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The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced

BACKGROUND: The global pandemic COVID-19 caused by the new coronavirus SARS-CoV-2 has already caused about 1.4 million deaths, and to date, there are no effective or direct antiviral vaccines. Some vaccines are in the last stages of testing. Overall mortality rates vary between countries, for exampl...

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Autores principales: Vitiello, Antonio, La Porta, Raffaele, D’Aiuto, Vilma, Ferrara, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838235/
https://www.ncbi.nlm.nih.gov/pubmed/34777865
http://dx.doi.org/10.1186/s43066-021-00082-y
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author Vitiello, Antonio
La Porta, Raffaele
D’Aiuto, Vilma
Ferrara, Francesco
author_facet Vitiello, Antonio
La Porta, Raffaele
D’Aiuto, Vilma
Ferrara, Francesco
author_sort Vitiello, Antonio
collection PubMed
description BACKGROUND: The global pandemic COVID-19 caused by the new coronavirus SARS-CoV-2 has already caused about 1.4 million deaths, and to date, there are no effective or direct antiviral vaccines. Some vaccines are in the last stages of testing. Overall mortality rates vary between countries, for example, from a minimum of 0.05% in Singapore to a maximum of 9.75 in Mexico; however, mortality and severity of COVID-19 are higher in the elderly and in those with comorbidities already present such as diabetes, hypertension, and heart disease. MAIN TEXT: Recent evidence has shown that an underlying liver disease can also be a risk factor, and SARS-CoV-2 itself can cause direct or indirect damage to liver tissue through multisystem inflammation generated especially in the more severe stages. In the current pandemic, liver dysfunction has been observed in 14–53% of patients with severe COVID-19. In addition, drugs administered during infection may be an additional factor of liver damage. The mechanism of cellular penetration of the virus that occurs by viral entry is through the receptors of the angiotensin 2 conversion enzyme (ACE-2) host that are abundantly present in type II pneumocytes, heart cells, but also liver cholangiocytes. CONCLUSION: In this manuscript, we describe the clinical management aimed at preserving the liver or reducing the damage caused by COVID-19 and anti-COVID-19 drug treatments.
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spelling pubmed-78382352021-01-28 The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced Vitiello, Antonio La Porta, Raffaele D’Aiuto, Vilma Ferrara, Francesco Egypt Liver Journal Review BACKGROUND: The global pandemic COVID-19 caused by the new coronavirus SARS-CoV-2 has already caused about 1.4 million deaths, and to date, there are no effective or direct antiviral vaccines. Some vaccines are in the last stages of testing. Overall mortality rates vary between countries, for example, from a minimum of 0.05% in Singapore to a maximum of 9.75 in Mexico; however, mortality and severity of COVID-19 are higher in the elderly and in those with comorbidities already present such as diabetes, hypertension, and heart disease. MAIN TEXT: Recent evidence has shown that an underlying liver disease can also be a risk factor, and SARS-CoV-2 itself can cause direct or indirect damage to liver tissue through multisystem inflammation generated especially in the more severe stages. In the current pandemic, liver dysfunction has been observed in 14–53% of patients with severe COVID-19. In addition, drugs administered during infection may be an additional factor of liver damage. The mechanism of cellular penetration of the virus that occurs by viral entry is through the receptors of the angiotensin 2 conversion enzyme (ACE-2) host that are abundantly present in type II pneumocytes, heart cells, but also liver cholangiocytes. CONCLUSION: In this manuscript, we describe the clinical management aimed at preserving the liver or reducing the damage caused by COVID-19 and anti-COVID-19 drug treatments. Springer Berlin Heidelberg 2021-01-27 2021 /pmc/articles/PMC7838235/ /pubmed/34777865 http://dx.doi.org/10.1186/s43066-021-00082-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Vitiello, Antonio
La Porta, Raffaele
D’Aiuto, Vilma
Ferrara, Francesco
The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced
title The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced
title_full The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced
title_fullStr The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced
title_full_unstemmed The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced
title_short The risks of liver injury in COVID-19 patients and pharmacological management to reduce or prevent the damage induced
title_sort risks of liver injury in covid-19 patients and pharmacological management to reduce or prevent the damage induced
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838235/
https://www.ncbi.nlm.nih.gov/pubmed/34777865
http://dx.doi.org/10.1186/s43066-021-00082-y
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