Lux Robert L, Gettes Leonard S
Cardiovascular Research and Training Institute, University of Utah, Salt Lake City, UT 84112-5000, USA.
J Electrocardiol. 2011 Nov-Dec;44(6):730-5. doi: 10.1016/j.jelectrocard.2011.08.001. Epub 2011 Sep 14.
Repolarization heterogeneity and rate dependency have long been established as factors contributing to arrhythmogenic risk. However, there are conflicting observations regarding the nature and extent of ventricular repolarization heterogeneity that complicate understanding of arrhythmogenic mechanisms. To explore these disparate findings, we studied ventricular repolarization heterogeneity and rate dependency in a canine, rapid pacing model of heart failure.
We studied ventricular repolarization heterogeneity and rate dependency in 10 canine hearts (5 normal and 5 after 1 month of rapid pacing at 240 beats per minute) by analyzing 64 body surface electrocardiograms, 64 epicardial, and 190 intramural plunge electrograms. We estimated mean ventricular depolarization and repolarization times from R- and T-wave peaks of the root-mean-square electrocardiogram (body surface) and local depolarization and repolarization times using activation-recovery interval (ARI) methods from recordings obtained during a range of fixed rate pacing. In addition, we estimated local epicardial and transmural gradients of ARIs to assess cardiac locations of greatest spatial repolarization heterogeneity. We compared changes in repolarization at different rates between normal and heart failure hearts. Findings documented prolongation of repolarization, repolarization rate dependency, and increased repolarization gradients in the heart failure hearts compared with control as observed from body surface, epicardial, and transmural measurements. Maximum local epicardial and intramural ARI gradients were comparable both in heart failure and control hearts. Intramural ARI distributions tended to be more irregular in the heart failure hearts compared with the systematic epicardium to endocardium ARI increase observed in control animals.
This study documented prolongation of repolarization, increase in both epicardial and transmural repolarization gradients, and irregularity of transmural distribution in a rapid pacing canine model of heart failure compared with control animals. The findings support previously published results of increased repolarization heterogeneity and repolarization prolongation observed in rapid pacing models of heart failure. New findings are the irregularity of transmural heterogeneity and the ability of noninvasive root-mean-square electrocardiogram R-T intervals to estimate mean ventricular repolarization duration in the setting of rapid pacing models of heart failure. These findings suggest increased arrhythmogenic risk in this model and potentially in patients with heart failure.
复极异质性和心率依赖性长期以来一直被认为是导致心律失常风险的因素。然而,关于心室复极异质性的性质和程度存在相互矛盾的观察结果,这使得对心律失常机制的理解变得复杂。为了探究这些不同的发现,我们在犬类快速起搏心力衰竭模型中研究了心室复极异质性和心率依赖性。
我们通过分析64份体表心电图、64份心外膜电图和190份心内膜下针电极电图,研究了10只犬心脏(5只正常犬和5只在每分钟240次快速起搏1个月后的犬)的心室复极异质性和心率依赖性。我们从均方根心电图(体表)的R波和T波峰值估计平均心室去极化和复极时间,并使用激活-恢复间期(ARI)方法从一系列固定心率起搏期间获得的记录中估计局部去极化和复极时间。此外,我们估计了ARI的心外膜和跨壁梯度,以评估最大空间复极异质性的心脏位置。我们比较了正常心脏和心力衰竭心脏在不同心率下复极的变化。从体表、心外膜和跨壁测量结果来看,与对照组相比,心力衰竭心脏的复极延长、复极心率依赖性以及复极梯度增加。心力衰竭心脏和对照心脏的心外膜最大局部ARI梯度和心内膜下ARI梯度相当。与对照动物中观察到的心外膜到心内膜ARI系统性增加相比,心力衰竭心脏的心内膜下ARI分布往往更不规则。
本研究证明,与对照动物相比,在快速起搏犬类心力衰竭模型中,复极延长、心外膜和跨壁复极梯度增加以及跨壁分布不规则。这些发现支持了先前在心力衰竭快速起搏模型中观察到的复极异质性增加和复极延长的结果。新发现是跨壁异质性的不规则性以及无创均方根心电图R-T间期在心力衰竭快速起搏模型中估计平均心室复极持续时间的能力。这些发现表明该模型以及可能的心力衰竭患者的心律失常风险增加。