Pirillo Angela, Catapano Alberico Luigi
Center for the Study of Atherosclerosis, Bassini Hospital, Cinisello Balsamo, Italy ; IRCCS Multimedica, Milan, Italy.
IRCCS Multimedica, Milan, Italy ; Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.
Drug Des Devel Ther. 2015 Apr 10;9:2129-37. doi: 10.2147/DDDT.S67551. eCollection 2015.
High levels of plasma triglycerides (TG) are a risk factor for cardiovascular diseases, often associated with anomalies in other lipids or lipoproteins. Hypertriglyceridemia (HTG), particularly at very high levels, significantly increases also the risk of acute pancreatitis. Thus, interventions to lower TG levels are required to reduce the risk of pancreatitis and cardiovascular disease. Several strategies may be adopted for TG reduction, including lifestyle changes and pharmacological interventions. Among the available drugs, the most commonly used for HTG are fibrates, nicotinic acid, and omega-3 polyunsaturated fatty acids (usually a mixture of eicosapentaenoic acid, or EPA, and docosahexaenoic acid, or DHA). These last are available under different concentrated formulations containing high amounts of omega-3 fatty acids, including a mixture of EPA and DHA or pure EPA. The most recent formulation contains a free fatty acid (FFA) form of EPA and DHA, and exhibits a significantly higher bioavailability compared with the ethyl ester forms contained in the other formulations. This is due to the fact that the ethyl ester forms, to be absorbed, need to be hydrolyzed by the pancreatic enzymes that are secreted in response to fat intake, while the FFA do not. This higher bioavailability translates into a higher TG-lowering efficacy compared with the ethyl ester forms at equivalent doses. Omega-3 FFA are effective in reducing TG levels and other lipids in hypertriglyceridemic patients as well as in high cardiovascular risk patients treated with statins and residual HTG. Currently, omega-3 FFA formulation is under evaluation to establish whether, in high cardiovascular risk subjects, the addition of omega-3 to statin therapy may prevent or reduce major cardiovascular events.
高水平的血浆甘油三酯(TG)是心血管疾病的一个危险因素,常与其他脂质或脂蛋白异常相关。高甘油三酯血症(HTG),尤其是在甘油三酯水平非常高时,也会显著增加急性胰腺炎的风险。因此,需要采取降低TG水平的干预措施来降低胰腺炎和心血管疾病的风险。可以采用多种策略来降低TG水平,包括生活方式改变和药物干预。在现有药物中,最常用于治疗HTG的是贝特类药物、烟酸和ω-3多不饱和脂肪酸(通常是二十碳五烯酸,即EPA,和二十二碳六烯酸,即DHA的混合物)。最后这些物质有不同的高浓度制剂可供选择,这些制剂含有大量的ω-3脂肪酸,包括EPA和DHA的混合物或纯EPA。最新的制剂含有EPA和DHA的游离脂肪酸(FFA)形式,与其他制剂中含有的乙酯形式相比,其生物利用度显著更高。这是因为乙酯形式在被吸收时需要被胰腺酶水解,胰腺酶是在摄入脂肪后分泌的,而FFA则不需要。与同等剂量的乙酯形式相比,这种更高的生物利用度转化为更高的降低TG的疗效。ω-3 FFA在降低高甘油三酯血症患者以及接受他汀类药物治疗且仍有HTG的高心血管风险患者的TG水平和其他脂质方面是有效的。目前,正在对ω-3 FFA制剂进行评估,以确定在高心血管风险受试者中,在他汀类药物治疗中添加ω-3是否可以预防或减少主要心血管事件。