Admixture mapping of quantitative trait loci for blood lipids in African-Americans

被引:24
作者
Basu, Analabha [1 ]
Tang, Hua [3 ]
Lewis, Cora E. [5 ]
North, Kari [6 ]
Curb, J. David [7 ]
Quertermous, Thomas [4 ,8 ]
Mosley, Thomas H.
Boerwinkle, Eric [9 ]
Zhu, Xiaofeng [10 ]
Risch, Neil J. [1 ,2 ,11 ]
机构
[1] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[3] Stanford Univ, Dept Genet, Palo Alto, CA USA
[4] Stanford Univ, Dept Med, Palo Alto, CA USA
[5] Univ Alabama, Dept Med, Birmingham, W Midlands, England
[6] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC USA
[7] Univ Hawaii, John A Burns Sch Med, Dept Geriatr Med, Honolulu, HI 96822 USA
[8] Univ Mississippi, Med Ctr, Jackson, MS 39216 USA
[9] Univ Texas Hlth Sci Ctr, Sch Publ Hlth, Houston, TX USA
[10] Case Western Reserve Univ, Sch Med, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[11] Kaiser Permanente, Div Res, Oakland, CA USA
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; ISCHEMIC-HEART-DISEASE; MULTILOCUS GENOTYPE DATA; GENOME-WIDE ASSOCIATION; CORONARY-ARTERY-DISEASE; HDL CHOLESTEROL; RISK-FACTORS; ENVIRONMENTAL-FACTORS; CELLULAR CHOLESTEROL; METABOLIC SYNDROME;
D O I
10.1093/hmg/ddp122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Blood lipid levels, including low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and triglycerides (TG), are highly heritable traits and major risk factors for atherosclerotic cardiovascular disease (CVD). Using individual ancestry estimates at marker locations across the genome, we present a novel quantitative admixture mapping analysis of all three lipid traits in a large sample of African-Americans from the Family Blood Pressure Program. Regression analysis was performed with both total and marker-location-specific European ancestry as explanatory variables, along with demographic covariates. Robust permutation analysis was used to assess statistical significance. Overall European ancestry was significantly correlated with HDL-C (negatively) and TG (positively), but not with LDL-C. We found strong evidence for a novel locus underlying HDL-C on chromosome 8q, which correlated negatively with European ancestry (P = .0014); the same location also showed positive correlation of European ancestry with TG levels. A region on chromosome 14q also showed significant negative correlation between HDL-C levels and European ancestry. On chromosome 15q, a suggestive negative correlation of European ancestry with TG and positive correlation with HDL-C was observed. Results with LDL-C were less significant overall. We also found significant evidence for genome-wide ancestry effects underlying the joint distribution of HDL-C and TG, not fully explained by the locus on chromosome 8. Our results are consistent with a genetic contribution to and may explain the healthier HDL-C and TG profiles found in Blacks versus Whites. The identified regions provide locations for follow-up studies of genetic variants underlying lipid variation in African-Americans and possibly other populations.
引用
收藏
页码:2091 / 2098
页数:8
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