Back to Search Start Over

Sex specific EEG signatures associated with cerebrospinal fluid biomarkers in mild cognitive impairment.

Authors :
Chino-Vilca B
Rodríguez-Rojo IC
Torres-Simón L
Cuesta P
Vendrell AC
Piñol-Ripoll G
Huerto R
Tahan N
Maestú F
Source :
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology [Clin Neurophysiol] 2022 Oct; Vol. 142, pp. 190-198. Date of Electronic Publication: 2022 Aug 24.
Publication Year :
2022

Abstract

Objective: The use of the electroencephalography (EEG) technique in Alzheimer's disease (AD) diagnosis is scarce due to a lack of validation of its neurophysiological information with current biomarkers. Therefore, our goal was to assess correlations between brain spectral power signatures and cerebrospinal fluid markers (CSF) such as amyloid-β 42 load (Aβ-42), total tau (t-tau), and phosphorylated tau (p-tau) in a mild cognitive impairment (MCI) population. Furthermore, given the AD sex-dependent vulnerability related to CSF biomarkers, we went a little forward looking for different electrophysiological correlations for males and females independently.<br />Methods: A data-driven approach was employed to determine bidimensional spectral power signatures (space-frequency) that correlated (Spearman) significantly with any of the three CSF markers in 27 patients with MCI in any of the two sex-dependent subsamples (i.e., 12 females and 15 males).<br />Results: Our main significant outcomes evidenced 1) a negative correlation of Aβ-42 load with central-posterior theta power and a negative correlation of t-tau with widespread alpha power within the male subsample, and 2) a significant negative correlation between t-tau and widespread beta power in the female subgroup.<br />Conclusions: There is a distinctive profile of correlations between resting-state electrophysiological signatures and CSF markers in male and female individuals.<br />Significance: The combination of these two measures would be pointing out the need of a more personalized approach to promote early AD diagnosis.<br /> (Copyright © 2022 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-8952
Volume :
142
Database :
MEDLINE
Journal :
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Publication Type :
Academic Journal
Accession number :
36063668
Full Text :
https://doi.org/10.1016/j.clinph.2022.08.007