TY - JOUR
T1 - Source-space EEG alpha activity reveals brain age gaps due to neurodegeneration and disparity
AU - Otero, Mónica
AU - Carriel-Rubilar, Felipe I.
AU - Hernandez, Hernan
AU - Cuadros, Jhosmary
AU - Condado, Jorge G.
AU - Sainz-Ballesteros, Agustin
AU - Santamaria-Garcia, Hernando
AU - Legaz, Agustina
AU - Birba, Agustina
AU - Fittipaldi, Sol
AU - Lopera, Francisco
AU - Ochoa-Gómez, John
AU - Aguillon, David
AU - González-Hernández, Alfredis
AU - Bonilla-Santos, Jasmin
AU - Gonzalez-Montealegre, Rodrigo A.
AU - Yener, Görsev G.
AU - Güntekin, Bahar
AU - Kıyı, İlayda
AU - Aktürk, Tuba
AU - Yıldırım, Ebru
AU - Hanoğlu, Lütfü
AU - Anghinah, Renato
AU - Valdes-Sosa, Pedro A.
AU - Garcia-Reyes, Ronaldo
AU - Escudero, Javier
AU - Lopez, Susanna
AU - Whelan, Robert
AU - Fernández, Alberto
AU - García, Adolfo M.
AU - Huepe, David
AU - Soto-Añari, Marcio
AU - Herrera, Eduar
AU - Abasolo, Daniel
AU - Rubido, Nicolás
AU - Clark, Ruaridh A.
AU - El-Deredy, Wael
AU - Cortes, Jesús M.
AU - Parra, Mario A.
AU - Babiloni, Claudio
AU - Ibanez, Agustin
AU - Prado, Pavel
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026/12
Y1 - 2026/12
N2 - Brain clocks are promising tools for evaluating brain health. However, most current methods rely on structural neuroimaging. Functionally based approaches remain scarce, especially for assessing age-related neurodegenerative diseases. This study examines whether the brain age gap (BAG), the difference between chronological and predicted brain age, reflects neurodegeneration when estimated from electroencephalographic resting-state (rsEEG) α-oscillations, a well-established marker of brain functional aging. It also explores whether α-based brain clocks reflect sociodemographic diversity and structural inequality. The BAG was computed using spectral descriptors of α-activity in the rsEEG source space of 1228 healthy participants, individuals with mild cognitive impairment (MCI), and patients with Alzheimer’s disease or behavioral variant frontotemporal dementia, residing in 10 countries with varying levels of structural inequality. BAGs are increased in MCI and dementia groups, particularly in posterior cortical regions. Structural inequality emerges as the strongest predictor of BAG, surpassing cognition, education, and sex. The findings indicate that an α-oscillation-based brain clock provides a sensitive functional marker of brain aging, capable of capturing neurodegenerative processes as well as the impact of social disparities. This scalable, accessible approach to brain health shows promise for translational use and population-wide screening in underserved, resource-limited settings. (Figure presented.)
AB - Brain clocks are promising tools for evaluating brain health. However, most current methods rely on structural neuroimaging. Functionally based approaches remain scarce, especially for assessing age-related neurodegenerative diseases. This study examines whether the brain age gap (BAG), the difference between chronological and predicted brain age, reflects neurodegeneration when estimated from electroencephalographic resting-state (rsEEG) α-oscillations, a well-established marker of brain functional aging. It also explores whether α-based brain clocks reflect sociodemographic diversity and structural inequality. The BAG was computed using spectral descriptors of α-activity in the rsEEG source space of 1228 healthy participants, individuals with mild cognitive impairment (MCI), and patients with Alzheimer’s disease or behavioral variant frontotemporal dementia, residing in 10 countries with varying levels of structural inequality. BAGs are increased in MCI and dementia groups, particularly in posterior cortical regions. Structural inequality emerges as the strongest predictor of BAG, surpassing cognition, education, and sex. The findings indicate that an α-oscillation-based brain clock provides a sensitive functional marker of brain aging, capable of capturing neurodegenerative processes as well as the impact of social disparities. This scalable, accessible approach to brain health shows promise for translational use and population-wide screening in underserved, resource-limited settings. (Figure presented.)
UR - https://www.scopus.com/pages/publications/105040756265
U2 - 10.1038/s42003-026-10205-z
DO - 10.1038/s42003-026-10205-z
M3 - Article
C2 - 42162258
AN - SCOPUS:105040756265
SN - 2399-3642
VL - 9
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 740
ER -