Genetics and Epigenetics of Atrial Fibrillation.
Estefanía Lozano-VelascoDiego FrancoAmelia AranegaHouria DaimiPublished in: International journal of molecular sciences (2020)
Atrial fibrillation (AF) is known to be the most common supraventricular arrhythmia affecting up to 1% of the general population. Its prevalence exponentially increases with age and could reach up to 8% in the elderly population. The management of AF is a complex issue that is addressed by extensive ongoing basic and clinical research. AF centers around different types of disturbances, including ion channel dysfunction, Ca2+-handling abnormalities, and structural remodeling. Genome-wide association studies (GWAS) have uncovered over 100 genetic loci associated with AF. Most of these loci point to ion channels, distinct cardiac-enriched transcription factors, as well as to other regulatory genes. Recently, the discovery of post-transcriptional regulatory mechanisms, involving non-coding RNAs (especially microRNAs), DNA methylation, and histone modification, has allowed to decipher how a normal heart develops and which modifications are involved in reshaping the processes leading to arrhythmias. This review aims to provide a current state of the field regarding the identification and functional characterization of AF-related epigenetic regulatory networks.
Keyphrases
- atrial fibrillation
- catheter ablation
- genome wide
- dna methylation
- transcription factor
- genome wide association
- left atrial
- oral anticoagulants
- left atrial appendage
- direct oral anticoagulants
- gene expression
- heart failure
- percutaneous coronary intervention
- copy number
- genome wide identification
- high throughput
- bioinformatics analysis
- genome wide association study
- oxidative stress
- heat shock protein
- heat shock
- acute coronary syndrome
- case control
- mitral valve
- protein kinase
- heat stress