josyf C. Mychaleckyj(University of Virginia)
PLoS Genetics
April 12, 2012
Cited by 105Open Access
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Abstract

Using ~60,000 SNPs selected for minimal linkage disequilibrium, we perform population structure analysis of 1,374 unrelated Hispanic individuals from the Multi-Ethnic Study of Atherosclerosis (MESA), with self-identification corresponding to Central America (n = 93), Cuba (n = 50), the Dominican Republic (n = 203), Mexico (n = 708), Puerto Rico (n = 192), and South America (n = 111). By projection of principal components (PCs) of ancestry to samples from the HapMap phase III and the Human Genome Diversity Panel (HGDP), we show the first two PCs quantify the Caucasian, African, and Native American origins, while the third and fourth PCs bring out an axis that aligns with known South-to-North geographic location of HGDP Native American samples and further separates MESA Mexican versus Central/South American samples along the same axis. Using k-means clustering computed from the first four PCs, we define four subgroups of the MESA Hispanic cohort that show close agreement with self-identification, labeling the clusters as primarily Dominican/Cuban, Mexican, Central/South American, and Puerto Rican. To demonstrate our recommendations for genetic analysis in the MESA Hispanic cohort, we present pooled and stratified association analysis of triglycerides for selected SNPs in the LPL and TRIB1 gene regions, previously reported in GWAS of triglycerides in Caucasians but as yet unconfirmed in Hispanic populations. We report statistically significant evidence for genetic association in both genes, and we further demonstrate the importance of considering population substructure and genetic heterogeneity in genetic association studies performed in the United States Hispanic population.


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