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245 changes: 245 additions & 0 deletions paper.bib
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Expand Up @@ -40,4 +40,249 @@ @article{DeLeener201724
doi = "https://doi.org/10.1016/j.neuroimage.2016.10.009",
url = "http://www.sciencedirect.com/science/article/pii/S1053811916305560",
author = "De Leener, Benjamin and Lévy, Simon and Dupont, Sara M. and Fonov, Vladimir S. and Stikov, Nikola and Collins, D. Louis and Callot, Virginie and Cohen-Adad, Julien",
}

@ARTICLE{Kearney2015-py,
title = "Spinal cord {MRI} in multiple sclerosis--diagnostic, prognostic
and clinical value",
author = "Kearney, Hugh and Miller, David H and Ciccarelli, Olga",
abstract = "Multiple sclerosis (MS) is an inflammatory disorder of the CNS
that affects both the brain and the spinal cord. MRI studies in
MS focus more often on the brain than on the spinal cord, owing
to the technical challenges in imaging this smaller, mobile
structure. However, spinal cord abnormalities at disease onset
have important implications for diagnosis and prognosis.
Furthermore, later in the disease course, in progressive MS,
myelopathy becomes the primary characteristic of the clinical
presentation, and extensive spinal cord pathology--including
atrophy, diffuse abnormalities and numerous focal lesions--is
common. Recent spinal cord imaging studies have employed
increasingly sophisticated techniques to improve detection and
quantification of spinal cord lesions, and to elucidate their
relationship with physical disability. Quantitative MRI measures
of cord size and tissue integrity could be more sensitive to the
axonal loss and other pathological processes in the spinal cord
than is conventional MRI, putting quantitative MRI in a key role
to elucidate the association between disability and spinal cord
abnormalities seen in people with MS. In this Review, we
summarize the most recent MS spinal cord imaging studies and
discuss the new insights they have provided into the mechanisms
of neurological impairment. Finally, we suggest directions for
further and future research.",
journal = "Nat. Rev. Neurol.",
volume = 11,
number = 6,
pages = "327--338",
month = jun,
year = 2015,
language = "en"
}

@ARTICLE{David2019-jy,
title = "Traumatic and nontraumatic spinal cord injury: pathological
insights from neuroimaging",
author = "David, Gergely and Mohammadi, Siawoosh and Martin, Allan R and
Cohen-Adad, Julien and Weiskopf, Nikolaus and Thompson, Alan and
Freund, Patrick",
abstract = "Pathophysiological changes in the spinal cord white and grey
matter resulting from injury can be observed with MRI techniques.
These techniques provide sensitive markers of macrostructural and
microstructural tissue integrity, which correlate with
histological findings. Spinal cord MRI findings in traumatic
spinal cord injury (tSCI) and nontraumatic spinal cord injury -
the most common form of which is degenerative cervical myelopathy
(DCM) - have provided important insights into the
pathophysiological processes taking place not just at the focal
injury site but also rostral and caudal to the spinal injury.
Although tSCI and DCM have different aetiologies, they show
similar degrees of spinal cord pathology remote from the injury
site, suggesting the involvement of similar secondary
degenerative mechanisms. Advanced quantitative MRI protocols that
are sensitive to spinal cord pathology have the potential to
improve diagnosis and, more importantly, predict outcomes in
patients with tSCI or nontraumatic spinal cord injury. This
Review describes the insights into tSCI and DCM that have been
revealed by neuroimaging and outlines current activities and
future directions for the field.",
journal = "Nat. Rev. Neurol.",
volume = 15,
number = 12,
pages = "718--731",
month = dec,
year = 2019,
language = "en"
}

@MISC{Ibrahim2001-xt,
title = "Dielectric resonances and {B1} field inhomogeneity in {UHF}
{MRI}: computational analysis and experimental findings",
author = "Ibrahim, Tamer S and Lee, Robert and Abduljalil, Amir M and
Baertlein, Brian A and Robitaille, Pierre-Marie L",
year = 2001,
note = "Accessed: 2020-8-10"
}

