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Pushing the boundaries of MEG based on optically pumped magnetometers towards early human life

View ORCID ProfilePierre Corvilain, View ORCID ProfileVincent Wens, View ORCID ProfileMathieu Bourguignon, View ORCID ProfileChiara Capparini, Lauréline Fourdin, View ORCID ProfileMaxime Ferez, View ORCID ProfileOdile Feys, View ORCID ProfileXavier De Tiège, View ORCID ProfileJulie Bertels
doi: https://doi.org/10.1101/2023.10.28.564455
Pierre Corvilain
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
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  • For correspondence: [email protected]
Vincent Wens
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
2Université libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Department of Translational Neuroimaging, Brussels, Belgium
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Mathieu Bourguignon
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
3Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratory of Neurophysiology and Movement Biomechanics, Brussels, Belgium
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Chiara Capparini
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
4Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), ULBabyLab – Center for Research in Cognition and Neurosciences (CRCN), Brussels, Belgium
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Lauréline Fourdin
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
4Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), ULBabyLab – Center for Research in Cognition and Neurosciences (CRCN), Brussels, Belgium
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Maxime Ferez
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
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Odile Feys
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
2Université libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Department of Translational Neuroimaging, Brussels, Belgium
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Xavier De Tiège
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
2Université libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Department of Translational Neuroimaging, Brussels, Belgium
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Julie Bertels
1Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Laboratoire de Neuroimagerie et Neuroanatomie translationnelles (LN2T), Brussels, Belgium
4Université libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), ULBabyLab – Center for Research in Cognition and Neurosciences (CRCN), Brussels, Belgium
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Abstract

Characterizing the early development of the human brain is critical from both fundamental and clinical perspectives. However, existing neuroimaging techniques are either not well suited to infants or have limited spatial or temporal resolution. The advent of optically pumped magnetometers (OPMs) has revolutionized magnetoencephalography (MEG) by enabling wearable and thus more naturalistic recordings while maintaining excellent sensitivity and spatiotemporal resolution. Nevertheless, its adaptation to studying neural activity in infancy poses several challenges. In this work, we present an original close-to-scalp OPM-MEG setup that successfully recorded brain responses to sounds in newborns. We exposed one-month-old infants to continuous streams of tones and observed significant evoked responses, which peaked ∼250 ms poststimulus at bilateral auditory cortices. When tones were presented at a steady fixed pace with an oddball tone every fourth tone, significant neural responses were found both at the frequency of the standard tones (3 Hz) and of the oddball tones (0.75 Hz). The latter reflects the ability of the newborn brain to detect auditory change and synchronize to regular auditory patterns. Additional analyses support the added value of triaxial OPMs to increase the number of channels on small heads. Finally, OPM-MEG responses were validated with those obtained from the same participants using an adult-sized cryogenic MEG. This study demonstrates the applicability of OPM-MEG to study early postnatal periods; a crucial step towards future OPM investigations of typical and pathological early brain development.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • This version of the manuscript has been revised to include an investigation of the hemispheric lateralization of the auditory responses, as well as more Supplemental Material, which now include e.g. information about the lengths of the recordings and the preprocessing

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted November 21, 2024.
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Pushing the boundaries of MEG based on optically pumped magnetometers towards early human life
Pierre Corvilain, Vincent Wens, Mathieu Bourguignon, Chiara Capparini, Lauréline Fourdin, Maxime Ferez, Odile Feys, Xavier De Tiège, Julie Bertels
bioRxiv 2023.10.28.564455; doi: https://doi.org/10.1101/2023.10.28.564455
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Pushing the boundaries of MEG based on optically pumped magnetometers towards early human life
Pierre Corvilain, Vincent Wens, Mathieu Bourguignon, Chiara Capparini, Lauréline Fourdin, Maxime Ferez, Odile Feys, Xavier De Tiège, Julie Bertels
bioRxiv 2023.10.28.564455; doi: https://doi.org/10.1101/2023.10.28.564455

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