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Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity

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 at...

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Autores principales: Ferreira, Francisca, Akram, Harith, Ashburner, John, Zrinzo, Ludvic, Zhang, Hui, Lambert, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960999/
https://www.ncbi.nlm.nih.gov/pubmed/34089871
http://dx.doi.org/10.1016/j.neuroimage.2021.118231
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author Ferreira, Francisca
Akram, Harith
Ashburner, John
Zrinzo, Ludvic
Zhang, Hui
Lambert, Christian
author_facet Ferreira, Francisca
Akram, Harith
Ashburner, John
Zrinzo, Ludvic
Zhang, Hui
Lambert, Christian
author_sort Ferreira, Francisca
collection PubMed
description 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 identify 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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spelling pubmed-89609992022-04-26 Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity Ferreira, Francisca Akram, Harith Ashburner, John Zrinzo, Ludvic Zhang, Hui Lambert, Christian Neuroimage Article 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 identify 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. Academic Press 2021-09 /pmc/articles/PMC8960999/ /pubmed/34089871 http://dx.doi.org/10.1016/j.neuroimage.2021.118231 Text en © 2021 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ferreira, Francisca
Akram, Harith
Ashburner, John
Zrinzo, Ludvic
Zhang, Hui
Lambert, Christian
Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity
title Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity
title_full Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity
title_fullStr Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity
title_full_unstemmed Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity
title_short Ventralis intermedius nucleus anatomical variability assessment by MRI structural connectivity
title_sort ventralis intermedius nucleus anatomical variability assessment by mri structural connectivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960999/
https://www.ncbi.nlm.nih.gov/pubmed/34089871
http://dx.doi.org/10.1016/j.neuroimage.2021.118231
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