School of Natural Sciences and Queensland Micro- and Nanotechnology Centre, Griffith University, Nathan, Queensland, 4111, Australia.
School of Natural Sciences and Queensland Micro- and Nanotechnology Centre, Griffith University, Nathan, Queensland, 4111, Australia.
Comput Biol Med. 2018 Apr 1;95:75-89. doi: 10.1016/j.compbiomed.2018.02.003. Epub 2018 Feb 10.
There is considerable interest in simulating ischaemia in the ventricle and its effect on the electrocardiogram, because a better understanding of the connection between the two may lead to improvements in diagnosis of myocardial ischaemia. In this work we studied subendocardial ischaemia, in a simplified half-ellipsoidal bidomain model of a ventricle, and its effect on ST segment epicardial potential distributions (EPDs). We found that the EPD changed as the ischaemic depth increased, from a single minimum (min1) over the ischaemic region to a maximum (max) there, with min1 over the border of the region. Lastly, a second minimum (min2) developed on the opposite side of the ischaemic region, in addition to min1 and max. We replicated these results in a realistic ventricular model and showed that the min1 only case could be found for ischaemic depths of up to around 35% of the ventricular wall. In addition, we systematically examined the sensitivity of EPD parameters, such as the potentials and positions of min1, max and min2, to various inputs to the half-ellipsoidal model, such as fibre rotation angle, ischaemic depth and conductivities. We found that the EPD parameters were not sensitive to the blood or transverse bidomain conductivities and were most sensitive to either ischaemic depth and/or fibre rotation angle. This allowed us to conclude that the asynchronous development of the two minima might provide a way of distinguishing between low and high thickness subendocardial ischaemia, and that this method may well be valid despite variability in the population.
人们对模拟心室中的缺血及其对心电图的影响非常感兴趣,因为更好地理解两者之间的关系可能会导致心肌缺血的诊断得到改善。在这项工作中,我们研究了心室简化的半椭圆双域模型中的心内膜下缺血及其对心外膜 ST 段电位分布(EPD)的影响。我们发现,随着缺血深度的增加,EPD 会发生变化,从缺血区域的单个最小值(min1)变为最大值(max),min1 位于区域边界上。最后,在缺血区域的对面还会出现第二个最小值(min2),除了 min1 和 max。我们在一个现实的心室模型中复制了这些结果,并表明仅在缺血深度达到心室壁的约 35%左右时,才会出现 min1 情况。此外,我们系统地检查了 EPD 参数的敏感性,例如 min1、max 和 min2 的电位和位置,这些参数对双域模型的各种输入(如纤维旋转角度、缺血深度和电导率)敏感。我们发现,EPD 参数对血液或横向双域电导率不敏感,而对缺血深度和/或纤维旋转角度最为敏感。这使我们得出结论,两个最小值的异步发展可能提供了一种区分低和高厚度心内膜下缺血的方法,尽管人群存在变异性,但这种方法可能仍然有效。