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辛伐他汀在一大群老年高胆固醇血症患者中的长期疗效及耐受性

Long-term efficacy and tolerability of simvastatin in a large cohort of elderly hypercholesterolemic patients.

作者信息

Lansberg P J, Mitchel Y B, Shapiro D, Kastelein J J, Altman R, Jerums G, Bolzano K, Giannini S, Davignon J, DeWailly P

机构信息

Center for Hemostasis, Thrombosis, Atherosclerosis and Inflammation, Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Atherosclerosis. 1995 Aug;116(2):153-62. doi: 10.1016/0021-9150(95)05523-y.

Abstract

The long-term efficacy and tolerability of simvastatin, a 3-hydroxy-3-methylglutaryl-co-enzyme A (HMG-CoA) reductase inhibitor, was assessed during a 24-month follow-up period in 168 elderly hypercholesterolemic patients. After completing a 4 week double blind dose ranging study with simvastatin, 47 males and 122 females over 62 years of age with type II hyperlipidemia, a total cholesterol level above 6.5 mmol/l and clinically manifest cardiovascular disease were included in this extended study. A total of 159 patients completed the 12-month follow-up period and 141 patients were monitored over the full 24 months. All patients were started on 10 mg simvastatin once daily and the dosage was increased until the target levels of low density lipoprotein (LDL) cholesterol between 2.3 mmol/l (90 mg/dl) and 3.6 mmol/l (140 mg/dl) were reached. Fifty percent of patients reached the targeted LDL cholesterol goal of < 3.6 mmol/l (140 mg/dl) during the study. At study completion, 65 patients (39%) were taking 40 mg simvastatin per day, 56 patients (33%) 20 mg, 42 patients (25%) 10 mg and 5 patients (3%) only used 5 mg per day. Sixteen patients (9%) received concomitant lipid lowering therapy. Over 2 years, the mean decrease in LDL cholesterol ranged from 36% to 38%, the median decrease in triglycerides was 12% to 19% and the mean increase in high density lipoprotein (HDL) cholesterol ranged from 9% to 10%, respectively. Seven patients discontinued simvastatin because of adverse clinical or laboratory events, but only in two (1.1%) was this considered to be drug-related. Side-effects were mild and most frequently gastrointestinal in nature. Mean changes in asparate aminotransferase (AST) were not significantly different from zero and mean changes in alanine aminotransferase (ALT) and creatine phosphokinase (CPK) showed a small increase. We conclude that simvastatin is an efficacious and well-tolerated treatment for hypercholesterolemia in elderly individuals for extended periods.

摘要

在一项针对168例老年高胆固醇血症患者的24个月随访研究中,评估了3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂辛伐他汀的长期疗效和耐受性。在完成辛伐他汀为期4周的双盲剂量范围研究后,本项扩展研究纳入了47例男性和122例62岁以上患有II型高脂血症、总胆固醇水平高于6.5 mmol/l且有临床症状的心血管疾病患者。共有159例患者完成了12个月的随访期,141例患者接受了完整24个月的监测。所有患者均开始每日一次服用10 mg辛伐他汀,并增加剂量直至低密度脂蛋白(LDL)胆固醇达到2.3 mmol/l(90 mg/dl)至3.6 mmol/l(140 mg/dl)的目标水平。在研究期间,50%的患者达到了LDL胆固醇目标值<3.6 mmol/l(140 mg/dl)。在研究结束时,65例患者(39%)每天服用40 mg辛伐他汀,56例患者(33%)服用20 mg,42例患者(25%)服用10 mg,5例患者(3%)每天仅服用5 mg。16例患者(9%)接受了联合降脂治疗。在两年多的时间里,LDL胆固醇的平均降幅为36%至38%,甘油三酯的中位数降幅为12%至19%,高密度脂蛋白(HDL)胆固醇的平均增幅为9%至10%。7例患者因不良临床或实验室事件停用辛伐他汀,但只有2例(1.1%)被认为与药物有关。副作用较轻,最常见的是胃肠道反应。天冬氨酸转氨酶(AST)的平均变化与零无显著差异,丙氨酸转氨酶(ALT)和肌酸磷酸激酶(CPK)的平均变化略有升高。我们得出结论,辛伐他汀对老年个体的高胆固醇血症是一种长期有效且耐受性良好的治疗方法。

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