Mäkiranta Minna, Ruohonen Jyrki, Suominen Kalervo, Niinimäki Jaakko, Sonkajärvi Eila, Kiviniemi Vesa, Seppänen Tapio, Alahuhta Seppo, Jäntti Ville, Tervonen Osmo
Department of Diagnostic Radiology, University of Oulu, Kajaanintie 50, 90220 Oulu, Finland.
Neuroimage. 2005 Oct 1;27(4):715-24. doi: 10.1016/j.neuroimage.2005.05.025.
In 40-60% of cases with interictal activity in EEG, fMRI cannot locate any focus or foci with simultaneous EEG/fMRI. In experimental focal epilepsy, a priori knowledge exists of the location of the epileptogenic area. This study aimed to develop and to test an experimental focal epilepsy model, which includes dynamic induction of epileptic activity, simultaneous EEG/fMRI, and deep anesthesia. Reported results are from seven pigs (23 +/- 2 kg) studied under isoflurane anesthesia (1.2-1.6 MAC, burst-suppression EEG) and muscle relaxant. Hypo- and hypercapnia were tested in one pig. Penicillin (6000 IU) was injected via a plastic catheter (inserted into the somatosensory cortex) during fMRI (GRE-EPI, TE = 40 ms, 300 ms/two slices, acquisition delay 1700 ms) in 1.5 T (N = 6). Epileptic spikes between acquisition artifacts were reviewed and EEG total power calculated. Cross-correlation between voxel time series and three model functions resembling induced spike activity were tested. Activation map averages were calculated. Development of penicillin induced focal epileptic activity was associated with linear increase and saturation up to approximately 10-20%, in BOLD activation map average. Its initial linear increase reached 2.5-10% at the appearance of the first distinguished spike in ipsilateral EEG in all six animals. Correlated voxels were located mainly in the vicinity of the penicillin injection site and midline, but few in the thalamus. In conclusion, development of focal epileptic activity can be detected as a BOLD signal change, even preceding the spike activity in scalp EEG. This experimental model contains potential for development and testing different localization methods and revealing the characteristic time sequence of epileptic activity with fMRI during deep anesthesia.
在脑电图(EEG)发作间期有活动的病例中,40%-60%的情况下,功能磁共振成像(fMRI)无法通过同步EEG/fMRI定位任何病灶。在实验性局灶性癫痫中,癫痫发作起源区的位置存在先验知识。本研究旨在开发并测试一种实验性局灶性癫痫模型,该模型包括癫痫活动的动态诱导、同步EEG/fMRI以及深度麻醉。报告的结果来自七头猪(体重23±2千克),在异氟烷麻醉(1.2-1.6 MAC,爆发抑制脑电图)和肌肉松弛剂作用下进行研究。对一头猪进行了低碳酸血症和高碳酸血症测试。在1.5T磁共振成像(GRE-EPI,TE = 40毫秒,300毫秒/两层,采集延迟1700毫秒)期间,通过塑料导管(插入体感皮层)向六头猪注射青霉素(6000国际单位)。对采集伪影之间的癫痫棘波进行了复查,并计算了脑电图总功率。测试了体素时间序列与三种类似于诱导棘波活动的模型函数之间的互相关性。计算了激活图平均值。青霉素诱导的局灶性癫痫活动的发展与血氧水平依赖(BOLD)激活图平均值的线性增加和饱和度增加有关,饱和度最高可达约10%-20%。在所有六只动物同侧脑电图中首次出现明显棘波时,其最初的线性增加达到2.5%-10%。相关体素主要位于青霉素注射部位附近和中线,但丘脑部位较少。总之,局灶性癫痫活动的发展可被检测为BOLD信号变化,甚至早于头皮脑电图中的棘波活动。该实验模型具有开发和测试不同定位方法以及揭示深度麻醉期间fMRI检测癫痫活动特征时间序列的潜力。