Mol M J, Erkelens D W, Gevers Leuven J A, Schouten J A, Stalenhoef A F
Department of Internal Medicine, University Hospital, Nijmegen, The Netherlands.
Atherosclerosis. 1988 Feb;69(2-3):131-7. doi: 10.1016/0021-9150(88)90006-8.
Simvastatin (MK-733), a new inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, was administered to 38 patients with heterozygous familial hypercholesterolaemia for 24 weeks. A dose of 40 mg per day produced a mean reduction in low density lipoprotein cholesterol of 43-45% and in triglycerides of 21-31%. Mean high density lipoprotein cholesterol increased significantly by 10-13%. There were no major differences in response whether the drug was taken in one or two doses. MK-733 was tolerated well. Adverse effects were infrequent and limited to slight increases of alanine aminotransferase, creatine phosphokinase and bilirubin. This drug appears to be a potent inhibitor of cholesterol synthesis and has produced the largest therapeutic response as monotherapy in patients with familial hypercholesterolaemia.
辛伐他汀(MK - 733)是一种新型3 - 羟基 - 3 - 甲基戊二酰辅酶A还原酶抑制剂,对38例杂合子家族性高胆固醇血症患者进行了为期24周的治疗。每日40毫克的剂量使低密度脂蛋白胆固醇平均降低43% - 45%,甘油三酯降低21% - 31%。高密度脂蛋白胆固醇平均显著升高10% - 13%。无论该药是分一次还是两次服用,疗效均无重大差异。MK - 733耐受性良好。不良反应很少,仅限于丙氨酸转氨酶、肌酸磷酸激酶和胆红素略有升高。这种药物似乎是胆固醇合成的有效抑制剂,作为家族性高胆固醇血症患者的单一疗法产生了最大的治疗反应。