Fibre-Orientation-based Contrast for Thalamic Subnuclei Targeting using MR-guided Focused Ultrasound

Poster No:

1295 

Submission Type:

Abstract Submission 

Authors:

Eric Pierre1, Chris Kokkinos1, Wesley Thevathasan2,3, Kristian Bulluss4,3,5, Arthur Thevathasan2,3, Robert Smith1,3, David Vaughan1,3, David Abbott1,3, Heath Pardoe1,3, Graeme Jackson1,3

Institutions:

1The Florey Institute of Neuroscience and Mental Health, Melbourne, Australia, 2Department of Neurology, Austin Health, Melbourne, Australia, 3The University of Melbourne, Melbourne, Australia, 4Department of Neurosurgery, Austin Health, Melbourne, Australia, 5Department of Neurosurgery, St Vincent’s Hospital, Melbourne, Australia

First Author:

Eric Pierre  
The Florey Institute of Neuroscience and Mental Health
Melbourne, Australia

Co-Author(s):

Chris Kokkinos  
The Florey Institute of Neuroscience and Mental Health
Melbourne, Australia
Wesley Thevathasan  
Department of Neurology, Austin Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia
Kristian Bulluss  
Department of Neurosurgery, Austin Health|The University of Melbourne|Department of Neurosurgery, St Vincent’s Hospital
Melbourne, Australia|Melbourne, Australia|Melbourne, Australia
Arthur Thevathasan  
Department of Neurology, Austin Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia
Robert Smith  
The Florey Institute of Neuroscience and Mental Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia
David Vaughan  
The Florey Institute of Neuroscience and Mental Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia
David Abbott, PhD  
The Florey Institute of Neuroscience and Mental Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia
Heath Pardoe, PhD  
The Florey Institute of Neuroscience and Mental Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia
Graeme Jackson  
The Florey Institute of Neuroscience and Mental Health|The University of Melbourne
Melbourne, Australia|Melbourne, Australia

Introduction:

The major target for MR-guided Focused Ultrasound (MRgFUS) for treatment of essential tremor (ET) is the ventral intermediate nucleus (Vim) of the thalamus. Accurate MRI visualization of the Vim is still an active topic of research (Jameel et al., 2024).

Most proposed methods include structural MRI techniques like susceptibility-weighted imaging (Abosch et al., 2010), quantitative susceptibility mapping (Deistung et al., 2013), or white-matter nulled T1 imaging, e.g. FGATIR (Sudhyadhom et al., 2009). Other approaches make use of Diffusion-Weighted Imaging (DWI) to probe the thalamic microstructure, e.g. via tractography (Tian et al., 2018).

To circumvent the usual drawbacks of tractography, a combination of both approaches has been recently proposed to produce a synthetic FAT1 contrast, based on high-resolution T1-weighted images and DWI metrics (Goedemans et al., 2024).

However, DWI methods proposed thus far rely on tensor-based analysis for probing fibre-bundle orientation, with known modelling limits. This work applies more modern DWI techniques to represent fibre bundles within voxels (Jeurissen et al., 2014), combined with structural contrast for enhanced visualization of Thalamic microstructure.

Methods:

Three patients undergoing MRgFUS ablation for ET underwent scanning on a Siemens 3T Vida Scanner for pre-operative planning and 1-day post-operation. Acquisitions included a T1-weighted and FGATIR volume at 1mm isotropic resolution, and a DWI dataset of 105 directions over b-values (0, 1000 & 3000 s/mm²) at 2mm resolution, interpolated to 1.3mm in-plane. The clinical team used FGATIR images for final Vim targeting and was blinded to the DWI data.

DWI preprocessing included denoising, Gibbs ringing removal, distortion & motion correction. Fibre Orientation Distributions (FODs) were computed from the DWI dataset using MRtrix3 software (Tournier et al., 2019). FAT1 contrast was also computed for comparison (Figure 1).
For each voxel, we averaged the FOD peak of all fibre populations, weighted by their apparent fibre density. The resulting average peak was given a direction-encoded colour, with intensity corresponding to the averaged peak's height. The average fibre direction map was overlayed onto the FGATIR volume.

