Preventive Cardiology, Sterling Rock Falls Clinic, Sterling, Illinois 61081, USA.
Drugs. 2010 Jul 30;70(11):1363-79. doi: 10.2165/10898610-000000000-00000.
Mammalian sterol and lipid metabolism depends on a large number of highly evolved biochemical and histological processes responsible for the absorption, distribution and steady-state anabolic/catabolic handling of these substances. Lipoproteins are complex polymolecular assemblies comprising phospholipids, cholesterol and cholesterol esters, triglycerides and a variety of apolipoproteins. The primary function of lipoproteins is to facilitate the systemic distribution of sterols and lipids. Abnormalities in lipoprotein metabolism are quite common and are attributable to a large number of genetic mutations, metabolic derangements such as insulin resistance or thyroid dysfunction, and excess availability of cholesterol and fat from dietary sources. Dyslipidaemic states facilitate endothelial dysfunction and atherogenesis. Dyslipidaemia is recognized as a risk factor for cardiovascular disease in both men and women, and people of all racial and ethnic groups throughout the world. Dyslipidaemia is modifiable with dietary change and the use of medications that impact on lipid metabolism through a variety of mechanisms. Reducing atherogenic lipoprotein burden in serum is associated with significant and meaningful reductions in risk for a variety of cardiovascular endpoints, including myocardial infarction, ischaemic stroke, development of peripheral arterial disease and mortality. This review provides an overview on how to best position lipid-lowering drugs when attempting to normalize serum lipid profiles and reduce risk for cardiovascular disease. HMG-CoA reductase inhibitors (statins) are widely accepted to be the agents of choice for reducing serum levels of low-density lipoprotein cholesterol (LDL-C) in both the primary and secondary prevention settings. Ezetimibe and bile acid sequestrants are both effective agents for reducing LDL-C, either used alone or in combination with statins. The statins, fibric acid derivatives (fibrates) and niacin raise high-density lipoprotein cholesterol to different extents depending upon genetic and metabolic background. Fibrates, niacin and omega-3 fish oils are efficacious therapies for reducing serum triglycerides. Combinations of these drugs are frequently required for normalizing mixed forms of dyslipidaemia.
哺乳动物的甾醇和脂质代谢依赖于大量高度进化的生化和组织学过程,这些过程负责这些物质的吸收、分布和稳态合成代谢/分解代谢处理。脂蛋白是由磷脂、胆固醇和胆固醇酯、甘油三酯和各种载脂蛋白组成的复杂多分子组装体。脂蛋白的主要功能是促进甾醇和脂质的全身分布。脂蛋白代谢异常相当常见,归因于大量基因突变、代谢紊乱(如胰岛素抵抗或甲状腺功能障碍)以及膳食来源胆固醇和脂肪的过度供应。血脂异常状态促进内皮功能障碍和动脉粥样硬化形成。血脂异常被认为是男性和女性以及世界各地所有种族和民族人群心血管疾病的危险因素。通过改变饮食和使用通过多种机制影响脂质代谢的药物,可以改变血脂异常。降低血清中致动脉粥样硬化脂蛋白的负担与多种心血管终点(包括心肌梗死、缺血性中风、外周动脉疾病发展和死亡率)风险的显著和有意义降低相关。本综述提供了关于如何在尝试使血清脂质谱正常化并降低心血管疾病风险时最佳定位降脂药物的概述。羟甲基戊二酰辅酶 A 还原酶抑制剂(他汀类药物)被广泛认为是降低原发性和二级预防环境中血清低密度脂蛋白胆固醇(LDL-C)水平的首选药物。依折麦布和胆汁酸螯合剂都是降低 LDL-C 的有效药物,可单独使用或与他汀类药物联合使用。他汀类药物、纤维酸衍生物(贝特类药物)和烟酸根据遗传和代谢背景不同程度地升高高密度脂蛋白胆固醇。贝特类药物、烟酸和欧米伽-3 鱼油可有效降低血清甘油三酯。为了使混合形式的血脂异常正常化,通常需要联合使用这些药物。