Lewis S J, Sacks F M, Mitchell J S, East C, Glasser S, Kell S, Letterer R, Limacher M, Moye L A, Rouleau J L, Pfeffer M A, Braunwald E
Legacy Good Samaritan Hospital, Portland Cardiovascular Institute, Oregon, USA.
J Am Coll Cardiol. 1998 Jul;32(1):140-6. doi: 10.1016/s0735-1097(98)00202-2.
We sought to determine the effect of pravastatin on recurrent cardiovascular events in women with average cholesterol levels after myocardial infarction (MI).
Little information is available on the effectiveness of lipid lowering in secondary prevention of coronary heart disease (CHD) in women; in particular, those with CHD and average cholesterol levels.
In the Cholesterol and Recurrent Events (CARE) trial, 576 postmenopausal women, between 3 and 20 months after MI, with a total cholesterol level <240 mg/dl and a low density lipoprotein cholesterol level 115 to 174 mg/dl, were randomized to receive pravastatin 40 mg/day or matching placebo for a median follow-up period of 5 years. The main outcome measures were combined coronary events (coronary death, nonfatal MI, percutaneous transluminal coronary angioplasty [PTCA] or coronary artery bypass graft surgery [CABG]), the primary trial end point (coronary death or nonfatal MI) and stroke.
Women treated with pravastatin had a risk reduction of 43% for the primary end point (p = 0.035), 46% for combined coronary events (p = 0.001), 48% for PTCA (p = 0.025), 40% for CABG (p = 0.14) and 56% for stroke (p = 0.07). The 3,583 men in the CARE trial also showed a reduction in risk, but the magnitude tended to be less. Pravastatin improved plasma lipids similarly in men and women. There were no differences in risk of coronary events in the placebo group between men and women. Minor differences between men and women were present in baseline characteristics and treatment for MI, in general, conferring a higher risk status and a lower incidence of CABG in the women.
Pravastatin led to significant early reduction of a wide range of cardiovascular events in post-MI women with average cholesterol levels.
我们试图确定普伐他汀对心肌梗死(MI)后胆固醇水平正常的女性复发性心血管事件的影响。
关于女性冠心病(CHD)二级预防中降脂治疗有效性的信息较少;特别是那些患有冠心病且胆固醇水平正常的女性。
在胆固醇与复发性事件(CARE)试验中,576名绝经后女性在心肌梗死后3至20个月,总胆固醇水平<240mg/dl且低密度脂蛋白胆固醇水平为115至174mg/dl,被随机分为接受普伐他汀40mg/天或匹配的安慰剂治疗,中位随访期为5年。主要结局指标为联合冠状动脉事件(冠状动脉死亡、非致命性心肌梗死、经皮腔内冠状动脉成形术[PTCA]或冠状动脉旁路移植术[CABG])、主要试验终点(冠状动脉死亡或非致命性心肌梗死)和中风。
接受普伐他汀治疗的女性主要终点风险降低43%(p = 0.035),联合冠状动脉事件风险降低46%(p = 0.001),PTCA风险降低48%(p = 0.025),CABG风险降低40%(p = 0.14),中风风险降低56%(p = 0.07)。CARE试验中的3583名男性也显示风险降低,但降低幅度往往较小。普伐他汀对男性和女性的血脂改善相似。安慰剂组中男性和女性的冠状动脉事件风险没有差异。男性和女性在基线特征和心肌梗死治疗方面存在微小差异,总体而言,女性具有更高的风险状态和更低的CABG发生率。
普伐他汀可使心肌梗死后胆固醇水平正常的女性早期显著减少多种心血管事件。