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 |