Multilevel hybrid principal components analysis for region-referenced functional electroencephalography data.

Journal Article (Journal Article)

Electroencephalography experiments produce region-referenced functional data representing brain signals in the time or the frequency domain collected across the scalp. The data typically also have a multilevel structure with high-dimensional observations collected across multiple experimental conditions or visits. Common analysis approaches reduce the data complexity by collapsing the functional and regional dimensions, where event-related potential (ERP) features or band power are targeted in a pre-specified scalp region. This practice can fail to portray more comprehensive differences in the entire ERP signal or the power spectral density (PSD) across the scalp. Building on the weak separability of the high-dimensional covariance process, the proposed multilevel hybrid principal components analysis (M-HPCA) utilizes dimension reduction tools from both vector and functional principal components analysis to decompose the total variation into between- and within-subject variance. The resulting model components are estimated in a mixed effects modeling framework via a computationally efficient minorization-maximization algorithm coupled with bootstrap. The diverse array of applications of M-HPCA is showcased with two studies of individuals with autism. While ERP responses to match vs mismatch conditions are compared in an audio odd-ball paradigm in the first study, short-term reliability of the PSD across visits is compared in the second. Finite sample properties of the proposed methodology are studied in extensive simulations.

Full Text

Duke Authors

Cited Authors

  • Campos, E; Wolfe Scheffler, A; Telesca, D; Sugar, C; DiStefano, C; Jeste, S; Levin, AR; Naples, A; Webb, SJ; Shic, F; Dawson, G; Faja, S; McPartland, JC; ┼×entürk, D; Autism Biomarkers Consortium for Clinical Trials,

Published Date

  • August 30, 2022

Published In

Volume / Issue

  • 41 / 19

Start / End Page

  • 3737 - 3757

PubMed ID

  • 35611602

Pubmed Central ID

  • PMC9308678

Electronic International Standard Serial Number (EISSN)

  • 1097-0258

Digital Object Identifier (DOI)

  • 10.1002/sim.9445


  • eng

Conference Location

  • England