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载脂蛋白C-Ⅲ在心血管疾病中的研究进展 被引量:1

Progress of Apolipoprotein C-Ⅲ in Cardiovascular Diseases
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摘要 血脂异常会导致心血管疾病风险增加,降脂可减少动脉粥样硬化及其并发症的发生发展。他汀类药物能有效降低低密度脂蛋白,然而,许多患者在低密度脂蛋白很低的情况下仍发生心血管事件,载脂蛋白C-Ⅲ有直接导致动脉粥样硬化的作用,促发炎症因子的表达释放,是心血管疾病独立危险因素,因而载脂蛋白C-Ⅲ抑制剂为心血管疾病的治疗提供新的干预方式。 Dyslipidemia can increase the risk of cardiovascular disease, and lowering lipids may reduce the development of atheroscle- rosis and its complications. Statins can reduce low density lipoprotein, however, many patients with cardiovascular events still occur with ca- ses of low density lipoprotein. Apolipoprotein C-Ⅲ has a direct role in causing atherosclerosis, and it can prove the release of inflammatory factors. Also, it is an independent risk factor for cardiovascular disease. Thus apolipoprotein C-Ⅲ inhibitors provide new interventions for the treatment of cardiovascular diseases.
作者 冉丹 佘强
出处 《心血管病学进展》 CAS 2015年第5期613-616,共4页 Advances in Cardiovascular Diseases
关键词 载脂蛋白C-Ⅲ 血脂调节 心血管疾病 apolipoprotein C- Ⅲ lipid regulation cardiovascular disease
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  • 1Scandinavian Simvastatin Survival Study Group.Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease:the Scandinavian Simvas- tatin Survival Study(4S)[J].Lancet,1994,344(8934):1383-1389.
  • 2Gupta A,Smith DA.The 2013 American College of Cardiology/American Heart Association guidelines on treating blood cholesterol and assessing cardiovascular risk:a busy practitioners guide[J].Endocrinol Metab Clin North Am,2014,43(4):869-892.
  • 3Reiner Z.Managing the residual cardiovascular disease risk associated with HDL- cholesterol and triglycerides in statin-treated patients:a clinical update[J].Nutr Metab Cardiovasc Dis,2013,23(9):799-807.
  • 4TG and HDL Working Group of the Exome Sequencing Project,National Heart,Lung,and Blood Institute,Grosby J,et al.Loss-of-function mutations in AP0C3,triglycerides,and coronary disease[J].N Engl J Med,2014,371(1):22-31.
  • 5j0rgensen AB,Frikke-Schmidt R,Nordestgaard BG,et al.Loss-of-function mu- tations in APOC3 and risk of ischemic vascular disease[J].N Engl J Med,2014,371(1):3241.
  • 6Sehayek E,Eisenberg S.Mechanisms of inhibition by apolipoprotein C of apoli- poprotein E-dependent cellular metabolism of human triglyceride-rich lipopro- teins through the low density lipoprotein receptor pathway[J].J Biol Chem,1991,266(27):18259-18267.
  • 7Pollin TI,Damcott CM,Shen H,et al.A null mutation in human APOC3 con- fers a favorable plasma lipid profile and apparent cardioprotection[J].Science,2008,322(5908):1702-1705.
  • 8Crawford DC,Dumitrescu L,Goodloe R,et al.Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment(EAGLE)Study[J].Circ Cardiovasc Genet,2014,7(6):848-853.
  • 9Atzmon G,Rincon M,Schechter CB,et al.Lipoprotein genotype and con- served pathway for exceptional longevity in humans[J].PLoS Biol,2006,4(4):e113.
  • 10Luc G,Fievet C,Arveiler D,et al.Apolipoproteins C-Ⅲ and E in apoB-and non-apoB-containing lipoproteins in two populations at contrasting risk for myo- cardial infarction:the ECTIM study.Etude Cas T6moins sur' Infarctus du Myo- carde[J].J Lipid Res,1996,37(3):508-517.

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