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烟酸缓释片/辛伐他汀

Niacin extended-release/simvastatin.

作者信息

Sanford Mark, Curran Monique P

机构信息

Wolters Kluwer Health, Adis, Auckland, New Zealand.

出版信息

Drugs. 2008;68(16):2373-86. doi: 10.2165/0003495-200868160-00008.

Abstract

Niacin extended-release (ER)/simvastatin is a once-daily, fixed-dose combination of the HMG-CoA reductase inhibitor simvastatin and an ER formulation of niacin (a B-complex vitamin). In healthy volunteers who were given niacin ER/simvastatin 2000 mg/40 mg, niacin exposure was similar to that with niacin ER 2000 mg, while simvastatin exposure was increased compared to that with simvastatin 40 mg. In patients with elevated non-high-density lipoprotein cholesterol (non-HDL-C) but with low-density lipoprotein cholesterol (LDL-C) at or below the National Cholesterol Education Program (NCEP) goal after a > or = 2-week simvastatin 20 mg/day run-in period (SEACOAST I), 24 weeks of niacin ER/simvastatin 1000 mg/20 mg or 2000 mg/20 mg per day reduced median plasma non-HDL-C levels to a significantly greater extent than simvastatin 20 mg/day. In patients with elevated non-HDL-C and LDL-C at any level after a > or = 2-week simvastatin 40 mg/day run-in period (SEACOAST II), 24 weeks of niacin ER/simvastatin 1000 mg/40 mg or 2000 mg/40 mg per day was noninferior to simvastatin 80 mg/day in reducing median plasma non-HDL-C levels. Compared with simvastatin monotherapy, there was no significant difference in reduction in plasma LDL-C levels with niacin ER/simvastatin in SEACOAST I, and the noninferiority criterion for LDL-C was not met in SEACOAST II. However, plasma HDL-C levels increased more and triglyceride levels were lowered more than with simvastatin monotherapy (SEACOAST I and II). Niacin ER/simvastatin was generally well tolerated, with flushing being the most common adverse reaction.

摘要

缓释烟酸/辛伐他汀是一种每日服用一次的固定剂量复方制剂,由HMG-CoA还原酶抑制剂辛伐他汀和缓释烟酸(一种B族复合维生素)组成。在给予2000毫克/40毫克缓释烟酸/辛伐他汀的健康志愿者中,烟酸暴露量与2000毫克缓释烟酸相似,而辛伐他汀暴露量比40毫克辛伐他汀有所增加。在非高密度脂蛋白胆固醇(非HDL-C)升高但低密度脂蛋白胆固醇(LDL-C)在经过≥2周每天20毫克辛伐他汀导入期后处于或低于国家胆固醇教育计划(NCEP)目标的患者中(SEACOAST I),每天服用1000毫克/20毫克或2000毫克/20毫克缓释烟酸/辛伐他汀24周,使血浆非HDL-C水平中位数降低的程度显著大于每天20毫克辛伐他汀。在经过≥2周每天40毫克辛伐他汀导入期后非HDL-C和LDL-C在任何水平升高的患者中(SEACOAST II),每天服用1000毫克/40毫克或2000毫克/40毫克缓释烟酸/辛伐他汀24周,在降低血浆非HDL-C水平中位数方面不劣于每天80毫克辛伐他汀。与辛伐他汀单药治疗相比,SEACOAST I中缓释烟酸/辛伐他汀在降低血浆LDL-C水平方面无显著差异,且SEACOAST II中未达到LDL-C的非劣效性标准。然而,与辛伐他汀单药治疗相比,血浆HDL-C水平升高更多,甘油三酯水平降低更多(SEACOAST I和II)。缓释烟酸/辛伐他汀总体耐受性良好,潮红是最常见的不良反应。

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