The Epithelial Sodium Channel γ-Subunit Gene and Blood Pressure Family Based Association, Renal Gene Expression, and Physiological Analyses

被引:17
作者
Buesst, Cara J. [1 ]
Bloomer, Lisa D. S. [3 ]
Scurrah, Katrina J. [2 ]
Ellis, Justine A. [4 ]
Barnes, Timothy A. [3 ]
Charchar, Fadi J. [3 ,5 ]
Braund, Peter [3 ]
Hopkins, Paul N. [6 ]
Samani, Nilesh J. [3 ,7 ]
Hunt, Steven C. [6 ]
Tomaszewski, Maciej [3 ,7 ]
Harrap, Stephen B. [1 ]
机构
[1] Univ Melbourne, Dept Physiol, Melbourne, Vic, Australia
[2] Univ Melbourne, Ctr Mol Environm Genet & Analyt Epidemiol, Melbourne, Vic, Australia
[3] Univ Leicester, Dept Cardiovasc Sci, Leicester, Leics, England
[4] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[5] Univ Ballarat, Sch Sci & Engn, Ballarat, Vic 3353, Australia
[6] Univ Utah, Dept Internal Med, Cardiovasc Genet Div, Salt Lake City, UT 84112 USA
[7] Glenfield Hosp, Leicester Natl Inst Hlth Res Biomed Res Unit Card, Leicester, Leics, England
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
blood pressure; genetics; meta-analysis; risk factors; cardiovascular diseases; COMMON VARIANTS; LINKAGE DISEQUILIBRIUM; ESSENTIAL-HYPERTENSION; RECEPTOR GENE; POPULATION; LOCI; PEDIGREES; PATHWAY; RENIN; CELLS;
D O I
10.1161/HYPERTENSIONAHA.111.176370
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Variants in the gene encoding the gamma-subunit of the epithelial sodium channel (SCNN1G) are associated with both Mendelian and quantitative effects on blood pressure. Here, in 4 cohorts of 1611 white European families composed of a total of 8199 individuals, we undertook staged testing of candidate single-nucleotide polymorphisms for SCNN1G (supplemented with imputation based on data from the 1000 Genomes Project) followed by a meta-analysis in all of the families of the strongest candidate. We also examined relationships between the genotypes and relevant intermediate renal phenotypes, as well as expression of SCNN1G in human kidneys. We found that an intronic single-nucleotide polymorphism of SCNN1G (rs13331086) was significantly associated with age-, sex-, and body mass index-adjusted blood pressure in each of the 4 populations (P<0.05). In an inverse variance-weighted meta-analysis of this single-nucleotide polymorphism in all 4 of the populations, each additional minor allele copy was associated with a 1-mm Hg increase in systolic blood pressure and 0.52-mm Hg increase in diastolic blood pressure (SE=0.33, P=0.002 for systolic blood pressure; SE=0.21, P=0.011 for diastolic blood pressure). The same allele was also associated with higher 12-hour overnight urinary potassium excretion (P=0.04), consistent with increased epithelial sodium channel activity. Renal samples from hypertensive subjects showed a nonsignificant (P=0.07) 1.7-fold higher expression of SCNN1G compared with normotensive controls. These data provide genetic and phenotypic evidence in support of a role for a common genetic variant of SCNN1G in blood pressure determination. (Hypertension. 2011;58:1073-1078.). Online Data Supplement
引用
收藏
页码:1073 / U209
页数:14
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