ISSN# 1545-4428 | Published date: 19 April, 2024
You must be logged in to view entire program, abstracts, and syllabi
At-A-Glance Session Detail
   
White Matter & Spinal Cord
Digital Poster
Neuro
Tuesday, 07 May 2024
Exhibition Hall (Hall 403)
09:15 -  10:15
Session Number: D-131
No CME/CE Credit

Computer #
2513.
33Exploring the Efficacy of Different Combinations of B-Values and B-Tensor Shapes in Assessing Spinal Cord in MS and NMOSD Using Micro-FA
Masaaki Hori1,2, Akifumi Hagiwara2, Kouhei Kamiya1,2, Kazumasa Yokoyama3, Issei Fukunaga4, Katsuhiro Sano2, Koji Kamagata2, Katsutoshi Murata5, Shohei Fujita2, Christina Andica6, Akihiko Wada2, Julien Cohen-Adad7, and Shigeki Aoki2,6
1Toho University, Tokyo, Japan, 2Radiology, Faculty of Medicine, Juntendo University, Tokyo, Japan, 3Neurology, Faculty of Medicine, Juntendo University, Tokyo, Japan, 4Radiological Technology, Faculty of Health Science, Juntendo University, Tokyo, Japan, 5Siemens Japan K.K., Tokyo, Japan, 6Faculty of Health Data Science, Juntendo University, Chiba, Japan, 7NeuroPoly Lab, Polytechnique Montreal, Montréal, QC, Canada

Keywords: Spinal Cord, Spinal Cord

Motivation: The necessity to accurately delineate microstructural changes in the spinal cords of MS and NMOSD patients in vivo.

Goal(s): Assess if multiple b-tensor diffusion MRI data enhances the clinical utility of Micro Fractional Anisotropy (μFA) in distinguishing pathological variances in MS and NMOSD.

Approach: Comparative analysis of μFA values derived from planar tensor encoding data (DDE) and a combination of DDE with linear tensor encoding data was conducted.

Results: No significant μFA difference between MS and NMOSD was found, and additional linear tensor encoding data did not improve the results, highlighting the need for optimized imaging protocols.

Impact: This study elucidates the criticality of optimizing imaging protocols over merely aggregating data for precise diagnostic outcomes in MS and NMOSD. It prompts further investigation into refining imaging methodologies to uncover microstructural changes, enhancing diagnostic accuracy and subsequent patient management.

2514.
34Hyperplane-based tract parcellations for improved anatomical coherence in tractometry
Peter Neher1,2,3, Robin Peretzke1,4, and Klaus Maier-Hein1,2,3,5
1Medical Image Computing, German Cancer Research Center (DKFZ), Heidelberg, Germany, 2Pattern Analysis and Learning Group, Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany, 3German Cancer Consortium (DKTK), DKFZ, core center Heidelberg, Heidelberg, Germany, 4Medical Faculty Heidelberg, Heidelberg University, Heidelberg, Germany, 5National Center for Tumor Diseases (NCT), NCT Heidelberg, a partnership between DKFZ and the university medical center Heidelberg, Heidelberg, Germany

Keywords: White Matter, Tractography & Fibre Modelling, Tractometry, Parcellation

Motivation: The subdivision of WM tracts into individual parcels required for tractometry analysis, suffers from blurred parcel borders and wrong assignments of complete tract regions, particularly in fanning tracts.

Goal(s): The goal of this work is to overcome these limitations with a new parcellation approach that yields clearly delineated tract parcels and avoids wrong parcel assignments even in challenging tracts. 

Approach: We propose a self-supervised approach based on optimally separating hyperplanes, obtained using large-margin classifiers, to separate tracts into parcels.

Results: We compare our approach to two popular state-of-the-art approaches and clearly show markedly improved results in 24 tracts and 98 subjects.

