Department of Medicine, Section of Cardiovascular Research, Baylor College of Medicine, Houston, TX, USA.
Department of Medicine, Section of Cardiology, Baylor College of Medicine, Houston, TX, USA.
Curr Atheroscler Rep. 2020 Jun 3;22(7):25. doi: 10.1007/s11883-020-00846-8.
This review focuses on recent evidence examining the role triglycerides (TG) and triglyceride-enriched lipoproteins (TGRL) play in atherosclerotic cardiovascular disease (ASCVD). It also provides a succinct overview of current and future TG-lowering therapies for ASCVD risk reduction.
Epidemiological and Mendelian randomization studies have consistently shown that TGRL are strongly associated with ASCVD. REDUCE-IT demonstrated cardiovascular benefit with icosapent ethyl in high-risk patients with hypertriglyceridemia on statin therapy. Polymorphisms in APOC3 and ANGPTL3 are associated with ASCVD and use of RNA-interfering therapies to target these proteins has shown TG lowering in early phase trials. TG and TGRL are causally associated with ASCVD. Lifestyle modifications and statin therapy can lower TG/TGRL and are considered first-line treatment for hypertriglyceridemia. Icosapent ethyl has been shown to reduce residual ASCVD risk in high-risk patients on maximally tolerated statins. Ongoing clinical trials will better define optimal therapy for patients on statins with residual hypertriglyceridemia.
本综述重点关注近期研究证据,探讨甘油三酯(TG)和富含甘油三酯的脂蛋白(TGRL)在动脉粥样硬化性心血管疾病(ASCVD)中的作用。本文还简要概述了目前和未来用于降低 ASCVD 风险的降 TG 治疗方法。
流行病学和孟德尔随机化研究一致表明,TGRL 与 ASCVD 密切相关。在接受他汀类药物治疗的高甘油三酯血症高危患者中,icosapent ethyl 可降低心血管风险,这证明了 REDUCE-IT 研究的结果。APOC3 和 ANGPTL3 的多态性与 ASCVD 相关,使用针对这些蛋白的 RNA 干扰疗法在早期临床试验中显示可降低 TG。TG 和 TGRL 与 ASCVD 有因果关系。生活方式的改变和他汀类药物治疗可以降低 TG/TGRL,被认为是高甘油三酯血症的一线治疗方法。icosapent ethyl 已被证明可降低最大耐受剂量他汀类药物治疗的高危患者的残余 ASCVD 风险。正在进行的临床试验将更好地确定他汀类药物治疗后残余高甘油三酯血症患者的最佳治疗方法。