Vaudano Anna Elisabetta, Olivotto Sara, Ruggieri Andrea, Gessaroli Giuliana, De Giorgis Valentina, Parmeggiani Antonia, Veggiotti Pierangelo, Meletti Stefano
Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy; N.O.C.S.A.E. Hospital, AUSL Modena, 41100 Modena, Italy.
Brain and Behavior Department, University of Pavia, Pavia, Italy.
Neuroimage Clin. 2016 Dec 21;13:446-454. doi: 10.1016/j.nicl.2016.12.026. eCollection 2017.
To provide imaging biomarkers of generalized spike-and-wave discharges (GSWD) in patients with GLUT1 deficiency syndrome (GLUT1DS).
Eighteen GLUT1DS patients with pathogenetic mutation in SLC2A1 gene were studied by means of Video-EEG simultaneously recorded with functional MRI (VideoEEG-fMRI). A control group of sex and age-matched patients affected by Genetic Generalized Epilepsy (GGE) with GSWD were investigated with the same protocol. Within and between groups comparison was performed as appropriated. For GLUT1DS, correlations analyses between the contrast of interest and the main clinical measurements were provided.
EEG during fMRI revealed interictal GSWD in 10 GLUT1DS patients. Group-level analysis showed BOLD signal increases at the premotor cortex and putamen. With respect to GGE, GLUT1DS patients demonstrated increased neuronal activity in the putamen, precuneus, cingulate cortex, SMA and paracentral lobule. Whole-brain correlation analyses disclosed a linear relationship between the GSWD-related BOLD changes and the levels of glycorrhachia at diagnosis over the sensory-motor cortex and superior parietal lobuli.
The BOLD dynamics related to GSWD in GLUT1DS are substantially different from typical GGE showing the former an increased activity in the premotor-striatal network and a decrease in the thalamus. The revealed hemodynamic maps might represent imaging biomarkers of GLUT1DS, being potentially useful for a precocious diagnosis of this genetic disorder.
提供葡萄糖转运蛋白1缺乏综合征(GLUT1DS)患者广泛性棘慢波放电(GSWD)的影像学生物标志物。
对18例SLC2A1基因发生致病突变的GLUT1DS患者进行视频脑电图与功能磁共振成像同步记录(视频脑电图-功能磁共振成像)研究。对一组年龄和性别匹配的患有伴有GSWD的遗传性全身性癫痫(GGE)的患者按照相同方案进行研究。在组内和组间进行适当比较。对于GLUT1DS,提供了感兴趣的对比与主要临床测量之间的相关性分析。
功能磁共振成像期间的脑电图显示10例GLUT1DS患者存在发作间期GSWD。组水平分析显示运动前皮质和壳核的血氧水平依赖(BOLD)信号增加。与GGE相比,GLUT1DS患者在壳核、楔前叶、扣带回皮质、辅助运动区和中央旁小叶的神经元活动增加。全脑相关性分析揭示了GSWD相关的BOLD变化与诊断时感觉运动皮质和顶上小叶的脑脊液糖水平之间的线性关系。
GLUT1DS中与GSWD相关的BOLD动力学与典型GGE有显著不同,前者表现为运动前-纹状体网络活动增加和丘脑活动减少。所揭示的血流动力学图谱可能代表GLUT1DS的影像学生物标志物,对这种遗传性疾病的早期诊断可能有帮助。