TY - JOUR
T1 - Admixture mapping for hypertension loci with genome-scan markers
AU - Zhu, Xiaofeng
AU - Luke, Amy
AU - Cooper, Richard S.
AU - Quertermous, Tom
AU - Hanis, Craig
AU - Mosley, Tom
AU - Gu, C. Charles
AU - Tang, Hua
AU - Rao, Dabeeru C.
AU - Risch, Neil
AU - Weder, Alan
N1 - Funding Information:
We thank D. Kan for his assistance in programming. This work was supported by grants awarded to the Family Blood Pressure Program, which is supported by a series of cooperative agreements from the National Heart, Lung and Blood Institute to GenNet, HyperGEN, GENOA and SAPPHIRe. The work was also supported by the Reynolds Cardiovascular Clinical Research Center at the University of Texas Southwestern, Dallas, Texas, USA. Genotype data for the Nigerian samples are available on request from R.S.C. ([email protected]).
PY - 2005/2
Y1 - 2005/2
N2 - Identification of genetic variants that contribute to risk of hypertension is challenging. As a complement to linkage and candidate gene association studies, we carried out admixture mapping using genome-scan microsatellite markers among the African American participants in the US National Heart, Lung, and Blood Institute's Family Blood Pressure Program. This population was assumed to have experienced recent admixture from ancestral groups originating in Africa and Europe. We used a set of unrelated individuals from Nigeria to represent the African ancestral population and used the European Americans in the Family Blood Pressure Program to provide estimates of allele frequencies for the European ancestors. We genotyped a common set of 269 microsatellite markers in the three groups at the same laboratory. The distribution of marker location-specific African ancestry, based on multipoint analysis, was shifted upward in hypertensive cases versus normotensive controls, consistent with linkage to genes conferring susceptibility. This shift was largely due to a small number of loci, including five adjacent markers on chromosome 6q and two on chromosome 21q. These results suggest that chromosome 6q24 and 21q21 may contain genes influencing risk of hypertension in African Americans.
AB - Identification of genetic variants that contribute to risk of hypertension is challenging. As a complement to linkage and candidate gene association studies, we carried out admixture mapping using genome-scan microsatellite markers among the African American participants in the US National Heart, Lung, and Blood Institute's Family Blood Pressure Program. This population was assumed to have experienced recent admixture from ancestral groups originating in Africa and Europe. We used a set of unrelated individuals from Nigeria to represent the African ancestral population and used the European Americans in the Family Blood Pressure Program to provide estimates of allele frequencies for the European ancestors. We genotyped a common set of 269 microsatellite markers in the three groups at the same laboratory. The distribution of marker location-specific African ancestry, based on multipoint analysis, was shifted upward in hypertensive cases versus normotensive controls, consistent with linkage to genes conferring susceptibility. This shift was largely due to a small number of loci, including five adjacent markers on chromosome 6q and two on chromosome 21q. These results suggest that chromosome 6q24 and 21q21 may contain genes influencing risk of hypertension in African Americans.
UR - http://www.scopus.com/inward/record.url?scp=13944250687&partnerID=8YFLogxK
U2 - 10.1038/ng1510
DO - 10.1038/ng1510
M3 - Article
C2 - 15665825
AN - SCOPUS:13944250687
SN - 1061-4036
VL - 37
SP - 177
EP - 181
JO - Nature Genetics
JF - Nature Genetics
IS - 2
ER -