Abstract Type II diabetes mellitus (T2DM) is a multidimensional metabolic disorder driven by insulin resistance, chronic inflammation and β-cell dysfunction. Emerging evidence shows that epigenetic mechanisms i.e., DNA methylation, histone acetylation and noncoding RNAs, form a key nexus between genetic predisposition and environmental factors including diet, oxidative stress and obesity. These inheritable yet reversible modifications shape transcriptional control of key genes involved in inflammatory signalling, glucose metabolism and insulin secretion. Altered methylation of PDX1 and GLP-1R genes, overexpression of histone deacetylases, impairment of miRNA expression (e.g., miR-21, miR-146a) and lncRNAs (e.g., MALAT) cumulatively impair insulin sensitivity and β-cell identity. In addition, transgenerational epigenetic inheritance reveals how parental nutrition choices and metabolic status can predispose offspring to metabolic memory of T2DM risk. Emerging evidence highlights the promise of targeting epigenetic modifiers e.g., DNMT, HDAC inhibitors and miRNA-based strategies to reverse the abnormalities and regain normal gene expression and metabolic balance. Complementarily, the Wnt/ β-catenin and GLP-1 signalling pathways are key interfaces of epigenetic modulation of β-cell function. Understanding these mechanisms is a gateway for precision medicine that goes beyond glycaemic control in the direction of disease modification and prevention. Integrating epigenetic profiling into clinical management can redefine patients care therapies covering both molecular and heritable dimensions of T2DM.
Chaudhry et al. (Wed,) studied this question.