4.7 Article

Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity

Journal

NEUROIMAGE
Volume 238, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2021.118231

Keywords

Connectivity; Functional neurosurgery; Tremor; Individualized targeting; Probabilistic tractography

Funding

  1. Engineering and Physical Sciences Research Council (EPSRC) [EP/L016476/1, EP/S021930/1]
  2. Brain Research UK
  3. University College London Hospitals NIHR Biomedical Research Centre
  4. Parkinson's Appeal
  5. Sainsbury Monument Trust
  6. MRC Clinician Scientist award [MR/R006504/1]
  7. Wellcome Trust [203147/Z/16/Z]
  8. MRC [MR/R006504/1] Funding Source: UKRI

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The study found that the location of cd-Vim was more variable on the right during the reconstruction of DTCp using probabilistic tractography, and no significant effect of any confounds was observed. This work demonstrates significant individual anatomical variability of the cd-Vim that atlas-based targeting fails to capture.
The ventralis intermedius nucleus (Vim) is centrally placed in the dentato-thalamo-cortical pathway (DTCp) and is a key surgical target in the treatment of severe medically refractory tremor. It is not visible on conventional MRI sequences; consequently, stereotactic targeting currently relies on atlas-based coordinates. This fails to capture individual anatomical variability, which may lead to poor long-term clinical efficacy. Probabilistic tractography, combined with known anatomical connectivity, enables localisation of thalamic nuclei at an individual subject level. There are, however, a number of confounds associated with this technique that may influence results. Here we focused on an established method, using probabilistic tractography to reconstruct the DTCp, to iden-tify the connectivity-defined Vim (cd-Vim) in vivo . Using 100 healthy individuals from the Human Connectome Project, our aim was to quantify cd-Vim variability across this population, measure the discrepancy with atlas-defined Vim (ad-Vim), and assess the influence of potential methodological confounds. We found no significant effect of any of the confounds. The mean cd-Vim coordinate was located within 1.88 mm (left) and 2.12 mm (right) of the average midpoint and 3.98 mm (left) and 5.41 mm (right) from the ad-Vim coordinates. cd-Vim location was more variable on the right, which reflects hemispheric asymmetries in the probabilistic DTC reconstructed. The method was reproducible, with no significant cd-Vim location differences in a separate test-retest cohort. The superior cerebellar peduncle was identified as a potential source of artificial variance. This work demonstrates significant individual anatomical variability of the cd-Vim that atlas-based coordinate targeting fails to capture. This variability was not related to any methodological confound tested. Lateralisation of cerebellar functions, such as speech, may contribute to the observed asymmetry. Tractography-based methods seem sensitive to individual anatomical variability that is missed by conventional neurosurgical targeting; these findings may form the basis for translational tools to improve efficacy and reduce side-effects of thalamic surgery for tremor.

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