Automated slice-specific z-shimming for functional magnetic resonance imaging of the human spinal cord.


Journal

Human brain mapping
ISSN: 1097-0193
Titre abrégé: Hum Brain Mapp
Pays: United States
ID NLM: 9419065

Informations de publication

Date de publication:
15 12 2022
Historique:
revised: 21 06 2022
received: 25 04 2022
accepted: 24 06 2022
pubmed: 9 8 2022
medline: 1 12 2022
entrez: 8 8 2022
Statut: ppublish

Résumé

Functional magnetic resonance imaging (fMRI) of the human spinal cord faces many challenges, such as signal loss due to local magnetic field inhomogeneities. This issue can be addressed with slice-specific z-shimming, which compensates for the dephasing effect of the inhomogeneities using a slice-specific gradient pulse. Here, we aim to address outstanding issues regarding this technique by evaluating its effects on several aspects that are directly relevant for spinal fMRI and by developing two automated procedures in order to improve upon the time-consuming and subjective nature of manual selection of z-shims: one procedure finds the z-shim that maximizes signal intensity in each slice of an EPI reference-scan and the other finds the through-slice field inhomogeneity for each EPI-slice in field map data and calculates the required compensation gradient moment. We demonstrate that the beneficial effects of z-shimming are apparent across different echo times, hold true for both the dorsal and ventral horn, and are also apparent in the temporal signal-to-noise ratio (tSNR) of EPI time-series data. Both of our automated approaches were faster than the manual approach, lead to significant improvements in gray matter tSNR compared to no z-shimming and resulted in beneficial effects that were stable across time. While the field-map-based approach performed slightly worse than the manual approach, the EPI-based approach performed as well as the manual one and was furthermore validated on an external corticospinal data-set (N > 100). Together, automated z-shimming may improve the data quality of future spinal fMRI studies and lead to increased reproducibility in longitudinal studies.

Identifiants

pubmed: 35938527
doi: 10.1002/hbm.26018
pmc: PMC9704784
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5389-5407

Subventions

Organisme : Medical Research Council
ID : MR/N026969/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 203963/Z/16/Z
Pays : United Kingdom

Informations de copyright

© 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.

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Auteurs

Merve Kaptan (M)

Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

S Johanna Vannesjo (SJ)

Department of Physics, Norwegian University of Science and Technology, Trondheim, Norway.

Toralf Mildner (T)

Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Ulrike Horn (U)

Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Ronald Hartley-Davies (R)

Department of Medical Physics, University Hospitals Bristol and Weston, Bristol, UK.

Valeria Oliva (V)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.

Jonathan C W Brooks (JCW)

School of Psychology, University of East Anglia Wellcome Wolfson Brain Imaging Centre (UWWBIC), Norwich, UK.

Nikolaus Weiskopf (N)

Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Felix Bloch Institute for Solid State Physics, Faculty of Physics and Earth Sciences, Leipzig University, Leipzig, Germany.

Jürgen Finsterbusch (J)

Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Falk Eippert (F)

Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

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