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应用腔内影像评估前蛋白转化酶枯草溶菌素9抑制剂对冠状动脉斑块特征影响的研究进展 被引量:1

Research progress on the effects of proprotein convertase subtilisin kexin type 9 inhibitors on coronary plaques evaluated by intravascular imaging
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摘要 前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂可在他汀类药物基础上进一步降低低密度脂蛋白胆固醇水平约60%。LDL-C降低能减少主要不良心血管事件的发生,也可促使动脉粥样硬化斑块的消退,但目前为止应用PCSK9抑制剂对冠状动脉斑块影响的研究仍比较有限。本综述回顾了PCSK9抑制剂对冠状动脉斑块的影响,基于血管内超声和光学相干断层扫描等腔内影像技术观察到PCSK9抑制剂对于斑块具有良好的稳定作用,表现为动脉粥样硬化体积百分比和标准化总动脉粥样硬化体积降低、纤维帽厚度增加、脂质池缩小、巨噬细胞减少、薄纤维帽粥样硬化斑块比例降低和富脂斑块消退。 Proprotein convertase subtilisin Kexin type 9(PCSK9)inhibitors can further reduce low-density lipoprotein cholesterol(LDL-C)level by about 60%on the base of statins.The reduction of LDL-C can reduce the occurrence of major adverse cardiovascular events(MACE)and also promote the regression of the atherosclerotic plaques.However,studies about the effects of PCSK9 inhibitors on the coronary plaques are still limited so far.The effects of PCSK9 inhibitors on the coronary plaque,based on intravascular imaging techniques such as intravascular ultrasound(IVUS)and optical coherence tomography(OCT),are reviewed in this paper.PCSK9 inhibitors have been observed to have good stability for the plaques,reflected in the decreased percent atheroma volume(PAV)and standardized total atheroma volume(TAV),the increased fibrous cap thickness(FCT)and the decreased lipid pool,macrophages,proportion of thin-cap fibroatheroma(TCFA)as well the regression of lipid-rich plaques.
作者 韩思睿 南楠 宋现涛 HAN Si-rui;NAN Nan;SONG Xian-tao(The Sixth Clinical Medical School,Capital Medical University,Beijing 100069,China;Department of Cardiology,Beijing Anzhen Hospital,Capital Medical University,Beijing 100029,China)
出处 《中国心血管病研究》 CAS 2022年第7期656-661,共6页 Chinese Journal of Cardiovascular Research
基金 中国心血管健康联盟进阶基金(2019-CCA-ACCESS-077)。
关键词 前蛋白转化酶枯草溶菌素9抑制剂 冠状动脉斑块 血管内超声 光学相干断层扫描 Proprotein convertase subtilisin kexin type 9 inhibitors Coronary plaque Intravascular ultrasound Optical coherence tomography
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  • 1Cannon CP, Braunwald E, McCabe CH, et al. Intensive versus moderate lipid lowering with statins after acute coronary syndromes. N Engl J Med. 2004;350:1495-1504.
  • 2LaRosa JC, Grundy SM, Waters DD, et al; Treating to New Targets (TNT) Investigators. Intensive lipid lowering with atorvastatin in patients with stable coronary disease. N Engl J Med. 2005;352:1425-1435.
  • 3Pedersen TR, Faergeman O, Kastelein J J, et al; Incremental Decrease in End Points Through Aggressive Lipid Lowedng (IDEAL) Study Group. High-dose atorvastatin vs usual-dose simvastatin for secondary prevention after myocardial infarction: the IDEAL study:a randomized controlled trial. JAMA. 2005;294:2437-2445.
  • 4Grundy SM, Cleeman JI, Merz CN, et al; Coordinating Committee of the National Cholesterol Education Program. Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel Ⅲ Guidelines. J Am Coll Cardiol. 2004;44:720-732.
  • 5Blankenhom DH, Azen SP, Kramsch DM, et al;MARS Research Group. Coronary angiographic changes with Iovastatin therapy: the Monitored Atherosclerosis Regression Study (MARS). Ann Intern Med.1993;119:969-976.
  • 6Waters D, Higginson L, Gladstone P, et al. Effects of monotherapy with HMG-CoA reductase inhibitor on the progression of coronary atherosclerosis as assessed be serial quantitaUve arteriography: the Canadian Coronary Atherosclerosis Intervention Trial(CCAIT). Circulation. 1994;89:959-968.
  • 7Jukema JW, Bruschke AV, van Boven A J, et al. Effects of lipid lowering by pravastatin on progression and regression of coronary artery disease in symptomatic men with normal to moderately elevated serum cholesterol levels: the Regression Growth Evaluation Statin Study (REGRESS). Circulation. 1995;91:2528-2540.
  • 8Pitt B, Mancini GB, Ellis SG, Rosrnan HS, Park J-S,McGovem ME. Pravastatin limitaUon of atherosclerosis in the coronary arteries (PLAC Ⅰ): reduction in atherosclerosis progression and clinical events. J Am Coll Cardiol. 1995;26:1133-1139.
  • 9Brown G, Albers J J, Fisher LD, et al. Regression of coronary artery disease as a result of intensive lipidlowering therapy in men with high levels of apolipoprotein B. N Engl J Med. 1990;323:1289-1298.
  • 10MAAS Study Group. Effect of simvastatin on coronary atheroma: the Multicentre Anti-atheroma Study( MAAS). Lancet. 1994;344:633 -638.

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