Department of Clinical and Experimental Medicine, University of Pisa, Italy.
Epilepsia. 2014 Jul;55(7):1038-47. doi: 10.1111/epi.12634. Epub 2014 May 23.
Juvenile myoclonic epilepsy (JME) is a young-onset electroclinical syndrome, characterized by myoclonic, generalized tonic-clonic, and possibly typical absence seizures. Interictal electroencephalography (EEG) displays 3-6 Hz spike/polyspike and wave pattern. Photosensitivity is common. Our aim was to explore the blood oxygen level-dependent (BOLD) response evoked by a highly provocative photic stimulus in a cohort of people with JME compared to a group of nonphotosensitive healthy controls, and to investigate the hemodynamic phenomena seen in patients with photosensitive JME.
We studied 13 JME patients and 18 healthy controls using EEG-functional magnetic resonance imaging (fMRI) performed during low luminance intermittent photic stimulation (IPS). The BOLD response to IPS was investigated both in JME and control groups. In photosensitive JME subjects, we also performed a dynamic evaluation of BOLD signal changes evoked by the photoparoxysmal response (PPR) in a time frame ranging from 10 s before the onset of the EEG paroxysm up until 10 s afterward.
The IPS evoked a positive BOLD response in striate and extrastriate visual areas, which was less in JME patients than in controls. Moreover, people with JME had a reduced positive BOLD response in the frontoparietal areas and putamen but a stronger negative BOLD response in the primary sensorimotor cortex (SM1) and in cortical regions belonging to the default mode network (DMN). In JME, the dynamic evaluation of BOLD signal changes related to PPR revealed an early positive response in the putamen and SM1, followed by BOLD signal decrements in the putamen, caudate nuclei, thalami, and SM1.
Our results confirm the hypothesis that people with JME might have an altered interaction between the motor circuit and other neuronal networks, with prominent involvement of basal ganglia circuitry. The PPR could be a final expression of pathogenic phenomena occurring in the striato-thalamocortical system, possibly a core feature of system epilepsy JME.
青少年肌阵挛癫痫(JME)是一种年轻起病的电临床综合征,其特征为肌阵挛、全面强直-阵挛和可能的典型失神发作。发作间期脑电图(EEG)显示 3-6 Hz 棘波/多棘波和波模式。光敏感性很常见。我们的目的是探索与非光敏感健康对照组相比,一组 JME 患者对高度刺激性光刺激的血氧水平依赖(BOLD)反应,并研究光敏性 JME 患者的血液动力学现象。
我们使用 EEG 功能磁共振成像(fMRI)研究了 13 名 JME 患者和 18 名健康对照者,这些患者在低亮度间歇性光刺激(IPS)期间进行。研究了 JME 和对照组对 IPS 的 BOLD 反应。在光敏性 JME 患者中,我们还对光惊反射(PPR)引起的 BOLD 信号变化进行了动态评估,时间范围从 EEG 发作前 10 秒到发作后 10 秒。
IPS 在纹状和纹外视觉区域引起正 BOLD 反应,JME 患者的反应低于对照组。此外,JME 患者的额顶叶区域和壳核的正 BOLD 反应减弱,但初级感觉运动皮层(SM1)和默认模式网络(DMN)的皮质区域的负 BOLD 反应增强。在 JME 中,与 PPR 相关的 BOLD 信号变化的动态评估显示,壳核和 SM1 中存在早期正反应,随后壳核、尾状核、丘脑和 SM1 中 BOLD 信号减少。
我们的结果证实了这样一种假设,即 JME 患者可能存在运动回路与其他神经元网络之间的交互作用改变,基底节回路的参与尤为突出。PPR 可能是纹状体-丘脑-皮质系统中发生的致病现象的最终表现,可能是 JME 系统癫痫的核心特征。