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阿托伐他汀。其在高脂血症管理中的药理学及治疗潜力综述。

Atorvastatin. A review of its pharmacology and therapeutic potential in the management of hyperlipidaemias.

作者信息

Lea A P, McTavish D

机构信息

Adis International Limited, Auckland, New Zealand.

出版信息

Drugs. 1997 May;53(5):828-47. doi: 10.2165/00003495-199753050-00011.

Abstract

Atorvastatin is a synthetic HMG-CoA reductase inhibitor which lowers plasma cholesterol levels by inhibiting endogenous cholesterol synthesis. It also reduces triglyceride levels through an as yet unproven mechanism. Dose-dependent reductions in total cholesterol, low density lipoprotein (LDL)-cholesterol and triglyceride levels have been observed with atorvastatin in patients with hypercholesterolaemia and in patients with hypertriglyceridaemia. In large trials involving patients with hypercholesterolaemia, atorvastatin produced greater reductions in total cholesterol, LDL-cholesterol, apolipoprotein B and triglyceride levels than lovastatin, pravastatin and simvastatin. In patients with primary hypercholesterolaemia, the combination of atorvastatin and colestipol tended to produce larger reductions in LDL-cholesterol levels and smaller reductions in triglyceride levels than atorvastatin monotherapy. Although atorvastatin induced smaller reductions in triglyceride levels and more modest increases in high density lipoprotein (HDL)-cholesterol levels than either fenofibrate or nicotinic acid in patients with combined hyperlipidaemia, it produced larger reductions in total cholesterol and LDL-cholesterol. As with other HMG-CoA reductase inhibitors, the most frequently reported adverse events associated with atorvastatin are gastrointestinal effects. In comparative trials, atorvastatin had a similar adverse event profile to that of other HMG-CoA reductase inhibitors. Clinical data with atorvastatin are limited at present. However, with its ability to markedly reduce LDL-cholesterol levels, atorvastatin is likely to join other members of its class as a first-line agent for the treatment of patients with hypercholesterolaemia, if changes in lipid levels with atorvastatin convert to reductions in CHD mortality and morbidity. Atorvastatin may be particularly suitable for patients with heterozygous or homozygous familial hypercholesterolaemia because of the marked reductions in LDL-cholesterol experienced with the drug. Additionally, because of its triglyceride-lowering properties, atorvastatin appears to have the potential to become an appropriate treatment for patients with combined hyperlipidaemia or hypertriglyceridaemia.

摘要

阿托伐他汀是一种合成的HMG-CoA还原酶抑制剂,通过抑制内源性胆固醇合成来降低血浆胆固醇水平。它还通过一种尚未得到证实的机制降低甘油三酯水平。在高胆固醇血症患者和高甘油三酯血症患者中,已观察到阿托伐他汀可使总胆固醇、低密度脂蛋白(LDL)胆固醇和甘油三酯水平呈剂量依赖性降低。在涉及高胆固醇血症患者的大型试验中,阿托伐他汀在降低总胆固醇、LDL胆固醇、载脂蛋白B和甘油三酯水平方面比洛伐他汀、普伐他汀和辛伐他汀更有效。在原发性高胆固醇血症患者中,与阿托伐他汀单药治疗相比,阿托伐他汀与考来替泊联合使用往往能更大程度地降低LDL胆固醇水平,而降低甘油三酯水平的幅度较小。在混合性高脂血症患者中,尽管阿托伐他汀降低甘油三酯水平的幅度小于非诺贝特或烟酸,且使高密度脂蛋白(HDL)胆固醇水平升高的幅度较小,但它降低总胆固醇和LDL胆固醇的幅度更大。与其他HMG-CoA还原酶抑制剂一样,与阿托伐他汀相关的最常见不良事件是胃肠道反应。在比较试验中,阿托伐他汀的不良事件谱与其他HMG-CoA还原酶抑制剂相似。目前关于阿托伐他汀的临床数据有限。然而,如果阿托伐他汀引起的血脂变化能转化为冠心病死亡率和发病率的降低,那么由于其能够显著降低LDL胆固醇水平,阿托伐他汀可能会与该类药物的其他成员一样,成为治疗高胆固醇血症患者的一线药物。由于阿托伐他汀可使LDL胆固醇显著降低,它可能特别适用于杂合子或纯合子家族性高胆固醇血症患者。此外,由于其降低甘油三酯的特性,阿托伐他汀似乎有可能成为混合性高脂血症或高甘油三酯血症患者的合适治疗药物。

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