Impact: A new method to parcellate tracts for fiber tractometry, avoiding frequent errors of state-of-the-art approaches, particularly in complex tracts with a fanning topology. This might lead to improved tractometry analysis and potentially insights that were not possible with previous approaches.

2515.
35Fast Single-Point Macromolecular Proton Fraction Mapping using a 0.3 T MRI System
Yasuhiro Fujiwara1, Shoma Eitoku2, Nobutaka Sakae3, Takahisa Izumi4, Yuuki Motoyama5, Hiroyuki Kumazoe5, and Mika Kitajima1
1Department of Medical Image Sciences, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan, 2Department of Radiology, Hospital of the University of Occupational and Environmental Health, Fukuoka, Japan, 3Department of Neurology, National Hospital Organization Omuta National Hospital, Fukuoka, Japan, 4Department of Radiology, National Hospital Organization Kumamoto Saishun Medical Center, Kumamoto, Japan, 5Department of Radiology, National Hospital Organization Omuta National Hospital, Fukuoka, Japan

Keywords: Other Neurodegeneration, CEST & MT

Motivation: Quantifying myelin content in 0.3 T low-field MRI presents a challenge owing to prolonged imaging times and a low signal-to-noise ratio.

Goal(s): The study aimed to validate the practical feasibility of macromolecular proton fraction (MPF) mapping in the brain using a 0.3 T MRI system.

Approach: A phantom study with protein samples and an in vivo investigation were conducted.

Results: The study findings indicate a robust correlation between 0.3 T MPF in brain tissue, MPF at 3.0 T, and previously reported MPF at 0.5 T.

Impact: The fast single-point MPF mapping using a 0.3 T MRI exhibited the capacity to accurately measure brain MPF in a clinically feasible timeframe, providing a valuable tool for assessing myelin content. 

2516.
36Cross Site Reproducibility for standard and ultra-high b-value diffusion imaging in high-performance gradient (MAGNUS 3T) MRI systems.
Nastaren Abad1, Chitresh Bhushan1, Luca Marinelli1, Eric Fiveland1, Eric Budesheim1, Keith Park1, Justin Ricci1, Vincent M Magnotta2, Merry Mani2, James H. Holmes2, Matthew Sodoma2, Alan McCarville2, Andrew Alexander3, Steven R Kecskemeti3, Michael J Anderle3, Jose Guerrero Gonzalez3, Lisette LeMerise3, Jeffrey McGovern4, and Thomas K.F. Foo1
1Technology & Innovation Center, GE HealthCare, Niskayuna, NY, United States, 2University of Iowa, Iowa City, IA, United States, 3University of Wisconsin - Madison, Madison, WI, United States, 4GE HealthCare, Waukesha, WI, United States

Keywords: White Matter, Diffusion/other diffusion imaging techniques, High performance gradient inserts, cross-site, repeatability, reproducibility

Motivation: Cross-site reproducibility of ultra-high b-value diffusion MRI across multiple MAGNUS MRI systems is important for multi-site studies

Goal(s): To disentangle the contributions of physiological fluctuations vs. manufacturing tolerances to inform future cross-site studies for advanced and novel brain microstructural modelling and quantification

Approach: A traveling volunteer was recruited and imaged at three different MAGNUS (2nd generation) systems. An expanded multi-shell parameter space ranging from b=500-30,000 s/mm2 was analysed quantitatively to assess cross-site reproducibility. 

Results: Statistical comparisons across sites for global white matter and white matter parcels highlight good agreement without harmonization efforts.

Impact: This dataset is expected to lay the ground work for multicenter collaboration for novel and advanced brain microstructural modelling and quantification. It can further be used to evaluate differences across scanners and to show the consistency of pipeline outputs.

