Roles of different methylation modifications in cardiovascular disease
Peer-Reviewed Publication
Updates every hour. Last Updated: 22-Jun-2026 12:16 ET (22-Jun-2026 16:16 GMT/UTC)
Cardiovascular disease remains the leading cause of mortality worldwide, necessitating deeper insights into its molecular underpinnings beyond genetic predisposition. Epigenetic modifications, particularly methylation changes affecting DNA, proteins, and RNA, have emerged as critical regulators of gene expression implicated in cardiac pathophysiology. These heritable yet reversible chemical alterations govern chromatin architecture, transcriptional activity, and post-transcriptional processing without changing underlying nucleotide sequences. Within the spectrum of cardiovascular pathology—including ischemic heart disease, cardiac hypertrophy, heart failure, and atherosclerosis—dysregulated methylation patterns contribute substantially to disease initiation, progression, and phenotypic manifestation. Understanding the distinct and convergent roles of these three major methylation modalities offers promising avenues for developing novel diagnostic biomarkers and targeted therapeutic interventions that could transform precision medicine in cardiology.
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