Van Paesschen W, Duncan J S, Connelly A
University Department of Clinical Neurology, National Hospital for Neurology and Neurosurgery, London, UK.
Epilepsy Res. 1998 Jan;29(2):155-60. doi: 10.1016/s0920-1211(97)00077-6.
Magnetic resonance (MR)-based T2 relaxation time measurement is a sensitive technique to detect neuropathological changes such as intramyelinic edema in vivo.
To determine whether vigabatrin (VGB) causes an increase in T2 relaxation time in patients with newly diagnosed localization-related epilepsy over 1 year.
Patients with newly diagnosed localization-related epilepsy who participated in a VGB-carbamazepine (CBZ) monotherapy trial were included. All were scanned on a 1.5 T Siemens SP63 Magnetom scanner. T2 maps of the brain were obtained at baseline and at follow-up 1 year later. Nine control subjects had repeated hippocampal T2 maps with a median interval of approximately 2 years.
23 patients (12 on VGB and 11 on CBZ) were included. There were no increased T2 relaxation times in the VGB treated group at follow-up and no significant differences between the two antiepileptic drug groups. There was a trend for the temporal and frontal white matter T2 relaxation times to be lower on follow-up in the patients compared to the control subjects.
The findings do not suggest that intramyelinic edema occurs in patients taking monotherapy VGB for 1 year.
基于磁共振(MR)的T2弛豫时间测量是一种在体内检测神经病理变化(如髓鞘内水肿)的敏感技术。
确定在新诊断的局灶性癫痫患者中,vigabatrin(VGB)是否会导致1年内T2弛豫时间增加。
纳入参与VGB - 卡马西平(CBZ)单药治疗试验的新诊断局灶性癫痫患者。所有患者均在1.5T西门子SP63 Magnetom扫描仪上进行扫描。在基线和1年后随访时获取脑部T2图谱。9名对照受试者重复进行海马T2图谱检查,中位间隔时间约为2年。
纳入23例患者(12例服用VGB,11例服用CBZ)。随访时VGB治疗组的T2弛豫时间未增加,两组抗癫痫药物组之间无显著差异。与对照受试者相比,患者随访时颞叶和额叶白质T2弛豫时间有降低趋势。
研究结果并不表明接受VGB单药治疗1年的患者会发生髓鞘内水肿。