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首页> 外文期刊>Metabolism: Clinical and Experimental >Intensive insulin therapy reduces small dense low-density lipoprotein particles in patients with type 2 diabetes mellitus: relationship to triglyceride-rich lipoprotein subspecies.
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Intensive insulin therapy reduces small dense low-density lipoprotein particles in patients with type 2 diabetes mellitus: relationship to triglyceride-rich lipoprotein subspecies.

机译:强化胰岛素治疗可减少2型糖尿病患者中小的致密的低密度脂蛋白颗粒:与富含甘油三酸酯的脂蛋白亚种的关系。

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It remains unclear whether insulin improves dyslipidemia in patients with type 2 diabetes mellitus. Small dense low-density lipoprotein (sd-LDL) particles are recognized as a powerful risk factor for coronary heart disease and are often elevated in type 2 diabetes mellitus. We examined the effect of intensive insulin therapy on sd-LDL particles and triglyceride (TG)-rich lipoprotein subspecies. Intensive insulin therapy (insulin aspart [NovoRapid, Tokyo, Japan] before each meal and isophane insulin suspension at bedtime) was given to poorly controlled type 2 diabetic patients (n = 46) who were on high doses of sulfonylureas. Fasting serum samples were collected before and 14 days after the commencement of insulin therapy. Low-density lipoprotein size was measured by gradient gel electrophoresis, and the small dense LDL cholesterol (sd-LDL-C) concentration was measured by a new precipitation method. Chylomicrons (Svedberg flotation unit >400), very low-density lipoprotein 1 (VLDL1) (Sf, 60-400), and VLDL2 (Sf, 20-60) were separated by ultracentrifugation. Serum apolipoprotein B-48 and lipoprotein lipase levels were measured by the enzyme immunoassay method. Serum glucose and glycoalbumin levels were substantially decreased by insulin treatment. The LDL size increased (25.8-26.0 nm, P < .05) and the sd-LDL-C level was significantly reduced (44-34 mg/dL, P < .005). Apolipoproteins B-48 and C-III were decreased, whereas lipoprotein lipase was increased. Triglyceride levels in chylomicrons, VLDL1, and VLDL2 all showed a decrease. Changes of sd-LDL-C or LDL size were associated with changes of the TG levels in the major TG-rich lipoprotein subspecies. These results suggest that intensive insulin therapy decreases atherogenic sd-LDL particles by reducing TG in TG-rich lipoproteins. We did not find any specific relationship between VLDL1 and sd-LDL during insulin treatment.
机译:尚不清楚胰岛素是否能改善2型糖尿病患者的血脂异常。小而密集的低密度脂蛋白(sd-LDL)颗粒被认为是冠心病的重要危险因素,在2型糖尿病中通常升高。我们检查了强化胰岛素治疗对sd-LDL颗粒和富含甘油三酸酯(TG)的脂蛋白亚种的影响。强化胰岛素治疗(每餐前胰岛素门冬胰岛素[NovoRapid,东京,日本],就寝时间加异佛康胰岛素悬浮液)用于控制不佳的2型糖尿病患者(n = 46),他们接受大剂量的磺酰脲类药物治疗。在胰岛素治疗开始之前和之后的14天收集空腹血清样品。通过梯度凝胶电泳测量低密度脂蛋白的大小,并通过新的沉淀方法测量低密度LDL胆固醇(sd-LDL-C)的浓度。通过超速离心分离了乳糜微粒(Svedberg浮选单元> 400),极低密度脂蛋白1(VLDL1)(Sf,60-400)和VLDL2(Sf,20-60)。通过酶免疫法测定血清载脂蛋白B-48和脂蛋白脂肪酶的水平。胰岛素治疗可显着降低血清葡萄糖和糖蛋白水平。 LDL大小增加(25.8-26.0 nm,P <.05),并且sd-LDL-C水平显着降低(44-34 mg / dL,P <.005)。载脂蛋白B-48和C-III减少,而脂蛋白脂肪酶增加。乳糜微粒,VLDL1和VLDL2中的甘油三酸酯水平均降低。 sd-LDL-C或LDL大小的变化与富含TG的主要脂蛋白亚种中TG水平的变化有关。这些结果表明,强化胰岛素治疗可通过减少富含TG的脂蛋白中的TG来减少动脉粥样硬化sd-LDL颗粒。我们在胰岛素治疗期间未发现VLDL1和sd-LDL之间有任何特定关系。

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