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Infections at the nexus of metabolic-associated fatty liver disease. | LitMetric

AI Article Synopsis

  • * The progression of MAFLD can be accelerated by factors such as diet, lifestyle, genetics, certain medications, male gender, and infections, which often complicate the disease landscape.
  • * This review highlights how specific infections, including COVID-19 and hepatitis C, interact with MAFLD and its risk factors, potentially worsening the condition and contributing to an underreporting of combined disease cases.

Article Abstract

Metabolic-associated fatty liver disease (MAFLD) is a chronic liver disease that affects about a quarter of the world population. MAFLD encompasses different disease stadia ranging from isolated liver steatosis to non-alcoholic steatohepatitis (NASH), fibrosis, cirrhosis and hepatocellular carcinoma. Although MAFLD is considered as the hepatic manifestation of the metabolic syndrome, multiple concomitant disease-potentiating factors can accelerate disease progression. Among these risk factors are diet, lifestyle, genetic traits, intake of steatogenic drugs, male gender and particular infections. Although infections often outweigh the development of fatty liver disease, pre-existing MAFLD could be triggered to progress towards more severe disease stadia. These combined disease cases might be underreported because of the high prevalence of both MAFLD and infectious diseases that can promote or exacerbate fatty liver disease development. In this review, we portray the molecular and cellular mechanisms by which the most relevant viral, bacterial and parasitic infections influence the progression of fatty liver disease and steatohepatitis. We focus in particular on how infectious diseases, including coronavirus disease-19, hepatitis C, acquired immunodeficiency syndrome, peptic ulcer and periodontitis, exacerbate MAFLD. We specifically underscore the synergistic effects of these infections with other MAFLD-promoting factors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141380PMC
http://dx.doi.org/10.1007/s00204-021-03069-1DOI Listing

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