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Safety and Tolerability of PCSK9 Inhibitors: Current Insights
The current era of preventive cardiology continues to emphasize on low-density lipoprotein cholesterol (LDL-C) reduction to alleviate the burden of atherosclerotic cardiovascular disease (ASCVD). In this regard, the pharmacological inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737942/ https://www.ncbi.nlm.nih.gov/pubmed/33335431 http://dx.doi.org/10.2147/CPAA.S288831 |
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author | Kosmas, Constantine E Skavdis, Andreas Sourlas, Andreas Papakonstantinou, Evangelia J Peña Genao, Edilberto Echavarria Uceta, Rogers Guzman, Eliscer |
author_facet | Kosmas, Constantine E Skavdis, Andreas Sourlas, Andreas Papakonstantinou, Evangelia J Peña Genao, Edilberto Echavarria Uceta, Rogers Guzman, Eliscer |
author_sort | Kosmas, Constantine E |
collection | PubMed |
description | The current era of preventive cardiology continues to emphasize on low-density lipoprotein cholesterol (LDL-C) reduction to alleviate the burden of atherosclerotic cardiovascular disease (ASCVD). In this regard, the pharmacological inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) enzyme via monoclonal antibodies has emerged as a novel lipid-lowering therapy, leading to a marked reduction in circulating LDL-C levels and subsequent improvement of cardiovascular outcomes. As these agents are increasingly used in current clinical practice, mounting scientific and clinical evidence supports that PCSK9 inhibitors offer an excellent safety and tolerability profile with a low incidence of adverse events. Notably, the most frequently reported side effects are injection-site reactions. In contrast to statins, PCSK9 inhibitors do not appear to exert a detrimental effect on glycemic control or to increase the incidence of new-onset diabetes mellitus. Accumulating evidence also indicates that PCSK9 inhibitors are a safe, well-tolerated and effective therapeutic strategy for patients with statin intolerance. On the other hand, as PCSK9 inhibitors reduce LDL-C to unprecedented low levels, a large body of current research has examined the effects of their long-term administration on neurocognition and on levels of vitamin E and other fat-soluble vitamins, providing encouraging results. This review aims to present and discuss the current clinical and scientific evidence pertaining to the safety and tolerability of PCSK9 inhibitors. |
format | Online Article Text |
id | pubmed-7737942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-77379422020-12-16 Safety and Tolerability of PCSK9 Inhibitors: Current Insights Kosmas, Constantine E Skavdis, Andreas Sourlas, Andreas Papakonstantinou, Evangelia J Peña Genao, Edilberto Echavarria Uceta, Rogers Guzman, Eliscer Clin Pharmacol Review The current era of preventive cardiology continues to emphasize on low-density lipoprotein cholesterol (LDL-C) reduction to alleviate the burden of atherosclerotic cardiovascular disease (ASCVD). In this regard, the pharmacological inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) enzyme via monoclonal antibodies has emerged as a novel lipid-lowering therapy, leading to a marked reduction in circulating LDL-C levels and subsequent improvement of cardiovascular outcomes. As these agents are increasingly used in current clinical practice, mounting scientific and clinical evidence supports that PCSK9 inhibitors offer an excellent safety and tolerability profile with a low incidence of adverse events. Notably, the most frequently reported side effects are injection-site reactions. In contrast to statins, PCSK9 inhibitors do not appear to exert a detrimental effect on glycemic control or to increase the incidence of new-onset diabetes mellitus. Accumulating evidence also indicates that PCSK9 inhibitors are a safe, well-tolerated and effective therapeutic strategy for patients with statin intolerance. On the other hand, as PCSK9 inhibitors reduce LDL-C to unprecedented low levels, a large body of current research has examined the effects of their long-term administration on neurocognition and on levels of vitamin E and other fat-soluble vitamins, providing encouraging results. This review aims to present and discuss the current clinical and scientific evidence pertaining to the safety and tolerability of PCSK9 inhibitors. Dove 2020-12-11 /pmc/articles/PMC7737942/ /pubmed/33335431 http://dx.doi.org/10.2147/CPAA.S288831 Text en © 2020 Kosmas et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Kosmas, Constantine E Skavdis, Andreas Sourlas, Andreas Papakonstantinou, Evangelia J Peña Genao, Edilberto Echavarria Uceta, Rogers Guzman, Eliscer Safety and Tolerability of PCSK9 Inhibitors: Current Insights |
title | Safety and Tolerability of PCSK9 Inhibitors: Current Insights |
title_full | Safety and Tolerability of PCSK9 Inhibitors: Current Insights |
title_fullStr | Safety and Tolerability of PCSK9 Inhibitors: Current Insights |
title_full_unstemmed | Safety and Tolerability of PCSK9 Inhibitors: Current Insights |
title_short | Safety and Tolerability of PCSK9 Inhibitors: Current Insights |
title_sort | safety and tolerability of pcsk9 inhibitors: current insights |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737942/ https://www.ncbi.nlm.nih.gov/pubmed/33335431 http://dx.doi.org/10.2147/CPAA.S288831 |
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