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Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome.依洛尤单抗与急性冠脉综合征后的心血管结局。
N Engl J Med. 2018 Nov 29;379(22):2097-2107. doi: 10.1056/NEJMoa1801174. Epub 2018 Nov 7.
2
Efficacy and safety of bempedoic acid added to ezetimibe in statin-intolerant patients with hypercholesterolemia: A randomized, placebo-controlled study.在不能耐受他汀类药物的高胆固醇血症患者中,添加苯扎贝特酸与依折麦布联合治疗的疗效和安全性:一项随机、安慰剂对照研究。
Atherosclerosis. 2018 Oct;277:195-203. doi: 10.1016/j.atherosclerosis.2018.06.002. Epub 2018 Jun 12.
3
Relationship between "LDL-C", estimated true LDL-C, apolipoprotein B-100, and PCSK9 levels following lipoprotein(a) lowering with an antisense oligonucleotide.载脂蛋白(a)降低后 LDL-C、估计真实 LDL-C、载脂蛋白 B-100 和 PCSK9 水平的关系。 采用反义寡核苷酸。
J Clin Lipidol. 2018 May-Jun;12(3):702-710. doi: 10.1016/j.jacl.2018.02.014. Epub 2018 Mar 1.
4
Heart Disease and Stroke Statistics-2018 Update: A Report From the American Heart Association.《2018年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2018 Mar 20;137(12):e67-e492. doi: 10.1161/CIR.0000000000000558. Epub 2018 Jan 31.
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2017 Focused Update of the 2016 ACC Expert Consensus Decision Pathway on the Role of Non-Statin Therapies for LDL-Cholesterol Lowering in the Management of Atherosclerotic Cardiovascular Disease Risk: A Report of the American College of Cardiology Task Force on Expert Consensus Decision Pathways.2017 年对 2016 年美国心脏病学会专家共识决策途径的重点更新:非他汀类药物在降低动脉粥样硬化性心血管疾病风险管理中的作用:美国心脏病学会专家组的专家共识决策途径报告。
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6
Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.血管生成素样蛋白3的基因和药物失活与心血管疾病
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Lipoprotein(a) and inhibitors of proprotein convertase subtilisin/kexin type 9.脂蛋白(a)与前蛋白转化酶枯草杆菌蛋白酶/kexin 9型抑制剂
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他汀类药物后脂质治疗学:综述

Poststatin Lipid Therapeutics: A Review.

作者信息

Jia Xiaoming, Lorenz Patrick, Ballantyne Christie M

机构信息

BAYLOR COLLEGE OF MEDICINE, HOUSTON, TEXAS.

出版信息

Methodist Debakey Cardiovasc J. 2019 Jan-Mar;15(1):32-38. doi: 10.14797/mdcj-15-1-32.

DOI:10.14797/mdcj-15-1-32
PMID:31049147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6489602/
Abstract

Low-density lipoprotein cholesterol (LDL-C) is a well-established risk factor for atherosclerotic cardiovascular disease (ASCVD). Statins remain the first-line therapy for patients with elevated LDL-C and increased risk. However, many at-risk patients do not achieve adequate LDL-C lowering with statin monotherapy or do not tolerate statins because of side effects. Recent cardiovascular outcome trials involving ezetimibe and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have demonstrated efficacy of nonstatin therapies in further reducing LDL-C levels and ASCVD risk. This review highlights the available nonstatin therapeutic options and explores important novel therapeutic approaches currently under development.

摘要

低密度脂蛋白胆固醇(LDL-C)是动脉粥样硬化性心血管疾病(ASCVD)公认的危险因素。他汀类药物仍然是LDL-C升高且风险增加患者的一线治疗药物。然而,许多高危患者使用他汀类药物单药治疗无法充分降低LDL-C水平,或者由于副作用而不耐受他汀类药物。最近涉及依折麦布和前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)抑制剂的心血管结局试验证明了非他汀类疗法在进一步降低LDL-C水平和ASCVD风险方面的疗效。本综述重点介绍了现有的非他汀类治疗选择,并探讨了目前正在研发的重要新型治疗方法。