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Altered Mitochondrial Function in MASLD: Key Features and Promising Therapeutic Approaches.

Tatjana Radosavljevic1, Milica Brankovic2, Janko Samardzic2

  • 1Institute of Pathophysiology "Ljubodrag Buba Mihailovic", Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.

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|August 29, 2024
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Summary

Metabolic dysfunction-associated steatotic liver disease (MASLD) involves mitochondrial dysfunction, impacting liver health. Enhancing mitochondrial function offers a promising therapeutic avenue for MASLD and metabolic-associated steatohepatitis (MASH).

Keywords:
MASHMASLDmetabolic syndromemitochondriamitochondrial dysfunctionmitochondrial quality controloxidative stress

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Area of Science:

  • Hepatology and Metabolic Disorders
  • Mitochondrial Biology and Disease

Background:

  • Metabolic dysfunction-associated steatotic liver disease (MASLD), previously nonalcoholic fatty liver disease (NAFLD), is a spectrum of liver conditions with increasing global prevalence, particularly in patients with metabolic syndrome.
  • MASLD pathogenesis involves complex factors including metabolic dysregulation, inflammation, oxidative stress, genetic predispositions, and critically, mitochondrial dysfunction.

Purpose of the Study:

  • To elucidate the pivotal role of mitochondrial dysfunction in the progression of MASLD.
  • To explore novel and existing therapeutic strategies targeting mitochondrial function for MASLD and metabolic-associated steatohepatitis (MASH) treatment.

Main Methods:

  • Review of recent scientific literature focusing on MASLD pathogenesis and mitochondrial dysfunction.
  • Analysis of therapeutic interventions, including lifestyle modifications, pharmacological agents, and emerging strategies like gene editing.

Main Results:

  • Mitochondrial dysfunction is a key driver in the progression of MASLD from steatosis to more severe forms like MASH.
  • Therapeutic enhancement of mitochondrial function, alongside lifestyle changes, shows promise for MASLD management.
  • FDA approval of resmetirom for MASH with fibrosis signifies a therapeutic advancement.

Conclusions:

  • A deeper understanding of MASLD-related mitochondrial dysfunction is crucial for developing effective treatments.
  • Innovative approaches, including drug repurposing and targeting novel pathways, are needed to address the growing global burden of MASLD.
  • Combined strategies involving lifestyle interventions and targeted therapies hold potential for improved patient outcomes.