Research Service, VA New York Harbor Healthcare System, New York, NY, USA; Department of Neurology, New York University Langone Medical Center, New York, NY, USA.
Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Epilepsy Behav. 2018 Nov;88:315-324. doi: 10.1016/j.yebeh.2018.06.047. Epub 2018 Oct 27.
Excitotoxic injury involving N-methyl-d-aspartate (NMDA) receptor hyperactivity contributes to epilepsy-related memory dysfunction (ERMD). Current treatment strategies for ERMD have limited efficacy and fail to target the underlying pathophysiology. The present pilot study evaluated the efficacy of memantine, an NMDA receptor antagonist, for the treatment of ERMD in adults with focal-onset seizures.
Subjects underwent cognitive testing at baseline, after a 13-week randomized, parallel-group, double-blinded phase (of memantine titrated to 10 mg bid or placebo), and following a 13-week open-label extension phase (of memantine titrated to 10 mg bid). The selective reminding test (SRT) continuous long-term retrieval (CLTR) score and 7/24 Spatial Recall Test learning score served as the primary outcome measures. Secondary measures included tests of attention span, fluency, visual construction, and response inhibition, as well as assessments of quality of life, depression, sleepiness, and side effects.
Seventeen subjects contributed data to the blinded phase (n = 8 memantine, n = 9 placebo). No significant differences were seen between groups on the primary or secondary outcome measures. Pooled data at the end of the open-label phase from 10 subjects (initially randomized to memantine n = 3 or placebo n = 7) demonstrated statistically significant improvement from baseline in CLTR score, memory-related quality of life, spatial span, and response inhibition. No significant changes were evident in depression, sleepiness, side effects, or seizure frequency throughout the trial.
Results demonstrated no significant effect of memantine on cognition when assessed at the end of the blinded period. Pooled data at the end of the open-label phase showed significant improvement over baseline performance in measures of verbal memory, frontal-executive function, and memory-related quality of life. These improvements, however, may be due to practice effects and should be interpreted cautiously. Findings suggest a favorable safety profile of memantine in the setting of epilepsy.
涉及 N-甲基-D-天冬氨酸(NMDA)受体过度活跃的兴奋性毒性损伤导致与癫痫相关的记忆功能障碍(ERMD)。目前针对 ERMD 的治疗策略疗效有限,无法针对潜在的病理生理学进行治疗。本初步研究评估了 NMDA 受体拮抗剂美金刚治疗局灶性发作性癫痫成人 ERMD 的疗效。
受试者在基线时、13 周随机、平行组、双盲期(美金刚滴定至 10mg bid 或安慰剂)后以及 13 周开放标签扩展期(美金刚滴定至 10mg bid)后进行认知测试。选择性提醒测试(SRT)连续长期检索(CLTR)评分和 7/24 空间回忆测试学习评分作为主要结局指标。次要指标包括注意力跨度、流畅性、视觉构建和反应抑制测试,以及生活质量、抑郁、嗜睡和副作用评估。
17 名受试者参与了盲法期(n=8 美金刚,n=9 安慰剂)的数据。主要或次要结局指标上,两组之间无显著差异。10 名受试者(最初随机分为美金刚 n=3 或安慰剂 n=7)在开放标签期结束时的汇总数据显示,CLTR 评分、记忆相关生活质量、空间跨度和反应抑制从基线开始有统计学意义的改善。整个试验过程中,抑郁、嗜睡、副作用或癫痫发作频率均无明显变化。
结果表明,在盲法期结束时评估时,美金刚对认知没有显著影响。开放标签期结束时的汇总数据显示,在言语记忆、额叶执行功能和记忆相关生活质量方面,与基线相比,有显著改善。然而,这些改善可能是由于练习效应,应谨慎解释。研究结果表明,在癫痫的情况下,美金刚具有良好的安全性。