TY - JOUR
T1 - Blood pressure response to potassium supplementation is associated with genetic variation in endothelin 1 and interactions with e selectin in rural Chinese
AU - Montasser, May E.
AU - Shimmin, Lawrence C.
AU - Gu, Donfeng
AU - Chen, Jing
AU - Gu, Charles
AU - Kelly, Tanika N.
AU - Jaquish, Cashell E.
AU - Rice, Treva
AU - Rao, D. C.
AU - Cao, Jie
AU - Chen, Jichun
AU - Liu, De Pei
AU - Whelton, Paul
AU - He, Jiang
AU - Hixson, James E.
PY - 2010/4
Y1 - 2010/4
N2 - Objective Although beneficial effects of potassium intake on blood pressure (BP) are well established, little is known about genetic factors that underlie interindividual variability in BP response to dietary potassium. In a previous study, we reported the first evidence for significant heritabilities for BP response in a dietary intervention study in rural Chinese. In this report, we extend our genetic studies to examine associations with polymorphisms in genes in vascular endothelial pathways. Methods We genotyped study participants for 23 single nucleotide polymorphisms (SNPs) in endothelin 1 (EDN1), nitric oxide synthase 3, and E selectin (SELE). We tested 17 of these SNPs for associations with BP response to potassium supplementation in 1843 participants. Association tests used population-based [generalized estimation equation (GEE)] and family-based (quantitative transmission disequilibrium test) methods, as well as tests for gene-by-gene (G×G) interaction (generalized multifactor dimensionalilty reduction and GEE). Results Single SNP analysis identified significant associations for several SNPs in EDN1 with multiple measures of BP response to potassium supplementation. The cumulative effects of the minor EDN1 alleles that showed significant associations were to reduce measures of BP response by 0.5-0.9 mmHg. We found significant evidence for effects of GxG interactions between EDN1 and SELE, even in the absence of individual associations with SELE variants. Conclusion Our results implicate variability in EDN1 and SELE as genetic factors that influence BP response to potassium intake. Although such epidemiological studies do not allow direct determination of physiologic mechanisms, our findings of joint effects identify EDN1 and SELE as targets for functional studies to determine their interactions in BP response to potassium intake.
AB - Objective Although beneficial effects of potassium intake on blood pressure (BP) are well established, little is known about genetic factors that underlie interindividual variability in BP response to dietary potassium. In a previous study, we reported the first evidence for significant heritabilities for BP response in a dietary intervention study in rural Chinese. In this report, we extend our genetic studies to examine associations with polymorphisms in genes in vascular endothelial pathways. Methods We genotyped study participants for 23 single nucleotide polymorphisms (SNPs) in endothelin 1 (EDN1), nitric oxide synthase 3, and E selectin (SELE). We tested 17 of these SNPs for associations with BP response to potassium supplementation in 1843 participants. Association tests used population-based [generalized estimation equation (GEE)] and family-based (quantitative transmission disequilibrium test) methods, as well as tests for gene-by-gene (G×G) interaction (generalized multifactor dimensionalilty reduction and GEE). Results Single SNP analysis identified significant associations for several SNPs in EDN1 with multiple measures of BP response to potassium supplementation. The cumulative effects of the minor EDN1 alleles that showed significant associations were to reduce measures of BP response by 0.5-0.9 mmHg. We found significant evidence for effects of GxG interactions between EDN1 and SELE, even in the absence of individual associations with SELE variants. Conclusion Our results implicate variability in EDN1 and SELE as genetic factors that influence BP response to potassium intake. Although such epidemiological studies do not allow direct determination of physiologic mechanisms, our findings of joint effects identify EDN1 and SELE as targets for functional studies to determine their interactions in BP response to potassium intake.
KW - Blood pressure response
KW - Dietary intervention
KW - Gene-by-gene interaction
KW - Genetic association
KW - Hypertension
KW - Potassium
UR - http://www.scopus.com/inward/record.url?scp=78650782558&partnerID=8YFLogxK
U2 - 10.1097/HJH.0b013e3283355672
DO - 10.1097/HJH.0b013e3283355672
M3 - Article
C2 - 19996987
AN - SCOPUS:78650782558
SN - 0263-6352
VL - 28
SP - 748
EP - 755
JO - Journal of Hypertension
JF - Journal of Hypertension
IS - 4
ER -