Circulating microRNAs and DNA Methylation as Regulators of Direct Oral Anticoagulant Response in Atrial Fibrillation and Key Elements for the Identification of the Mechanism of Action (miR-CRAFT): Study Design and Patient Enrolment.
Georgia RagiaThomas ThomopoulosGeorgios K ChalikiasAthanasios TrikasDimitrios N TziakasVangelis G ManolopoulosPublished in: Journal of personalized medicine (2024)
Direct oral anticoagulants (DOACs) are the standard treatment for thromboembolic protection in atrial fibrillation (AF) patients. Epigenetic modifications, such as DNA methylation and microRNAs, have emerged as potential biomarkers of AF. The epigenetics of DOACs is still an understudied field. It is largely unknown whether epigenetic modifications interfere with DOAC response or whether DOAC treatment induces epigenetic modifications. To fill this gap, we started the miR-CRAFT (Circulating microRNAs and DNA methylation as regulators of Direct Oral Anticoagulant Response in Atrial Fibrillation) research study. In miR-CRAFT, we follow, over time, changes in DNA methylation and microRNAs expression in naïve AF patients starting DOAC treatment. The ultimate goal of miR-CRAFT is to identify the molecular pathways epigenetically affected by DOACs, beyond the coagulation cascade, that are potentially mediating DOAC pleiotropic actions and to propose specific microRNAs as novel circulating biomarkers for DOAC therapy monitoring. We herein describe the study design and briefly present the progress in participant enrolment.
Keyphrases
- direct oral anticoagulants
- atrial fibrillation
- dna methylation
- venous thromboembolism
- catheter ablation
- oral anticoagulants
- left atrial
- gene expression
- cell proliferation
- left atrial appendage
- long non coding rna
- long noncoding rna
- genome wide
- heart failure
- end stage renal disease
- ejection fraction
- newly diagnosed
- poor prognosis
- chronic kidney disease
- prognostic factors
- transcription factor
- stem cells
- peritoneal dialysis
- health insurance
- replacement therapy
- bone marrow
- binding protein
- coronary artery disease