Mipomersen: A Safe and Effective Antisense Therapy Adjunct to Statins in Patients With Hypercholesterolemia

被引:43
作者
Ricotta, Daniel N. [2 ]
Frishman, William [1 ]
机构
[1] New York Med Coll, Dept Med, Westchester Med Ctr, Valhalla, NY 10595 USA
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Med, Boston, MA 02215 USA
关键词
mipomersen; antisense oligonucleotide; hyperlipidemia; familial hypercholesterolemia; TRIGLYCERIDE TRANSFER PROTEIN; DENSITY-LIPOPROTEIN CHOLESTEROL; HUMAN APOLIPOPROTEIN B-100; PLACEBO-CONTROLLED TRIAL; CORONARY-HEART-DISEASE; LOWER LDL CHOLESTEROL; FAMILIAL HYPOBETALIPOPROTEINEMIA; HEPATIC STEATOSIS; MESSENGER-RNA; B SECRETION;
D O I
10.1097/CRD.0b013e31823424be
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mipomersen is an antisense oligonucleotide inhibitor of apolipoprotein (apo) B-100 currently in phase 3 of development for the treatment of hyperlipidemia in patients with a high risk for cardiovascular disease. The drug acts by inhibiting the production of apoB-100, which is the structural core for all atherogenic lipids, including low-density lipoprotein cholesterol (LDL-C). The agent has been shown to produce significant reductions in LDL-C from baseline values compared with placebos. Clinical trials have demonstrated that mipomersen reduces LDL-C up to 44% in patients with familial hypercholesterolemia and patients with significantly elevated LDL despite taking maximum doses of statins. Unlike other medications that target apoB-100, such as microsomal triglyceride transfer proteins, mipomersen does not cause hepatic steatosis or intestinal steatosis and does not affect dietary fat absorption. Adverse side effects encountered with mipomersen include flu-like symptoms, injection site reactions, and elevated liver transaminases. If future studies continue to show such promising results, mipomersen would likely be a viable additional lipid-lowering therapy for patients who are at high cardiovascular risk, intolerant to statins, and/or not at target lipid levels despite maximum doses of statin therapy. Clinical outcome studies looking at cardiovascular disease end points still need to be done.
引用
收藏
页码:90 / 95
页数:6
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