Local Ancestry and Clinical Cardiovascular Events Among African Americans From the Atherosclerosis Risk in Communities Study

被引:21
|
作者
Shendre, Aditi [2 ]
Irvin, Marguerite R. [2 ]
Wiener, Howard [2 ]
Zhi, Degui [3 ]
Limdi, Nita A. [4 ]
Overton, Edgar T. [1 ]
Shrestha, Sadeep [2 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Infect Dis, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Epidemiol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Biostat, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Dept Neurol, UAB Stn, Birmingham, AL 35294 USA
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2017年 / 6卷 / 04期
关键词
admixture mapping; association studies; cardiovascular events; genetic epidemiology; genetics; genome-wide association scan; race and ethnicity; GENOME-WIDE ASSOCIATION; CORONARY-ARTERY-DISEASE; STUDY 100K PROJECT; ISCHEMIC-STROKE; MATRIX METALLOPROTEINASES; AGING RESEARCH; CELL-DEATH; HEART; ADMIXTURE; GENES;
D O I
10.1161/JAHA.116.004739
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Local ancestry in relation to clinical cardiovascular events (CVEs) among African Americans can provide insight into their genetic susceptibility to the disease. Methods and Results-We examined local European ancestry (LEA) association with CVEs among 3000 African Americans from the Atherosclerosis Risk in Communities Study (ARIC). We estimated LEA using Local Ancestry Inference in adMixed Populations using Linkage Disequilibrium (LAMP-LD) and examined its association with myocardial infarction, stroke, coronary heart disease and its composite and cardiovascular disease composite using logistic regression. Genome-wide significance was achieved by 121 LEA regions in relation to myocardial infarction and 2 in relation to the cardiovascular disease composite. The LEA region downstream of 4q32.1 was significantly associated with 2 times higher odds of myocardial infarction (P=1.45x 10(-6)). The LEA region upstream of 6q 11.1 was associated with 0.37 times lower odds of fatal coronary heart disease (P=7.34x 10(-4)), whereas the LEA region downstream of 21q21.1 was associated with 1.55 times higher odds of composite coronary heart disease (P= 3.45x 10(-4)). Association of LEA with stroke was observed in the region upstream of 6p22.3 with a 1.57 times higher odds of stroke (P=9.69x 10(-4)). Likewise, the LEA region on 4q32.3 was associated with a 1.53 times higher odds of composite cardiovascular disease (P= 3.04x 10(-4)). We also found 20 of the LEA regions at previously significant cardiovascular disease single-nucleotide polymorphisms to be associated with CVE in our study. Conclusions-Future studies are needed to replicate and/or determine the causal variants driving our associations and explore clinical applications for those consistently associated with CVEs.
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页数:183
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