Metabolic dysfunction associated fatty liver disease and coronavirus disease 2019: clinical relationship and current management

Lipids Health Dis. 2021 Oct 3;20(1):126. doi: 10.1186/s12944-021-01564-z.

Abstract

The coronavirus disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2). At present, the COVID-19 has been prevalent worldwide for more than a year and caused more than four million deaths. Liver injury was frequently observed in patients with COVID-19. Recently, a new definition of metabolic dysfunction associated fatty liver disease (MAFLD) was proposed by a panel of international experts, and the relationship between MAFLD and COVID-19 has been actively investigated. Several previous studies indicated that the patients with MAFLD had a higher prevalence of COVID-19 and a tendency to develop severe type of respiratory infection, and others indicated that liver injury would be exacerbated in the patients with MAFLD once infected with COVID-19. The mechanism underlying the relationship between MAFLD and COVID-19 infection has not been thoroughly investigated, and recent studies indicated that multifactorial mechanisms, such as altered host angiotensin converting enzyme 2 (ACE2) receptor expression, direct viral attack, disruption of cholangiocyte function, systemic inflammatory reaction, drug-induced liver injury, hepatic ischemic and hypoxic injury, and MAFLD-related glucose and lipid metabolic disorders, might jointly contribute to both of the adverse hepatic and respiratory outcomes. In this review, we discussed the relationship between MAFLD and COVID-19 based on current available literature, and summarized the recommendations for clinical management of MAFLD patients during the pandemic of COVID-19.

Keywords: COVID-19; Fatty liver; Liver injury; MAFLD; SARS-CoV-2.

Publication types

  • Review

MeSH terms

  • Age Factors
  • Angiotensin-Converting Enzyme 2 / genetics
  • Angiotensin-Converting Enzyme 2 / metabolism
  • Anti-Inflammatory Agents / therapeutic use*
  • COVID-19 / complications*
  • COVID-19 / pathology
  • COVID-19 / virology
  • COVID-19 Drug Treatment
  • Chemical and Drug Induced Liver Injury / complications*
  • Chemical and Drug Induced Liver Injury / drug therapy
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury / virology
  • Cytokines / genetics
  • Cytokines / metabolism
  • Dipeptides / therapeutic use
  • Gene Expression Regulation
  • Glucose / metabolism
  • Glycyrrhizic Acid / therapeutic use
  • Humans
  • Hypoxia / complications*
  • Hypoxia / drug therapy
  • Hypoxia / pathology
  • Hypoxia / virology
  • Liver / drug effects
  • Liver / metabolism*
  • Liver / pathology
  • Liver / virology
  • Lung / drug effects
  • Lung / metabolism
  • Lung / pathology
  • Lung / virology
  • Non-alcoholic Fatty Liver Disease / complications*
  • Non-alcoholic Fatty Liver Disease / drug therapy
  • Non-alcoholic Fatty Liver Disease / pathology
  • Non-alcoholic Fatty Liver Disease / virology
  • Receptors, Virus / genetics
  • Receptors, Virus / metabolism
  • SARS-CoV-2 / pathogenicity*
  • Severity of Illness Index

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Dipeptides
  • Receptors, Virus
  • Glycyrrhizic Acid
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Glucose
  • ornithylaspartate