Roney Caroline H, Bayer Jason D, Zahid Sohail, Meo Marianna, Boyle Patrick M J, Trayanova Natalia A, Haïssaguerre Michel, Dubois Rémi, Cochet Hubert, Vigmond Edward J
IHU Liryc, Electrophysiology and Heart Modeling Institute, foundation Bordeaux Université, F-33600 Pessac- Bordeaux, France.
Univ. Bordeaux, IMB UMR 5251, CNRS, F-33400 Talence, France.
Europace. 2016 Dec;18(suppl 4):iv146-iv155. doi: 10.1093/europace/euw365.
Catheter ablation is an effective technique for terminating atrial arrhythmia. However, given a high atrial fibrillation (AF) recurrence rate, optimal ablation strategies have yet to be defined. Computer modelling can be a powerful aid but modelling of fibrosis, a major factor associated with AF, is an open question. Several groups have proposed methodologies based on imaging data, but no comparison to determine which methodology best corroborates clinically observed reentrant behaviour has been performed. We examined several methodologies to determine the best method for capturing fibrillation dynamics.
Patient late gadolinium-enhanced magnetic resonance imaging data were transferred onto a bilayer atrial computer model and used to assign fibrosis distributions. Fibrosis was modelled as conduction disturbances (lower conductivity, edge splitting, or percolation), transforming growth factor-β1 ionic channel effects, myocyte-fibroblast coupling, and combinations of the preceding. Reentry was induced through pulmonary vein ectopy and the ensuing rotor dynamics characterized. Non-invasive electrocardiographic imaging data of the patients in AF was used for comparison. Electrograms were computed and the fractionation durations measured over the surface. Edge splitting produced more phase singularities from wavebreaks than the other representations. The number of phase singularities seen with percolation was closer to the clinical values. Addition of fibroblast coupling had an organizing effect on rotor dynamics. Simple tissue conductivity changes with ionic changes localized rotors over fibrosis which was not observed with clinical data.
The specific representation of fibrosis has a large effect on rotor dynamics and needs to be carefully considered for patient specific modelling.
导管消融是终止房性心律失常的有效技术。然而,鉴于房颤(AF)复发率较高,最佳消融策略尚未明确。计算机建模可能是一种强大的辅助手段,但对与房颤相关的主要因素——纤维化进行建模仍是一个悬而未决的问题。多个研究小组提出了基于成像数据的方法,但尚未进行比较以确定哪种方法最能证实临床观察到的折返行为。我们研究了几种方法以确定捕捉颤动动态的最佳方法。
将患者的延迟钆增强磁共振成像数据传输到双层心房计算机模型上,并用于指定纤维化分布。纤维化被建模为传导障碍(较低的电导率、边缘分裂或渗流)、转化生长因子-β1离子通道效应、心肌细胞-成纤维细胞耦合以及上述因素的组合。通过肺静脉异位诱发折返,并对随之产生的转子动态进行表征。使用房颤患者的非侵入性心电图成像数据进行比较。计算心内电图并测量表面的碎裂持续时间。与其他表示形式相比,边缘分裂从波破裂产生的相位奇点更多。渗流所见的相位奇点数量更接近临床值。添加成纤维细胞耦合对转子动态有组织作用。简单的组织电导率随离子变化而改变,使转子定位于纤维化区域,而临床数据未观察到这种情况。
纤维化的具体表示形式对转子动态有很大影响,在针对患者的建模中需要仔细考虑。