Yoshikawa Yukie, Nakayama Tomohiro, Saito Kosuke, Hui Peng, Morita Akihiko, Sato Naoyuki, Takahashi Teruyuki, Tamura Masaaki, Sato Ichiro, Aoi Noriko, Doba Nobutaka, Hinohara Shigeaki, Soma Masayoshi, Usami Ron
Division of Molecular Diagnostics, Department of Advanced Medical Science, Nihon University School of Medicine, Tokyo, Japan.
Hypertens Res. 2007 Sep;30(9):789-96. doi: 10.1291/hypres.30.789.
Uroguanylin (gene name: guanylate cyclase activator 2B, GUCA2B) is a peptide regulator of intestinal salt and water transport. It has been reported that the uroguanylin knockout mouse exhibits elevated blood pressure. Therefore, the GUCA2B gene is thought to be a susceptibility gene for essential hypertension (EH). Despite extensive studies, however, the relationship between the GUCA2B gene and EH has not yet been defined. The aim of this study was to assess the association between the human GUCA2B gene and EH. Using four single nucleotide polymorphisms (SNPs), we conducted a genetic association study in 281 EH patients and 279 age-matched normotensive (NT1) individuals. To derive more reliable data, we performed a duplicate case-control study in which we recruited another normotensive group (NT2). There was no significant difference in the overall distribution of alleles for any of the SNPs between the EH and NT1 groups, or between the EH and NT2 groups. Therefore, these four SNPs cannot be the genetic markers for EH. The occurrences of the C-A haplotype (rs883062-rs1047047) and the C-A-G haplotype (rs883062-rs1047047-rs2297566) were significantly higher in the EH group than in the NT1 group (p<0.0001) or the NT2 group (p<0.0001). These results suggest that the C-A haplotype and the C-A-G haplotype of the GUCA2B gene are the genetic markers for EH, and that GUCA2B or a neighboring gene might be a susceptibility gene for EH.
尿鸟苷素(基因名称:鸟苷酸环化酶激活剂2B,GUCA2B)是肠道盐和水转运的一种肽调节剂。据报道,尿鸟苷素基因敲除小鼠的血压会升高。因此,GUCA2B基因被认为是原发性高血压(EH)的一个易感基因。然而,尽管进行了广泛研究,但GUCA2B基因与EH之间的关系尚未明确。本研究的目的是评估人类GUCA2B基因与EH之间的关联。我们利用四个单核苷酸多态性(SNP),对281例EH患者和279例年龄匹配的血压正常(NT1)个体进行了基因关联研究。为了获得更可靠的数据,我们进行了一项重复病例对照研究,招募了另一个血压正常组(NT2)。在EH组与NT1组之间,以及EH组与NT2组之间,任何一个SNP的等位基因总体分布均无显著差异。因此,这四个SNP不能作为EH的遗传标记。EH组中C-A单倍型(rs883062-rs1047047)和C-A-G单倍型(rs883062-rs1047047-rs2297566)的出现频率显著高于NT1组(p<0.0001)或NT2组(p<0.0001)。这些结果表明,GUCA2B基因的C-A单倍型和C-A-G单倍型是EH的遗传标记,并且GUCA2B或其邻近基因可能是EH的一个易感基因。