2517.
37Investigating brain correlates of neural plasticity with visual-motor sequence learning: Preliminary observations using 3.0T MAGNUS
Nastaren Abad1, Mika Kaeja2, Jing Zhang3, Christopher Steele2, and Thomas K.F. Foo1
1Technology & Innovation Center, GE HealthCare, Niskayuna, NY, United States, 2Concordia University, Montreal, QC, Canada, 3GE HealthCare, Mississauga, ON, Canada

Keywords: White Matter, Brain Connectivity, High performance gradient MRI, WM plasticity, Learning, Dynamic white matter plasticity

Motivation: To investigated whether white matter microstructural changes after adaptive short-term training can be detected in a limited sample size with a high-performance gradient system that allows for increased sensitivity to underlying brain micro-architecture.

Goal(s): Demonstrate that with task complexity and short-term training, the dynamic-location-specific neuroplastic changes can be detected.

Approach: Advanced structural and functional MRI sequences in <60-min examination with a pre- and post-design paradigm were used in a high-performance head gradient system that allows for increased sensitivity to the underlying brain micro-architecture.

Results: In this pilot study microstructural changes were noted on a group basis underlying primary motor and sensorimotor cortices. 

Impact: This study highlights the role of dynamic brain processes following short term visual motor sequencing learning (VMSL). The adult brain preserves dynamic characteristics that are altered by short-term learning experiences that can be detected with dMRI.

2518.
38Piloting individualised probabilistic tractography to measure motor system integrity and rehabilitation potential in cerebral palsy
Bronwyn Gavine1, Foteini Mavrommati2, Matthew Weightmann1, Rachel Buckingham3, Cherry Kilbride4, Martin Smith3, Tim Theologis3,5, Dido Green4,6, Ned Jenkinson7, Jennifer Ryan8, Liana Nagy4, Heidi Johansen-Berg1, Helen Dawes2,9, and Melanie K Fleming1
1Wellcome Centre for Integrative Neuroimaging, Nuffield Department of Clinical Neurosciences, University Of Oxford, Oxford, United Kingdom, 2Movement Science Group, Oxford Brookes University, Oxford, United Kingdom, 3Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom, 4Department of Health Sciences, Brunel University London, London, United Kingdom, 5Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, University Of Oxford, Oxford, United Kingdom, 6Department of Rehabilitation, Jönköping University, Jönköping, Sweden, 7School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, United Kingdom, 8Department of Epidemiology and Public Health Medicine, Royal College of Surgeons in Ireland, Dublin, Ireland, 9National Institute for Health Research Exeter Biomedical Research Centre, University of Exeter, Exeter, United Kingdom

Keywords: Neuro, Diffusion Tensor Imaging, Cerebral palsy

Motivation: A biomarker of motor system function is needed to assist with treatment selection for children with cerebral palsy (CP).

Goal(s): We aimed to pilot an automated tractography tool in a clinical trial cohort of adolescents with CP, and determine if corticospinal tract (CST) integrity could be used as a biomarker for baseline function and treatment response.

Approach: A customised probabilistic tractography pipeline was used to quantify CST integrity. Hand function was assessed at baseline and after a motor training intervention.

Results: We demonstrated feasibility, and found that CST integrity was positively correlated with baseline hand function, and negatively correlated with improvement after training. 

Impact: Automated individualised native-space tractography is feasible in a clinical population of adolescents with cerebral palsy. Tractography-derived corticospinal tract integrity predicts baseline hand function impairment and may be useful as a predictive biomarker for rehabilitation response.

2519.
39Myelin Water Imaging on MAGNUS (high-performance Mesoscale Anatomy Gradient for Neuroimaging with Ultrafast Scanning) system
Jing Zhang1, Nastaren Abad2, Suchandrima Banerjee3, Alexander MacKay4, and Thomas K.F. Foo2
1GE Healthcare, Mississauga, ON, Canada, 2Technology & Innovation Center, GE HealthCare, Niskayuna, NY, United States, 3Global MR Applications & Workflow, GE HealthCare, Menlo Park, CA, United States, 4Department of Radiology, University of British Columbia, Vancouver, BC, Canada

Keywords: White Matter, Brain, myelin water imaging, Gradient Echo Spin Echo (GRASE))

Motivation: Myelin water fraction (MWF) is conventionally measured using the T2 decay curve. Due to hardware limitations, for spin-echo based sequences, TR and TE times were restricted by SAR and gradient slew rate.

