首页> 外文期刊>Journal of clinical lipidology >Achievement of specified low-density lipoprotein cholesterol, non-high-density lipoprotein cholesterol apolipoprotein B, and high-sensitivity C-reactive protein levels with ezetimibe/simvastatin or atorvastatin in metabolic syndrome patients with and without atherosclerotic vascular disease (from the VYMET study)
【24h】

Achievement of specified low-density lipoprotein cholesterol, non-high-density lipoprotein cholesterol apolipoprotein B, and high-sensitivity C-reactive protein levels with ezetimibe/simvastatin or atorvastatin in metabolic syndrome patients with and without atherosclerotic vascular disease (from the VYMET study)

机译:依泽替米贝/辛伐他汀或阿托伐他汀在有或没有动脉粥样硬化性血管疾病的代谢综合征患者中达到特定的低密度脂蛋白胆固醇,非高密度脂蛋白胆固醇载脂蛋白B和高敏感性C反应蛋白水平(来自VYMET研究)

获取原文
获取原文并翻译 | 示例
           

摘要

Background: Metabolic syndrome (MetS) and atherosclerotic vascular disease (AVD) are associated with increased coronary heart disease risk. Objective: To assess percent change from baseline in lipids and high-sensitivity C-reactive protein (hs-CRP) levels and the proportion of subjects reaching specified low-density lipoprotein cholesterol (LDL-C), non-high-density lipoprotein cholesterol (HDL-C) and apolipoprotein B (Apo B) single, dual, and triple targets and hs-CRP <2 mg/L among subjects with and without AVD treated with ezetimibe/simvastatin or atorvastatin for 6 weeks. Methods: Adults (N = 1143) with MetS and hypercholesterolemia were randomized to starting and next higher doses of ezetimibe/simvastatin (10/20 or 10/40 mg) or atorvastatin (10, 20, or 40 mg). Results: Ezetimibe/simvastatin produced significantly greater reductions in evaluated lipids than atorvastatin for most prespecified dose comparisons. More subjects without AVD achieved LDL-C levels <100 mg/dL, non-HDL-C levels <130 mg/dL, and dual LDL-Con-HDL targets (83%-92% vs 62%-76%) and Apo B <90 mg/dL or triple targets (65%-75% vs 41%-49%) with 40 mg of atorvastatin or 10/20-40 mg of ezetimibe/simvastatin compared with 10 or 20 mg of atorvastatin, respectively. More subjects with AVD achieved LDL-C<70 mg/dL and non-HDL-C<100 mg/dL single and dual targets (65%-80%) and Apo B <80 mg/dL (53%-63%) with 10/20-40 mg of ezetimibe/simvastatin than with 40 mg of atorvastatin (40%-49%). More subjects achieved triple lipid targets with 10/20-40 mg of ezetimibe/simvastatin versus 10-40 mg of atorvastatin (50%-63% vs 24%-40%). Achievement of hs-CRP <2 mg/L was similar across all doses regardless of AVD status. Conclusions: More intensive therapy was required for >80% of subjects to achieve LDL-C <100 mg/dL and non-HDL-C <130 mg/dL and for the majority of subjects to achieve lower levels of LDL-C <70 mg/dL, non-HDL-C <100 mg/dL, and/or Apo B <90 mg/dL. The effect of ezetimibe on cardiovascular risk reduction has yet to be established.
机译:背景:代谢综合征(MetS)和动脉粥样硬化性血管疾病(AVD)与冠心病风险增加相关。目的:评估脂质和高敏C反应蛋白(hs-CRP)水平相对于基线的变化百分比,以及达到指定的低密度脂蛋白胆固醇(LDL-C),非高密度脂蛋白胆固醇( HDZ-C)和载脂蛋白B(Apo B)的单一,双重和三重靶标,且在接受和未接受ezetimibe / simvastatin或阿托伐他汀治疗的AVD患者中,hs-CRP <2 mg / L达6周。方法:将患有MetS和高胆固醇血症的成年人(N = 1143)随机分配至开始和下一个更高剂量的依泽替米贝/辛伐他汀(10/20或10/40 mg)或阿托伐他汀(10、20或40 mg)。结果:对于大多数预先设定的剂量比较,依泽替米贝/辛伐他汀产生的脂质减少量明显大于阿托伐他汀。更多无AVD的受试者达到LDL-C水平<100 mg / dL,非HDL-C水平<130 mg / dL和双重LDL-C /非HDL目标(83%-92%vs 62%-76%)和Apo B <90 mg / dL或三重靶点(65%-75%对41%-49%)用40 mg阿托伐他汀或10 / 20-40 mg依泽替米贝/辛伐他汀分别比较10或20 mg阿托伐他汀。越来越多的AVD患者达到LDL-C <70 mg / dL和非HDL-C <100 mg / dL单和双重目标(65%-80%)和Apo B <80 mg / dL(53%-63%)含10 / 20-40毫克的依折麦布/辛伐他汀比40毫克的阿托伐他汀(40%-49%)。与10-40 mg阿托伐他汀相比,更多的受试者使用10 / 20-40 mg依泽替米贝/辛伐他汀实现了三重脂质目标(50%-63%对24%-40%)。不论AVD状态如何,所有剂量的hs-CRP均<2 mg / L达到相似。结论:> 80%的受试者需要更深入的治疗以达到LDL-C <100 mg / dL和非HDL-C <130 mg / dL,并且大多数受试者需要达到更低的LDL-C <70 mg / dL,非HDL-C <100 mg / dL和/或Apo B <90 mg / dL。依泽替米贝对降低心血管风险的作用尚未确定。

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