Literature DB >> 33572429

Hepatotropic Properties of SARS-CoV-2-Preliminary Results of Cross-Sectional Observational Study from the First Wave COVID-19 Pandemic.

Hanna Wiśniewska1, Karolina Skonieczna-Żydecka2, Miłosz Parczewski3, Jolanta Niścigorska-Olsen3, Ewa Karpińska1, Monika Hornung1, Krzysztof Jurczyk1, Magdalena Witak-Jędra3, Łukasz Laurans1, Katarzyna Maciejewska3, Łukasz Socha1, Agnieszka Leonciuk3, Dorota Bander1, Malwina Karasińska-Cieślak3, Bogusz Aksak-Wąs3, Marta Wawrzynowicz-Syczewska1.   

Abstract

Liver injury-expressed as elevated liver enzymes-is common in patients with COVID-19. Little is known about the potential mechanisms of liver damage by SARS-CoV-2. A direct cytopathic effect on hepatocytes as well as injury related to hypoxia or hepatotoxicity are being considered. The aim of the study was to compare the clinical characteristic of COVID-19 disease in patients with normal and abnormal liver enzymes activity. A group of 150 patients with COVID-19, hospitalized in our center, was analyzed. Patients with the known liver comorbidities were excluded (n = 15). Clinical features and laboratory parameters were compared between patients with normal and abnormal aminotransferase values. Liver injury expressed as any alanine aminotransferase (ALT) elevation was noted in 45.6% of patients hospitalized due to COVID-19. The frequencies of aspartate aminotransferase (AST) elevation were lower. It was noted that elevated ALT/AST unfavorably affected other parameters related to liver function such as albumin level; gamma-glutamyl transpeptidase (GGTP); and partly, ALP activity and influenced inflammation-related parameters. The most probable cause of mild hepatitis during COVID-19 was anoxia and immune-mediated damage due to the inflammatory response following SARS-CoV-2 infection. A direct cytopathic effect of SARS-CoV-2 on hepatocytes, albeit less probable, can be considered as well. The use of potentially hepatotoxic drugs may contribute to liver damage.

Entities:  

Keywords:  COVID-19; SARS-CoV-2 infection; liver dysfunction; liver enzyme abnormality

Year:  2021        PMID: 33572429      PMCID: PMC7916209          DOI: 10.3390/jcm10040672

Source DB:  PubMed          Journal:  J Clin Med        ISSN: 2077-0383            Impact factor:   4.241


  26 in total

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5.  A Novel Coronavirus from Patients with Pneumonia in China, 2019.

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Review 8.  Angiotensin-Converting Enzyme 2: SARS-CoV-2 Receptor and Regulator of the Renin-Angiotensin System: Celebrating the 20th Anniversary of the Discovery of ACE2.

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10.  Clinical Best Practice Advice for Hepatology and Liver Transplant Providers During the COVID-19 Pandemic: AASLD Expert Panel Consensus Statement.

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  8 in total

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Review 2.  Immune Signature of COVID-19: In-Depth Reasons and Consequences of the Cytokine Storm.

Authors:  Paulina Niedźwiedzka-Rystwej; Adam Majchrzak; Sara Kurkowska; Paulina Małkowska; Olga Sierawska; Rafał Hrynkiewicz; Miłosz Parczewski
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3.  Effectiveness of Tocilizumab in Patients with Severe or Critical Lung Involvement in COVID-19: A Retrospective Study.

Authors:  Daniel Chober; Bogusz Aksak-Wąs; Katarzyna Bobrek-Lesiakowska; Anna Budny-Finster; Ewa Hołda; Joanna Mieżyńska-Kurtycz; Grzegorz Jamro; Miłosz Parczewski
Journal:  J Clin Med       Date:  2022-04-20       Impact factor: 4.241

4.  Association of non-alcoholic fatty liver disease with coronary artery calcification progression: a systematic review and meta-analysis.

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Journal:  Prz Gastroenterol       Date:  2021-09-17

5.  Clinical, Laboratory, and Imaging Findings of Pregnant Women with Possible Vertical Transmission of SARS-CoV-2-Case Series.

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Journal:  Diagnostics (Basel)       Date:  2022-01-04

Review 8.  Abnormal Liver Biochemistry Tests and Acute Liver Injury in COVID-19 Patients: Current Evidence and Potential Pathogenesis.

Authors:  Donovan A McGrowder; Fabian Miller; Melisa Anderson Cross; Lennox Anderson-Jackson; Sophia Bryan; Lowell Dilworth
Journal:  Diseases       Date:  2021-07-01
  8 in total

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