IHU LIRYC, L'Institut des maladies du RYthme Cardiaque, Fondation Bordeaux Université, Bordeaux, France; University of Bordeaux, Inserm, Centre de Recherche Cardio-Thoracique de Bordeaux, Bordeaux, France.
IHU LIRYC, L'Institut des maladies du RYthme Cardiaque, Fondation Bordeaux Université, Bordeaux, France; University of Bordeaux, Inserm, Centre de Recherche Cardio-Thoracique de Bordeaux, Bordeaux, France.
JACC Clin Electrophysiol. 2024 Jul;10(7 Pt 1):1424-1438. doi: 10.1016/j.jacep.2024.03.002. Epub 2024 Apr 24.
Recent clinical studies have indicated the presence of localized electrical abnormalities in idiopathic ventricular fibrillation and J-wave syndrome patients.
This study aims to characterize the specific electrical signatures of localized repolarization and conduction heterogeneities and their respective role in vulnerability to arrhythmias.
Optical mapping was performed in porcine right ventricles with local: 1) repolarization shortening; 2) conduction slowing; or 3) structural heterogeneity induced by locally perfusing: 1) pinacidil (20 μmol/L, n = 13); or 2) flecainide (2 μmol/L, n = 13) via an epicardial catheter; or 3) by local epicardial tissue destruction (9 radiofrequency lesions n = 12). Electrograms were recorded (n = 5 in each group) and spontaneous and induced arrhythmias were quantified and optically mapped.
Electrograms were normal in (1) but showed local fragmentation in 40% of preparations in (2) with greater effects observed at high pacing frequencies dependent on the wavefront direction. In (3), the structural substrate alone increased the width and number of peaks in the electrograms, and addition of flecainide induced pronounced fragmentation (≥3 peaks and ≥70 ms) in all cases. Occurrence of spontaneous arrhythmias was significantly increased in (1) and (2) (P < 0.0001 and 0.05, respectively, vs baseline) and were triggered by ectopies. Vulnerability to arrhythmias at high pacing frequencies (≥2 Hz) was the lowest in (1) and greatest in (2).
Microstructural substrates have the most pronounced impact on electrograms, especially when combined with sodium channel blockers, whereas local action potential duration shortening does not lead to electrogram fragmentation even though it is associated with the highest prevalence of spontaneous arrhythmias.
最近的临床研究表明,特发性室颤和 J 波综合征患者存在局部电异常。
本研究旨在描述局部复极和传导异质性的特定电特征及其在心律失常易感性中的各自作用。
通过心外膜导管局部灌注:1)吡那地尔(20 μmol/L,n=13);或 2)氟卡尼(2 μmol/L,n=13);或 3)局部心外膜组织破坏(9 个射频消融灶 n=12),在猪右心室中进行光学标测,局部表现为 1)复极缩短;2)传导减慢;或 3)结构异质性。记录心外膜电图(n=每组 5),并定量和光学标测自发和诱发的心律失常。
电描记图在(1)中正常,但在(2)中 40%的标本中显示局部碎裂,在依赖波阵面方向的较高起搏频率下观察到更大的影响。在(3)中,结构基质本身增加了电描记图中的波宽和波峰数量,并且在所有情况下,氟卡尼的加入都会引起明显的碎裂(≥3 个波峰和≥70ms)。在(1)和(2)中自发心律失常的发生率显著增加(P<0.0001 和 0.05,分别与基线相比),并由异位搏动触发。在较高起搏频率(≥2Hz)下心律失常的易感性在(1)中最低,在(2)中最高。
微结构基质对电描记图的影响最为显著,尤其是与钠通道阻滞剂联合使用时,而局部动作电位时程缩短不会导致电描记图碎裂,尽管它与自发性心律失常的最高发生率相关。