Toth Peter P, Farnier Michel, Tomassini Joanne E, Foody JoAnne M, Tershakovec Andrew M
CGH Medical Center, Sterling, Illinois, & Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Lipid Clinic, Point Médical, Dijon, France.
Future Cardiol. 2016 May;12(3):289-315. doi: 10.2217/fca-2015-0011. Epub 2016 Apr 15.
In numerous clinical trials, lowering LDL-C with statin therapy has been demonstrated to reduce the risk of cardiovascular disease (CVD) in primary and secondary prevention settings. Guidelines recommend statins for first-line therapy in cholesterol-lowering management of patients with CVD risk. Despite increased statin monotherapy use over the last decade, a number of patients with high CVD risk do not achieve optimal LDL-C lowering. Guidelines recommend consideration of statin combination therapy with nonstatin agents for these patients. However, combination therapy approaches have been hampered by neutral findings. Recently, ezetimibe added to simvastatin therapy reduced cardiovascular events in acute coronary syndrome patients, more than simvastatin alone. This article provides an overview of various agents in combination with statin therapy on cardiovascular outcomes. Other lipid-lowering agents in development, including PCSK9 and CETP inhibitors in development, are also described.
在众多临床试验中,他汀类药物治疗降低低密度脂蛋白胆固醇(LDL-C)已被证明可降低一级和二级预防环境中心血管疾病(CVD)的风险。指南推荐他汀类药物作为心血管疾病风险患者降脂管理的一线治疗药物。尽管在过去十年中他汀类单药治疗的使用有所增加,但许多心血管疾病高风险患者并未实现最佳的LDL-C降低。指南建议考虑对这些患者采用他汀类药物与非他汀类药物的联合治疗。然而,联合治疗方法一直受到中性结果的阻碍。最近,依折麦布联合辛伐他汀治疗比单独使用辛伐他汀更能减少急性冠脉综合征患者的心血管事件。本文概述了与他汀类药物联合治疗的各种药物对心血管结局的影响。还描述了其他正在研发的降脂药物,包括正在研发的前蛋白转化酶枯草溶菌素9(PCSK9)和胆固醇酯转运蛋白(CETP)抑制剂。