Plehn J F, Davis B R, Sacks F M, Rouleau J L, Pfeffer M A, Bernstein V, Cuddy T E, Moyé L A, Piller L B, Rutherford J, Simpson L M, Braunwald E
Section of Cardiology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Circulation. 1999 Jan 19;99(2):216-23. doi: 10.1161/01.cir.99.2.216.
The role of lipid modification in stroke prevention is controversial, although increasing evidence suggests that HMG-CoA reductase inhibition may reduce cerebrovascular events in patients with prevalent coronary artery disease.
To test the hypothesis that cholesterol reduction with pravastatin may reduce stroke incidence after myocardial infarction, we followed 4159 subjects with average total and LDL serum cholesterol levels (mean, 209 and 139 mg/dL, respectively) who had sustained an infarction an average of 10 months before study entry and who were randomized to pravastatin 40 mg/d or placebo in the Cholesterol and Recurrent Events (CARE) trial. Using prospectively defined criteria, we assessed the incidence of stroke, a prespecified secondary end point, and transient ischemic attack (TIA) over a median 5-year follow-up period. Patients were well matched for stroke risk factors and the use of antiplatelet agents (85% of subjects in each group). Compared with placebo, pravastatin lowered total serum cholesterol by 20%, LDL cholesterol by 32%, and triglycerides by 14% and raised HDL cholesterol by 5% over the course of the trial. A total of 128 strokes (52 on pravastatin, 76 on placebo) and 216 strokes or TIAs (92 on pravastatin, 124 on placebo) were observed, representing a 32% reduction (95% CI, 4% to 52%, P=0.03) in all-cause stroke and 27% reduction in stroke or TIA (95% CI, 4% to 44%, P=0.02). All categories of strokes were reduced, and treatment effect was similar when adjusted for age, sex, history of hypertension, cigarette smoking, diabetes, left ventricular ejection fraction, and baseline total, HDL, and LDL cholesterol and triglyceride levels. There was no increase in hemorrhagic stroke in patients on pravastatin compared with placebo (2 versus 6, respectively).
Pravastatin significantly reduced stroke and stroke or TIA incidence after myocardial infarction in patients with average serum cholesterol levels despite the high concurrent use of antiplatelet therapy.
尽管越来越多的证据表明,抑制HMG - CoA还原酶可能会降低患有冠状动脉疾病患者的脑血管事件发生率,但脂质修饰在预防中风中的作用仍存在争议。
为了验证普伐他汀降低胆固醇可能会降低心肌梗死后中风发生率这一假设,我们对4159名受试者进行了随访。这些受试者血清总胆固醇和低密度脂蛋白胆固醇平均水平分别为209mg/dL和139mg/dL,在研究开始前平均10个月发生过心肌梗死,并在胆固醇与再发事件(CARE)试验中被随机分为每日服用40mg普伐他汀组或安慰剂组。我们采用前瞻性定义的标准,在中位5年的随访期内评估中风(一个预先设定的次要终点)和短暂性脑缺血发作(TIA)的发生率。患者在中风危险因素和抗血小板药物使用方面匹配良好(每组85%的受试者)。在试验过程中与安慰剂相比,普伐他汀使血清总胆固醇降低了20%,低密度脂蛋白胆固醇降低了32%,甘油三酯降低了14%,高密度脂蛋白胆固醇升高了5%。共观察到128例中风(普伐他汀组52例,安慰剂组76例)和216例中风或TIA(普伐他汀组92例,安慰剂组124例),这表明全因中风发生率降低了32%(95%CI,4%至52%,P = 0·03),中风或TIA发生率降低了27%(95%CI,4%至44%,P = 0·02)。所有类型的中风均减少,在调整年龄、性别、高血压病史、吸烟、糖尿病、左心室射血分数以及基线总胆固醇、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇和甘油三酯水平后,治疗效果相似。与安慰剂相比,服用普伐他汀的患者出血性中风没有增加(分别为2例和6例)。
尽管同时大量使用抗血小板治疗,但对于血清胆固醇水平正常的心肌梗死后患者,普伐他汀显著降低了中风及中风或TIA的发生率。