The Relationship between Pathogenesis and Possible Treatments for the MASLD-Cirrhosis Spectrum
- PMID: 38673981
- PMCID: PMC11050641
- DOI: 10.3390/ijms25084397
The Relationship between Pathogenesis and Possible Treatments for the MASLD-Cirrhosis Spectrum
Abstract
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a term that entails a broad spectrum of conditions that vary in severity. Its development is influenced by multiple factors such as environment, microbiome, comorbidities, and genetic factors. MASLD is closely related to metabolic syndrome as it is caused by an alteration in the metabolism of fatty acids due to the accumulation of lipids because of an imbalance between its absorption and elimination in the liver. Its progression to fibrosis is due to a constant flow of fatty acids through the mitochondria and the inability of the liver to slow down this metabolic load, which generates oxidative stress and lipid peroxidation, triggering cell death. The development and progression of MASLD are closely related to unhealthy lifestyle habits, and nutritional epigenetic and genetic mechanisms have also been implicated. Currently, lifestyle modification is the first-line treatment for MASLD and nonalcoholic steatohepatitis; weight loss of ≥10% produces resolution of steatohepatitis and fibrosis regression. In many patients, body weight reduction cannot be achieved; therefore, pharmacological treatment should be offered in particular populations.
Keywords: diet; fibrosis; hepatic steatosis; metabolic syndrome; sedentarism; steatohepatitis.
Conflict of interest statement
We confirm that this work is original and has not been published, is not currently under consideration for publication elsewhere, in whole or in part, and we have not had any competing financial interests or commercial relationships that might pose conflicts of interest.
Figures
Similar articles
-
Molecular pathogenesis of metabolic dysfunction-associated steatotic liver disease, steatohepatitis, hepatic fibrosis and liver cirrhosis.J Cell Mol Med. 2024 Jun;28(12):e18491. doi: 10.1111/jcmm.18491. J Cell Mol Med. 2024. PMID: 38894579 Free PMC article.
-
Genetic Ablation of STE20-Type Kinase MST4 Does Not Alleviate Diet-Induced MASLD Susceptibility in Mice.Int J Mol Sci. 2024 Feb 19;25(4):2446. doi: 10.3390/ijms25042446. Int J Mol Sci. 2024. PMID: 38397122 Free PMC article.
-
Influence of Lipid Class Used for Omega-3 Fatty Acid Supplementation on Liver Fat Accumulation in MASLD.Physiol Res. 2024 Aug 31;73(Suppl 1):S295-S320. doi: 10.33549/physiolres.935396. Epub 2024 Jul 17. Physiol Res. 2024. PMID: 39016154 Free PMC article. Review.
-
Metabolic Dysfunction-Associated Steatotic Liver Disease: From Pathogenesis to Current Therapeutic Options.Int J Mol Sci. 2024 May 22;25(11):5640. doi: 10.3390/ijms25115640. Int J Mol Sci. 2024. PMID: 38891828 Free PMC article. Review.
-
An unbiased ranking of murine dietary models based on their proximity to human metabolic dysfunction-associated steatotic liver disease (MASLD).Nat Metab. 2024 Jun;6(6):1178-1196. doi: 10.1038/s42255-024-01043-6. Epub 2024 Jun 12. Nat Metab. 2024. PMID: 38867022 Free PMC article.
Cited by
-
Management of Metabolic-Associated Fatty Liver Disease/Metabolic Dysfunction-Associated Steatotic Liver Disease: From Medication Therapy to Nutritional Interventions.Nutrients. 2024 Jul 11;16(14):2220. doi: 10.3390/nu16142220. Nutrients. 2024. PMID: 39064665 Free PMC article. Review.
References
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical