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. 2021 Feb 9;10(4):672.
doi: 10.3390/jcm10040672.

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

Affiliations

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

Hanna Wiśniewska et al. J Clin Med. .

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.

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

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Conflict of interest statement

All authors report no relevant conflicts of interest, financial or otherwise.

Figures

Figure 1
Figure 1
Study flow chart.
Figure 2
Figure 2
ALT (alanine aminotransferase) change over time by gender. Middle lines represent medians and central boxes stand for IQRs. Tx—treatment. Dots and squares represent outside and far out values.
Figure 3
Figure 3
AST (aspartate aminotransferase) change over time by gender. Middle lines represent medians and central boxes stand for IQRs. Tx-treatment. Dots and squares represent outside and far out values.

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