Table 2.
Potential areas for clinical application of genetic discoveries in atrial fibrillation (AF) management
Area | Example | Potential utility | Limitations |
---|---|---|---|
Risk prediction | Predict new-onset AF or AF-related morbidity (stroke, heart failure, mortality risk) | Benchmark for clinical trial development | Absence of known preventive strategies for AF |
Facilitate AF and clinical outcome prevention | Cohorts for genetic risk score derivation predominantly of European ancestry | ||
Small relative risks of discovered variants | |||
Complexity of incorporation into clinical practice | |||
Cost | |||
Untested | |||
Predict AF progression | Early antiarrhythmic or ablation intervention | Unclear relations between AF progression and morbidity and mortality | |
Untested | |||
Patient management | Pharmacogenetics | Maximize efficacy, minimize adverse effects | Development of novel agents with wide therapeutic margins |
Thromboembolism prophylaxis | Ablation and mechanical interventions as alternatives | ||
Antiarrhythmic therapy | Complexity of incorporation into clinical practice | ||
Cost | |||
Untested |