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机构地区:[1]中山医科大学附属第一医院内分泌科
出 处:《中华内分泌代谢杂志》1997年第4期229-232,共4页Chinese Journal of Endocrinology and Metabolism
摘 要:我们观察了羟甲基戊二酰辅酶A(HMGCoA)还原酶抑制剂乐瓦停对31例胆固醇增高的2型糖尿病病人的降胆固醇作用,结果显示每日睡前服乐瓦停20mg,3个月后平均降低血清总胆固醇30.5%、低密度脂蛋白胆固醇29.8%,并对高密度脂蛋白胆固醇降低者有升高其高密度脂蛋白胆固醇的作用;同时也有明显的降低载脂蛋白B100(P<0.01)和载脂蛋白CIII(P<0.05)的作用,但对载脂蛋白AI与载脂蛋白AII水平无影响。在观察期间未发现对血糖与糖基化血红蛋白A1c有影响,提示在2型糖尿病病人中。The effect of lovastatin, a potent inhibitor of 3_hydroxy_3_methylglutaryl_coenzyme A reductase was assessed in 31 type 2 diabetes mellitus patients with moderate elevation of plasma cholesterol. Each patient received 20mg of lovastatin peroral daily for 3 months. The results showed that lovastatin reduced total cholesterol by 30.5% and low_density lipoprotein cholesterol (LDL_C) by 29.8%. Lovastatin therapy also reduced apolipoprotein B100 and apolipoprotein CIII and elevated high_density lipoprotein cholesterol level in type 2 diabetes mellitus patients with hypohigh_density lipoprotein cholesterol and glycemic control was well_maintained. However, Lovastatin had no effect on apolipoprotein AI and apolipoprotein AII. No side effects or abnormalities in serum hepatic enzyme concentration or CPK were noted during short_term lovastatin therapy. The data suggest that lovastatin has beneficial effect to decrease plasma cholesterol level in patients with type 2 diabetes mellitus.
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