Low-density Lipoprotein-Cholesterol Lowering Strategies for Prevention of Atherosclerotic Cardiovascular Disease: Focus on siRNA Treatment Targeting PCSK9 (Inclisiran)
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作者:
Sinning, David
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机构:
Charite Univ Med Berlin, Campus Benjamin Franklin, Dept Cardiol, Berlin, GermanyCharite Univ Med Berlin, Campus Benjamin Franklin, Dept Cardiol, Berlin, Germany
Sinning, David
[1
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Landmesser, Ulf
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机构:
Charite Univ Med Berlin, Campus Benjamin Franklin, Dept Cardiol, Berlin, Germany
Berlin Inst Hlth BIH, Hindenburgdamm 30, D-12203 Berlin, Germany
German Ctr Cardiovasc Res DZHK, Partner Site Berlin, Berlin, GermanyCharite Univ Med Berlin, Campus Benjamin Franklin, Dept Cardiol, Berlin, Germany
Landmesser, Ulf
[1
,2
,3
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机构:
[1] Charite Univ Med Berlin, Campus Benjamin Franklin, Dept Cardiol, Berlin, Germany
[2] Berlin Inst Hlth BIH, Hindenburgdamm 30, D-12203 Berlin, Germany
[3] German Ctr Cardiovasc Res DZHK, Partner Site Berlin, Berlin, Germany
Purpose of Review The aim of low-density lipoprotein-cholesterol (LDL-C) lowering therapies is to safely achieve a consistent and long-term reduction in exposure of the vasculature to atherogenic lipoproteins in order to reduce the risk of atherosclerotic cardiovascular (CV) disease and the associated CV events, such as myocardial infarctions and ischemic strokes. This review summarizes the concept and clinical development of a novel molecular approach to efficiently lower LDL-C, a synthetic small interfering ribonucleic acid (siRNA)-inclisiran-directed against proprotein convertase subtilisin-kexin type 9 (PCSK9). Recent Findings The understanding of genes regulating atherogenic lipoproteins and their causal role in the development of atherosclerotic CV disease has substantially advanced over the past years. This has opened the possibility for development of molecular therapies targeting these atherogenic lipoproteins, in particular by RNA-targeted treatment approaches. The most advanced clinical development program is the siRNA-treatment targeting PCSK9 (inclisiran), involving more than 4000 patients in clinical studies. Phase 1 and 2 studies have identified the dose of 300 mg inclisiran for efficient LDL-C lowering. Most recently, three phase 3 studies demonstrated that a regimen of inclisiran every 6 months was feasible and reduced LDL-C by approximately 50% in patients at high or very high CV risk or with familial hypercholesterolemia. Adverse events were similar in the inclisiran and the placebo groups, except for more frequent transient injection site reactions with inclisiran than with placebo. siRNA therapy targeting PCSK9 (inclisiran) applied twice a year efficiently reduced LDL-C by approximately 50% and was safe in recent phase 3 studies. The effects of this treatment on CV outcome are currently further assessed in a large ongoing CV outcome trial.
机构:
Rey Juan Carlos Univ, Univ Hosp Alcorcon Fdn, Internal Med Unit, Budapest 1, Madrid 28922, SpainRey Juan Carlos Univ, Univ Hosp Alcorcon Fdn, Internal Med Unit, Budapest 1, Madrid 28922, Spain
机构:
Stanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Stanford Univ, Ctr Digital Hlth, Stanford, CA USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Rodriguez, F.
Koren, M.
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Jacksonville Ctr Clin Res, Jacksonville, FL USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Koren, M.
East, C.
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Baylor Scott & White Res Inst, Soltero Cardiovasc Res Ctr, Dallas, TX USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
East, C.
Ali, Y.
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机构:
Novartis Pharmaceut, Novartis, E Hanover, NJ USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Ali, Y.
Kleeman, K.
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机构:
Novartis Pharmaceut, Novartis, E Hanover, NJ USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Kleeman, K.
Sarwat, S.
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机构:
Novartis Pharmaceut, Novartis, E Hanover, NJ USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Sarwat, S.
Abbas, C.
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机构:
Novartis Pharmaceut, Novartis, E Hanover, NJ USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
Abbas, C.
Toth, P. P.
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机构:
CGH Med Ctr, Preventat Cardiol, Rock Falls, IL USAStanford Univ, Sch Med, Div Cardiovasc Med, Stanford, CA USA
机构:
UCL, Dept Clin Biochem, Univ Coll London Med Sch, London NW3 2QG, England
Univ Ioannina, Sch Med, Dept Internal Med, GR-45110 Ioannina, GreeceUCL, Dept Clin Biochem, Univ Coll London Med Sch, London NW3 2QG, England
Kostapanos, Michael S.
Katsiki, Niki
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机构:
Agios Dimitrios Gen Hosp, Dept Internal Med 1, Thessaloniki, GreeceUCL, Dept Clin Biochem, Univ Coll London Med Sch, London NW3 2QG, England
Katsiki, Niki
Elisaf, Moses S.
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机构:
Univ Ioannina, Sch Med, Dept Internal Med, GR-45110 Ioannina, GreeceUCL, Dept Clin Biochem, Univ Coll London Med Sch, London NW3 2QG, England
Elisaf, Moses S.
Mikhailidis, Dimitri P.
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机构:
UCL, Dept Clin Biochem, Univ Coll London Med Sch, London NW3 2QG, EnglandUCL, Dept Clin Biochem, Univ Coll London Med Sch, London NW3 2QG, England