A. I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Sapienza University of Rome, Rome, Italy.
Epilepsia. 2022 Jul;63(7):1849-1861. doi: 10.1111/epi.17264. Epub 2022 May 12.
This study was undertaken to identify prognostic biomarkers for posttraumatic epileptogenesis derived from parameters related to the hippocampal position and orientation.
Data were derived from two preclinical magnetic resonance imaging (MRI) follow-up studies: EPITARGET (156 rats) and Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx; University of Eastern Finland cohort, 43 rats). Epileptogenesis was induced with lateral fluid percussion-induced traumatic brain injury (TBI) in adult male Sprague Dawley rats. In the EPITARGET cohort, -weighted MRI was performed at 2, 7, and 21 days and in the EpiBioS4Rx cohort at 2, 9, and 30 days and 5 months post-TBI. Both hippocampi were segmented using convolutional neural networks. The extracted segmentation mask was used for a geometric construction, extracting 39 parameters that described the position and orientation of the left and right hippocampus. In each cohort, we assessed the parameters as prognostic biomarkers for posttraumatic epilepsy (PTE) both individually, using repeated measures analysis of variance, and in combination, using random forest classifiers.
The extracted parameters were highly effective in discriminating between sham-operated and TBI rats in both the EPITARGET and EpiBioS4Rx cohorts at all timepoints (t; balanced accuracy > .9). The most discriminating parameter was the inclination of the hippocampus ipsilateral to the lesion at t = 2 days and the volumes at t ≥ 7 days after TBI. Furthermore, in the EpiBioS4Rx cohort, we could effectively discriminate epileptogenic from nonepileptogenic animals with a longer MRI follow-up, at t = 150 days (area under the curve = .78, balanced accuracy = .80, p = .0050), based on the orientation of both hippocampi. We found that the ipsilateral hippocampus rotated outward on the horizontal plane, whereas the contralateral hippocampus rotated away from the vertical direction.
We demonstrate that assessment of TBI-induced hippocampal deformation by clinically translatable MRI methodologies detects subjects with prior TBI as well as those at high risk of PTE, paving the way toward subject stratification for antiepileptogenesis studies.
本研究旨在确定源自海马位置和方向相关参数的创伤后癫痫发生的预后生物标志物。
数据来自两项临床前磁共振成像(MRI)随访研究:EPITARGET(156 只大鼠)和癫痫生物信息学研究以评估抗癫痫发生治疗(EpiBioS4Rx;东芬兰大学队列,43 只大鼠)。采用侧方液压诱导性创伤性脑损伤(TBI)诱导成年雄性 Sprague Dawley 大鼠癫痫发生。在 EPITARGET 队列中,在 TBI 后 2、7 和 21 天进行 T2 加权 MRI,在 EpiBioS4Rx 队列中在 2、9 和 30 天和 5 个月时进行 MRI。使用卷积神经网络对双侧海马进行分割。提取的分割掩模用于几何构建,提取了 39 个参数,描述了左、右海马的位置和方向。在每个队列中,我们使用重复测量方差分析分别评估这些参数作为创伤后癫痫(PTE)的预后生物标志物,并使用随机森林分类器进行组合评估。
在 EPITARGET 和 EpiBioS4Rx 队列中,在所有时间点(t;平衡准确性>.9),提取的参数均能有效区分假手术和 TBI 大鼠。最具区分性的参数是损伤对侧海马的倾斜度,以及 TBI 后 7 天以上的体积。此外,在 EpiBioS4Rx 队列中,我们可以基于双侧海马的方向,在更长的 MRI 随访中(t=150 天,曲线下面积[AUC] =.78,平衡准确性 =.80,p=.0050),有效区分致痫和非致痫动物。我们发现,损伤对侧的海马在水平面上向外旋转,而对侧的海马则远离垂直方向。
我们证明,通过临床可转化的 MRI 方法评估 TBI 引起的海马变形,可以检测到既往 TBI 患者以及 PTE 风险较高的患者,为抗癫痫发生研究的患者分层铺平了道路。