Association of Genetic Variants in the Apelin-APJ System and ACE2 With Blood Pressure Responses to Potassium Supplementation: The GenSalt Study

被引:41
作者
Zhao, Qi [1 ]
Gu, Dongfeng [2 ,3 ,4 ]
Kelly, Tanika N. [1 ]
Hixson, James E. [5 ]
Rao, Dabeeru C. [6 ]
Jaquish, Cashell E. [7 ]
Chen, Jing [8 ]
Huang, Jianfeng [2 ,3 ,4 ]
Chen, Chung-Shivan [1 ]
Gu, C. Charles [6 ]
Whelton, Paul K. [9 ]
He, Jiang [1 ,8 ]
机构
[1] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Epidemiol, New Orleans, LA 70118 USA
[2] Chinese Acad Med Sci, Cardiovasc Inst, Fuwai Hosp, Beijing 100037, Peoples R China
[3] Peking Union Med Coll, Beijing 100021, Peoples R China
[4] Chinese Natl Ctr Cardiovasc Dis Control & Res, Beijing, Peoples R China
[5] Univ Texas Sch Publ Hlth, Dept Epidemiol, Houston, TX USA
[6] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[7] NHLBI, Div Cardiovasc Sci, Bethesda, MD 20892 USA
[8] Tulane Univ, Sch Med, Dept Med, New Orleans, LA 70112 USA
[9] Loyola Univ Med Ctr, Off President, Maywood, IL 60153 USA
基金
美国国家卫生研究院;
关键词
ACE2; apelin; apelin receptor; blood pressure; hypertension; polymorphism; potassium supplement; RENIN-ANGIOTENSIN SYSTEM; IN-VIVO; AGTRL1; GENE; HYPERTENSION; POLYMORPHISMS; POPULATION; RECEPTOR; DISEASE; CHINESE; INFARCTION;
D O I
10.1038/ajh.2010.36
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
BACKGROUND Genetic factors may influence blood pressure (BP) responses to dietary potassium intake. We examined the association of genetic variants in the apelin-APJ system and angiotensin-converting enzyme 2 (ACE2) with BP responses to potassium supplementation. METHODS We conducted a 7-day potassium supplementation (60 mmol/day) intervention among 1,906 Chinese adults who participated in the Genetic Epidemiology Network of Salt-Sensitivity (GenSalt) study. Tag single-nucleotide polymorphisms (SNPs) based on HapMap data and potential functional SNPs were selected in the APLN, APLNR, and ACE2 genes. Because the ACE2 and APLN genes are located on the X chromosome, men and women were analyzed separately. RESULTS In women, SNP rs2235306 in the APLN gene was significantly associated with diastolic BP (DBP) response to potassium supplementation (P=0.0009).The DBP responses (95% confidence interval (Cl)) among those with genotypes T/T,T/C, and C/C were -2.22 (-2.74, -1.70), -1.69 (-2.20, -1.19), and -0.81 (-1.54, -0.09) mm Hg, respectively. In men, SNP rs4646174 of the ACE2 gene was significantly associated with systolic BP (SBP), DBP, and mean arterial pressure (MAP) responses to potassium supplementation (P=0.0001, P=0.001, and P=3.0 x 10(-6), respectively). The SBP, DBP, and MAP responses (95% Cl) were -0.79 (-2.27,0.69) vs.-3.53 (-3.94, -3.12), 1.07 (-0.34, 2.49) vs.-1.06 (-1.43, -0.69), and 0.44 (-0.60, 1.48) vs.-1.89 (-2.22,-1.55) mm Hg among men with minor G allele compared to those with major C allele of rs4646174, respectively. CONCLUSION Our study indicates that genetic variation of APLN and ACE2 may influence BP response to potassium intake.
引用
收藏
页码:606 / 613
页数:8
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