@ARTICLE{Collins2005-za,
title = "Central brightening due to constructive interference with,
without, and despite dielectric resonance",
author = "Collins, Christopher M and Liu, Wanzhan and Schreiber, Weston and
Yang, Qing X and Smith, Michael B",
abstract = "PURPOSE: To aid in discussion about the mechanism for central
brightening in high field magnetic resonance imaging (MRI),
especially regarding the appropriateness of using the term
dielectric resonance to describe the central brightening seen in
images of the human head. MATERIALS AND METHODS: We present both
numerical calculations and experimental images at 3 T of a
35-cm-diameter spherical phantom of varying salinity both with
one surface coil and with two surface coils on opposite sides,
and further numerical calculations at frequencies corresponding
to dielectric resonances for the sphere. RESULTS: With two
strategically placed surface coils it is possible to create
central brightening even when one coil alone excites an image
intensity pattern either bright on one side only or bright on
both sides with central darkening. This central brightening can
be created with strategic coil placement even when the resonant
pattern would favor central darkening. Results in a conductive
sample show that central brightening can similarly be achieved in
weakly conductive dielectric materials where any true resonances
would be heavily damped, such as in human tissues. CONCLUSION:
Constructive interference and wavelength effects are likely
bigger contributors to central brightening in MR images of weakly
conductive biological samples than is true dielectric resonance.",
journal = "J. Magn. Reson. Imaging",
volume = 21,
number = 2,
pages = "192--196",
month = feb,
year = 2005,
language = "en"
}

@MISC{Ibrahim2001-xt,
title = "Dielectric resonances and {B1} field inhomogeneity in {UHF}
{MRI}: computational analysis and experimental findings",
author = "Ibrahim, Tamer S and Lee, Robert and Abduljalil, Amir M and
Baertlein, Brian A and Robitaille, Pierre-Marie L",
year = 2001,
note = "Accessed: 2020-8-10"
}

@ARTICLE{Papp_undated-xl,
title = "Universal pulses for the cervical spinal cord at 7T: a feasibility
study",
author = "Papp, Daniel and Boulant, Nicolas and Massire, Aurelien and
Mauconduit, Frank and Gras, Vincent and Cohen-Adad, Julien"
}

@ARTICLE{Kearney2015-py,
title = "Spinal cord {MRI} in multiple sclerosis--diagnostic, prognostic
and clinical value",
author = "Kearney, Hugh and Miller, David H and Ciccarelli, Olga",
abstract = "Multiple sclerosis (MS) is an inflammatory disorder of the CNS
that affects both the brain and the spinal cord. MRI studies in
MS focus more often on the brain than on the spinal cord, owing
to the technical challenges in imaging this smaller, mobile
structure. However, spinal cord abnormalities at disease onset
have important implications for diagnosis and prognosis.
Furthermore, later in the disease course, in progressive MS,
myelopathy becomes the primary characteristic of the clinical
presentation, and extensive spinal cord pathology--including
atrophy, diffuse abnormalities and numerous focal lesions--is
common. Recent spinal cord imaging studies have employed
increasingly sophisticated techniques to improve detection and
quantification of spinal cord lesions, and to elucidate their
relationship with physical disability. Quantitative MRI measures
of cord size and tissue integrity could be more sensitive to the
axonal loss and other pathological processes in the spinal cord
than is conventional MRI, putting quantitative MRI in a key role
to elucidate the association between disability and spinal cord
abnormalities seen in people with MS. In this Review, we
summarize the most recent MS spinal cord imaging studies and
discuss the new insights they have provided into the mechanisms
of neurological impairment. Finally, we suggest directions for
further and future research.",
journal = "Nat. Rev. Neurol.",
volume = 11,
number = 6,
pages = "327--338",
month = jun,
year = 2015,
language = "en"
}

