TY - JOUR
T1 - Detection of subclinical epileptiform discharges in Alzheimer's disease using long-term outpatient EEG monitoring
AU - Musaeus, Christian Sandøe
AU - Frederiksen, Kristian Steen
AU - Andersen, Birgitte Bo
AU - Høgh, Peter
AU - Kidmose, Preben
AU - Fabricius, Martin
AU - Hribljan, Melita Cacic
AU - Hemmsen, Martin Christian
AU - Rank, Mike Lind
AU - Waldemar, Gunhild
AU - Kjær, Troels Wesenberg
N1 - Copyright © 2023. Published by Elsevier Inc.
PY - 2023/7
Y1 - 2023/7
N2 - BACKGROUND: In patients with Alzheimer's disease (AD) without clinical seizures, up to half have epileptiform discharges on long-term in-patient electroencephalography (EEG) recordings. Long-term in-patient monitoring is obtrusive, and expensive as compared to outpatient monitoring. No studies have so far investigated if long-term outpatient EEG monitoring is able to identify epileptiform discharges in AD. Our aim is to investigate if epileptiform discharges as measured with ear-EEG are more common in patients with AD compared to healthy elderly controls (HC).METHODS: In this longitudinal observational study, 24 patients with mild to moderate AD and 15 age-matched HC were included in the analysis. Patients with AD underwent up to three ear-EEG recordings, each lasting up to two days, within 6 months.RESULTS: The first recording was defined as the baseline recording. At baseline, epileptiform discharges were detected in 75.0% of patients with AD and in 46.7% of HC (p-value = 0.073). The spike frequency (spikes or sharp waves/24 h) was significantly higher in patients with AD as compared to HC with a risk ratio of 2.90 (CI: 1.77-5.01, p < 0.001). Most patients with AD (91.7%) showed epileptiform discharges when combining all ear-EEG recordings.CONCLUSIONS: Long-term ear-EEG monitoring detects epileptiform discharges in most patients with AD with a three-fold increased spike frequency compared to HC, which most likely originates from the temporal lobes. Since most patients showed epileptiform discharges with multiple recordings, elevated spike frequency should be considered a marker of hyperexcitability in AD.
AB - BACKGROUND: In patients with Alzheimer's disease (AD) without clinical seizures, up to half have epileptiform discharges on long-term in-patient electroencephalography (EEG) recordings. Long-term in-patient monitoring is obtrusive, and expensive as compared to outpatient monitoring. No studies have so far investigated if long-term outpatient EEG monitoring is able to identify epileptiform discharges in AD. Our aim is to investigate if epileptiform discharges as measured with ear-EEG are more common in patients with AD compared to healthy elderly controls (HC).METHODS: In this longitudinal observational study, 24 patients with mild to moderate AD and 15 age-matched HC were included in the analysis. Patients with AD underwent up to three ear-EEG recordings, each lasting up to two days, within 6 months.RESULTS: The first recording was defined as the baseline recording. At baseline, epileptiform discharges were detected in 75.0% of patients with AD and in 46.7% of HC (p-value = 0.073). The spike frequency (spikes or sharp waves/24 h) was significantly higher in patients with AD as compared to HC with a risk ratio of 2.90 (CI: 1.77-5.01, p < 0.001). Most patients with AD (91.7%) showed epileptiform discharges when combining all ear-EEG recordings.CONCLUSIONS: Long-term ear-EEG monitoring detects epileptiform discharges in most patients with AD with a three-fold increased spike frequency compared to HC, which most likely originates from the temporal lobes. Since most patients showed epileptiform discharges with multiple recordings, elevated spike frequency should be considered a marker of hyperexcitability in AD.
KW - Alzheimer's disease
KW - Device
KW - Ear-EEG
KW - EEG
KW - Long-term EEG
KW - Subclinical epileptiform discharges
KW - Wearable
UR - http://www.scopus.com/inward/record.url?scp=85160360807&partnerID=8YFLogxK
U2 - 10.1016/j.nbd.2023.106149
DO - 10.1016/j.nbd.2023.106149
M3 - Journal article
C2 - 37196736
SN - 0969-9961
VL - 183
JO - Neurobiology of Disease
JF - Neurobiology of Disease
M1 - 106149
ER -