Cheng-Lai Angela
Department of Pharmacy, Montefiore Medical Center, Bronx, New York 10461, USA.
Heart Dis. 2003 Jan-Feb;5(1):72-8. doi: 10.1097/01.HDX.0000050417.89309.F8.
Because of their excellent tolerability and their positive impact on lipid parameters, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) have become the drugs of first choice for many patients with dyslipidemia. Rosuvastatin is an investigational statin in the U.S. with a number of favorable characteristics, which include low lipophilicity, high hepatocyte selectivity, minimal metabolism, and a low propensity for cytochrome P450 drug interactions. Rosuvastatin has been studied at doses ranging from 1 to 80 mg. In comparative clinical trials, rosuvastatin given at 5 to 10 mg/day reduced low-density lipoprotein cholesterol to a significantly greater extent than atorvastatin 10 mg/day, pravastatin 20 mg/day, and simvastatin 20 mg/day. In addition, rosuvastatin exhibited beneficial effects on other lipid parameters such as high-density lipoprotein cholesterol and triglycerides. Rosuvastatin's safety profile was demonstrated to be similar to those of other statins. Given its favorable pharmacokinetic and pharmacodynamic characteristics, rosuvastatin is likely to become a valuable addition to the statin drug class. The author reviews the pharmacologic and pharmacokinetic properties of this new statin.
由于其出色的耐受性以及对脂质参数的积极影响,3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂(他汀类药物)已成为许多血脂异常患者的首选药物。瑞舒伐他汀在美国是一种处于研究阶段的他汀类药物,具有许多有利特性,包括低亲脂性、高肝细胞选择性、最小限度的代谢以及细胞色素P450药物相互作用的可能性低。瑞舒伐他汀已在1至80毫克的剂量范围内进行了研究。在比较临床试验中,每天服用5至10毫克的瑞舒伐他汀比每天服用10毫克的阿托伐他汀、20毫克的普伐他汀和20毫克的辛伐他汀能更显著地降低低密度脂蛋白胆固醇。此外,瑞舒伐他汀对其他脂质参数如高密度脂蛋白胆固醇和甘油三酯也有有益作用。瑞舒伐他汀的安全性与其他他汀类药物相似。鉴于其有利的药代动力学和药效学特性,瑞舒伐他汀很可能成为他汀类药物类别中的一种有价值的补充药物。作者综述了这种新型他汀类药物的药理和药代动力学特性。