@ARTICLE{Roschmann1987-om,
title = "Radiofrequency penetration and absorption in the human body:
limitations to high-field whole-body nuclear magnetic resonance
imaging",
author = "R{\"o}schmann, P",
abstract = "This study presents experimental results about the effective
depth of penetration and about the radiofrequency (rf) power
absorption in humans as a function of frequency. The frequency
range investigated covers 10 up to 220 MHz. For the main part,
the results were derived from bench measurements of the quality
factor Q, and of the resonance frequency shift due to the loading
of the coil. Different types of head-, body-, and surface coils
were investigated loaded with volunteers or metallic phantoms.
For spin-echo imaging at 2 T (85 MHz), the local specific
absorption rate (SAR) was found to be approximately equal to 0.05
W/kg using a pi pulse of 1-ms duration and pulse repetition time
TR = 1 s. Measurements of the quality factor Q as a function of
frequency show that the SAR depends upon the frequency f
according to approximately f2.15. The effective depth of rf
penetration as derived drops from 17 cm at 85 MHz to 7 cm at 220
MHz. Head imaging with B1 penetrating from practically all sides
into the object should be possible up to 220 MHz (5 T) with SAR
values staying within the local limit of 2 W/kg as set by the
FDA. Whole-body imaging of large subjects as well as surface coil
imaging is depth limited above 100-MHz frequency. Perturbation
methods are applied in order to separate the total rf power
deposition in the patient into dielectric and magnetic
contributions. The observed effects due to interactions of rf
magnetic fields with biological tissue contradict predictions
based on homogeneous tissue models. A refined tissue model with
regions of high electrical conductivity, subdivided by
quasi-insulating adipose layers, provides a rationale for a
better understanding of the underlying processes. At frequencies
below 100 MHz, the rf power deposition in patients is apparently
more evenly distributed over the exposed body volume than
currently assumed.",
journal = "Med. Phys.",
volume = 14,
number = 6,
pages = "922--931",
month = nov,
year = 1987,
language = "en"
}

@ARTICLE{Yang2002-ui,
title = "Analysis of wave behavior in lossy dielectric samples at high
field",
author = "Yang, Qing X and Wang, Jinghua and Zhang, Xiaoliang and Collins,
Christopher M and Smith, Michael B and Liu, Haiying and Zhu,
Xiao-Hong and Vaughan, J Thomas and Ugurbil, Kamil and Chen, Wei",
abstract = "Radiofrequency (RF) field wave behavior and associated nonuniform
image intensity at high magnetic field strengths are examined
experimentally and numerically. The RF field produced by a
10-cm-diameter surface coil at 300 MHz is evaluated in a
16-cm-diameter spherical phantom with variable salinity, and in
the human head. Temporal progression of the RF field indicates
that the standing wave and associated dielectric resonance
occurring in a pure water phantom near 300 MHz is greatly
dampened in the human head due to the strong decay of the
electromagnetic wave. The characteristic image intensity
distribution in the human head is the result of spatial phase
distribution and amplitude modulation by the interference of the
RF traveling waves determined by a given sample-coil
configuration. The numerical calculation method is validated with
experimental results. The general behavior of the RF field with
respect to the average brain electrical properties in a frequency
range of 42-350 MHz is also analyzed.",
journal = "Magn. Reson. Med.",
volume = 47,
number = 5,
pages = "982--989",
month = may,
year = 2002,
language = "en"
}
78 changes: 60 additions & 18 deletions paper.md
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@@ -1,48 +1,90 @@
---
title: 'RF Shimming 7T'
title: Analysis code for the paper "RF shimming in the cervical spinal cord at 7T"

