Functional network dynamics revealed by EEG microstates reflect cognitive decline in amyotrophic lateral sclerosis

Author:

Metzger Marjorie1ORCID,Dukic Stefan12,McMackin Roisin13,Giglia Eileen1,Mitchell Matthew1,Bista Saroj1,Costello Emmet1,Peelo Colm1,Tadjine Yasmine1,Sirenko Vladyslav1,Plaitano Serena1,Coffey Amina1,McManus Lara1,Farnell Sharp Adelais1,Mehra Prabhav1,Heverin Mark1,Bede Peter1,Muthuraman Muthuraman4,Pender Niall15,Hardiman Orla16,Nasseroleslami Bahman17ORCID

Affiliation:

1. Academic Unit of Neurology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin University of Dublin Dublin Ireland

2. Department of Neurology, University Medical Centre Utrecht Brain Centre Utrecht University Utrecht The Netherlands

3. Discipline of Physiology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin University of Dublin Dublin Ireland

4. Neural Engineering with Signal Analytics and Artificial Intelligence, Department of Neurology University of Würzburg Würzburg Germany

5. Department of Psychology Beaumont Hospital Dublin Ireland

6. Department of Neurology Beaumont Hospital Dublin Ireland

7. FutureNeuro ‐ SFI Research Centre for Chronic and Rare Neurological Diseases Royal College of Surgeons Dublin Ireland

Abstract

AbstractRecent electroencephalography (EEG) studies have shown that patterns of brain activity can be used to differentiate amyotrophic lateral sclerosis (ALS) and control groups. These differences can be interrogated by examining EEG microstates, which are distinct, reoccurring topographies of the scalp's electrical potentials. Quantifying the temporal properties of the four canonical microstates can elucidate how the dynamics of functional brain networks are altered in neurological conditions. Here we have analysed the properties of microstates to detect and quantify signal‐based abnormality in ALS. High‐density resting‐state EEG data from 129 people with ALS and 78 HC were recorded longitudinally over a 24‐month period. EEG topographies were extracted at instances of peak global field power to identify four microstate classes (labelled A‐D) using K‐means clustering. Each EEG topography was retrospectively associated with a microstate class based on global map dissimilarity. Changes in microstate properties over the course of the disease were assessed in people with ALS and compared with changes in clinical scores. The topographies of microstate classes remained consistent across participants and conditions. Differences were observed in coverage, occurrence, duration, and transition probabilities between ALS and control groups. The duration of microstate class B and coverage of microstate class C correlated with lower limb functional decline. The transition probabilities A to D, C to B and C to B also correlated with cognitive decline (total ECAS) in those with cognitive and behavioural impairments. Microstate characteristics also significantly changed over the course of the disease. Examining the temporal dependencies in the sequences of microstates revealed that the symmetry and stationarity of transition matrices were increased in people with late‐stage ALS. These alterations in the properties of EEG microstates in ALS may reflect abnormalities within the sensory network and higher‐order networks. Microstate properties could also prospectively predict symptom progression in those with cognitive impairments.

Funder

Fondation Thierry Latran

Iris O'Brien Foundation

Irish Institute of Clinical Neuroscience

Irish Research Council

Perrigo Company Charitable Foundation

Science Foundation Ireland

Publisher

Wiley

Subject

Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology,Anatomy

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