Key result
Elevated stimulated PRD linked to ~230% greater risk of new device-detected AF in pacemaker patients.
Why the study?
The relationship between periodic repolarisation dynamics, reflecting cardiac autonomic dysfunction, and atrial arrhythmias including atrial fibrillation remains unclear.
Does elevated stimulated Periodic Repolarisation Dynamics predict new-onset device-detected atrial fibrillation in patients with implanted pacemakers?
Does elevated stimulated Periodic Repolarisation Dynamics predict new-onset device-detected atrial fibrillation in patients with implanted pacemakers?
Elevated stimulated Periodic Repolarisation Dynamics is a significant predictor of new-onset device-detected atrial fibrillation in pacemaker patients, highlighting the role of autonomic dysfunction in arrhythmogenesis.
Background Periodic Repolarisation Dynamics (PRD) is a novel ECG-based risk marker reflecting low-frequency oscillations in cardiac repolarisation, caused by efferent sympathetic nervous system activity. Elevated PRD (≥ 5.75 deg²) predicts malignant arrhythmias and sudden cardiac death in both ischaemic and non-ischaemic cardiomyopathy. The relationship between PRD and atrial arrhythmias, particularly atrial fibrillation (AF), remains unclear despite growing evidence of cardiac autonomic dysfunction (c-AD) in AF pathogenesis. This study examines the relationship between c-AD, as measured by PRD, and the incidence of device-detected atrial fibrillation (DDAF) in patients with implanted cardiac pacemakers. Methods In the observational ACasA study, patients with implanted cardiac pacemakers were prospectively enrolled. High-resolution ECG recordings under native (AAI) and stimulated (DDD) conditions were used to calculate PRD at the baseline visit. c-AD was defined by native PRD ≥ 5.75 deg² and stimulated PRD > 4.3 deg², as determined by the Youden index method. DDAF episodes (≥ 6 minutes) were identified via continuous telemedical pacemaker monitoring. The primary endpoint was time to first DDAF episode, analysed with Kaplan-Meier curves and Cox regression to assess the relationship between PRD and DDAF, adjusting for potential confounders. Results Between November 2021 and January 2024, a total of 233 patients were prospectively enrolled. Patients with known clinical AF were excluded. Overall, 13,801 patient-days of 111 patients (median age 76 years, 44% female) were analysed. Of the 111 patients analysed, 60 had c-AD (median stimulated PRD: 7.7 [5.7–8.6] deg²) and 51 did not (median stimulated PRD: 3.8 [2.0–7.3] deg²). During a 120-day follow-up, DDAF occurred in 41.2% of patients with c-AD, compared to 21.7% in those without c-AD (hazard ratio [HR], 3.3; 95% confidence interval [CI], 1.3–8.5; p = 0.009). However, native PRD showed no significant effect on the incidence of DDAF (HR, 1.27; 95% CI, 0.4–4.0). Conclusion Elevated stimulated PRD predicts the occurrence of DDAF in pacemaker patients without prior clinical AF, highlighting cardiac autonomic dysfunction’s role in atrial arrhythmogenesis. Native PRD did not show a significant association with DDAF, suggesting stimulated PRD may offer better predictive value. Further research is needed to explore the relationship between pacing modalities, autonomic function, and arrhythmogenesis.
No takes yet. Share an insight, caveat, or question.
Spitaler et al. (2025) studied this question. Elevated stimulated PRD (>4.3 deg²) tripled risk of device-detected atrial fibrillation (HR 3.3, p=0.009) in pacemaker patients without prior AF.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: