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首页> 外文期刊>Heart and vessels: An international journal >Impact of decreased insulin resistance by ezetimibe on postprandial lipid profiles and endothelial functions in obese, non-diabetic-metabolic syndrome patients with coronary artery disease
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Impact of decreased insulin resistance by ezetimibe on postprandial lipid profiles and endothelial functions in obese, non-diabetic-metabolic syndrome patients with coronary artery disease

机译:ezetimibe对血液后脂质谱对肥胖后脂质曲线和内皮功能的影响,非糖尿病代谢综合征患者冠状动脉疾病患者的影响

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The association between insulin resistance and lipid dysmetabolism after consuming a meal is unclear. We aimed at assessing the effects of ezetimibe on postprandial hyperlipidemia and hyperinsulinemia and to find out whether the medication improves endothelial function in obese metabolic syndrome (MetS) patients with coronary artery disease (CAD). We obtained oral fat loading test results (4 and 6 h after load) and brachial flow-mediated vasodilation (FMD) measurements before and 24 weeks after ezetimibe treatment initiation from 27 MetS patients with CAD and from 68 control patients with CAD alone. Serum triglyceride (TG) and insulin levels (2 h after the loading dose) were significantly higher in MetS patients than in control patients. The incremental areas under the curve (iAUCs) for these levels decreased significantly after ezetimibe treatment in MetS patients but not in control patients. Treatment with ezetimibe resulted in significant FMD changes in MetS patients (from 3.4 to 4.9%, P = 0.002), but not in control patients (from 5.1 to 5.4%, P = 0.216). When MetS patients were divided into two groups based on the median insulin iAUC reduction rate (higher group >= 34%, n = 14; lower group < 34%, n = 13), those in the higher group showed a significantly higher rate of change in the iAUCs of TG and FMD than those in the lower group (TG, 31.0% vs. 10.8%; P = 0.033; FMD, 39.2% vs. 9.8%; P = 0.037). These results suggest that ezetimibe may reverse insulin resistance, reducing lipid dysmetabolism after a meal and endothelial dysfunction in MetS patients with CAD.
机译:胰岛蛋白抗性和脂质多蛋白蛋白酶消耗后的关联尚不清楚。我们旨在评估ezetimibe对餐后高脂血症和高胰岛素血症的影响,并了解药物是否改善肥胖代谢综合征(Mets)冠状动脉疾病患者的内皮功能(CAD)。我们在ezetimibe治疗开始于27名METS患者和单独的CAD 68患者之前,获得口服脂肪加载试验结果(载荷后的载荷后4和6小时)和肱骨介导的血管介导的血管介导的血管介导(FMD)测量。血清甘油三酯(Tg)和胰岛素水平(在载入剂量后2小时)在METS患者中显着高于对照患者。在Metss患者的ezetimibe治疗后,这些水平下的曲线(IAC)下的增量区域显着下降,但不控制患者。鉴定欧元治疗导致Mets患者的显着FMD变化(从3.4〜4.9%,P = 0.002),但不在对照患者(从5.1〜5.4%,P = 0.216)。当METS患者基于中位胰岛素IAC IAC的还原率(高于= 34%)分为两组时(= 34%,N = 14;低群<34%,N = 13),那些在更高组中的那些表现出显着更高的速率TG和FMD的IAC的变化比下组(TG,31.0%与10.8%; P = 0.033; FMD,39.2%与9.8%; P = 0.037)。这些结果表明,依泽替米贝可能会逆转胰岛素抵抗,降低膳食和CAD患者的膳食和内皮功能障碍后降低脂质多蛋白酶。

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