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Resting state EEG power spectrum and functional connectivity in autism: a cross-sectional analysis

Authors :
Pilar Garcés
Sarah Baumeister
Luke Mason
Christopher H. Chatham
Stefan Holiga
Juergen Dukart
Emily J. H. Jones
Tobias Banaschewski
Simon Baron-Cohen
Sven Bölte
Jan K. Buitelaar
Sarah Durston
Bob Oranje
Antonio M. Persico
Christian F. Beckmann
Thomas Bougeron
Flavio Dell’Acqua
Christine Ecker
Carolin Moessnang
Tony Charman
Julian Tillmann
Declan G. M. Murphy
Mark Johnson
Eva Loth
Daniel Brandeis
Joerg F. Hipp
The EU-AIMS LEAP group authorship
Source :
Molecular Autism, Vol 13, Iss 1, Pp 1-16 (2022)
Publication Year :
2022
Publisher :
BMC, 2022.

Abstract

Abstract Background Understanding the development of the neuronal circuitry underlying autism spectrum disorder (ASD) is critical to shed light into its etiology and for the development of treatment options. Resting state EEG provides a window into spontaneous local and long-range neuronal synchronization and has been investigated in many ASD studies, but results are inconsistent. Unbiased investigation in large and comprehensive samples focusing on replicability is needed. Methods We quantified resting state EEG alpha peak metrics, power spectrum (PS, 2–32 Hz) and functional connectivity (FC) in 411 children, adolescents and adults (n = 212 ASD, n = 199 neurotypicals [NT], all with IQ > 75). We performed analyses in source-space using individual head models derived from the participants’ MRIs. We tested for differences in mean and variance between the ASD and NT groups for both PS and FC using linear mixed effects models accounting for age, sex, IQ and site effects. Then, we used machine learning to assess whether a multivariate combination of EEG features could better separate ASD and NT participants. All analyses were embedded within a train-validation approach (70%–30% split). Results In the training dataset, we found an interaction between age and group for the reactivity to eye opening (p = .042 uncorrected), and a significant but weak multivariate ASD vs. NT classification performance for PS and FC (sensitivity 0.52–0.62, specificity 0.59–0.73). None of these findings replicated significantly in the validation dataset, although the effect size in the validation dataset overlapped with the prediction interval from the training dataset. Limitations The statistical power to detect weak effects—of the magnitude of those found in the training dataset—in the validation dataset is small, and we cannot fully conclude on the reproducibility of the training dataset’s effects. Conclusions This suggests that PS and FC values in ASD and NT have a strong overlap, and that differences between both groups (in both mean and variance) have, at best, a small effect size. Larger studies would be needed to investigate and replicate such potential effects.

Details

Language :
English
ISSN :
20402392
Volume :
13
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Molecular Autism
Publication Type :
Academic Journal
Accession number :
edsdoj.b81ea07e96244b0897ba1df29043f8e
Document Type :
article
Full Text :
https://doi.org/10.1186/s13229-022-00500-x