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Association of the G protein beta3 subunit T allele with insulin resistance in essential hypertension.

机译:在原发性高血压中,G蛋白beta3亚基T等位基因与胰岛素抵抗相关。

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A polymorphism (C825T) in the gene encoding the G protein beta3 subunit (GNB3) has recently been associated with hypertension and obesity in several populations. The aim of the study was to analyse the relationship between this polymorphism and insulin sensitivity, an hypothesised unifying factor for hypertension and obesity. One hundred thirty unrelated patients with essential hypertension, 70 female and 60 male, aged 58 +/- 1 years with systolic blood pressure of 173 +/- 2 mm Hg and diastolic blood pressure of 105 +/- 1 mm Hg, were genotyped for the GNB3 polymorphism by PCR and restriction digestion with BseDI, and classified in two groups according to the genotypes CC and CT + TT. Body mass index (BMI) was significantly higher in patients with the T allele as compared with patients without the T allele (29.3 +/- 0.4 vs. 26.7 +/- 0.6 kg/m2, p<0.001). On the contrary, there were no differences in the level of systolic or diastolic blood pressure among the genotypes. Insulin sensitivity was measured in a subgroup of 35 patients by means of an euglycemic hyperinsulinemic clamp test. In this subgroup, patients with the T allele displayed lower insulin sensitivity index (1.6 +/- 0.3 vs. 2.7 +/- 0.3 mg/kg/min, p = 0.022), higher fasting serum insulin (121 +/- 16 vs. 77 +/- 11 pmol/L, p = 0.032), higher serum glucose 120 min after 75 g load (9.8 +/- 1.2 vs. 7.0 +/- 0.5 mmol/L, p = 0.038), and higher glycosilated haemoglobin (5.7 +/- 0.4 vs. 4.7 +/- 0.2%; p = 0.042) as compared with patients without the T allele. A regression analysis showed that the association between the T allele and insulin sensitivity was independent of BMI (beta coefficient -0.386, p = 0.022). These results suggest a relationship between the 825T allele of GNB3 and insulin resistance in the essential hypertensive patients studied, which seems to be independent of BMI.
机译:最近,在一些人群中,编码G蛋白beta3亚基(GNB3)的基因中的多态性(C825T)与高血压和肥胖有关。该研究的目的是分析这种多态性与胰岛素敏感性之间的关系,胰岛素敏感性是假设的高血压和肥胖的统一因素。对133例原发性高血压无关患者,70名女性和60名男性,年龄58 +/- 1岁,收缩压为173 +/- 2 mm Hg,舒张压为105 +/- 1 mm Hg。通过PCR和BseDI的限制性酶切鉴定发现GNB3多态性,并根据基因型CC和CT + TT分为两类。具有T等位基因的患者的体重指数(BMI)与没有T等位基因的患者相比明显更高(29.3 +/- 0.4 vs. 26.7 +/- 0.6 kg / m2,p <0.001)。相反,基因型之间的收缩压或舒张压水平没有差异。在35名患者的亚组中,通过正常血糖高胰岛素钳夹试验测量了胰岛素敏感性。在该亚组中,T等位基因患者的胰岛素敏感性指数较低(1.6 +/- 0.3 vs. 2.7 +/- 0.3 mg / kg / min,p = 0.022),空腹血清胰岛素较高(121 +/- 16vs。 77 +/- 11 pmol / L,p = 0.032),75 g负荷后120分钟时血糖升高(9.8 +/- 1.2 vs. 7.0 +/- 0.5 mmol / L,p = 0.038),糖化血红蛋白更高(与没有T等位基因的患者相比,5.7 +/- 0.4 vs. 4.7 +/- 0.2%; p = 0.042)。回归分析显示,T等位基因与胰岛素敏感性之间的关联与BMI无关(β系数-0.386,p = 0.022)。这些结果表明,在研究的原发性高血压患者中,GNB3的825T等位基因与胰岛素抵抗之间存在相关性,这似乎与BMI无关。

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