Goal(s): Our objective is to reduce the total scan time by shortening the TR time. A shorter TE time should also capture more signal from the short T2 components of myelin water.

Approach: We implemented myelin water imaging (MWI) on the MAGNUS system with reduced TR and TE times.

Results: When implemented on the MAGNUS system, MWI could be carried out in a shorter time and the MWF were slightly larger.

Impact: The work aims to optimize MWI by shortening scan times. It successfully achieves this, leading to quicker, high-quality MWI acquisition, benefiting medical diagnostics and research efficiency.

2520.
40A Matched Case Control Study of Early Cervical Spondylotic Myelopathy Based on Diffusion Magnetic Resonance Imaging
Ming Ni1, Shujing Li1, Xianchang Zhang2, Ning Lang1, Liang Jiang3, and Huishu Yuan1
1Department of Radiology, Peking University Third Hospital, BeiJing, China, 2MR Collaboration, Siemens Healthineers Ltd., BeiJing, China, 3Department of Orthopedics, Peking University Third Hospital, BeiJing, China

Keywords: Spinal Cord, Spinal Cord, Cervical Spondylotic Myelopathy; Diffusion Magnetic Resonance Imaging

Motivation: Early cervical spondylotic myelopathy (CSM) is challenging to diagnose and easily missed. 

Goal(s): To explore the value of diffusion MRI (dMRI) in diagnosing early-stage CSM and evaluating uncompressed segments in patients with early CSM.

Approach:  Using diffusion tensor imaging (DTI), diffusion kurtosis imaging (DKI), and neurite orientation dispersion and density imaging (NODDI), a 1:1 matched case control study was conducted.

Results: The orientation division index (ODI) was positively correlated with early CSM, and the anisotropic water fraction (AWF) was negatively correlated. The ODI and AWF can assist in identifying the scope of early CSM involvement.

Impact: The orientation division index (ODI) was positively correlated with early CSM, and the anisotropic water fraction (AWF) was negatively correlated. The ODI and AWF can assist in identifying the scope of early CSM involvement.

2521.
41Monitoring of therapeutic response using lesion segmentation and DTI in adult cerebral adrenoleukodystrophy treated with Leriglitazone
Marianne Golse1, Isabelle Weinhofer2, Bernardo Blanco 3, Magali Barbier3, Camille Huiban3, Silvia Pascual4, Marc Martinell4, Johannes Berger2, Vincent Perlbarg5, Damien Galanaud6, and Fanny Mochel7
1Sorbonne Université, INSERM, CNRS, Laboratoire d'Imagerie Biomédicale, Paris, France, 23Department of Pathobiology of the Nervous System, Center for Brain Research, Medical University of Vienna, Vienna, Austria, 3Department of Medical Genetics, Reference Centers for Adult Neurometabolic diseases and Adult Leukodystrophies, AP-HP, Pitié-Salpêtrière University Hospita, Paris, France, 4Minoryx Therapeutics, Barcelona, Spain, 5Braintale (Software As a Service), Paris, France, 6Department of Neuroradiology, AP-HP, Pitié-Salpêtrière University Hospital, Paris, France, 7Department of Medical Genetics, Reference Centers for Adult Neurometabolic diseases and Adult Leukodystrophies, AP-HP, Pitié-Salpêtrière University Hospital, Paris, France

Keywords: White Matter, Brain, Adrenoleukodystrophy, Leriglitazone, Volumetric analysis, Diffusion Tensor Imaging

Motivation: Cerebral adrenoleukodystrophy (CALD) is a rare and devastating demyelinating disease. The standard of care is hematopoeitic stem cell transplantation (HCST), which efficacy is limited to early-stage patients.

