Genuine high-order interactions in brain networks and neurodegeneration.

Biomarkers High-order interactions Machine learning Neural networks Neurodegeneration Neuroimaging

Journal

Neurobiology of disease
ISSN: 1095-953X
Titre abrégé: Neurobiol Dis
Pays: United States
ID NLM: 9500169

Informations de publication

Date de publication:
12 2022
Historique:
received: 13 08 2022
revised: 18 10 2022
accepted: 03 11 2022
pubmed: 15 11 2022
medline: 17 12 2022
entrez: 14 11 2022
Statut: ppublish

Résumé

Brain functional networks have been traditionally studied considering only interactions between pairs of regions, neglecting the richer information encoded in higher orders of interactions. In consequence, most of the connectivity studies in neurodegeneration and dementia use standard pairwise metrics. Here, we developed a genuine high-order functional connectivity (HOFC) approach that captures interactions between 3 or more regions across spatiotemporal scales, delivering a more biologically plausible characterization of the pathophysiology of neurodegeneration. We applied HOFC to multimodal (electroencephalography [EEG], and functional magnetic resonance imaging [fMRI]) data from patients diagnosed with behavioral variant of frontotemporal dementia (bvFTD), Alzheimer's disease (AD), and healthy controls. HOFC revealed large effect sizes, which, in comparison to standard pairwise metrics, provided a more accurate and parsimonious characterization of neurodegeneration. The multimodal characterization of neurodegeneration revealed hypo and hyperconnectivity on medium to large-scale brain networks, with a larger contribution of the former. Regions as the amygdala, the insula, and frontal gyrus were associated with both effects, suggesting potential compensatory processes in hub regions. fMRI revealed hypoconnectivity in AD between regions of the default mode, salience, visual, and auditory networks, while in bvFTD between regions of the default mode, salience, and somatomotor networks. EEG revealed hypoconnectivity in the γ band between frontal, limbic, and sensory regions in AD, and in the δ band between frontal, temporal, parietal and posterior areas in bvFTD, suggesting additional pathophysiological processes that fMRI alone can not capture. Classification accuracy was comparable with standard biomarkers and robust against confounders such as sample size, age, education, and motor artifacts (from fMRI and EEG). We conclude that high-order interactions provide a detailed, EEG- and fMRI compatible, biologically plausible, and psychopathological-specific characterization of different neurodegenerative conditions.

Identifiants

pubmed: 36375407
pii: S0969-9961(22)00310-2
doi: 10.1016/j.nbd.2022.105918
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105918

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interests Authors declare that they have no competing interests.

Auteurs

Rubén Herzog (R)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile; Fundación para el Estudio de la Conciencia Humana (EcoH), Chile.

Fernando E Rosas (FE)

Fundación para el Estudio de la Conciencia Humana (EcoH), Chile; Centre for Psychedelic Research, Department of Brain Sciences, Imperial College London, UK; Data Science Institute, Imperial College London, UK; Centre for Complexity Science, Imperial College London, UK; Department of Informatics, University of Sussex, Brighton, UK.

Robert Whelan (R)

Global Brain Health Institute (GBHI), Trinity College Dublin, Dublin 2, Ireland.

Sol Fittipaldi (S)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile; Global Brain Health Institute (GBHI), Trinity College Dublin, Dublin 2, Ireland; Cognitive Neuroscience Center (CNC), Universidad de San Andrés & CONICET, Buenos Aires, Argentina.

Hernando Santamaria-Garcia (H)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile.

Josephine Cruzat (J)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile; Fundación para el Estudio de la Conciencia Humana (EcoH), Chile.

Agustina Birba (A)

Cognitive Neuroscience Center (CNC), Universidad de San Andrés & CONICET, Buenos Aires, Argentina.

Sebastian Moguilner (S)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile.

Enzo Tagliazucchi (E)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile; Buenos Aires Physics Institute and Physics Department, University of Buenos Aires, Buenos Aires, Argentina.

Pavel Prado (P)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile. Electronic address: pavel.prado@uai.cl.

Agustin Ibanez (A)

Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Santiago, Chile; Global Brain Health Institute (GBHI), Trinity College Dublin, Dublin 2, Ireland; Cognitive Neuroscience Center (CNC), Universidad de San Andrés & CONICET, Buenos Aires, Argentina; Global Brain Health Institute (GBHI), University of California San Francisco (UCSF), CA, USA. Electronic address: agustin.ibanez@gbhi.org.

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Classifications MeSH