Lipoprotein(a): Medical Treatment Options for an Elusive Molecule

被引：7

作者：

Parhofer, Klaus G. ^{[1
]}

机构：

[1] Univ Munich, Dept Med 2, D-81377 Munich, Germany

来源：

CURRENT PHARMACEUTICAL DESIGN | 2011年 / 17卷 / 09期

关键词：

Apoprotein(a); carnitine; ascorbic acid; mipomersen; statin; eprotirome; anacetrapib; dalcetrapib; HORMONE REPLACEMENT THERAPY; LOW-DENSITY-LIPOPROTEIN; EXTENDED-RELEASE NIACIN; HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; CORONARY-HEART-DISEASE; C-REACTIVE PROTEIN; PLASMA LIPOPROTEIN(A); SERUM LIPOPROTEIN(A); L-CARNITINE; APOLIPOPROTEIN(A) GENE;

D O I：

暂无

中图分类号：

R9 [药学];

学科分类号：

100702 [药剂学];

摘要：

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.

引用

页码：871 / 876

页数：6

共 80 条

[1]

Akaike M, 2002, CLIN CHEM, V48, P1454

[2]

Effect of Mipomersen, an Apolipoprotein B Synthesis Inhibitor, on Low-Density Lipoprotein Cholesterol in Patients With Familial Hypercholesterolemia [J].