Kitsios Georgios D, Zintzaras Elias
Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Tufts University School of Medicine, 800 Washington Street, Tufts MC no. 63, Boston, MA 02111, USA.
Int J Hypertens. 2010 Mar 25;2010:865031. doi: 10.4061/2010/865031.
The endothelial nitric oxide synthase gene (NOS3) has been implicated in the development of hypertension, although the specific role of variants and haplotypes has not been clarified. In this study, the association of three polymorphisms (promoter T786C, intronic 4a/b, and nonsynonymous G894T) was tested in a case-control sample of 230 patients with essential hypertension and 306 healthy controls. Haplotype analysis was also performed. The mutant allele a(∗) of the 4a/b polymorphism showed a protective effect against hypertension under a dominant model (odds ratio = 0.64, 95% confidence interval (0.44-0.93)), although this effect was not significant after the adjustment for covariates (P = 0.06). The estimated frequency of the haplotype composed of the T786(∗), 4a(∗), and G894(∗) alleles was significantly higher in controls (5.5%) compared to cases (2%). These results indicate that although individual NOS3 polymorphisms are not associated with hypertension, a rare haplotype of the gene might be protective against the development of hypertension.
内皮型一氧化氮合酶基因(NOS3)被认为与高血压的发生有关,尽管其变异体和单倍型的具体作用尚未明确。在本研究中,我们在一个包含230例原发性高血压患者和306例健康对照的病例对照样本中,检测了三个多态性位点(启动子T786C、内含子4a/b和非同义G894T)的关联性。同时也进行了单倍型分析。在显性模型下,4a/b多态性的突变等位基因a()对高血压具有保护作用(优势比=0.64,95%置信区间(0.44 - 0.93)),尽管在对协变量进行调整后,这种效应并不显著(P = 0.06)。由T786()、4a()和G894()等位基因组成的单倍型在对照组中的估计频率(5.5%)显著高于病例组(2%)。这些结果表明,尽管单个NOS3多态性与高血压无关,但该基因的一种罕见单倍型可能对高血压的发生具有保护作用。