Goal(s): We studied the efficacy of Leriglitazone in CALD patients, either not eligible or awaiting HSCT.

Approach: Leriglitazone was administered to thirteen adult male patients. They underwent brain MRI every 3 months, with a quantitative analysis of lesion volumes on FLAIR, diffusion tensor parameters and gadolinium enhancements.  

Results: The disease stabilized in all patients awaiting HSCT. Corticospinal tract lesions downsized in most patients and turned gadolinium-negative, showing a selective effect of this molecule on motor pathways. 

Impact: Cerebral adrenoleukodystrophy is a devastating demyelinating disease, fatal for all patients without early stem cell transplantation. We showed that Leriglitazone represents a therapeutic alternative, allowing clinical and radiological stabilization in ten men. Remarkably, motor pathways lesions downsized and turned gadolinium-negative.  

2522.
42Quantitative and Comparative Evaluation of 2D Reduced-FOV Multi-shot Diffusion Tensor Imaging in Spinal Cord
Chenglang Yuan1, Shihui Chen1, Liyuan Liang1,2, Xiaorui Xu3, Hailin Xiong1, Tianbaige Liu1, Yi Li1, and Hing-Chiu Chang1,2
1Department of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong, China, 2Multi-Scale Medical Robotics Center, Hong Kong, China, 3Department of Diagnostic Radiology, The University of Hong Kong, Hong Kong, China

Keywords: Spinal Cord, Spinal Cord, reduced-FOV, multi-shot DTI

Motivation: To our best knowledge, there has yet to be a comprehensive evaluation of the combination of cardiac triggering, reduced-FOV, or multi-shot techniques together for improving spinal cord DTI. 

Goal(s): This study aims to compare the performances of spinal cord DTI with different parametric combinations.

Approach: Extensive and comparative experiments in five aspects were conducted.

Results: Results demonstrate that multi-shot DTI with MUSE could achieve better reconstruction in the spinal cord. A combination of reduced-FOV and multi-shot techniques could be adopted simultaneously in pursuit of ultimate distortion correction. In addition, cardiac triggering should be equipped to reduce the influences on cerebrospinal fluid pulsation.

Impact: Multi-shot DTI with MUSE and cardiac triggering might be the optimal combination for clinical diagnosis of the spinal cord if available on commercial MRI scanners. Future coil design could focus on customized coil arrangement of the spinal cord for optimization.

2523.
43Spinal cord injury-induced changes in thoracolumbar microarchitecture: a semi-automated DTI pipeline for improved clinical translation
Georgia E. Bright1,2, Angela Walls3,4,5, Thorsten Feiweier6, Wickramaarchchigeige Lakshantha3,5,7, Patrick Stroman8,9,10, Jillian M. Clark1,2, and Ryan L. O'Hare Doig1,2,3,5
1School of Medicine, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia, 2Neil Sachse Centre for Spinal Cord Research, Lifelong Health Theme, South Australian Health and Medical Research Institute, Adelaide, Australia, 3Preclinical, Imaging and Research Laboratories, South Australian Health and Medical Research Institute, Adelaide, Australia, 4Clinical & Research Imaging Centre, South Australian Health and Medical Research Institute, Adelaide, Australia, 5National Imaging Facility, South Australian Node, Adelaide, Australia, 6Siemens Healthcare GmbH, Erlangen, Germany, 7Australian Cancer Research Foundation Molecular Theranostics Laboratory, Centenary Institute, Sydney, Australia, 8Centre for Neuroscience Studies, Queens University, Kingston, ON, Canada, 9Department of Biomedical and Molecular Sciences, Queens University, Kingston, ON, Canada, 10Department of Physics, Queens University, Kingston, ON, Canada

Keywords: Spinal Cord, Microstructure, Diffusion Tensor Imaging

Motivation: While diffusion tensor imaging (DTI) is sensitive to spinal cord injury (SCI)-induced microstructural changes, manual pre-processing of thoracolumbar spinal cord (TL-SC) data precludes its clinical translation.

