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The Future of Lipid-Lowering Therapy
The recent introduction of inhibitors of proprotein convertase subtilisin/kexin 9 to lower low-density lipoprotein (LDL) cholesterol on top of statins or as monotherapy is rapidly changing the landscape of treatment of atherosclerotic cardiovascular disease (ASCVD). However, existing lipid-lowering...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678580/ https://www.ncbi.nlm.nih.gov/pubmed/31340607 http://dx.doi.org/10.3390/jcm8071085 |
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author | van Zwol, Willemien Rimbert, Antoine Kuivenhoven, Jan Albert |
author_facet | van Zwol, Willemien Rimbert, Antoine Kuivenhoven, Jan Albert |
author_sort | van Zwol, Willemien |
collection | PubMed |
description | The recent introduction of inhibitors of proprotein convertase subtilisin/kexin 9 to lower low-density lipoprotein (LDL) cholesterol on top of statins or as monotherapy is rapidly changing the landscape of treatment of atherosclerotic cardiovascular disease (ASCVD). However, existing lipid-lowering drugs have little impact on lipoprotein(a) (Lp(a)) or plasma triglycerides, two other risk factors for ASCVD. This review summarizes the evidence and the rationale to target Lp(a) and triglycerides and provides an overview of currently tested strategies to lower Lp(a), apolipoprotein C-III and angiopoietin-like protein 3. In addition, it summarizes new findings on the use of omega-3 fatty acids (OM3FA) to fight ASCVD. With the exception of OM3FA supplementation, the promise of the experimental drugs discussed here depends on the long-term safety and efficacy of monoclonal antibodies and/or antisense oligonucleotides Clinical outcome trials will ultimately prove whether these new therapeutic modalities will reduce ASCVD risk. |
format | Online Article Text |
id | pubmed-6678580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66785802019-08-19 The Future of Lipid-Lowering Therapy van Zwol, Willemien Rimbert, Antoine Kuivenhoven, Jan Albert J Clin Med Review The recent introduction of inhibitors of proprotein convertase subtilisin/kexin 9 to lower low-density lipoprotein (LDL) cholesterol on top of statins or as monotherapy is rapidly changing the landscape of treatment of atherosclerotic cardiovascular disease (ASCVD). However, existing lipid-lowering drugs have little impact on lipoprotein(a) (Lp(a)) or plasma triglycerides, two other risk factors for ASCVD. This review summarizes the evidence and the rationale to target Lp(a) and triglycerides and provides an overview of currently tested strategies to lower Lp(a), apolipoprotein C-III and angiopoietin-like protein 3. In addition, it summarizes new findings on the use of omega-3 fatty acids (OM3FA) to fight ASCVD. With the exception of OM3FA supplementation, the promise of the experimental drugs discussed here depends on the long-term safety and efficacy of monoclonal antibodies and/or antisense oligonucleotides Clinical outcome trials will ultimately prove whether these new therapeutic modalities will reduce ASCVD risk. MDPI 2019-07-23 /pmc/articles/PMC6678580/ /pubmed/31340607 http://dx.doi.org/10.3390/jcm8071085 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review van Zwol, Willemien Rimbert, Antoine Kuivenhoven, Jan Albert The Future of Lipid-Lowering Therapy |
title | The Future of Lipid-Lowering Therapy |
title_full | The Future of Lipid-Lowering Therapy |
title_fullStr | The Future of Lipid-Lowering Therapy |
title_full_unstemmed | The Future of Lipid-Lowering Therapy |
title_short | The Future of Lipid-Lowering Therapy |
title_sort | future of lipid-lowering therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678580/ https://www.ncbi.nlm.nih.gov/pubmed/31340607 http://dx.doi.org/10.3390/jcm8071085 |
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