Global DNA methylation patterns in Alcohol Use Disorder.
Jaqueline B SchuchCibele E BandeiraJorge L S JuniorDiana MüllerMariele F CharãoBruna S da SilvaEugenio H GrevetFelix H P KesslerLisia von DiemenDiego L RovarisClaiton Henrique Dotto BauPublished in: Genetics and molecular biology (2024)
Alcohol Use Disorder (AUD) is a highly prevalent condition worldwide that produces a wide range of pathophysiological consequences, with a critical impact on health and social issues. Alcohol influences gene expression through epigenetic changes mainly through DNA methylation. In this sense, levels of 5-methylcytosine (5-mC), namely Global DNA methylation (GMe), which can be influenced by environmental and hormonal effects, represent a putative biological mechanism underlying alcohol effects. Our aim was to investigate the influence of AUD diagnosis and alcohol patterns (i.e., years of addiction, use in the last 30 days, and alcohol severity) on GMe levels. The sample consisted of 256 men diagnosed with AUD and 361 men without AUD. DNA samples from peripheral blood were used to assess GMe levels, measured through the levels of 5-mC using high-performance liquid chromatography. Results from multiple linear regression analysis indicated that the presence of AUD was associated with lower GMe levels (beta=-0.155, p=0.011). Other alcohol-related outcomes were not associated with DNA methylation. Our findings are consistent with the hypothesis that the impact of chronic and heavy alcohol use in GMe could be a potential mechanism mediating the multiple organ damages related to AUD.
Keyphrases
- alcohol use disorder
- dna methylation
- gene expression
- genome wide
- high performance liquid chromatography
- alcohol consumption
- peripheral blood
- healthcare
- public health
- human health
- type diabetes
- skeletal muscle
- risk assessment
- mass spectrometry
- tandem mass spectrometry
- adipose tissue
- drug induced
- middle aged
- circulating tumor
- insulin resistance
- circulating tumor cells
- weight loss