Incidence and impact of subclinical epileptiform activity in Alzheimer's disease.
Incidence and impact of subclinical epileptiform activity in Alzheimer's disease.
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DOI:
10.1002/ana.24794
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发表时间:
2016-12
影响因子:
11.2
通讯作者:
Nagarajan, Srikantan S.
中科院分区:
文献类型:
--
作者:
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.
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 and a one-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.
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影响因子:
29
作者:
Donohue, Michael C.;Sperling, Reisa A.;Salmon, David P.;Rentz, Dorene M.;Raman, Rema;Thomas, Ronald G.;Weiner, Michael;Aisen, Paul S.
通讯作者:
Aisen, Paul S.
DOI:
10.1016/j.jalz.2011.03.005
发表时间:
2011-05
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
McKhann GM;Knopman DS;Chertkow H;Hyman BT;Jack CR Jr;Kawas CH;Klunk WE;Koroshetz WJ;Manly JJ;Mayeux R;Mohs RC;Morris JC;Rossor MN;Scheltens P;Carrillo MC;Thies B;Weintraub S;Phelps CH
通讯作者:
Phelps CH
DOI:
10.1073/pnas.0812697106
发表时间:
2009-02-10
影响因子:
11.1
作者:
Agosta, Federica;Vossel, Keith A.;Gorno-Tempini, Maria Luisa
通讯作者:
Gorno-Tempini, Maria Luisa
影响因子:
16.2
作者:
Bakker A;Krauss GL;Albert MS;Speck CL;Jones LR;Stark CE;Yassa MA;Bassett SS;Shelton AL;Gallagher M
通讯作者:
Gallagher M
影响因子:
4.2
作者:
Bakker, Arnold;Albert, Marilyn S.;Krauss, Gregory;Speck, Caroline L.;Gallagher, Michela
通讯作者:
Gallagher, Michela