Ksiazek Piotr, Wojewoda Pawel, Muc Kamil, Buraczynska Monika
Laboratory for Molecular Diagnostics of Multifactorial Diseases, Department of Nephrology, University Medical School, Lublin, Poland.
Mol Diagn. 2003;7(2):119-23. doi: 10.1007/BF03260027.
Endothelial nitric oxide synthase (ecNOS) is a key regulator of vascular nitric oxide production. Polymorphism in intron 4 of the ecNOS gene is implicated in cardiovascular and renal diseases. We investigated a potential involvement of this polymorphism in the development of type 2 diabetes mellitus and its renal complications.
This preliminary study involved 410 individuals with type 2 diabetes and 330 healthy control subjects. From the diabetes group 178 patients had diabetic nephropathy. All subjects were genotyped for the ecNOS4 polymorphism by the polymerase chain reaction (PCR) followed by gel electrophoresis. Genotype and allele frequencies were compared between diabetes patients with and without nephropathy and the control group. All calculations were performed using the Statistical Package for the Social Sciences (SPSS, Inc., Chicago, IL, USA) for Windows 5.0. The chi-square test and Fisher's exact test were used for case-control comparisons. The Kruskal-Wallis test was used for the comparison of subgroups of patients with diabetes.
The analysis revealed that patients with diabetes, regardless of their nephropathy status, were significantly different in genotype distribution and 4a allele frequencies compared with controls (p < 0.05). The frequency of aa genotype was 8.2% in diabetic patients without nephropathy, 8.4% with those with nephropathy and 1.2% in controls. The 4a allele showed a significant effect on diabetic nephropathy, with odds ratio of 2.24 (95% confidence interval 1.12-3.40). There were no significant differences in the 4a allele frequency between the normotensive and hypertensive patients with diabetes.
Our results suggest that the ecNOS gene polymorphism can serve as a useful genetic marker of increased susceptibility to type 2 diabetes and its renal complications.
内皮型一氧化氮合酶(ecNOS)是血管一氧化氮生成的关键调节因子。ecNOS基因第4内含子的多态性与心血管疾病和肾脏疾病有关。我们研究了这种多态性在2型糖尿病及其肾脏并发症发生发展中的潜在作用。
这项初步研究纳入了410例2型糖尿病患者和330例健康对照者。糖尿病组中有178例患者患有糖尿病肾病。所有受试者均通过聚合酶链反应(PCR)结合凝胶电泳对ecNOS4多态性进行基因分型。比较了有和无肾病的糖尿病患者以及对照组之间的基因型和等位基因频率。所有计算均使用适用于Windows 5.0的社会科学统计软件包(SPSS,美国伊利诺伊州芝加哥市SPSS公司)进行。卡方检验和Fisher精确检验用于病例对照比较。Kruskal-Wallis检验用于糖尿病患者亚组的比较。
分析显示,无论肾病状态如何,糖尿病患者在基因型分布和4a等位基因频率方面与对照组相比均有显著差异(p < 0.05)。无肾病的糖尿病患者中aa基因型频率为8.2%,有肾病的糖尿病患者中为8.4%,对照组中为1.2%。4a等位基因对糖尿病肾病有显著影响,优势比为2.24(95%置信区间1.12 - 3.40)。糖尿病患者中血压正常者和高血压者的4a等位基因频率无显著差异。
我们的结果表明,ecNOS基因多态性可作为2型糖尿病及其肾脏并发症易感性增加的有用遗传标记。