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2
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本文引用的文献

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Effect of CC chemokine receptor 2 CCR2 blockade on serum C-reactive protein in individuals at atherosclerotic risk and with a single nucleotide polymorphism of the monocyte chemoattractant protein-1 promoter region.CC 趋化因子受体 2(CCR2)阻断对动脉粥样硬化风险个体和单核细胞趋化蛋白-1 启动子区域单核苷酸多态性患者血清 C 反应蛋白的影响。
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Randomized trial of an inhibitor of secretory phospholipase A2 on atherogenic lipoprotein subclasses in statin-treated patients with coronary heart disease.随机对照试验研究了在冠心病他汀类药物治疗患者中,一种抑制分泌型磷脂酶 A2 的药物对致动脉粥样硬化脂蛋白亚类的影响。
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Part 9: Acute coronary syndromes: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.第9部分:急性冠状动脉综合征:2010年心肺复苏和心血管急救科学与治疗建议国际共识。
Circulation. 2010 Oct 19;122(16 Suppl 2):S422-65. doi: 10.1161/CIRCULATIONAHA.110.985549.
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Hyperlipidemia-triggered neutrophilia promotes early atherosclerosis.高脂血症触发的中性粒细胞增多促进早期动脉粥样硬化。
Circulation. 2010 Nov 2;122(18):1837-45. doi: 10.1161/CIRCULATIONAHA.110.961714. Epub 2010 Oct 18.
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Study design and rationale for the clinical outcomes of the STABILITY Trial (STabilization of Atherosclerotic plaque By Initiation of darapLadIb TherapY) comparing darapladib versus placebo in patients with coronary heart disease.STABILITY 试验(通过起始 darapladib 治疗稳定动脉粥样硬化斑块)的临床结果研究设计和原理,该试验比较了 darapladib 与安慰剂在冠心病患者中的疗效。
Am Heart J. 2010 Oct;160(4):655-61. doi: 10.1016/j.ahj.2010.07.006.
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Contribution of 30 biomarkers to 10-year cardiovascular risk estimation in 2 population cohorts: the MONICA, risk, genetics, archiving, and monograph (MORGAM) biomarker project.30 种生物标志物对 2 个人群队列 10 年心血管风险评估的贡献:MONICA、风险、遗传学、存档和专论(MORGAM)生物标志物项目。
Circulation. 2010 Jun 8;121(22):2388-97. doi: 10.1161/CIRCULATIONAHA.109.901413. Epub 2010 May 24.
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Cholesterol efflux potential and antiinflammatory properties of high-density lipoprotein after treatment with niacin or anacetrapib.烟酸或阿昔单抗治疗后高密度脂蛋白的胆固醇外排潜力和抗炎特性。
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Lipoprotein-associated phospholipase A(2) and risk of coronary disease, stroke, and mortality: collaborative analysis of 32 prospective studies.脂蛋白相关磷脂酶 A(2)与冠心病、卒中和死亡风险:32 项前瞻性研究的协作分析。
Lancet. 2010 May 1;375(9725):1536-44. doi: 10.1016/S0140-6736(10)60319-4.
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Pleiotropic effects of statins. - Basic research and clinical perspectives -.他汀类药物的多效性作用。-基础研究和临床视角-。
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Phospholipase A2s: developing drug targets for atherosclerosis.磷脂酶 A2 酶:动脉粥样硬化的药物靶点开发。
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抗动脉粥样硬化炎症治疗策略。

Anti-inflammatory therapeutics for the treatment of atherosclerosis.

机构信息

Gladstone Institute of Cardiovascular Disease, 1650 Owens Street #149, San Francisco, California 94158, USA.

出版信息

Nat Rev Drug Discov. 2011 May;10(5):365-76. doi: 10.1038/nrd3444.

DOI:10.1038/nrd3444
PMID:21532566
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3947588/
Abstract

Atherosclerosis is the primary cause of heart disease and stroke and is thus the underlying pathology of the leading causes of death in the western world. Although risk can be reduced by lowering lipid levels, the equally important contribution of inflammation to the development of cardiovascular disease is not adequately addressed by existing therapies. Here, we summarize the evidence supporting a role for inflammation in the pathogenesis of atherosclerosis, discuss agents that are currently in the clinic and provide a perspective on the challenges faced in the development of drugs that target vascular inflammation.

摘要

动脉粥样硬化是心脏病和中风的主要病因,因此也是西方世界主要死亡原因的潜在病理学基础。尽管通过降低血脂水平可以降低风险,但现有疗法并不能充分解决炎症对心血管疾病发展的同等重要贡献。在这里,我们总结了支持炎症在动脉粥样硬化发病机制中起作用的证据,讨论了目前在临床使用的药物,并对靶向血管炎症的药物开发所面临的挑战提供了一个视角。