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ABSTRACT: Background
Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease worldwide, but its pathophysiological mechanisms remain elusive. It is a progressive disease, encompassing hepatic steatosis, steatohepatitis with (out) fibrosis, and ultimately cirrhosis and hepatocellular carcinoma. DNA methylation (DNAm) is dysregulated in MASLD and may play a central role in its pathogenesis. Additionally, aging is associated with MASLD and shares common processes of chronic inflammation and oxidative stress. Therefore, this study focuses on DNAm changes in relation to MASLD progression and epigenetic age acceleration (EAA).Results
Liver biopsies from 22 individuals with varying MASLD status were analyzed using Infinium MethylationEPIC Be
SUBMITTER: Van Dijck E
PROVIDER: S-EPMC12323057 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature