Hayashi Toshiyuki, Hirano Tsutomu, Yamamoto Takeshi, Ito Yasuki, Adachi Mitsuru
First Department of Internal Medicine, Showa University School of Medicine, Shinagawa-ku, Tokyo 142-8666, Japan.
Metabolism. 2006 Jul;55(7):879-84. doi: 10.1016/j.metabol.2006.02.014.
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.
胰岛素是否能改善2型糖尿病患者的血脂异常仍不清楚。小而密的低密度脂蛋白(sd-LDL)颗粒被认为是冠心病的一个强大危险因素,并且在2型糖尿病患者中常常升高。我们研究了强化胰岛素治疗对sd-LDL颗粒和富含甘油三酯(TG)的脂蛋白亚类的影响。对46例使用大剂量磺脲类药物但血糖控制不佳的2型糖尿病患者给予强化胰岛素治疗(每餐饭前注射门冬胰岛素[NovoRapid,日本东京],睡前注射低精蛋白胰岛素混悬液)。在胰岛素治疗开始前和开始后14天采集空腹血清样本。通过梯度凝胶电泳测量低密度脂蛋白大小,通过一种新的沉淀法测量小而密的低密度脂蛋白胆固醇(sd-LDL-C)浓度。通过超速离心分离乳糜微粒(斯维德伯格漂浮单位>400)、极低密度脂蛋白1(VLDL1)(Sf,60 - 400)和VLDL2(Sf,20 - 60)。采用酶免疫分析法测量血清载脂蛋白B-48和脂蛋白脂肪酶水平。胰岛素治疗使血清葡萄糖和糖化白蛋白水平大幅降低。低密度脂蛋白大小增加(25.8 - 26.0 nm,P < 0.05),sd-LDL-C水平显著降低(44 - 34 mg/dL,P < 0.005)。载脂蛋白B-48和C-III降低,而脂蛋白脂肪酶增加。乳糜微粒、VLDL1和VLDL2中的甘油三酯水平均下降。sd-LDL-C或低密度脂蛋白大小的变化与主要富含TG的脂蛋白亚类中TG水平的变化相关。这些结果表明,强化胰岛素治疗通过降低富含TG的脂蛋白中的TG来减少致动脉粥样硬化的sd-LDL颗粒。我们未发现胰岛素治疗期间VLDL1和sd-LDL之间存在任何特定关系。