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Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up
Inhibition of PCSK9 is a novel therapeutic strategy aimed at reducing low-density-lipoprotein cholesterol (LDL-C) and cardiovascular risk. Evolocumab is a fully humanized monoclonal antibody that inhibits PCSK9, an enzyme that binds to LDL receptors and prevents them from recycling to the hepatocyte...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513834/ https://www.ncbi.nlm.nih.gov/pubmed/28744103 http://dx.doi.org/10.2147/DDDT.S114091 |
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author | Dixon, Dave L Buckley, Leo F Trankle, Cory R Kadariya, Dinesh Abbate, Antonio |
author_facet | Dixon, Dave L Buckley, Leo F Trankle, Cory R Kadariya, Dinesh Abbate, Antonio |
author_sort | Dixon, Dave L |
collection | PubMed |
description | Inhibition of PCSK9 is a novel therapeutic strategy aimed at reducing low-density-lipoprotein cholesterol (LDL-C) and cardiovascular risk. Evolocumab is a fully humanized monoclonal antibody that inhibits PCSK9, an enzyme that binds to LDL receptors and prevents them from recycling to the hepatocyte surface. Clinical trials have demonstrated 50%–70% reductions in LDL-C with evolocumab when used in combination with statin therapy. The recent FOURIER trial demonstrated that evolocumab further reduces cardiovascular events, but not mortality, in high-risk patients already receiving statin therapy. Furthermore, evolocumab did not affect neurocognitive function and was not associated with antidrug-antibody production in over 60,000 patient-years of drug exposure. Appropriate candidates for evolocumab primarily are individuals at high cardiovascular risk, including those with familial hypercholesterolemia and/or established cardiovascular disease, who are already on statin therapy. At this time, the use of evolocumab monotherapy seems appropriate only for individuals deemed statin-intolerant despite attempting several statins. Consideration must be given toward patient willingness to self-inject evolocumab and issues concerning third-party coverage, given the current costs of evolocumab. |
format | Online Article Text |
id | pubmed-5513834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55138342017-07-25 Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up Dixon, Dave L Buckley, Leo F Trankle, Cory R Kadariya, Dinesh Abbate, Antonio Drug Des Devel Ther Review Inhibition of PCSK9 is a novel therapeutic strategy aimed at reducing low-density-lipoprotein cholesterol (LDL-C) and cardiovascular risk. Evolocumab is a fully humanized monoclonal antibody that inhibits PCSK9, an enzyme that binds to LDL receptors and prevents them from recycling to the hepatocyte surface. Clinical trials have demonstrated 50%–70% reductions in LDL-C with evolocumab when used in combination with statin therapy. The recent FOURIER trial demonstrated that evolocumab further reduces cardiovascular events, but not mortality, in high-risk patients already receiving statin therapy. Furthermore, evolocumab did not affect neurocognitive function and was not associated with antidrug-antibody production in over 60,000 patient-years of drug exposure. Appropriate candidates for evolocumab primarily are individuals at high cardiovascular risk, including those with familial hypercholesterolemia and/or established cardiovascular disease, who are already on statin therapy. At this time, the use of evolocumab monotherapy seems appropriate only for individuals deemed statin-intolerant despite attempting several statins. Consideration must be given toward patient willingness to self-inject evolocumab and issues concerning third-party coverage, given the current costs of evolocumab. Dove Medical Press 2017-07-11 /pmc/articles/PMC5513834/ /pubmed/28744103 http://dx.doi.org/10.2147/DDDT.S114091 Text en © 2017 Dixon et al. 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. |
spellingShingle | Review Dixon, Dave L Buckley, Leo F Trankle, Cory R Kadariya, Dinesh Abbate, Antonio Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
title | Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
title_full | Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
title_fullStr | Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
title_full_unstemmed | Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
title_short | Clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
title_sort | clinical utility of evolocumab in the management of hyperlipidemia: patient selection and follow-up |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513834/ https://www.ncbi.nlm.nih.gov/pubmed/28744103 http://dx.doi.org/10.2147/DDDT.S114091 |
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