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Multicenter Study
. 2025 Sep;94(3):1339-1355.
doi: 10.1002/mrm.30551. Epub 2025 May 20.

Multi-center benchmarking of cervical spinal cord RF coils for 7 T MRI: A traveling spines study

Affiliations
Multicenter Study

Multi-center benchmarking of cervical spinal cord RF coils for 7 T MRI: A traveling spines study

Eva Alonso-Ortiz et al. Magn Reson Med. 2025 Sep.

Abstract

Purpose: The depth within the body, small diameter, long length, and varying tissue surrounding the spinal cord impose specific considerations when designing RF coils. The optimal coil configuration for 7 T cervical spinal cord MRI is unknown and currently there are very few coil options. The purpose of this work was (1) to establish a quality control protocol for evaluating 7 T cervical spinal cord coils, and (2) to use that protocol to evaluate the performance of four different coil designs.

Methods: Three healthy volunteers and a custom anthropomorphic phantom (the traveling spines cohort) were scanned at seven 7 T imaging centers using a common protocol and each center's specific cervical spinal cord coil. Four different coil designs were tested (two in-house, one Rapid Biomedical, and one MRI.TOOLS design).

Results: The Rapid Biomedical coil was found to have the highest B 1 + $$ {\mathrm{B}}_1^{+} $$ efficiency, whereas one of the in-house designs (NeuroPoly Lab) had the highest SNR and the largest spinal cord coverage. The MRI.TOOLS coil had the most uniform B 1 + $$ {\mathrm{B}}_1^{+} $$ profile along the cervical spinal cord; however, it was limited in its ability to provide the requested flip angles (especially for larger individuals). The latter was also the case for the second in-house coil (MSSM).

Conclusion: The results of this study serve as a guide for the spinal cord MRI community in selecting the most suitable coil based on specific requirements and offer a standardized protocol for assessing future coils.

Keywords: B 1 + $$ {\mathrm{B}}_1^{+} $$ ; MRI; SNR; g‐factor; hardware; spinal cord.

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Conflict of interest statement

Since January 2024, Dr. Barry has been employed by the National Institute of Biomedical Imaging and Bioengineering at the NIH. This work was coauthored by Robert Barry in his personal capacity. The opinions expressed in this study are his own and do not necessarily reflect the views of the NIH, the Department of Health and Human Services, or the U.S. government. Since September 2023, Daniel Papp has been an employee of Siemens Healthineers Sweden AB but was a postdoctoral researcher at NeuroPoly Lab during the time of the study and initial preparation of this abstract. This work was coauthored by Daniel Papp in his personal capacity, and no company resources were used. Opinions expressed in this study do not necessarily reflect the view of Siemens Healthineers Sweden or Siemens Healthcare.

Figures

FIGURE 1
FIGURE 1
(A) Coil element layout for the four tested designs. Coil 1: Rapid Biomedical, coil 2: NeuroPoly (in‐house), coil 3: MRI.TOOLS, coil 4: MSSM (in‐house). Tx‐only coils are shown in red, Rx‐only in blue, and Tx/Rx in purple. The site(s) possessing a coil design that was included in this comparative study is indicated below the coil description, as well as the corresponding 7 T system. (B) Spinoza V6 phantom. Rx, receive; Tx, transmit.
FIGURE 2
FIGURE 2
Phantom SC mask creation workflow. The leftmost image is the CRMBM phantom scan that was coregistered onto a representative human anatomical scan. The red dots represent SC labels that were joined (red ROI) to form a path that was dilated, resulting in a phantom SC mask (yellow ROI), covering roughly from brainstem to T5–T6 vertebral level. CRMBM, Centre de Résonance Magnétique Biologique et Médicale; SC, spinal cord.
FIGURE 3
FIGURE 3
Co‐registration of phantom scans across sites.
FIGURE 4
FIGURE 4
(A) Spinoza TFL B1+ maps at each participating site and measured B1+ along the SC mask (white outline) for each site. (B) In vivo TFL B1+ maps at each participating site for the same representative subject (subject 3). TFL, turboFLASH.
FIGURE 5
FIGURE 5
(A) Spinoza DREAM B1+ maps at each participating site and measured B1+ along the SC mask (white outline) for each site. (B) In vivo DREAM B1+ maps at each participating site for the same representative subject (subject 3). DREAM, dual refocusing echo acquisition mode.
FIGURE 6
FIGURE 6
(A) TFL B1+ along the SC from C1‐T2 across sites for each subject. (B) DREAM B1+ along the SC from C1‐T2 across sites for each subject. TFL, turboFLASH; C1, cervical level 1; T2, thoracic level 2.
FIGURE 7
FIGURE 7
(A) CoV across C1‐T2 in the spinal cord of TFL B1+ for each subject, across sites. (B) SNR90 averaged across vertebral levels in the spinal cord. The average B1+ CoV and SNR90 across subjects is shown as a black horizontal line. CoV, coefficient of variation.
FIGURE 8
FIGURE 8
(A) SNR maps measured with the Spinoza phantom at each participating site and measured SNR90 along the SC mask (white outline in the B1+ maps) for each site. (B) SNR for a single representative subject across all sites (subject 3).
FIGURE 9
FIGURE 9
SNR90 along the spinal cord from C1 to T2 across sites for each subject.
FIGURE 10
FIGURE 10
(A) 1/g sagittal maps with RF/H × RA/p  = 2 × 2 of Spinoza at each site, except for MSSM. (B) 1/g‐factor maps with RF/H × RA/p  = 2 × 2 for a single representative subject across all sites (subject 2).

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