ASSOCIATION OF GENOTYPES OF POLYMORPHISM NOS3 WITH MACROANGIOPATHIES IN PATIENTS WITH HYPERTONIC DISEASE COMBINED WITH TYPE 2 DIABETES MELLITUS

E. Shorikov, D. Shorikova, O. Khukhlina, V. O. Shuper, I. Trefanenko
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Abstract

The purpose - to study the probability of association of genotypes of polymorphism NOS3 with macroangiopathies in patients with artherial hypertension (AH) with type 2 diabetes mellitus (DM). Material and methods . 100 patients with AH and type 2 DM and were examined. In all persons the lesions of the arteries of mixed type were verified. The alleles of the polymorphic sites of the synthetase gene of nitric oxide 3 (NOS3, Gene ID: 4846, locus-7q36, polymorphism -786T> C transversion, dbSNP-rs2070744) were studied. Results. The distribution of genotypes NOS3 polymorphism in AG and DM2 group characterized by a probable deviation from the Hardy-Weinberg equilibrium (p<0.01). In monolocal analysis of NOS3 alleles and genotypes with risk of macroangiopathy, a significant difference was found (p <0.05). The allele -786C associated with an increased risk (2.55) of mixed-type vascular lesions vs. control group (OR = 4,27; 95% CI=1,86 - 9.77; p<0.05). It was set decreased (4,46 times) frequency of protective allele -786T in AG and DM 2 (p<0.05), and homozygous "risk" allele C (2 times) vs. control group (95% CI=0.10-0,50; p<0.05). Conclusions. It was set the probable differences and decreased the frequency of "protective" alleles and genotypes in patients with hypertension and diabetes mellitus with macroangiopathy.
多态基因型nos3与高渗病合并2型糖尿病患者大血管病变的关系
目的:研究NOS3基因型多态性与2型糖尿病(DM)合并动脉性高血压(AH)患者大血管病变的相关性。材料和方法。对100例AH合并2型糖尿病患者进行了检查。所有患者均证实了混合型动脉病变。对一氧化氮3合成酶基因多态性位点(NOS3,基因ID: 4846,位点-7q36,多态性-786T> C翻转,dbSNP-rs2070744)的等位基因进行了研究。结果。AG和DM2组NOS3基因型多态性分布可能偏离Hardy-Weinberg平衡(p<0.01)。在大血管病变风险基因型和NOS3等位基因单区域分析中,差异有统计学意义(p <0.05)。与对照组相比,-786C等位基因与混合型血管病变风险增加(2.55)相关(OR = 4,27;95% ci =1,86 - 9.77;p < 0.05)。与对照组相比,保护性等位基因-786T和纯合子“危险”等位基因C的频率分别降低了4.46倍(p<0.05)和2倍(95% CI=0.10 ~ 0.50;p < 0.05)。结论。确定了高血压和糖尿病合并大血管病变患者“保护性”等位基因和基因型的可能差异,并降低了它们的频率。
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