Klimontov V V, Shevchenko V A, Bulumbaeva M D, Prokof 'ev F V, Konenkov I V
Scientific Institute of Clinical and Experimental Lymphology.
Kardiologiia. 2017 Aug;57(8):5-10. doi: 10.18087/cardio.2017.8.10011.
To examine associations between ischemic heart disease (IHD) and polymorphisms in cytokine genes (IL-1B, IL-4, IL-6, IL-10, TNFA, VEGF) and matrix metalloproteinase genes (MMP2, MMP3, MMP9) in patients with type 2 diabetes.
We studied 232 Caucasian diabetic subjects (33 men and 199 women aged 50-70 years). In 93 patients IHD was verified by treadmill test and/or coronary angiography (86 subjects with stable angina, 19 with previous myocardial infarction). Thirteen polymorphisms localized in the promoters of IL-1B (rs1143627), IL-4 (rs2243250), IL-6 (rs1800795), IL-10 (rs1800872, rs1800896), TNFA (rs361525, rs1800629, rs1800630), VEGF (rs699947, rs3025039), MMP2 (rs243865), MMP3 (rs3025058) and MMP9 (rs3918242) were investigated.
Prevalence of G-allele and GG-genotype at -308 position of TNFA (rs1800629), as well as C-allele and CC-genotype at position +936 of VEGF (rs3025039) was higher in patients with IHD as compared to patients without IHD (OR=2.0, OR=2.2, OR=2.1, OR=2.4, respectively, all p=0.02). In logistic regression analysis, TNFA -308 A/G and VEGF +936 C/T polymorphisms showed associations with IHD (both p=0.009). These polymorphisms along with age, body mass index, duration of diabetes, low density and high density lipoprotein cholesterol were associated with IHD in multivariate models (p=0.0002 and p=0.00008, respectively). Nine combinations of TNFA -308 GG-genotype and variants of other genes demonstrated associations with IHD (p≤0.002).
The polymorphisms in promoter regions of TNFA (rs1800629) and VEGF (rs3025039) are associated with IHD in patients with type 2 diabetes.
研究2型糖尿病患者缺血性心脏病(IHD)与细胞因子基因(IL-1B、IL-4、IL-6、IL-10、TNFA、VEGF)及基质金属蛋白酶基因(MMP2、MMP3、MMP9)多态性之间的关联。
我们研究了232名白种糖尿病患者(33名男性和199名女性,年龄50 - 70岁)。93例患者通过平板运动试验和/或冠状动脉造影确诊为IHD(86例稳定型心绞痛患者,19例既往有心肌梗死患者)。研究了位于IL-1B(rs1143627)、IL-4(rs2243250)、IL-6(rs1800795)、IL-10(rs1800872、rs1800896)、TNFA(rs361525、rs1800629、rs1800630)、VEGF(rs699947、rs3025039)、MMP2(rs243865)、MMP3(rs3025058)和MMP9(rs3918242)启动子区域的13种多态性。
与无IHD的患者相比,IHD患者中TNFA(rs1800629)-308位点的G等位基因和GG基因型以及VEGF(rs3025039)+936位点的C等位基因和CC基因型的患病率更高(OR分别为2.0、2.2、2.1、2.4,均p = 0.02)。在逻辑回归分析中,TNFA -308 A/G和VEGF +936 C/T多态性与IHD相关(均p = 0.009)。在多变量模型中,这些多态性连同年龄、体重指数、糖尿病病程、低密度和高密度脂蛋白胆固醇与IHD相关(分别p = 0.0002和p = 0.00008)。TNFA -308 GG基因型与其他基因变异的9种组合与IHD相关(p≤0.002)。
TNFA(rs1800629)和VEGF(rs3025039)启动子区域的多态性与2型糖尿病患者的IHD相关。