TY - JOUR
T1 - Scalp attached tangential magnetoencephalography using tunnel magneto-resistive sensors
AU - Kanno, Akitake
AU - Nakasato, Nobukazu
AU - Oogane, Mikihiko
AU - Fujiwara, Kosuke
AU - Nakano, Takafumi
AU - Arimoto, Tadashi
AU - Matsuzaki, Hitoshi
AU - Ando, Yasuo
N1 - Funding Information:
This work was supported in part by the S-Innovation program, Japan Science and Technology Agency (No. 201106007) awarded to Y.A. and T.A.; the Grants-in-Aid for Scientific Research (No. 16H05435) from the Japan Society for the Promotion of Science awarded to N.N., A.K., and Y.A.; Spin Sensing Factory; and KONICA MINOLTA, INC. We would like to remember †Mr. Takuo Nishikawa, who died July 3, 2014, as he first had the vision of room temperature TMR-MEG and initiated all the coauthors into this project.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Non-invasive human brain functional imaging with millisecond resolution can be achieved only with magnetoencephalography (MEG) and electroencephalography (EEG). MEG has better spatial resolution than EEG because signal distortion due to inhomogeneous head conductivity is negligible in MEG but serious in EEG. However, this advantage has been practically limited by the necessary setback distances between the sensors and scalp, because the Dewar vessel containing liquid helium for superconducting quantum interference devices (SQUIDs) requires a thick vacuum wall. Latest developments of high critical temperature (high-Tc) SQUIDs or optically pumped magnetometers have allowed closer placement of MEG sensors to the scalp. Here we introduce the use of tunnel magneto-resistive (TMR) sensors for scalp-attached MEG. Improvement of TMR sensitivity with magnetic flux concentrators enabled scalp-tangential MEG at 2.6 mm above the scalp, to target the largest signal component produced by the neural current below. In a healthy subject, our single-channel TMR-MEG system clearly demonstrated the N20m, the initial cortical component of the somatosensory evoked response after median nerve stimulation. Multisite measurement confirmed a spatially and temporally steep peak of N20m, immediately above the source at a latency around 20 ms, indicating a new approach to non-invasive functional brain imaging with millimeter and millisecond resolutions.
AB - Non-invasive human brain functional imaging with millisecond resolution can be achieved only with magnetoencephalography (MEG) and electroencephalography (EEG). MEG has better spatial resolution than EEG because signal distortion due to inhomogeneous head conductivity is negligible in MEG but serious in EEG. However, this advantage has been practically limited by the necessary setback distances between the sensors and scalp, because the Dewar vessel containing liquid helium for superconducting quantum interference devices (SQUIDs) requires a thick vacuum wall. Latest developments of high critical temperature (high-Tc) SQUIDs or optically pumped magnetometers have allowed closer placement of MEG sensors to the scalp. Here we introduce the use of tunnel magneto-resistive (TMR) sensors for scalp-attached MEG. Improvement of TMR sensitivity with magnetic flux concentrators enabled scalp-tangential MEG at 2.6 mm above the scalp, to target the largest signal component produced by the neural current below. In a healthy subject, our single-channel TMR-MEG system clearly demonstrated the N20m, the initial cortical component of the somatosensory evoked response after median nerve stimulation. Multisite measurement confirmed a spatially and temporally steep peak of N20m, immediately above the source at a latency around 20 ms, indicating a new approach to non-invasive functional brain imaging with millimeter and millisecond resolutions.
UR - http://www.scopus.com/inward/record.url?scp=85128146856&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85128146856&partnerID=8YFLogxK
U2 - 10.1038/s41598-022-10155-6
DO - 10.1038/s41598-022-10155-6
M3 - Article
C2 - 35414691
AN - SCOPUS:85128146856
SN - 2045-2322
VL - 12
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 6106
ER -