Taskinen Marja-Riitta, Borén Jan
Heart and Lung Centre, Helsinki University Central Hospital and Research Programs' Unit, Diabetes & Obesity, University of Helsinki, Helsinki, Finland.
Department of Molecular and Clinical Medicine, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.
Curr Atheroscler Rep. 2016 Oct;18(10):59. doi: 10.1007/s11883-016-0614-1.
ApoC-III was discovered almost 50 years ago, but for many years, it did not attract much attention. However, as epidemiological and Mendelian randomization studies have associated apoC-III with low levels of triglycerides and decreased incidence of cardiovascular disease (CVD), it has emerged as a novel and potentially powerful therapeutic approach to managing dyslipidemia and CVD risk. The atherogenicity of apoC-III has been attributed to both direct lipoprotein lipase-mediated mechanisms and indirect mechanisms, such as promoting secretion of triglyceride-rich lipoproteins (TRLs), provoking proinflammatory responses in vascular cells and impairing LPL-independent hepatic clearance of TRL remnants. Encouraging results from clinical trials using antisense oligonucleotide, which selectively inhibits apoC-III, indicate that modulating apoC-III may be a potent therapeutic approach to managing dyslipidemia and cardiovascular disease risk.
载脂蛋白C-III(ApoC-III)于近50年前被发现,但多年来并未引起太多关注。然而,随着流行病学和孟德尔随机化研究将ApoC-III与低甘油三酯水平及心血管疾病(CVD)发病率降低联系起来,它已成为一种新型且可能有效的治疗血脂异常和CVD风险的方法。ApoC-III的致动脉粥样硬化作用归因于直接的脂蛋白脂肪酶介导机制和间接机制,如促进富含甘油三酯脂蛋白(TRL)的分泌、引发血管细胞中的促炎反应以及损害TRL残余物不依赖脂蛋白脂肪酶的肝脏清除。使用反义寡核苷酸(可选择性抑制ApoC-III)的临床试验取得了令人鼓舞的结果,表明调节ApoC-III可能是治疗血脂异常和心血管疾病风险的有效方法。