Bang Lynne M, Goa Karen L
Adis International Limited, Auckland, New Zealand.
Drugs Aging. 2003;20(14):1061-82. doi: 10.2165/00002512-200320140-00005.
Pravastatin (Pravachol) is a competitive, reversible HMG-CoA reductase inhibitor that lowers serum cholesterol levels by inhibiting de novo cholesterol synthesis and has antiatherogenic effects that appear to be partially independent of its lipid-lowering effects. Pravastatin 10-40 mg/day produced significant reductions (vs baseline or placebo) in serum total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) levels in elderly patients (aged >or=60 or >or= 65 years) with hypercholesterolaemia or normal cholesterol levels. Serum triglyceride and high-density lipoprotein cholesterol levels also improved in some studies, but not in others. Coadministration of cholestyramine, another lipid-lowering agent, further enhanced the lipid-lowering effects of pravastatin in elderly patients. Data from the large, long-term (3-6 years) PROspective Study Of Pravastatin in the Elderly at Risk (PROSPER), Cholesterol And Recurrent Events trial (CARE) and Long term Intervention with Pravastatin in Ischaemic Disease (LIPID) trials demonstrated that pravastatin 40 mg/day reduces coronary events in elderly patients with hypercholesterolaemia or normal cholesterol levels, with or at high risk of developing coronary heart disease (CHD). In these trials, the incidence of death from CHD or the combined endpoint of death from CHD or nonfatal myocardial infarction was significantly lower in pravastatin than in placebo recipients. Pravastatin is well tolerated in the elderly, and adverse effects considered related to therapy are minimal. The most commonly occurring adverse events included gastrointestinal events, renal or genital system events, respiratory disorders, headaches and musculoskeletal pain.
Pravastatin effectively lowers serum TC and LDL-C levels and, as demonstrated in major clinical outcome trials, reduces coronary events in elderly patients with hypercholesterolaemia or normal cholesterol levels. Pravastatin is well tolerated and as such should be considered a first-line agents for primary or secondary prevention in older individuals with evident CHD or multiple risk factors for CHD.
普伐他汀(普拉固)是一种竞争性、可逆性的HMG-CoA还原酶抑制剂,通过抑制胆固醇的从头合成来降低血清胆固醇水平,并且具有抗动脉粥样硬化作用,这种作用似乎部分独立于其降脂作用。对于患有高胆固醇血症或胆固醇水平正常的老年患者(年龄≥60岁或≥65岁),每天服用10 - 40毫克普伐他汀可使血清总胆固醇(TC)和低密度脂蛋白胆固醇(LDL-C)水平显著降低(与基线或安慰剂相比)。在一些研究中,血清甘油三酯和高密度脂蛋白胆固醇水平也有所改善,但在其他研究中并非如此。同时服用另一种降脂药物考来烯胺,可进一步增强普伐他汀在老年患者中的降脂效果。来自大型长期(3 - 6年)的老年高危人群普伐他汀前瞻性研究(PROSPER)、胆固醇与再发事件试验(CARE)以及缺血性疾病普伐他汀长期干预试验(LIPID)的数据表明,每天服用40毫克普伐他汀可降低患有高胆固醇血症或胆固醇水平正常、有或有发展为冠心病(CHD)高风险的老年患者的冠心病事件。在这些试验中,普伐他汀组中因冠心病死亡或冠心病死亡与非致命性心肌梗死联合终点的发生率显著低于安慰剂组。普伐他汀在老年人中耐受性良好,与治疗相关的不良反应极少。最常见的不良事件包括胃肠道事件、肾脏或生殖系统事件、呼吸系统疾病、头痛和肌肉骨骼疼痛。
普伐他汀可有效降低血清TC和LDL-C水平,并且如主要临床结局试验所示,可降低患有高胆固醇血症或胆固醇水平正常的老年患者的冠心病事件。普伐他汀耐受性良好,因此应被视为患有明显冠心病或有多个冠心病危险因素的老年个体进行一级或二级预防的一线药物。