Medical Department II, Grosshadern, University Munich, Munich, Germany.
Curr Pharm Des. 2011;17(9):871-6. doi: 10.2174/138161211795428777.
Elevated levels of lipoprotein(a) are causally related to premature atherosclerosis. It is therefore of interested to evaluate by which treatment modalities elevated lipoprotein(a) levels can be decreased. With the exception of niacin, currently available lipid modifying drugs have only little effect on lipoprotein(a) levels. Niacin can decrease lipoprotein(a) concentration in a dose dependent fashion by approximately 20-30%. Similarly, acetylsalicylic acid and L-carnitine as well as some medications in development (mipomersen, eprotirome, Proprotein convertase subtilisin/kexin type 9 (PCSK-9) inhibitors, Cholesterol-ester-transfer protein (CETP inhibitors) can decrease elevated lipoprotein(a) concentrations. It is unclear whether this lipoprotein(a) reduction also translates into a decreased cardio-vascular morbidity or mortality. Estrogen (with or without progesterone) and tibolone but not tamoxifene or raloxifene can also decrease elevated lipoprotein(a) concentrations. The most dramatic change in lipoprotein(a) concentration can be achieved with regular lipid apheresis.
脂蛋白(a)水平升高与早发性动脉粥样硬化有关。因此,评估哪些治疗方法可以降低脂蛋白(a)水平是很有意义的。除了烟酸以外,目前可用的调脂药物对脂蛋白(a)水平的影响很小。烟酸可以剂量依赖性地降低脂蛋白(a)浓度约 20-30%。同样,乙酰水杨酸和左旋肉碱以及一些正在开发的药物(米泊美生、依替膦酸、脯氨酸羧肽酶/激肽释放酶 9(PCSK-9)抑制剂、胆固醇酯转移蛋白(CETP)抑制剂)也可以降低升高的脂蛋白(a)浓度。目前尚不清楚这种脂蛋白(a)的降低是否也能转化为降低心血管发病率或死亡率。雌激素(无论是否联合孕激素)和替勃龙,但不是他莫昔芬或雷洛昔芬,也可以降低升高的脂蛋白(a)浓度。脂蛋白(a)浓度的最大变化可以通过定期的血脂吸附来实现。