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  • ISSN 1674-8301
  • CN 32-1810/R
Peter Metrakos, Tommy Nilsson. Non-alcoholic fatty liver disease–a chronic disease of the 21st century[J]. The Journal of Biomedical Research, 2018, 32(5): 327-335. DOI: 10.7555/JBR.31.20160153
Citation: Peter Metrakos, Tommy Nilsson. Non-alcoholic fatty liver disease–a chronic disease of the 21st century[J]. The Journal of Biomedical Research, 2018, 32(5): 327-335. DOI: 10.7555/JBR.31.20160153

Non-alcoholic fatty liver disease–a chronic disease of the 21st century

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  • Received Date: November 18, 2016
  • Revised Date: December 14, 2016
  • Non-alcoholic fatty liver disease (NAFLD) comprises a spectrum of metabolic states ranging from simple steatosis o inflammation with associated fibrosis to cirrhosis. Though accumulation of hepatic fat is not associated with a ignificant increase in mortality rates, hepatic inflammation is, as this augments the risk of terminal liver disease, i.e., cirrhosis, hepatic decompensation (liver failure) and/or hepatocellular carcinoma. Disease progression is usually low, over a decade or more and, for the most part, remains asymptomatic. Recent estimates suggest that the global prevalence of NAFLD is high, about one in four. In most cases, NAFLD overlaps with overweight, obesity, cardiovascular disease and the metabolic syndrome with numerous contributing parameters including a dysregulation of adipose tissue, insulin resistance, type 2 diabetes, changes in the gut microbiome, neuronal and hormonal dysregulation and metabolic stress. NAFLD is diagnosed incidentally, despite its high prevalence. Non-invasive maging techniques have emerged, making it possible to determine degree of steatosis as well asfibrosis. Despite this, he benefit of routine diagnostics remains uncertain. A better understanding of the (molecular) pathogenesis of NAFLD is needed combined with long-term studies where benefits of treatment can be assessed to determine cost benefit ratios. This review summarizes the current state of knowledge and possible areas of treatment.
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    1. Compagnoni C, Capelli R, Zelli V, et al. MiR-182-5p Is Upregulated in Hepatic Tissues from a Diet-Induced NAFLD/NASH/HCC C57BL/6J Mouse Model and Modulates Cyld and Foxo1 Expression. Int J Mol Sci, 2023, 24(11): 9239. DOI:10.3390/ijms24119239
    2. Errafii K, Khalifa O, Al-Akl NS, et al. Comparative Transcriptome Analysis Reveals That Exendin-4 Improves Steatosis in HepG2 Cells by Modulating Signaling Pathways Related to Lipid Metabolism. Biomedicines, 2022, 10(5): 1020. DOI:10.3390/biomedicines10051020
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    6. Pillai SS, Lakhani HV, Zehra M, et al. Predicting Nonalcoholic Fatty Liver Disease through a Panel of Plasma Biomarkers and MicroRNAs in Female West Virginia Population. Int J Mol Sci, 2020, 21(18): 6698. DOI:10.3390/ijms21186698
    7. Krishnasamy Y, Gooz M, Li L, et al. Role of mitochondrial depolarization and disrupted mitochondrial homeostasis in non-alcoholic steatohepatitis and fibrosis in mice. Int J Physiol Pathophysiol Pharmacol, 2019, 11(5): 190-204.
    8. Ok DP, Ko K, Bae JY. Exercise without dietary changes alleviates nonalcoholic fatty liver disease without weight loss benefits. Lipids Health Dis, 2018, 17(1): 207. DOI:10.1186/s12944-018-0852-z
    9. Im AR, Yang WK, Park YC, et al. Hepatoprotective Effects of Insect Extracts in an Animal Model of Nonalcoholic Fatty Liver Disease. Nutrients, 2018, 10(6): 735. DOI:10.3390/nu10060735
    10. Leibowitz A, Bier A, Gilboa M, et al. Saccharin Increases Fasting Blood Glucose but Not Liver Insulin Resistance in Comparison to a High Fructose-Fed Rat Model. Nutrients, 2018, 10(3): 341. DOI:10.3390/nu10030341
    11. Bocsan IC, Milaciu MV, Pop RM, et al. Cytokines Genotype-Phenotype Correlation in Nonalcoholic Steatohepatitis. Oxid Med Cell Longev, 2017, 2017: 4297206. DOI:10.1155/2017/4297206

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