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Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition
SARS-CoV-2 infection continues to cause increased morbidity and mortality, and due to the slow pace of vaccination COVID-19 will probably remain a global burden to health systems for a long time. Unfortunately, the necessary prevention and treatment strategies of COVID-19 have led to restriction mea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349422/ https://www.ncbi.nlm.nih.gov/pubmed/34622243 http://dx.doi.org/10.1016/j.athplu.2021.08.001 |
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author | Vuorio, Alpo Strandberg, Timo E. Raal, Frederik Santos, Raul D. Kovanen, Petri T. |
author_facet | Vuorio, Alpo Strandberg, Timo E. Raal, Frederik Santos, Raul D. Kovanen, Petri T. |
author_sort | Vuorio, Alpo |
collection | PubMed |
description | SARS-CoV-2 infection continues to cause increased morbidity and mortality, and due to the slow pace of vaccination COVID-19 will probably remain a global burden to health systems for a long time. Unfortunately, the necessary prevention and treatment strategies of COVID-19 have led to restriction measures that are hampering the routine care of common chronic metabolic conditions like hypercholesterolemia. It is of particular concern that during the acute phase of COVID-19, the control of pre-existing metabolic diseases tends to get worse which again increases the risk for complications and a poor outcome in these patients. A significant contributor to these complications is endothelial dysfunction which is associated with COVID-19. This Commentary will discuss the impact of COVID-19 on endothelial function particularly in patients with familial hypercholesterolemia (FH), a metabolic inherited disease known to in itself adversely affect endothelial function. There should be no hesitation to continue with statin therapy in severe hypercholesterolemic patients with COVID-19. We argue that in FH patients with COVID-19 the clinicians need even consider intensifying statin therapy as well as the addition of other lipid-lowering agents, such as proprotein convertase subtilisin/kexin type 9(PCSK9) inhibitors. In contrast to statins, the PCSK9 inhibitors lower lipoprotein(a) [Lp(a)] level, and, accordingly, these latter drugs need to be considered particularly in FH patients with an elevated level of Lp(a). This call applies to the in-hospital stay and also beyond. When considering that the vasculopathic effects of COVID-19 may persist, a long-term follow-up of individualized therapies in FH patients is warranted. |
format | Online Article Text |
id | pubmed-8349422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83494222021-08-09 Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition Vuorio, Alpo Strandberg, Timo E. Raal, Frederik Santos, Raul D. Kovanen, Petri T. Atheroscler Plus Article SARS-CoV-2 infection continues to cause increased morbidity and mortality, and due to the slow pace of vaccination COVID-19 will probably remain a global burden to health systems for a long time. Unfortunately, the necessary prevention and treatment strategies of COVID-19 have led to restriction measures that are hampering the routine care of common chronic metabolic conditions like hypercholesterolemia. It is of particular concern that during the acute phase of COVID-19, the control of pre-existing metabolic diseases tends to get worse which again increases the risk for complications and a poor outcome in these patients. A significant contributor to these complications is endothelial dysfunction which is associated with COVID-19. This Commentary will discuss the impact of COVID-19 on endothelial function particularly in patients with familial hypercholesterolemia (FH), a metabolic inherited disease known to in itself adversely affect endothelial function. There should be no hesitation to continue with statin therapy in severe hypercholesterolemic patients with COVID-19. We argue that in FH patients with COVID-19 the clinicians need even consider intensifying statin therapy as well as the addition of other lipid-lowering agents, such as proprotein convertase subtilisin/kexin type 9(PCSK9) inhibitors. In contrast to statins, the PCSK9 inhibitors lower lipoprotein(a) [Lp(a)] level, and, accordingly, these latter drugs need to be considered particularly in FH patients with an elevated level of Lp(a). This call applies to the in-hospital stay and also beyond. When considering that the vasculopathic effects of COVID-19 may persist, a long-term follow-up of individualized therapies in FH patients is warranted. Elsevier 2021-08-08 /pmc/articles/PMC8349422/ /pubmed/34622243 http://dx.doi.org/10.1016/j.athplu.2021.08.001 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vuorio, Alpo Strandberg, Timo E. Raal, Frederik Santos, Raul D. Kovanen, Petri T. Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition |
title | Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition |
title_full | Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition |
title_fullStr | Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition |
title_full_unstemmed | Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition |
title_short | Familial hypercholesterolemia and COVID-19: A menacing but treatable vasculopathic condition |
title_sort | familial hypercholesterolemia and covid-19: a menacing but treatable vasculopathic condition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349422/ https://www.ncbi.nlm.nih.gov/pubmed/34622243 http://dx.doi.org/10.1016/j.athplu.2021.08.001 |
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