<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>81(3)</volume><submitter>Tobaruela-Resola AL</submitter><funding>Universidad de Navarra</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly NAFLD, includes a range of conditions from steatosis to hepatocellular carcinoma and poses a significant health and economic burden. Circulating microRNAs (miRNAs) are key regulators of metabolic and inflammatory pathways involved in MASLD. However, their clinical utility as non-invasive biomarkers remain unclear. This review aims to clarify their diagnostic, prognostic, and therapeutic potential, addressing current gaps in the literature.&lt;h4>Methods&lt;/h4>Following PRISMA guidelines, we conducted a systematic review of 1149 studies from the PubMed and Scopus databases up to 2024, focused on circulating miRNAs in MASLD.&lt;h4>Results&lt;/h4>The most frequently studied miRNAs included miR-122 (35.56% of studies), miR-21 (18.89%), miR-34 (14.44%), and miR-192-5p (13.33%). Diagnostic accuracy varied among miRNAs, with miR-200 and miR-298 demonstrating AUROCs of 0.96 and 0.98, respectively, for MASLD detection. In MASH, miR-200, miR-298, and miR-342 exhibited near-perfect AUROCs of 0.99, while miR-122 showed values between 0.81 and 1.0. For HCC, miR-214 achieved an AUROC of 0.88, and miR-34a ranged from 0.73 to 0.76. Several miRNA panels demonstrated high diagnostic accuracy, with AUROCs up to 0.99, particularly in distinguishing HCC from other liver conditions. Prognostically, elevated miR-122 levels correlated with disease severity and fibrosis progression, while miR-21 and miR-223 were linked to obesity-associated MASH. Therapeutic interventions, including surgery, dietary modifications, and supplementation, were found to modulate miRNA profiles.&lt;h4>Conclusions&lt;/h4>MiRNAs exhibit strong potential as minimally invasive biomarkers for MASLD, contributing to improved diagnosis, prognosis, and therapeutic decision-making. Their stability and role in personalized medicine underscore their clinical relevance.</pubmed_abstract><journal>Journal of physiology and biochemistry</journal><pagination>589-609</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12373555</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The use of circulating miRNAs for the diagnosis, prognosis, and personalized treatment of MASLD.</pubmed_title><pmcid>PMC12373555</pmcid><pubmed_authors>Milagro FI</pubmed_authors><pubmed_authors>Mogna-Pelaez P</pubmed_authors><pubmed_authors>Moreno-Aliaga MJ</pubmed_authors><pubmed_authors>Tobaruela-Resola AL</pubmed_authors><pubmed_authors>Zulet MA</pubmed_authors><pubmed_authors>Abete I</pubmed_authors></additional><is_claimable>false</is_claimable><name>The use of circulating miRNAs for the diagnosis, prognosis, and personalized treatment of MASLD.</name><description>&lt;h4>Introduction&lt;/h4>Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly NAFLD, includes a range of conditions from steatosis to hepatocellular carcinoma and poses a significant health and economic burden. Circulating microRNAs (miRNAs) are key regulators of metabolic and inflammatory pathways involved in MASLD. However, their clinical utility as non-invasive biomarkers remain unclear. This review aims to clarify their diagnostic, prognostic, and therapeutic potential, addressing current gaps in the literature.&lt;h4>Methods&lt;/h4>Following PRISMA guidelines, we conducted a systematic review of 1149 studies from the PubMed and Scopus databases up to 2024, focused on circulating miRNAs in MASLD.&lt;h4>Results&lt;/h4>The most frequently studied miRNAs included miR-122 (35.56% of studies), miR-21 (18.89%), miR-34 (14.44%), and miR-192-5p (13.33%). Diagnostic accuracy varied among miRNAs, with miR-200 and miR-298 demonstrating AUROCs of 0.96 and 0.98, respectively, for MASLD detection. In MASH, miR-200, miR-298, and miR-342 exhibited near-perfect AUROCs of 0.99, while miR-122 showed values between 0.81 and 1.0. For HCC, miR-214 achieved an AUROC of 0.88, and miR-34a ranged from 0.73 to 0.76. Several miRNA panels demonstrated high diagnostic accuracy, with AUROCs up to 0.99, particularly in distinguishing HCC from other liver conditions. Prognostically, elevated miR-122 levels correlated with disease severity and fibrosis progression, while miR-21 and miR-223 were linked to obesity-associated MASH. Therapeutic interventions, including surgery, dietary modifications, and supplementation, were found to modulate miRNA profiles.&lt;h4>Conclusions&lt;/h4>MiRNAs exhibit strong potential as minimally invasive biomarkers for MASLD, contributing to improved diagnosis, prognosis, and therapeutic decision-making. Their stability and role in personalized medicine underscore their clinical relevance.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-08T20:11:44.761Z</modification><creation>2026-04-08T00:13:17.452Z</creation></dates><accession>S-EPMC12373555</accession><cross_references><pubmed>40668532</pubmed><doi>10.1007/s13105-025-01110-w</doi></cross_references></HashMap>