Optically pumped magnetometers detect altered maximal muscle activity in neuromuscular disease.
ATTR amyloidosis
Charcot-Marie-Tooth
electromyogram (EMG)
magnetomyography (MMG)
muscle activity
myotonia congenita
neuromuscular disease (NMD)
optically pumped magnetometers (OPM)
Journal
Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481
Informations de publication
Date de publication:
2022
2022
Historique:
received:
02
08
2022
accepted:
21
10
2022
entrez:
16
12
2022
pubmed:
17
12
2022
medline:
17
12
2022
Statut:
epublish
Résumé
Optically pumped magnetometers (OPM) are quantum sensors that enable the contactless, non-invasive measurement of biomagnetic muscle signals, i.e., magnetomyography (MMG). Due to the contactless recording, OPM-MMG might be preferable to standard electromyography (EMG) for patients with neuromuscular diseases, particularly when repetitive recordings for diagnostic and therapeutic monitoring are mandatory. OPM-MMG studies have focused on recording physiological muscle activity in healthy individuals, whereas research on neuromuscular patients with pathological altered muscle activity is non-existent. Here, we report a proof-of-principle study on the application of OPM-MMG in patients with neuromuscular diseases. Specifically, we compare the muscular activity during maximal isometric contraction of the left rectus femoris muscle in three neuromuscular patients with severe (Transthyretin Amyloidosis in combination with Pompe's disease), mild (Charcot-Marie-Tooth disease, type 2), and without neurogenic, but myogenic, damage (Myotonia Congenita). Seven healthy young participants served as the control group. As expected, and confirmed by using simultaneous surface electromyography (sEMG), a time-series analysis revealed a dispersed interference pattern during maximal contraction with high amplitudes. Furthermore, both patients with neurogenic damage (ATTR and CMT2) showed a reduced variability of the MMG signal, quantified as the signal standard deviation of the main component of the frequency spectrum, highlighting the reduced possibility of motor unit recruitment due to the loss of motor neurons. Our results show that recording pathologically altered voluntary muscle activity with OPM-MMG is possible, paving the way for the potential use of OPM-MMG in larger studies to explore the potential benefits in clinical neurophysiology.
Identifiants
pubmed: 36523432
doi: 10.3389/fnins.2022.1010242
pmc: PMC9745080
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1010242Informations de copyright
Copyright © 2022 Semeia, Middelmann, Baek, Sometti, Chen, Grimm, Lerche, Martin, Kronlage, Braun, Broser, Siegel, Breu and Marquetand.
Déclaration de conflit d'intérêts
JM received lecture fees and travel support from UCB, Eisai, Desitin, Alexion, and the German Society for Ultrasound (DEGUM), all unrelated to the current study. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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