首页> 外文期刊>BMC Medical Genetics >Correlation between gene polymorphism in angiotensin II type 1 receptor and type 2 diabetes mellitus complicated by hypertension in a population of Inner Mongolia
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Correlation between gene polymorphism in angiotensin II type 1 receptor and type 2 diabetes mellitus complicated by hypertension in a population of Inner Mongolia

机译:血管紧张素II型受体基因多态性与内蒙古群中高血压复杂化的基因多态性与2型糖尿病

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The role of angiotensin II type 1 receptor (AT1R) as a key player in type 2 diabetes mellitus (T2DM) complicated with hypertension remains controversial. The present case-control study systematically investigated the association between gene the correct variation type in the angiotensin II type 1 receptor (AT1R) gene and type 2 diabetes mellitus complicated with hypertension in the Han population from the Inner Mongolia region, China. Here, state which variants were analysis, including age, occupation, triglyceride, systolic, diastolic, sex, culture, marital status, smoking, alcohol, BMI (body mass index), SBP (systolic blood pressure), DBP (diastolic blood pressure), TG (triglyceride), TC (total cholesterol), HDL-C (high-density lipoprotein cholesterol), LDL-C (low-density lipoprotein cholesterol), FPG (fasting plasma glucose). Genomic DNA was extracted from samples from 202 type 2 diabetic patients with hypertension and 216 type 2 diabetic patients without hypertension. Non-conditional regression analysis showed that in comparison with the TT genotype, the presence of the CC genotype for the T573 site of the AT1R gene increased the risk for diabetes mellitus complicated with hypertension by 3.219-fold (OR?=?3.219, 95% CI: 1.042–9.941, P?=?0.042). The results from multivariate linear regression analysis suggested the rs5182 polymorphism in the AT1R gene to be associated with diastolic blood pressure (P?=?0.032). No other associations were found between the incidence of disease and the correct variation type at other sites of the AT1R gene. Our results suggest that the rs5182 polymorphism in the AT1R gene is associated with diabetes complicated by hypertension in the Han population of Inner Mongolia.
机译:血管紧张素II型的作用1受体(AT1R)作为2型糖尿病(T2DM)的关键球员复杂的高血压仍然存在争议。本病例对照研究系统地研究了基因之间的血管紧张素II型受体(AT1R)基因中的正确变异类型和2型糖尿病,以及来自中国内蒙古地区的汉族人口的高血压和2型糖尿病。在此,调节哪种变体分析,包括年龄,职业,甘油三酯,收缩,舒张,性别,培养,婚姻状况,吸烟,酒精,BMI(体重指数),SBP(收缩压),DBP(舒张压血压) ,Tg(甘油三酯),Tc(总胆固醇),HDL-C(高密度脂蛋白胆固醇),LDL-C(低密度脂蛋白胆固醇),FPG(空腹血浆葡萄糖)。从202型2型糖尿病患者的样品中提取基因组DNA,其高血压和216型糖尿病患者没有高血压。非条件性回归分析表明,与TT基因型相比,AT1R基因T573位点的CC基因型的存在增加了糖尿病的风险,使高血压复杂3.219倍(或?= 3.219,95% CI:1.042-9.941,p?= 0.042)。多变量线性回归分析的结果表明AT1R基因中的RS5182多态性与舒张压有关(P?= 0.032)。在AT1R基因的其他网站的疾病发病率和正确的变异类型之间没有发现其他关联。我们的研究结果表明,AT1R基因中的RS5182多态性与内蒙古汉族人群高血压复杂的糖尿病有关。

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