Thalamic subnuclei were manually segmented according to Schaltenbrand and Morel atlas references (Najdenovska et al. 2018). The day-1 post-operative T1-weighted volume was registered to the pre-operative planning FGATIR. An ROI of the necrotic core (Keil et al. 2020) was then segmented for lesion visualization.
Supporting Image: Figure1wtext.jpg
 

Results:

The proposed overlay is in good agreement with known neuroanatomy (Figure 1). In the internal capsule, cortico-spinal tracts appear in strong blue (high fibre density in superior-inferior direction), and purple (left right + superior-inferior direction) with thalamic radiations. ventral thalamic nuclei are more lightly shaded (less axonal density) in red (anteriorly) and purple (posteriorly). Anterior and medial groups appear in strong green (anterior-posterior direction). The use of FGATIR signal provides better contrast of Ventral Subnuclei compared to FAT1.

Figure 2 shows subnuclei segmentations for all three patients, transformed to the FGATIR volumes, with the day-1 necrotic core ROI additionally highlighted. All ROIs were close to the Vim/Ventralis Caudalis (VC) border, in agreement with multi-centre studies (Jameel et al., 2024).

All three patients showed significant tremor reduction on the corresponding treated side and are awaiting tremor reduction assessment at 3- and 12-months follow-up post-surgery.
Supporting Image: Figure2wtext.jpg
 

Conclusions:

We demonstrate an MRI overlay technique based on FOD maps and FGATIR contrast to better visualize thalamic subnuclei. The proposed method shows good agreement with expected neuroanatomy and surgical outcomes. While the small sample size precludes statistical analysis, initial results suggest potential value for surgical planning in MRgFUS thalamotomy, warranting validation in larger cohorts.

Brain Stimulation:

Sonic/Ultrasound 2

Disorders of the Nervous System:

Neurodegenerative/ Late Life (eg. Parkinson’s, Alzheimer’s)

Modeling and Analysis Methods:

Diffusion MRI Modeling and Analysis 1

Neuroanatomy, Physiology, Metabolism and Neurotransmission:

Subcortical Structures

Keywords:

Movement Disorder
MRI
Segmentation
STRUCTURAL MRI
Sub-Cortical
Thalamus
ULTRASOUND

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

Other

Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Patients

Was this research conducted in the United States?

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Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

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Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

Not applicable

Please indicate which methods were used in your research:

Structural MRI
Diffusion MRI
Computational modeling

For human MRI, what field strength scanner do you use?

3.0T

Which processing packages did you use for your study?

FSL
Other, Please list  -   MRtrix3

Provide references using APA citation style.

Abosch, A. (2010). An assessment of current brain targets for deep brain stimulation surgery with susceptibility-weighted imaging at 7 tesla. Neurosurgery, 67, 1745-1756.

Deistung, A. (2013). Toward in vivo histology: a comparison of quantitative susceptibility mapping (QSM) with magnitude-, phase-, and R2*-imaging at ultra-high magnetic field strength. Neuroimage, 65, 299-314.

Goedemans, T. (2024). FAT1 weighted MRI: Diffusion meets anatomical imaging and application in thalamic surgery for tremor. Imaging Neuroscience, 2024(2), 1–15.

Jameel, A. (2024). The evolution of ventral intermediate nucleus targeting in MRI guided focused ultrasound thalamotomy for essential tremor: an international multi center evaluation. Frontiers in Neurology, 15.

Jeurissen, B. (2014). Multi-tissue constrained spherical deconvolution for improved analysis of multi-shell diffusion MRI data. Neuroimage, 103, 411-426.

Keil, V.C. (2020). MRI follow-up after magnetic resonance-guided focused ultrasound for non-invasive thalamotomy: the neuroradiologist's perspective. Neuroradiology, 62(9), 1111-1122.

Najdenovska, E. (2018). In-vivo probabilistic atlas of human thalamic nuclei based on diffusion- weighted magnetic resonance imaging. Scientific Data, 5, 180270

Sudhyadhom, A. (2009). A high resolution and high contrast MRI for differentiation of subcortical structures for DBS targeting: the Fast Gray Matter Acquisition T1 Inversion Recovery (FGATIR). Neuroimage, 47(2), 44-52.

Tian, Q. (2018). Diffusion MRI tractography for improved transcranial MRI-guided focused ultrasound thalamotomy targeting for essential tremor. NeuroImage: Clinical, 19, 572-580.

Tournier, J.-D. (2019). MRtrix3: A fast, flexible and open software framework for medical image processing and visualisation. NeuroImage, 202, 116-137.

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