Plappert Felix, Wallman Mikael, Abdollahpur Mostafa, Platonov Pyotr G, Östenson Sten, Sandberg Frida
Department of Biomedical Engineering, Lund University, Lund, Sweden.
Department of Systems and Data Analysis, Fraunhofer-Chalmers Centre, Gothenburg, Sweden.
Front Physiol. 2022 Sep 15;13:976468. doi: 10.3389/fphys.2022.976468. eCollection 2022.
The response to atrial fibrillation (AF) treatment is differing widely among patients, and a better understanding of the factors that contribute to these differences is needed. One important factor may be differences in the autonomic nervous system (ANS) activity. The atrioventricular (AV) node plays an important role during AF in modulating heart rate. To study the effect of the ANS-induced activity on the AV nodal function in AF, mathematical modelling is a valuable tool. In this study, we present an extended AV node model that incorporates changes in autonomic tone. The extension was guided by a distribution-based sensitivity analysis and incorporates the ANS-induced changes in the refractoriness and conduction delay. Simulated RR series from the extended model driven by atrial impulse series obtained from clinical tilt test data were qualitatively evaluated against clinical RR series in terms of heart rate, RR series variability and RR series irregularity. The changes to the RR series characteristics during head-down tilt were replicated by a 10% decrease in conduction delay, while the changes during head-up tilt were replicated by a 5% decrease in the refractory period and a 10% decrease in the conduction delay. We demonstrate that the model extension is needed to replicate ANS-induced changes during tilt, indicating that the changes in RR series characteristics could not be explained by changes in atrial activity alone.
患者对房颤(AF)治疗的反应差异很大,因此需要更好地了解导致这些差异的因素。一个重要因素可能是自主神经系统(ANS)活动的差异。房室(AV)结在房颤期间对心率调节起着重要作用。为了研究ANS诱导的活动对房颤时房室结功能的影响,数学建模是一种有价值的工具。在本研究中,我们提出了一个扩展的房室结模型,该模型纳入了自主神经张力的变化。该扩展是由基于分布的敏感性分析指导的,并纳入了ANS诱导的不应期和传导延迟的变化。根据临床倾斜试验数据获得的心房冲动序列驱动扩展模型生成的模拟RR序列,在心率、RR序列变异性和RR序列不规则性方面与临床RR序列进行了定性评估。头低位倾斜期间RR序列特征的变化通过传导延迟降低10%来复制,而头高位倾斜期间的变化通过不应期降低5%和传导延迟降低10%来复制。我们证明需要模型扩展来复制倾斜期间ANS诱导的变化,这表明RR序列特征的变化不能仅用心房活动的变化来解释。