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

被引:70
作者
Manichaikul, Ani [1 ,2 ]
Palmas, Walter [3 ]
Rodriguez, Carlos J. [4 ,5 ]
Peralta, Carmen A. [6 ,7 ]
Divers, Jasmin [8 ]
Guo, Xiuqing [9 ]
Chen, Wei-Min [1 ,2 ]
Wong, Quenna [10 ]
Williams, Kayleen [10 ]
Kerr, Kathleen F. [10 ]
Taylor, Kent D. [9 ]
Tsai, Michael Y. [11 ]
Goodarzi, Mark O. [9 ]
Sale, Michele M. [1 ,12 ,13 ]
Diez-Roux, Ana V. [14 ]
Rich, Stephen S. [1 ]
Rotter, Jerome I. [9 ]
Mychaleckyj, Josyf C. [1 ]
机构
[1] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22903 USA
[2] Univ Virginia, Dept Publ Hlth Sci, Div Biostat & Epidemiol, Charlottesville, VA USA
[3] Columbia Univ, Dept Med, New York, NY USA
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Med, Winston Salem, NC 27103 USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Epidemiol, Winston Salem, NC USA
[6] Univ Calif San Francisco, Dept Med, Div Nephrol, San Francisco, CA USA
[7] San Francisco VA Med Ctr, Div Gen Internal Med, San Francisco, CA USA
[8] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27103 USA
[9] Cedars Sinai Med Ctr, Inst Med Genet, Los Angeles, CA 90048 USA
[10] Univ Washington, Dept Biostat, Sch Publ Hlth, Seattle, WA 98195 USA
[11] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[12] Univ Virginia, Dept Med, Charlottesville, VA USA
[13] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA USA
[14] Univ Michigan, Dept Epidemiol, Ctr Social Epidemiol & Populat Hlth, Ann Arbor, MI 48109 USA
来源
PLOS GENETICS | 2012年 / 8卷 / 04期
基金
美国国家环境保护局;
关键词
GENOME-WIDE ASSOCIATION; GENETIC-VARIATION; PATTERNS; RISK; LOCI; ACCULTURATION; INFERENCE; VARIANTS; PROFILE; AMAZON;
D O I
10.1371/journal.pgen.1002640
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Using similar to 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.
引用
收藏
页码:285 / 298
页数:14
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