A look at new therapeutic opportunities in patients with non-alcoholic fatty liver disease
Author(s) -
Ekaterina Е. Mishina,
Alexander Yur'evich Mayorov,
A. V. Bogolyubova,
Pavel Bogomolov,
Maria V. Matsievich,
K. Yu. Kokina
Publication year - 2019
Publication title -
obesity and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.154
H-Index - 5
eISSN - 2306-5524
pISSN - 2071-8713
DOI - 10.14341/omet9986
Subject(s) - farnesoid x receptor , fatty liver , dyslipidemia , metabolic syndrome , medicine , disease , steatohepatitis , nuclear receptor , bioinformatics , diabetes mellitus , endocrinology , pharmacology , transcription factor , biology , biochemistry , gene
Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease worldwide, and is considered to be the liver manifestation of metabolic syndrome. Currently, there is no etiotropic treatment of NAFLD, so an active research for new methods of treatment is underway. In the meantime, drugs are used to treat comorbid conditions, such as dyslipidemia, arterial hypertension, obesity, type 2 diabetes, which are present in varying degrees in patients. This review considers medications that are used in patients with NAFLD and related concomitant features, and also describes new strategies for regressing changes in liver tissue in NAFLD. In our opinion, one of the promising groups of drugs are agonists of the farnesoid X receptor (FXR). FXR belongs to the group of nuclear receptors, which are ligand-activated transcription factors that regulate the genes involved in metabolism. FXR agonists can claim to be a new promising drug for the treatment of NAFLD and related diseases influencing carbohydrate metabolism, fat metabolism, bile acid metabolism, as well as inflammatory processes in the liver to ensure metabolic homeostasis.
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