...
首页> 外文期刊>Current medical research and opinion >Safety and efficacy of colesevelam hydrochloride in combination with fenofibrate for the treatment of mixed hyperlipidemia.
【24h】

Safety and efficacy of colesevelam hydrochloride in combination with fenofibrate for the treatment of mixed hyperlipidemia.

机译:盐酸考来维仑联合非诺贝特治疗混合性高脂血症的安全性和有效性。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

OBJECTIVE: The aim of this study was to evaluate the amount of low-density lipoprotein cholesterol (LDL-C) reduction achieved by adding the specifically engineered bile acid sequestrant (SE-BAS) colesevelam HCl to a stable dose of fenofibrate in patients with mixed hyperlipidemia. RESEARCH DESIGN AND METHODS: Patients with mixed hyperlipidemia (n = 129) were enrolled in a randomized, double-blind, placebo-controlled, parallel-group study investigating the efficacy of fenofibrate plus colesevelam HCl versus fenofibrate monotherapy. After a 4- to 8-week washout period, subjects received fenofibrate 160 mg/day for 8 weeks and were then randomized to receive colesevelam HCl 3.75 g/day or placebo, in addition to fenofibrate 160 mg/day, for 6 weeks. MAIN OUTCOMES MEASURES: The primary efficacy endpoint was mean percent change in LDL-C during randomized treatment. Secondary endpoints included absolute and percent changes in mean levels of LDL-C, triglycerides (TGs), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, total cholesterol (TC), and apolipoproteins (apo) A-I and B during randomized treatment and from washout to end of randomized treatment. RESULTS: Of the 129 patients randomized to treatment, 119 completed the study. After 6 weeks of treatment, fenofibrate plus colesevelam HCl produced a mean percent change in LDL-C of -10.4% versus +2.3% with fenofibrate monotherapy (p < 0.0001). Fenofibrate plus colesevelam HCl was significantly more effective than fenofibrate alone at reducing levels of non-HDL-C, TC, and apo B (p < or = 0.0002). Colesevelam HCl did not significantly affect the TG-lowering effects of fenofibrate. Both treatment regimens were safe and well tolerated. CONCLUSIONS: Compared with fenofibrate monotherapy in patients with mixed hyperlipidemia, fenofibrate/colesevelam HCl combination therapy significantly reduced mean LDL-C, non-HDL-C, TC, and apo B levels without significantly affecting the TG-lowering or HDL-C-raising effects of fenofibrate. Fenofibrate/colesevelam HCl combination therapy is a safe, useful alternative for the treatment of mixed hyperlipidemia.
机译:目的:本研究的目的是评估在混合剂量患者中向稳定剂量的非诺贝特中加入特定工程设计的胆汁酸螯合剂(SE-BAS)考来维仑HCl所实现的低密度脂蛋白胆固醇(LDL-C)降低量高脂血症。研究设计和方法:混合性高脂血症患者(n = 129)参加了一项随机,双盲,安慰剂对照,平行组研究,研究非诺贝特联合盐酸西洛韦仑与非诺贝特单药治疗的疗效。在4到8周的清除期后,受试者接受160毫克/天的非诺贝特治疗8周,然后随机接受3,75 g /天的盐酸西洛韦仑或安慰剂,以及160毫克/天的非诺贝特治疗6周。主要观察指标:主要疗效终点是随机治疗期间LDL-C的平均变化百分比。次要终点包括LDL-C,甘油三酸酯(TGs),高密度脂蛋白胆固醇(HDL-C),非HDL-C,总胆固醇(TC)和载脂蛋白(apo)AI的绝对水平和百分比变化B在随机治疗期间以及从冲洗到随机治疗结束之间。结果:在随机分配的129例患者中,有119例完成了研究。治疗6周后,非诺贝特加盐酸西洛韦仑产生的LDL-C平均百分数变化为-10.4%,而非诺贝特单药治疗为+ 2.3%(p <0.0001)。非诺贝特加盐酸西洛韦仑在降低非HDL-C,TC和载脂蛋白B的水平上比单独使用非诺贝特显着更有效(p <或= 0.0002)。盐酸考来维仑未显着影响非诺贝特的降TG作用。两种治疗方案均安全且耐受性良好。结论:与非诺贝特单药治疗混合性高脂血症患者相比,非诺贝特/盐酸考来维仑联合治疗显着降低平均LDL-C,非HDL-C,TC和apo B水平,而不会显着降低TG降低或HDL-C升高非诺贝特的作用。非诺贝特/盐酸考来韦仑联合治疗是治疗混合性高脂血症的一种安全,有用的替代方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号