Scientific reports · 2026
Qualitative EEG abnormalities in ASD reflect inhibition-dominated brain dynamics.
СтатьяНазвание и аннотация: Перевод в очереди
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Avramiea Arthur-Ervin, Juarez-Martinez Erika L, Garcés Pilar, Hipp Joerg F, Poil Simon-Shlomo, Diachenko Marina, Mansvelder Huibert D, Jones Emily, Mason Luke, Murphy Declan, Loth Eva, Oakley Bethany, Charman Tony, Banaschewski Tobias, Oranje Bob, Buitelaar Jan, Bruining Hilgo, Linkenkaer-Hansen Klaus
Аннотация
Qualitative EEG abnormalities are common in Autism Spectrum Disorder (ASD) and hypothesized to reflect disrupted excitation/inhibition (E/I) balance. To test this, we recently introduced a functional measure of network-level E/I ratio (fE/I). Here, we applied fE/I and other EEG measures to alpha oscillations from source-reconstructed data in the EU-AIMS dataset (267 ASD, 209 controls). We analyzed these measures alongside qualitative EEG abnormalities ranging from slowing of activity to epileptiform patterns, aiming to replicate the findings from the SPACE-BAMBI study. Contrary to our previous report, we did not observe increased fE/I variability in ASD compared to controls. EEG abnormalities were rare in adults and could not be statistically assessed. ASD children-adolescents with EEG abnormalities exhibited lower relative alpha power and fE/I compared to those without. However, EEG-abnormality scoring did not stratify the behavioral heterogeneity of ASD using clinical measures. Surprisingly, several controls also exhibited qualitative EEG abnormalities with a strikingly similar anatomical distribution of reduced fE/I, reflecting inhibition-dominated network dynamics in sensory processing regions. The robustness of this association between EEG abnormalities and reduced fE/I was further supported by re-analysis of the SPACE-BAMBI study in source space. Stratification by the presence of EEG abnormalities and their effects on network activity may help understand neurodevelopmental physiological heterogeneity and the difficulties in implementing E/I targeting treatments in unselected cohorts.