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Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity
As far as comorbidity is concerned, cardiovascular diseases (CVD) appear to be accounted for the highest prevalence, severity, and fatality among COVID 19 patients. A wide array of causal links connecting CVD and COVID-19 baffle the overall prognosis as well as the efficacy of the given therapeutic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489295/ https://www.ncbi.nlm.nih.gov/pubmed/34649043 http://dx.doi.org/10.1016/j.jiph.2021.09.022 |
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author | Karim, Muhammad Manjurul Sultana, Shahnaz Sultana, Rokaia Rahman, Mohammad Tariqur |
author_facet | Karim, Muhammad Manjurul Sultana, Shahnaz Sultana, Rokaia Rahman, Mohammad Tariqur |
author_sort | Karim, Muhammad Manjurul |
collection | PubMed |
description | As far as comorbidity is concerned, cardiovascular diseases (CVD) appear to be accounted for the highest prevalence, severity, and fatality among COVID 19 patients. A wide array of causal links connecting CVD and COVID-19 baffle the overall prognosis as well as the efficacy of the given therapeutic interventions. At the centre of this puzzle lies ACE2 that works as a receptor for the SARS-CoV-2, and functional expression of which is also needed to minimize vasoconstriction otherwise would lead to high blood pressure. Furthermore, SARS-CoV-2 infection seems to reduce the functional expression of ACE2. Given these circumstances, it might be advisable to consider a treatment plan for COVID-19 patients with CVD in an approach that would neither aggravate the vasodeleterious arm of the renin-angiotensinogen-aldosterone system (RAAS) nor compromise the vasoprotective arm of RAAS but is effective to minimize or if possible, inhibit the viral replication. Given the immune modulatory role of Zn in both CVD and COVID-19 pathogenesis, zinc supplement to the selective treatment plan for CVD and COVID-19 comorbid conditions, to be decided by the clinicians depending on the cardiovascular conditions of the patients, might greatly improve the therapeutic outcome. Notably, ACE2 is a zinc metalloenzyme and zinc is also known to inhibit viral replication. |
format | Online Article Text |
id | pubmed-8489295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Authors. Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84892952021-10-04 Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity Karim, Muhammad Manjurul Sultana, Shahnaz Sultana, Rokaia Rahman, Mohammad Tariqur J Infect Public Health Review As far as comorbidity is concerned, cardiovascular diseases (CVD) appear to be accounted for the highest prevalence, severity, and fatality among COVID 19 patients. A wide array of causal links connecting CVD and COVID-19 baffle the overall prognosis as well as the efficacy of the given therapeutic interventions. At the centre of this puzzle lies ACE2 that works as a receptor for the SARS-CoV-2, and functional expression of which is also needed to minimize vasoconstriction otherwise would lead to high blood pressure. Furthermore, SARS-CoV-2 infection seems to reduce the functional expression of ACE2. Given these circumstances, it might be advisable to consider a treatment plan for COVID-19 patients with CVD in an approach that would neither aggravate the vasodeleterious arm of the renin-angiotensinogen-aldosterone system (RAAS) nor compromise the vasoprotective arm of RAAS but is effective to minimize or if possible, inhibit the viral replication. Given the immune modulatory role of Zn in both CVD and COVID-19 pathogenesis, zinc supplement to the selective treatment plan for CVD and COVID-19 comorbid conditions, to be decided by the clinicians depending on the cardiovascular conditions of the patients, might greatly improve the therapeutic outcome. Notably, ACE2 is a zinc metalloenzyme and zinc is also known to inhibit viral replication. The Authors. Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. 2021-11 2021-10-04 /pmc/articles/PMC8489295/ /pubmed/34649043 http://dx.doi.org/10.1016/j.jiph.2021.09.022 Text en © 2021 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Karim, Muhammad Manjurul Sultana, Shahnaz Sultana, Rokaia Rahman, Mohammad Tariqur Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity |
title | Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity |
title_full | Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity |
title_fullStr | Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity |
title_full_unstemmed | Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity |
title_short | Possible Benefits of Zinc supplement in CVD and COVID-19 Comorbidity |
title_sort | possible benefits of zinc supplement in cvd and covid-19 comorbidity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489295/ https://www.ncbi.nlm.nih.gov/pubmed/34649043 http://dx.doi.org/10.1016/j.jiph.2021.09.022 |
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