Long Ran, Wang Yuting, Chen Lizhou, Deng Dingmei, Mei Lan, Mou Jingping, Tang Guangcai, Han Fugang, Kemp Graham John, Gong Qiyong, Qiu Lihua
Department of Radiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Department of Radiology, The Second People's Hospital of Yibin, Yibin, China.
Front Neurol. 2021 Nov 30;12:744723. doi: 10.3389/fneur.2021.744723. eCollection 2021.
Despite evidence for microstructural brain alterations in epilepsy patients, little is known about how these develop with age and the progress of the disease. The aim of this study was to investigate microstructural abnormalities of the white matter (WM) in children with new-onset, untreated idiopathic-generalized epilepsy (IGE) using the MRI technique of diffusion tensor imaging (DTI). The study was approved by the institutional review board, and all individuals or their parents gave signed informed consent. In total, 45 patients with IGE (age 5-18 years, male: female 26:19) and 32 healthy controls (HCs; age 5-18 years, male: female 21:11) were included. Voxel-based analysis (VBA) was used to compare patients and controls, and Pearson correlation analysis was used to investigate relationships between altered DTI metrics and clinical parameters. Compared with controls, patients with IGE showed increased mean diffusivity (MD) in the left splenium of the corpus callosum, increased fractional anisotropy (FA) in the right WM of the superior and middle frontal gyri, increased axial diffusivity (AD) in the WM of right corona radiata and left occipital lobe, and decreased AD in the WM of the left thalamus and the right middle cerebellar peduncle. There was no correlation between the altered diffusion parameters and clinical measures. Our study demonstrated several distinct microstructural impairments in children with new-onset, untreated IGE, of which altered AD might be the most sensitive marker of dysmyelination. The increased FA in the IGE group might suggest an initiating or compensatory mechanism that is activated prior to cognitive decline in these children.
尽管有证据表明癫痫患者存在脑微结构改变,但对于这些改变如何随年龄和疾病进展而发展却知之甚少。本研究的目的是使用扩散张量成像(DTI)的MRI技术,研究新发、未经治疗的特发性全身性癫痫(IGE)儿童的白质(WM)微结构异常。该研究经机构审查委员会批准,所有个体或其父母均签署了知情同意书。总共纳入了45例IGE患者(年龄5 - 18岁,男∶女 = 26∶19)和32名健康对照者(HCs;年龄5 - 18岁,男∶女 = 21∶11)。基于体素的分析(VBA)用于比较患者和对照者,Pearson相关分析用于研究DTI指标改变与临床参数之间的关系。与对照者相比,IGE患者胼胝体左压部的平均扩散率(MD)增加,额上回和额中回右侧白质的分数各向异性(FA)增加,右侧放射冠和左侧枕叶白质的轴向扩散率(AD)增加,左侧丘脑和右侧小脑中脚白质的AD降低。扩散参数改变与临床指标之间无相关性。我们的研究证明了新发、未经治疗的IGE儿童存在几种不同的微结构损伤,其中AD改变可能是脱髓鞘最敏感的标志物。IGE组中FA增加可能提示在这些儿童认知功能下降之前激活的一种起始或代偿机制。