Antisense oligonucleotide targeting apolipoprotein(a) Treatment of lipoprotein disorders Treatment of cardiovascular diseases

被引:2
|
作者
Warden, Bruce A. [1 ]
Duell, P. Barton [1 ,2 ]
机构
[1] Oregon Hlth & Sci Univ, Ctr Prevent Cardiol, Knight Cardiovasc Inst, 3181 Sw Sam Jackson Pk Rd,Mail Code HRC5N, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Div Endocrinol Diabet & Clin Nutr, Portland, OR 97201 USA
关键词
Lipoprotein(a); Pharmacotherapy; Antisense oligonucleotide; Cardiovascular disease; Pelacarsen; AKCEA-APO(a)-L-Rx; IONIS-APO(a)-L-Rx; ISIS-681257; ISIS-APO(a)-L-Rx; TQJ-230; CORONARY-HEART-DISEASE; ELEVATED LIPOPROTEIN(A); REDUCES LIPOPROTEIN(A); RAISED LIPOPROTEIN(A); LIPID APHERESIS; INCREASED RISK; DOUBLE-BLIND; MASS LEVELS; PREVENTION; THERAPY;
D O I
10.1358/dof.2022.47.1.3369190
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Elevated levels of lipoprotein(a) [Lp(a)] are a prevalent and causative risk factor for atherosclerotic cardiovascular disease (ASCVD), but effective pharmacologic strategies for Lp(a) lowering are needed. Antisense oligonucleotides (ASOs) are effective for gene silencing and reducing production of unwanted proteins. Pelacarsen, a subcutaneously administered third-generation ASO directed against apolipoprotein(a) japo(a)J, prevents translation of and induces degradation of apo(a) messenger ribonucleic acid (mRNA). Pelacarsen has multiple side-chain modifications, including conjugation with N-acetylgalactosamine (GalNAc), which increases drug potency, half-life and drug tolerance. Pelacarsen significantly reduces Lp(a) concentrations by up to 80-90%, which may allow many patients to achieve normal Lp(a) levels. Pelacarsen has a good safety profile, bypassing toxicities associated with second-generation ASOs. The medical community awaits the results of the phase III Lp(a)HORIZON trial evaluating use of pelacarsen in patients with elevated Lp(a) and established ASCVD, which will provide the first definitive evidence of whether Lp(a) lowering reduces ASCVD risk.
引用
收藏
页码:11 / 25
页数:16
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