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首页> 外文期刊>Journal of human hypertension >Dysglycaemia in non-diabetic hypertensive patients: comparison of the impact of two different classifications of impaired fasting glucose on the cardiovascular risk profile.
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Dysglycaemia in non-diabetic hypertensive patients: comparison of the impact of two different classifications of impaired fasting glucose on the cardiovascular risk profile.

机译:非糖尿病高血压患者的血糖异常:两种不同分类的空腹血糖受损对心血管风险的影响比较。

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The clinical correlates and risk profile of prediabetes (fasting plasma glucose (FPG) values in the upper normal limits but below the diabetic threshold) in hypertension, an insulin-resistant, prodiabetogenic condition, are scarcely known. For this reason, we evaluated 982 non-diabetic (FPG,<126 mg 100 ml(-1) and no antidiabetic treatment) referred hypertensive patients without a history of cardiovascular disease grouped by mild (100-109 mg 100 ml(-1)) and advanced (110-125 mg 100 ml(-1)) dysglycaemia compared with normal FPG (<100 mg 100 ml(-1)). FPG, total and high density lipoprotein (HDL) cholesterol, triglycerides and total white blood cell count were assessed by standard methodologies; 10-year predicted coronary heart disease (CHD) risk was approximated by the Framingham risk score (FRS). Metabolic syndrome (MetS) was diagnosed by standard categorical criteria using either 110 or 100 mg 100 ml(-1) as a threshold for impaired fasting glucose (IFG). FPG was above 110 in 13% and between 100 and 109 in 20% of patients. In both dysglycaemic groups, perturbed glucose homeostasis was associated with abnormally high fasting triglycerides, low HDL cholesterol, obesity, worse CHD risk profile and higher white blood cell count. MetS was highly prevalent and its distribution pattern was markedly influenced by the definitions of IFG based on different FPG cutoffs. Thus, even mildly perturbed glucose homeostasis associates with atherogenic dyslipidaemia, obesity and adverse risk profile in non-diabetic hypertensive patients. Because of its prediabetic nature, dysglycaemia should prompt measures to prevent new-onset diabetes, although the role of IFG as an independent risk factor awaits specifically designed intervention trials.
机译:胰岛素抵抗,致糖尿病的高血压病前期糖尿病的临床相关性和风险特征(空腹血糖(FPG)值在正常上限但低于糖尿病阈值)几乎是未知的。因此,我们评估了982例无心血管疾病史的高血压非糖尿病患者(FPG,<126 mg 100 ml(-1),未进行抗糖尿病治疗),按轻度(100-109 mg 100 ml(-1))分组)和晚期(110-125 mg 100 ml(-1))的血糖异常,与正常FPG(<100 mg 100 ml(-1))相比。 FPG,总和高密度脂蛋白(HDL)胆固醇,甘油三酸酯和总白细胞计数通过标准方法进行评估; 10年预测的冠心病(CHD)风险通过Framingham风险评分(FRS)估算。代谢综合征(MetS)通过标准分类标准使用110或100 mg 100 ml(-1)作为空腹血糖受损(IFG)的阈值进行诊断。 FPG在13%的患者中高于110,在20%的患者中在100至109之间。在两个血糖不良组中,葡萄糖动态平衡异常与空腹高甘油三酯异常,低HDL胆固醇,肥胖,CHD危险性恶化和白细胞计数升高有关。 MetS非常流行,其分布模式受到基于不同FPG临界值的IFG定义的显着影响。因此,在非糖尿病性高血压患者中,即使是轻度扰动的葡萄糖稳态也与动脉粥样硬化性血脂异常,肥胖症和不良风险有关。由于其糖尿病前期性质,尽管IFG作为独立危险因素的作用正在等待专门设计的干预试验,但血糖过高应该提示采取措施预防新发糖尿病。

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