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
相关论文
共 50 条
  • [41] Treatment of ATTR cardiomyopathy with a TTR specific antisense oligonucleotide, inotersen
    Dasgupta, Noel R.
    Benson, Merrill D.
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2019, 26 : 20 - 21
  • [42] Antithrombotic Effect of Antisense Factor XI Oligonucleotide Treatment in Primates
    Crosby, Jeffrey R.
    Marzec, Ulla
    Revenko, Alexey S.
    Zhao, Chenguang
    Gao, Dacao
    Matafonov, Anton
    Gailani, David
    MacLeod, A. Robert
    Tucker, Erik I.
    Gruber, Andras
    Hanson, Stephen R.
    Monia, Brett P.
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2013, 33 (07) : 1670 - 1678
  • [43] Antisense oligonucleotide treatment prolongs survival in an ALS rat model
    Miller, Timothy M.
    Smith, Richard
    McAlonis-Downes, Melissa
    Szwajkowski, Gabrielle
    Bennett, Frank
    Cleveland, Don
    NEUROLOGY, 2007, 68 (12) : A91 - A91
  • [44] Antisense oligonucleotide suppression of transthyretin synthesis: A possible treatment for FAP
    Benson, MD
    Kluve-Beckerman, B
    Sloop, KW
    Bodenmiller, DM
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2005, 10 : 5 - 5
  • [45] Non-antisense oligonucleotide approaches for experimental treatment of glioblastoma
    Neckers, LM
    Kanekal, M
    Connell, Y
    ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1998, 8 (02): : 177 - 179
  • [46] Suppression of choroid plexus transthyretin levels by antisense oligonucleotide treatment
    Benson, Merrill D.
    Smith, Richard A.
    Hung, Gene
    Kluve-Beckerman, Barbara
    Showalter, Aaron D.
    Sloop, Kyle W.
    Monia, Brett P.
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2010, 17 (02): : 43 - 49
  • [47] Antisense oligonucleotide directed to human apolipoprotein B-100 reduces lipoprotein(a) levels and oxidized phospholipids on human apolipoprotein B-100 particles in lipoprotein(a) transgenic mice
    Merki, Esther
    Graham, Mark J.
    Mullick, Adam E.
    Miller, Elizabeth R.
    Crooke, Rosanne M.
    Pitas, Robert E.
    Witztum, Joseph L.
    Tsimikas, Sotirios
    CIRCULATION, 2008, 118 (07) : 743 - 753
  • [48] RVX-208, a stimulator of apolipoprotein AI gene expression for the treatment of cardiovascular diseases
    McNeill, Eileen
    CURRENT OPINION IN INVESTIGATIONAL DRUGS, 2010, 11 (03) : 357 - 364
  • [49] Volanesorsen, an antisense oligonucleotide to apolipoprotein C-III, increases lipoprotein lipase activity and lowers triglycerides in partial lipodystrophy
    Lightbourne, Marissa
    Startzell, Megan
    Bruce, Kimberley D.
    Brite, Brianna
    Muniyappa, Ranganath
    Skarulis, Monica
    Shamburek, Robert
    Gharib, Ahmed M.
    Ouwerkerk, Ronald
    Walter, Mary
    Eckel, Robert H.
    Brown, Rebecca J.
    JOURNAL OF CLINICAL LIPIDOLOGY, 2022, 16 (06) : 850 - 862
  • [50] A second generation antisense oligonucleotide directed to human apolipoprotein B-100 reduces lipoprotein(a) levels and oxidized phospholipids on apolipoprotein B-100 particles in lipoprotein(a)-transgenic mice
    Merki, Esther
    Graham, Mark J.
    Mullick, Adam
    Miller, Elizabeth R.
    Crooke, Roseanne M.
    Pitas, Robert
    Witztum, Joseph L.
    Tsimikas, Sotirios
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 51 (10) : A294 - A294