Department of Neurology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Epilepsy Res. 2012 Jun;100(1-2):59-66. doi: 10.1016/j.eplepsyres.2012.01.008. Epub 2012 Feb 2.
To characterize a biomarker for epileptogenesis based on cardiac interbeat interval characteristics.
Electrocardiograph (ECG) and electroencephalogram (EEG) signals were recorded from freely moving rats (n = 23) before status epilepticus (SE) induced by i.p. pilocarpine (PILO) injection as baseline, and on days 1, 3 and 7 after SE. We assessed several features from cardiac interbeat intervals, including linear, non-linear and frequency parameters of interbeat intervals, and power spectra of interpolated intervals during epileptogenesis. After thresholding, the altered values were applied to a non-linear classifier. The non-linear classifier divided animals into two groups; with and without epilepsy, based on all collected data.
We found that none of the single altered parameters in cardiac activity emerged as a sole biomarker for epileptogenesis. However, the non-linear classifier distinguished animals that later developed from those and did not develop epilepsy. The non-linear classification was performed on preliminary findings from 23 animals; six did not develop epilepsy and the rest did. The average positive predictive value (precision rate) was 78%. This was calculated based on the average sensitivity and specificity, which were 80.6% and 35.2% respectively, for the 100 classification passes. We also showed that these numbers would have increased as the number of subjects increased.
Changes to the brain caused by status epilepticus that lead to epileptogenesis have systemic effects, and alter cardiac activity. A non-linear classifier performed on several extracted features of cardiac interbeat intervals may be useful as a biomarker to identify animals with low and high probability of developing epilepsy after status epilepticus.
基于心动间隔特征来确定癫痫发生的生物标志物。
在腹腔注射匹罗卡品(PILO)诱导癫痫持续状态(SE)之前,从自由活动的大鼠(n = 23)中记录心电图(ECG)和脑电图(EEG)信号作为基线,并在 SE 后第 1、3 和 7 天记录。我们评估了心动间隔中的几个特征,包括心动间隔的线性、非线性和频率参数,以及癫痫发生过程中插值间隔的功率谱。经过阈值处理后,将改变的值应用于非线性分类器。非线性分类器根据所有收集的数据将动物分为有癫痫和无癫痫两组。
我们发现,心脏活动中没有一个单一的改变参数可以作为癫痫发生的唯一生物标志物。然而,非线性分类器可以区分后来发生癫痫和不发生癫痫的动物。非线性分类是在 23 只动物的初步发现上进行的;其中 6 只动物未发生癫痫,其余的发生了癫痫。平均阳性预测值(精度率)为 78%。这是基于平均敏感性和特异性计算得出的,敏感性和特异性分别为 80.6%和 35.2%,在 100 次分类通过中。我们还表明,随着研究对象数量的增加,这些数字将会增加。
SE 引起的大脑变化导致癫痫发生,具有系统性影响,并改变心脏活动。在心动间隔的几个提取特征上执行非线性分类器可能是一种有用的生物标志物,可用于识别 SE 后发生癫痫的低概率和高概率动物。