Goal(s): We aimed to optimise a semi-automatic TL-SC DTI protocol to detect SCI-induced microarchitectural changes.

Approach: TL-SC DTI data from two participants with diagnosed SCI and six healthy volunteers were pre-processed to equate the TL-SC microarchitecture and then compared to semi-automated analysis.

Results: Our optimised TL-SC DTI acquisition and semi-automatic analysis pipeline is sensitive to SCI-induced microstructural changes and may provide a more clinically viable method for TL-SC DTI analysis.

Impact: This study assessed and validated our newly developed thoracolumbar spinal cord (TL-SC) diffusion tensor imaging (DTI) pipeline in detecting spinal cord injury (SCI)-induced microstructural changes and offers an alternative semi-automatic pre-processing method for improved clinical translation.

2524.
44Demonstration of TE-dependence of lateralization of structural connectomes
Yifei He1, Xiaoming Liu2,3, Peng Sun4, Tenglong Wang1, Yizhe Zhang1, Jiaolong Qin1, Tao Zhou1, and Ye Wu1
1Nanjing University of Science and Technology, Nanjing, China, 2Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China, 3Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China, 4Philips Healthcare, Wuhan, China

Keywords: Tractography, Tractography & Fibre Modelling

Motivation: Lateralization of structural connectomes has become a widespread measurement for investigating brain asymmetry alterations during brain development, maturation and aging in health and disease. However, it is still unclear whether the acquisition parameters affect the lateralization measurement of structural connectomes.

Goal(s): We aim to investigate the TE-dependence of lateralization of structural connectomes.

Approach: We compared the lateral indices of structural connectivity generated by diffusion MRI on five different TEs.

Results: Diverse TE values in MRI scans lead to apparent differences in connectome lateralization, with more than 30% of connections of the same subject likely to have different lateral indices.

Impact: This research reveals the unknown relationship between TE and connectome lateralization and discover the potential influence of TE in connectome’s anatomy analysis, helping improve the acquisition protocol of future neuroimaging studies, especially in brain asymmetry during development, maturation and aging.

2525.
45Use of the Allen Human Brain spatial transcriptome for the validation of myelin content imaging using BMC-mcDESPOT.
Jonghyun Bae1, Zhaoyuan Gong1, Alex Guo1, Mary E Faulkner1, John P Laporte1, and Mustapha Bouhrara1
1National Institute on Aging, National Institute of Health, Baltimore, MD, United States

Keywords: Aging, Relaxometry, Transcriptomics, Myelin water fraction

Motivation: Myelin water imaging has demonstrated its ability to successfully detect changes of myelin content in different neuropathology. However, the validation of these measures remains challenging.

Goal(s): In this study, we aim to validate our MWF measurements with the gene expression that are relevant to myelin.

Approach: We utilized the Allen Human Brain Atlas (AHBA) transcriptomics dataset to validate our Myelin Water Fraction (MWF) measurements. We correlated the aggregated gene expression from AHBA with our derived MWF for different brain regions. 

Results: Our results demonstrate strong correlations of gene expression related to myelin and the transcription of myelin with derived MWF measurements.

Impact: We utilized transcriptomics to validate derived Myelin Water Fraction measures, which strongly correlated with the gene expression specific to myelin. The use of transcriptomics further supports on the molecular basis of myelin synthesis and transcriptional changes with aging.

