PCSK9 Inhibitors and Cardiovascular Disease: Impact on Cardiovascular Outcomes

Author:

Farmaki Paraskevi1,Damaskos Christos2,Garmpis Nikolaos2,Garmpi Anna3,Savvanis Spyridon4,Diamantis Evangelos5

Affiliation:

1. First Department of Pediatrics, Aghia Sophia Children's Hospital, Athens, Greece

2. Second Department of Propedeutic Surgery, Laiko General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece

3. Internal Medicine Department, Laiko General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece

4. Department of Internal Medicine, General Hospital of Athens "Elpis", Athens, Greece

5. Department of Endocrinology, Diabetes and Metabolism, Evangelismos Hospital, Athens, Greece

Abstract

Cardiovascular Disease (CVD) remains the leading cause of morbidity and mortality in the western world. Hypolipidemic drugs have long been used for the primary and secondary prevention of heart disease. However, the high frequency of recurrent events in patients despite hypolipidemic therapy has increased the need for new more targeted therapeutic approaches. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are monoclonal antibodies to the PCSK9 gene and represent a new class of drugs that have been shown to further decrease LDL-C when administered as a monotherapy or in combination with statins. In addition to LDL reduction, PCSK9 inhibitors are shown to decrease apolipoprotein B and lipoprotein (a) levels without major adverse effects. Whether or not PCSK9 inhibitors can actually reduce the incidence of cardiovascular events and ameliorate CVD prognosis is yet to be clarified. This review summarizes recent literature on the safety and efficacy of PCSK9 inhibitors on CVD outcome and its potential role in the management of patients with high-risk cardiovascular disease.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery

Reference74 articles.

1. Piepoli M.F.; Hoes A.W.; Agewall S.; Albus C.; Brotons C.; Catapano A.L.; Cooney M.T.; Corrà U.; Cosyns B.; Deaton C.; Graham I.; Hall M.S.; Hobbs F.D.R.; Løchen M.L.; Löllgen H.; Marques-Vidal P.; Perk J.; Prescott E.; Redon J.; Richter D.J.; Sattar N.; Smulders Y.; Tiberi M.; van der Worp H.B.; van Dis I.; Verschuren W.M.M.; Binno S.; 2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts)Developed with the special contribution of the European Association for Cardiovascular Prevention

2. Chasman D.I.; Giulianini F.; MacFadyen J.; Barratt B.J.; Nyberg F.; Ridker P.M.; Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial. Circ Cardiovasc Genet 2012,5(2),257-264

3. Murphy S.A.; Cannon C.P.; Wiviott S.D.; McCabe C.H.; Braunwald E.; Reduction in recurrent cardiovascular events with intensive lipid-lowering statin therapy compared with moderate lipid-lowering statin therapy after acute coronary syndromes from the PROVE IT-TIMI 22 (Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis In Myocardial Infarction 22) trial. J Am Coll Cardiol 2009,54(25),2358-2362

4. Baigent C.; Blackwell L.; Emberson J.; Holland L.E.; Reith C.; Bhala N.; Peto R.; Barnes E.H.; Keech A.; Simes J.; Collins R.; Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet 2010,376(9753),1670-1681

5. Baigent C.; Keech A.; Kearney P.M.; Blackwell L.; Buck G.; Pollicino C.; Kirby A.; Sourjina T.; Peto R.; Collins R.; Simes R.; Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins. Lancet 2005,366(9493),1267-1278

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