Human Genetics Center, School of Public Health, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
J Hypertens. 2010 Apr;28(4):748-55. doi: 10.1097/HJH.0b013e3283355672.
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.
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 (GxG) interaction (generalized multifactor dimensionalilty reduction and GEE).
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.
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.
尽管钾摄入对血压(BP)有益的确切效果已得到充分证实,但对于饮食钾对 BP 反应的个体差异背后的遗传因素知之甚少。在之前的研究中,我们报道了在对中国农村人群进行饮食干预研究中首次发现 BP 反应存在显著遗传可能性的证据。在本报告中,我们将遗传研究扩展到了检查血管内皮途径基因多态性与 BP 反应之间的关联。
我们对研究参与者的 23 个单核苷酸多态性(SNP)进行了基因分型,这些 SNP 分别位于内皮素 1(EDN1)、一氧化氮合酶 3 和 E 选择素(SELE)基因中。我们对 1843 名参与者的基因与钾补充对 BP 反应的关联进行了检测,共使用了基于人群的[广义估计方程(GEE)]和基于家庭的(定量传递不平衡检验)方法,以及基因与基因(GxG)相互作用(广义多因素维度还原和 GEE)的检验。
单 SNP 分析确定了 EDN1 中几个 SNP 与钾补充对 BP 反应的多个指标之间存在显著关联。这些与 BP 反应呈显著相关的 EDN1 次要等位基因的累积效应使 BP 反应的各项指标降低了 0.5-0.9mmHg。我们发现 EDN1 和 SELE 之间的 GxG 相互作用存在显著影响的证据,即使在 SELE 变异体没有单独关联的情况下也是如此。
我们的研究结果表明,EDN1 和 SELE 的变异性是影响钾摄入对 BP 反应的遗传因素。尽管此类流行病学研究不能直接确定生理机制,但我们的联合效应研究结果表明,EDN1 和 SELE 是功能研究的目标,以确定它们在钾摄入对 BP 反应中的相互作用。