Abnormal EEG Power Spectra in Acute Transient Global Amnesia: A Quantitative EEG Study.
Aged
Aged, 80 and over
Amnesia, Transient Global
/ physiopathology
Brain Mapping
/ methods
Electroencephalography
/ methods
Female
Frontal Lobe
/ physiopathology
Hippocampus
/ physiopathology
Humans
Male
Memory
/ physiology
Middle Aged
Parietal Lobe
/ physiopathology
Somatosensory Cortex
/ physiopathology
Temporal Lobe
/ physiopathology
EEG power spectra
MRI
diffusion-weighted imaging
eLORETA
quantitative EEG
transient global amnesia
Journal
Clinical EEG and neuroscience
ISSN: 2169-5202
Titre abrégé: Clin EEG Neurosci
Pays: United States
ID NLM: 101213033
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
pubmed:
8
6
2018
medline:
14
8
2019
entrez:
8
6
2018
Statut:
ppublish
Résumé
Transient global amnesia (TGA) is a clinical syndrome characterized by retrograde and anterograde amnesia without other neurological deficits. Although electroencephalography (EEG) methods are commonly used in both clinical and research setting with TGA patients, few studies have investigated neurophysiological pattern in TGA using quantitative EEG (qEEG). The main aim of the present study was to extend these previous findings by exploring EEG power spectra differences between patients with acute TGA and healthy controls using the exact low-resolution brain electromagnetic tomography software (eLORETA). EEG was recorded during 5 minutes of resting state. Sixteen patients (mean age: 66.81 ± 7.94 years) during acute TGA and 16 healthy subjects were enrolled. All patients showed hippocampal or parahippocampal signal abnormalities in diffusion-weighted magnetic resonance imaging performed from 2 to 5 days after the onset of TGA. Compared with healthy controls, TGA patients showed a decrease of theta power localized in the temporal lobe (Brodmann areas, BAs 21-22-38) and frontal lobe (BAs 8-9-44-45). A decrease of EEG beta power in the bilateral precuneus (BA 7) and in the bilateral postcentral gyrus (BAs 3-4-5) was also observed in TGA individuals. Taken together, our results could reflect the neurophysiological substrate of the severe impairment of both episodic memory and autobiographical memory which affect TGA patients during the acute phase.
Identifiants
pubmed: 29877098
doi: 10.1177/1550059418780780
doi:
Types de publication
Journal Article
Langues
eng