Meo Marianna, Bonizzi Pietro, Bear Laura R, Cluitmans Matthijs, Abell Emma, Haïssaguerre Michel, Bernus Olivier, Dubois Rémi
Institute of Electrophysiology and Heart Modeling (IHU Liryc), Foundation Bordeaux University, Pessac-Bordeaux, France.
University of Bordeaux, CRCTB, Bordeaux, France.
Front Physiol. 2020 Aug 13;11:933. doi: 10.3389/fphys.2020.00933. eCollection 2020.
Increased heterogeneity of ventricular repolarization is associated with life-threatening arrhythmia and sudden cardiac death (SCD). T-wave analysis through body surface potential mapping (BSPM) is a promising tool for risk stratification, but the clinical effectiveness of current electrocardiographic indices is still unclear, with limited experimental validation. This study aims to investigate performance of non-invasive state-of-the-art and novel T-wave markers for repolarization dispersion in an model.
Langendorff-perfused pig hearts ( = 7) were suspended in a human-shaped 256-electrode torso tank. Tank potentials were recorded during sinus rhythm before and after introducing repolarization inhomogeneities through local perfusion with dofetilide and/or pinacidil. Drug-induced repolarization gradients were investigated from BSPMs at different experiment phases. Dispersion of electrical recovery was quantified by duration parameters, i.e., the time interval between the peak and the offset of T-wave (T-T) and QT interval, and variability over time and electrodes was also assessed. The degree of T-wave symmetry to the peak was quantified by the ratio between the terminal and initial portions of T-wave area (). Morphological variability between left and right BSPM electrodes was measured by dynamic time warping (DTW). Finally, T-wave organization was assessed by the complexity of repolarization index (CR), i.e., the amount of energy non-preserved by the dominant eigenvector computed by principal component analysis (PCA), and the error between each multilead T-wave and its 3D PCA approximation (NMSE). Body surface indices were compared with global measures of epicardial dispersion of repolarization, and with local gradients between adjacent ventricular sites.
After drug intervention, both regional and global repolarization heterogeneity were significantly enhanced. On the body surface, T-T was significantly prolonged and less stable in time in all experiments, while QT interval showed higher variability across the interventions in terms of duration and spatial dispersion. The rising slope of the repolarization profile was steeper, and T-waves were more asymmetric than at baseline. Interventricular shape dissimilarity was enhanced by repolarization gradients according to DTW. Organized T-wave patterns were associated with abnormal repolarization, and they were properly described by the first principal components.
Repolarization heterogeneity significantly affects T-wave properties, and can be non-invasively captured by BSPM-based metrics.
心室复极异质性增加与危及生命的心律失常和心源性猝死(SCD)相关。通过体表电位标测(BSPM)进行T波分析是一种很有前景的风险分层工具,但目前心电图指标的临床有效性仍不明确,实验验证有限。本研究旨在研究非侵入性的先进和新型T波标记物在模型中对复极离散的性能。
将Langendorff灌注的猪心脏(n = 7)悬挂在人形256电极躯干槽中。在通过多非利特和/或吡那地尔局部灌注引入复极不均匀性之前和之后的窦性心律期间记录槽电位。在不同实验阶段从BSPM研究药物诱导的复极梯度。通过持续时间参数,即T波峰与偏移之间的时间间隔(T-T)和QT间期,量化电恢复的离散度,并评估随时间和电极的变异性。通过T波面积的终末部分与起始部分的比值()量化T波相对于峰的对称程度。通过动态时间规整(DTW)测量左右BSPM电极之间的形态变异性。最后,通过复极指数(CR)的复杂性评估T波组织,即主成分分析(PCA)计算的主导特征向量未保留的能量量,以及每个多导联T波与其3D PCA近似值之间的误差(NMSE)。将体表指标与心外膜复极离散的整体测量值以及相邻心室部位之间的局部梯度进行比较。
药物干预后,局部和整体复极异质性均显著增强。在体表,所有实验中T-T均显著延长且时间稳定性降低,而QT间期在持续时间和空间离散度方面在各干预措施中表现出更高的变异性。复极曲线的上升斜率更陡,T波比基线时更不对称。根据DTW,复极梯度增强了心室间形状的差异。有组织的T波模式与异常复极相关,并且它们由第一主成分恰当地描述。
复极异质性显著影响T波特性,并且可以通过基于BSPM的指标进行非侵入性捕获。