tags:
- shimming
- RF shimming
- spinal cord
- MRI
- high field
- 7T
authors:
- name: Daniel Papp
orcid:
affiliation: 1
- name: Kyle M. Gilbert
orcid:
affiliation: "2, 3"
- name: Gaspard Cereza
orcid:
affiliation: 1
- name: Alexandre D’Astous
orcid:
affiliation: 1
- name: Mathieu Boudreau
orcid:
affiliation: 1
- name: Marcus Couch
orcid:
affiliation: 4
- name: Pedram Yazdanbakhsh
orcid:
affiliation: 5
- name: Robert L. Barry
orcid:
affiliation: 6
- name: Eva Alonso Ortiz
orcid:
affiliation: 1
- name: Julien Cohen-Adad
orcid: 0000-0003-3662-9532
affiliation: "1, 2, 3, 4"
affiliation: "1, 7, 8"
affiliations:
- name: NeuroPoly Lab, Polytechnique Montréal, Montreal, Quebec, Canada
- name: NeuroPoly Lab, Institute of Biomedical Engineering, Polytechnique Montreal, Montreal, QC, Canada
index: 1
- name: Unité de Neuroimagerie Fonctionnelle (UNF), Centre de recherche de l’Institut Universitaire de Gériatrie de Montréal (CRIUGM), Montreal, Quebec, Canada
- name: Centre for Functional and Metabolic Mapping, The University of Western Ontario, London, ON, Canada
index: 2
- name: Mila - Quebec AI Institute, Montreal, QC, Canad
- name: Department of Medical Biophysics, The University of Western Ontario, London, ON, Canada
index: 3
- name: Centre de recherche du CHU Sainte-Justine, Université de Montréal, Montreal, QC, Canada
- name: Siemens Healthcare Limited, Montreal, QC, Canada
index: 4

date: 17 January 2024
- name: McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC, Canada
index: 5
- name: Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA
index: 6
- name: Mila - Quebec AI Institute, Montreal, QC, Canada
index: 7
- name: Functional Neuroimaging Unit, Centre de recherche de l'Institut universitaire de gériatrie de Montréal QC, Canada
index: 8

date: 2 February 2024
bibliography: paper.bib

---

# Summary

Text
Data was collected from five participants between two 7T sites with a custom 8Tx/20Rx parallel transmission (pTx) coil. We explored two RF shimming approaches from an MRI vendor and four from an open-source toolbox, showcasing their ability to enhance transmit field and signal homogeneity along the cervical spinal cord.

The results indicate significant improvements in B1+ efficiency and cerebrospinal fluid / spinal cord signal ratio across various RF shimming conditions compared to the vendor based methods.

The study's findings highlight the potential of RF shimming to advance 7T MRI's clinical utility for central nervous system imaging by enabling more homogenous and efficient spinal cord imaging. Additionally, the research incorporates a reproducible Jupyter Notebook, enhancing the study's transparency and facilitating peer verification. By also making the data openly accessible on OpenNeuro, we ensure that the scientific community can further explore, validate, and build upon our findings, contributing to the collective advancement in high-resolution imaging techniques.


# Statement of need

Text
Advancing the development of 7T MRI for spinal cord imaging is crucial for the enhanced diagnosis and monitoring of various neurodegenerative diseases [@Kearney2015-py] and traumas [@David2019-jy]. However, a significant challenge at this field strength is the transmit field inhomogeneity . Such inhomogeneity is particularly problematic for imaging the small, deep anatomical structures of[@Ibrahim2001-xt;@Collins2005-za;@Roschmann1987-om;@Yang2002-ui] the cervical spinal cord, as it can cause uneven signal intensity and elevate the local specific absorption ratio, compromising image quality. This multi-site study explores several radiofrequency (RF) shimming techniques in the cervical spinal cord at 7T.


# Figures

Figure

# Acknowledgements
![Overview of the RF shimming procedure.
\label{fig:overview}](featured.png)

Text

# Acknowledgements

1     |     INTRODUCTION
========================
Funded by the Canada Research Chair in Quantitative Magnetic Resonance Imaging [950-230815], the Canadian Institute of Health Research [CIHR FDN-143263], the Canada Foundation for Innovation [32454, 34824], the Fonds de Recherche du Québec - Santé [28826], the Natural Sciences and Engineering Research Council of Canada [RGPIN-2019-07244], the Canada First Research Excellence Fund (IVADO and TransMedTech), the Courtois NeuroMod project and the Quebec BioImaging Network [5886, 35450], and MITACS Accelerate Fellowship.

Test citation [@DAstous2023]

## References

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