TY - JOUR
T1 - Treatment effects on event-related EEG potentials and oscillations in Alzheimer's disease
AU - Yener, Görsev
AU - Hünerli-Gündüz, Duygu
AU - Yıldırım, Ebru
AU - Aktürk, Tuba
AU - Başar-Eroğlu, Canan
AU - Bonanni, Laura
AU - Del Percio, Claudio
AU - Farina, Francesca
AU - Ferri, Raffaele
AU - Güntekin, Bahar
AU - Hajós, Mihály
AU - Ibáñez, Agustín
AU - Jiang, Yang
AU - Lizio, Roberta
AU - Lopez, Susanna
AU - Noce, Giuseppe
AU - Parra, Mario A.
AU - Randall, Fiona
AU - Stocchi, Fabrizio
AU - Babiloni, Claudio
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/7
Y1 - 2022/7
N2 - Alzheimer's disease dementia (ADD) is the most diffuse neurodegenerative disorder belonging to mild cognitive impairment (MCI) and dementia in old persons. This disease is provoked by an abnormal accumulation of amyloid-beta and tauopathy proteins in the brain. Very recently, the first disease-modifying drug has been licensed with reserve (i.e., Aducanumab). Therefore, there is a need to identify and use biomarkers probing the neurophysiological underpinnings of human cognitive functions to test the clinical efficacy of that drug. In this regard, event-related electroencephalographic potentials (ERPs) and oscillations (EROs) are promising candidates. Here, an Expert Panel from the Electrophysiology Professional Interest Area of the Alzheimer's Association and Global Brain Consortium reviewed the field literature on the effects of the most used symptomatic drug against ADD (i.e., Acetylcholinesterase inhibitors) on ERPs and EROs in ADD patients with MCI and dementia at the group level. The most convincing results were found in ADD patients. In those patients, Acetylcholinesterase inhibitors partially normalized ERP P300 peak latency and amplitude in oddball paradigms using visual stimuli. In these same paradigms, those drugs partially normalize ERO phase-locking at the theta band (4–7 Hz) and spectral coherence between electrode pairs at the gamma (around 40 Hz) band. These results are of great interest and may motivate multicentric, double-blind, randomized, and placebo-controlled clinical trials in MCI and ADD patients for final cross-validation.
AB - Alzheimer's disease dementia (ADD) is the most diffuse neurodegenerative disorder belonging to mild cognitive impairment (MCI) and dementia in old persons. This disease is provoked by an abnormal accumulation of amyloid-beta and tauopathy proteins in the brain. Very recently, the first disease-modifying drug has been licensed with reserve (i.e., Aducanumab). Therefore, there is a need to identify and use biomarkers probing the neurophysiological underpinnings of human cognitive functions to test the clinical efficacy of that drug. In this regard, event-related electroencephalographic potentials (ERPs) and oscillations (EROs) are promising candidates. Here, an Expert Panel from the Electrophysiology Professional Interest Area of the Alzheimer's Association and Global Brain Consortium reviewed the field literature on the effects of the most used symptomatic drug against ADD (i.e., Acetylcholinesterase inhibitors) on ERPs and EROs in ADD patients with MCI and dementia at the group level. The most convincing results were found in ADD patients. In those patients, Acetylcholinesterase inhibitors partially normalized ERP P300 peak latency and amplitude in oddball paradigms using visual stimuli. In these same paradigms, those drugs partially normalize ERO phase-locking at the theta band (4–7 Hz) and spectral coherence between electrode pairs at the gamma (around 40 Hz) band. These results are of great interest and may motivate multicentric, double-blind, randomized, and placebo-controlled clinical trials in MCI and ADD patients for final cross-validation.
KW - Alzheimer
KW - Biomarker
KW - Dementia
KW - EEG
KW - EROs
KW - ERPs
KW - Event-related
KW - Mild cognitive impairment
KW - Monitoring
KW - Oscillations
KW - P300
KW - Treatment
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U2 - 10.1016/j.ijpsycho.2022.05.008
DO - 10.1016/j.ijpsycho.2022.05.008
M3 - Article
C2 - 35588964
AN - SCOPUS:85131441990
SN - 0167-8760
VL - 177
SP - 179
EP - 201
JO - International Journal of Psychophysiology
JF - International Journal of Psychophysiology
ER -