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PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia
Current guidelines for hypercholesterolemia treatment emphasize lifestyle modification and lipid‐modifying therapy to reduce the risk for cardiovascular disease. Statins are the primary class of agents used for the treatment of hypercholesterolemia. Although statins are effective for many patients,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215586/ https://www.ncbi.nlm.nih.gov/pubmed/27195910 http://dx.doi.org/10.1002/jcph.766 |
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author | Ito, Matthew K. Santos, Raul D. |
author_facet | Ito, Matthew K. Santos, Raul D. |
author_sort | Ito, Matthew K. |
collection | PubMed |
description | Current guidelines for hypercholesterolemia treatment emphasize lifestyle modification and lipid‐modifying therapy to reduce the risk for cardiovascular disease. Statins are the primary class of agents used for the treatment of hypercholesterolemia. Although statins are effective for many patients, they fail to achieve optimal reduction in lipids for some patients, including those who have or are at high risk for cardiovascular disease. The PCSK9 gene was identified in the past decade as a potential therapeutic target for the management of patients with hypercholesterolemia. Pharmacologic interventions to decrease PCSK9 levels are in development, with the most promising approach using monoclonal antibodies that bind to PCSK9 in the plasma. Two monoclonal antibodies, alirocumab and evolocumab, have recently been approved for the treatment of hypercholesterolemia, and a third one, bococizumab, is in phase 3 clinical development. All 3 agents achieve significant reductions in levels of low‐density lipoprotein cholesterol, as well as reductions in non‐high‐density lipoprotein cholesterol, apolipoprotein B, and lipoprotein(a). Long‐term outcome trials are under way to determine the sustained efficacy, safety, and tolerability of PCSK9 inhibitors and whether this novel class of agents decreases the risk for major cardiovascular events in patients on lipid‐modifying therapy. Available data suggest that PCSK9 inhibitors provide a robust reduction in atherogenic cholesterol levels with a good safety profile, especially for patients who fail to obtain an optimal clinical response to statin therapy, those who are statin intolerant or have contraindications to statin therapy, and those with familial hypercholesterolemia. |
format | Online Article Text |
id | pubmed-5215586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52155862017-01-18 PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia Ito, Matthew K. Santos, Raul D. J Clin Pharmacol Editor's choice: Review Current guidelines for hypercholesterolemia treatment emphasize lifestyle modification and lipid‐modifying therapy to reduce the risk for cardiovascular disease. Statins are the primary class of agents used for the treatment of hypercholesterolemia. Although statins are effective for many patients, they fail to achieve optimal reduction in lipids for some patients, including those who have or are at high risk for cardiovascular disease. The PCSK9 gene was identified in the past decade as a potential therapeutic target for the management of patients with hypercholesterolemia. Pharmacologic interventions to decrease PCSK9 levels are in development, with the most promising approach using monoclonal antibodies that bind to PCSK9 in the plasma. Two monoclonal antibodies, alirocumab and evolocumab, have recently been approved for the treatment of hypercholesterolemia, and a third one, bococizumab, is in phase 3 clinical development. All 3 agents achieve significant reductions in levels of low‐density lipoprotein cholesterol, as well as reductions in non‐high‐density lipoprotein cholesterol, apolipoprotein B, and lipoprotein(a). Long‐term outcome trials are under way to determine the sustained efficacy, safety, and tolerability of PCSK9 inhibitors and whether this novel class of agents decreases the risk for major cardiovascular events in patients on lipid‐modifying therapy. Available data suggest that PCSK9 inhibitors provide a robust reduction in atherogenic cholesterol levels with a good safety profile, especially for patients who fail to obtain an optimal clinical response to statin therapy, those who are statin intolerant or have contraindications to statin therapy, and those with familial hypercholesterolemia. John Wiley and Sons Inc. 2016-06-21 2017-01 /pmc/articles/PMC5215586/ /pubmed/27195910 http://dx.doi.org/10.1002/jcph.766 Text en © 2016, The Authors. The Journal of Clinical Pharmacology Published by Wiley Periodicals, Inc. on behalf of American College of Clinical Pharmacology This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Editor's choice: Review Ito, Matthew K. Santos, Raul D. PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia |
title | PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia |
title_full | PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia |
title_fullStr | PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia |
title_full_unstemmed | PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia |
title_short | PCSK9 Inhibition With Monoclonal Antibodies: Modern Management of Hypercholesterolemia |
title_sort | pcsk9 inhibition with monoclonal antibodies: modern management of hypercholesterolemia |
topic | Editor's choice: Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215586/ https://www.ncbi.nlm.nih.gov/pubmed/27195910 http://dx.doi.org/10.1002/jcph.766 |
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