2526.
46Recognition of Delayed Hypoxic Leukoencephalopathy after a Severe Drug Overdose Using a Divided Subtracted Inversion Recovery (dSIR) Sequence
Paul Condron1,2, Gil Newburn1, Maryam Tayebi1,2, Eryn Kwon1,2, Mark Griffin3, Miriam Scadeng1,2, Samantha J Holdsworth1,2, Daniel Cornfeld1,2, and Graeme M Bydder1,4
1Mātai Medical Research Institute, Tairāwhiti Gisborne, New Zealand, 2Department of Anatomy and Medical Imaging, Faculty of Medical and Health Sciences & Centre for Brain Research, University of Auckland, Auckland, New Zealand, 3Insight Research Services Associated, Gold Coast, Australia, 4University of California, San Diego, San Diego, CA, United States

Keywords: White Matter, Drugs, tMRI, Delayed Hypoxic Leukoencephalopathy, Drug Overdose

Motivation: Divided Subtracted Inversion Recovery (dSIR) sequences can show subtle abnormalities due to small increases in T1 that are not seen with conventional sequences,

Goal(s): To use dSIR sequences to examine the brain in a patient nine months after severe drug overdose associated with prolonged hypoxia and compare the dSIR images with T2-FLAIR images.

Approach: MRI scans obtained on an 18-y/o male control and a 19-y/o male patient. 2D IR FSE sequences were performed with TIs chosen to null WM, and a longer TIi producing dSIR images.

Results: Widespread abnormalities seen on dSIR images in areas of WM that appeared normal on T2-FLAIR images.

Impact: In a patient imaged nine months after a severe drug overdose, dSIR images showed extensive abnormalities in white matter that appeared normal on T2-FLAIR images. Widespread white matter changes may be common unrecognised sequelae of severe drug overdoses.

2527.
47Novel 3D myelin weighted imaging in the cervical spinal cord using myelin-sensitive inversion recovery (MySIR): a feasibility study
Minako Azuma1, Masahiro Enzaki2, Masami Yoneyama3, Yoshihito Kadota1, and Kengo Matsumura1
1Department of Radiology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan, 2Division of Radiology, Miyazaki University Hospital, Miyazaki, Japan, 3Philips Japan, Tokyo, Japan

Keywords: Spinal Cord, Spinal Cord

Motivation: Myelin water fraction (MWF) is a promising method for quantitative evaluation of myelin function in the brain. On the other hand, myelin-sensitive inversion recovery (MySIR) sequence is thought to show spinal myelin structure. 

Goal(s):  To evaluate the feasibility of MySIR imaging for myelin visualization in the cervical spinal cord. .

Approach: MySIR images were compared with MWF as the gold standard.

Results: We have demonstrated that MySIR showed similar results to MWF in evaluating the distribution of myelin in the spine. MySIR may be useful for evaluating the distribution of myelin.

Impact: MySIR gave us a novel contrast between grey matter and white matter. Additionally, MySIR showed similar results to MWF in evaluating myelin. We demonstrated the feasibility of MySIR for evaluating the distribution of myelin in cervical spine.

2528.
48Development of Quantitative Magnetization Transfer Imaging for the Human Cervical Spinal Cord at 3 Tesla
Ping Wang1,2, Zhiqiang Li1,2, and Richard D Dortch1,2
1Neuroimaging Innovation Center, Barrow Neurological Institute, Phoenix, AZ, United States, 2Translational Neuroscience, Barrow Neurological Institute, Phoenix, AZ, United States

Keywords: Spinal Cord, Relaxometry, Quantitative Magnetization Transfer, C-spine

Motivation: We proposed to use a method known as selective inversion recovery (SIR), which allows one to perform the entire QMT (quantitative magnetization transfer) experiment from a conventional inversion recovery sequence. 

Goal(s): To translate the SIR-QMT method to the spinal cord at 3T with optimized sampling schemes to yield high-resolution cervical spinal cord PSR (macromolecular pool-size-ratios) maps within clinically relevant scan times.

Approach: SIR-QMT was conducted on two healthy volunteers to calculate PSR and R1f.

Results: These results suggest that QMT imaging can be performed in the human cervical spinal cord at 3T.

Impact: The work has important clinical indication to study de/remyelination and nerve injuries/repairs in spinal cord disorders.