Arrhythmogenic activities more frequently co-localized with low-voltage areas than with delayed enhancement areas on MRI (78% vs. 63%, P=0.02).
Observational (n=16)
There is a significant spatial mismatch between MRI-detected delayed enhancement areas and electrophysiological low-voltage areas in persistent AF, with arrhythmogenic sites more frequently co-localizing with low-voltage areas.
Absolute Event Rate: 63% vs 78%
p-value: p=0.02
AIMS: Atrial fibrosis contributes to arrhythmogenesis in atrial fibrillation and can be detected by MRI or electrophysiological mapping. The current study compares the spatial correlation between delayed enhancement (DE) areas to low-voltage areas (LVAs) and to arrhythmogenic areas with spatio-temporal dispersion (ST-Disp) or continuous activity (CA) in atrial fibrillation (AF). METHODS AND RESULTS: Sixteen patients with persistent AF (nine long-standing) underwent DE-magnetic resonance imaging (1.25 mm × 1.25 mm × 2.5 mm) prior to pulmonary vein isolation. Left atrial (LA) voltage mapping was acquired in AF and the regional activation patterns of 7680 AF wavelets were analysed. Sites with ST-Disp or CA were characterized (voltage, duration) and their spatial relationship to DE areas and LVAs 0.5 mV). Spatio-temporal dispersion and CA more frequently co-localized with LVAs than with DE areas (78% vs. 63%, P = 0.02). Regional bipolar voltage of ST-Disp vs. CA was 0.64 ± 0.47 mV vs. 0.58 ± 0.51 mV. All 28 ST-Disp and 56 CA areas contained electrograms with prolonged duration (115 ± 14 ms) displaying low voltage (0.34 ± 0.11 mV). CONCLUSION: A small portion of DE areas and LVAs harbour the arrhythmogenic areas displaying ST-Disp or CA. Most arrhythmogenic activities co-localized with LVAs, while there was less co-localization with DE areas. There is an important mismatch between DE areas and LVAs which needs to be considered when used as target for catheter ablation.
Chen et al. (Mon,) conducted a observational in persistent atrial fibrillation (n=16). Delayed enhancement (DE) areas on MRI vs. Low-voltage areas (LVAs) on electrophysiological mapping was evaluated on Co-localization of spatio-temporal dispersion and continuous activity (p=0.02). Arrhythmogenic activities more frequently co-localized with low-voltage areas than with delayed enhancement areas on MRI (78% vs. 63%, P=0.02).