Vossel Keith A, Ranasinghe Kamalini G, Beagle Alexander J, Mizuiri Danielle, Honma Susanne M, Dowling Anne F, Darwish Sonja M, Van Berlo Victoria, Barnes Deborah E, Mantle Mary, Karydas Anna M, Coppola Giovanni, Roberson Erik D, Miller Bruce L, Garcia Paul A, Kirsch Heidi E, Mucke Lennart, Nagarajan Srikantan S
Memory and Aging Center, Department of Neurology, University of California, San Francisco, San Francisco, CA.
Gladstone Institute of Neurological Disease, San Francisco, CA.
Ann Neurol. 2016 Dec;80(6):858-870. doi: 10.1002/ana.24794. Epub 2016 Nov 7.
Seizures are more frequent in patients with Alzheimer's disease (AD) and can hasten cognitive decline. However, the incidence of subclinical epileptiform activity in AD and its consequences are unknown. Motivated by results from animal studies, we hypothesized higher than expected rates of subclinical epileptiform activity in AD with deleterious effects on cognition.
We prospectively enrolled 33 patients (mean age, 62 years) who met criteria for AD, but had no history of seizures, and 19 age-matched, cognitively normal controls. Subclinical epileptiform activity was assessed, blinded to diagnosis, by overnight long-term video-electroencephalography (EEG) and a 1-hour resting magnetoencephalography exam with simultaneous EEG. Patients also had comprehensive clinical and cognitive evaluations, assessed longitudinally over an average period of 3.3 years.
Subclinical epileptiform activity was detected in 42.4% of AD patients and 10.5% of controls (p = 0.02). At the time of monitoring, AD patients with epileptiform activity did not differ clinically from those without such activity. However, patients with subclinical epileptiform activity showed faster declines in global cognition, determined by the Mini-Mental State Examination (3.9 points/year in patients with epileptiform activity vs 1.6 points/year in patients without; p = 0.006), and in executive function (p = 0.01).
Extended monitoring detects subclinical epileptiform activity in a substantial proportion of patients with AD. Patients with this indicator of network hyperexcitability are at risk for accelerated cognitive decline and might benefit from antiepileptic therapies. These data call for more sensitive and comprehensive neurophysiological assessments in AD patient evaluations and impending clinical trials. Ann Neurol 2016;80:858-870.
癫痫发作在阿尔茨海默病(AD)患者中更为频繁,并且会加速认知功能衰退。然而,AD患者中亚临床癫痫样活动的发生率及其后果尚不清楚。受动物研究结果的启发,我们推测AD患者中亚临床癫痫样活动的发生率高于预期,且对认知有有害影响。
我们前瞻性地招募了33例符合AD标准但无癫痫发作史的患者(平均年龄62岁)以及19例年龄匹配、认知正常的对照者。在不知道诊断结果的情况下,通过夜间长期视频脑电图(EEG)以及1小时的静息脑磁图检查(同时记录EEG)来评估亚临床癫痫样活动。患者还接受了全面的临床和认知评估,并在平均3.3年的时间里进行纵向评估。
42.4%的AD患者检测到亚临床癫痫样活动,而对照组为10.5%(p = 0.02)。在监测时,有癫痫样活动的AD患者与无此类活动的患者在临床上并无差异。然而,有亚临床癫痫样活动的患者在简易精神状态检查中显示出整体认知功能下降更快(有癫痫样活动的患者每年下降3.9分,无癫痫样活动的患者每年下降1.6分;p = 0.006),执行功能也下降更快(p = 0.01)。
延长监测可在相当一部分AD患者中检测到亚临床癫痫样活动。有这种网络兴奋性过高指标的患者有认知衰退加速的风险,可能会从抗癫痫治疗中获益。这些数据呼吁在AD患者评估和即将进行的临床试验中进行更敏感和全面的神经生理学评估。《神经病学纪事》2016年;80:858 - 870。