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Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists

BACKGROUND: Atherosclerotic cardiovascular disease is a significant cause of morbidity and mortality worldwide. While use of statin therapy has improved management of lipids, an unmet need in reducing residual atherosclerotic cardiovascular disease risk and ischemic events persists. We provide an ov...

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Autores principales: Patel, Dhiren, Busch, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547235/
https://www.ncbi.nlm.nih.gov/pubmed/34191622
http://dx.doi.org/10.1177/10742484211023715
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author Patel, Dhiren
Busch, Robert
author_facet Patel, Dhiren
Busch, Robert
author_sort Patel, Dhiren
collection PubMed
description BACKGROUND: Atherosclerotic cardiovascular disease is a significant cause of morbidity and mortality worldwide. While use of statin therapy has improved management of lipids, an unmet need in reducing residual atherosclerotic cardiovascular disease risk and ischemic events persists. We provide an overview of the pharmacology of omega-3 fatty acids, omega-3 fatty acid cardiovascular outcomes trials, landmark clinical data and pharmacology of icosapent ethyl (a stable and highly purified ethyl ester of eicosapentaenoic acid), and the critical differences between fish oil supplements and prescription omega-3 fatty acids. METHOD: A PubMed literature review was conducted in April 2020 to identify articles discussing omega-3 fatty acid cardiovascular outcomes trials, pharmacology of icosapent ethyl, and the evaluation of fish oil dietary supplements and prescription omega-3 fatty acids. RESULTS: Both eicosapentaenoic acid and docosahexaenoic acid have been widely associated with positive health benefits; however, data are inconsistent regarding the benefit of combination eicosapentaenoic acid and docosahexaenoic acid in patients with cardiovascular disease. Eicosapentaenoic acid, and specifically icosapent ethyl, has demonstrated atherosclerotic cardiovascular disease risk reduction among statin-treated patients. Important clinical differences exist between dietary supplement and prescription omega-3 fatty acid products. CONCLUSIONS: As research regarding the optimal management of dyslipidemia continues, additional therapy beyond statins is necessary to reduce atherosclerotic cardiovascular disease risk. In large cardiovascular outcomes trials, eicosapentaenoic acid has demonstrated cardiovascular benefit. Icosapent ethyl possesses a favorable efficacy and safety profile and should be considered as an adjunct to statin therapy to reduce ischemic event risk.
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spelling pubmed-85472352021-10-27 Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists Patel, Dhiren Busch, Robert J Cardiovasc Pharmacol Ther Review Articles BACKGROUND: Atherosclerotic cardiovascular disease is a significant cause of morbidity and mortality worldwide. While use of statin therapy has improved management of lipids, an unmet need in reducing residual atherosclerotic cardiovascular disease risk and ischemic events persists. We provide an overview of the pharmacology of omega-3 fatty acids, omega-3 fatty acid cardiovascular outcomes trials, landmark clinical data and pharmacology of icosapent ethyl (a stable and highly purified ethyl ester of eicosapentaenoic acid), and the critical differences between fish oil supplements and prescription omega-3 fatty acids. METHOD: A PubMed literature review was conducted in April 2020 to identify articles discussing omega-3 fatty acid cardiovascular outcomes trials, pharmacology of icosapent ethyl, and the evaluation of fish oil dietary supplements and prescription omega-3 fatty acids. RESULTS: Both eicosapentaenoic acid and docosahexaenoic acid have been widely associated with positive health benefits; however, data are inconsistent regarding the benefit of combination eicosapentaenoic acid and docosahexaenoic acid in patients with cardiovascular disease. Eicosapentaenoic acid, and specifically icosapent ethyl, has demonstrated atherosclerotic cardiovascular disease risk reduction among statin-treated patients. Important clinical differences exist between dietary supplement and prescription omega-3 fatty acid products. CONCLUSIONS: As research regarding the optimal management of dyslipidemia continues, additional therapy beyond statins is necessary to reduce atherosclerotic cardiovascular disease risk. In large cardiovascular outcomes trials, eicosapentaenoic acid has demonstrated cardiovascular benefit. Icosapent ethyl possesses a favorable efficacy and safety profile and should be considered as an adjunct to statin therapy to reduce ischemic event risk. SAGE Publications 2021-06-30 2021-11 /pmc/articles/PMC8547235/ /pubmed/34191622 http://dx.doi.org/10.1177/10742484211023715 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review Articles
Patel, Dhiren
Busch, Robert
Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists
title Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists
title_full Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists
title_fullStr Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists
title_full_unstemmed Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists
title_short Omega-3 Fatty Acids and Cardiovascular Disease: A Narrative Review for Pharmacists
title_sort omega-3 fatty acids and cardiovascular disease: a narrative review for pharmacists
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547235/
https://www.ncbi.nlm.nih.gov/pubmed/34191622
http://dx.doi.org/10.1177/10742484211023715
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