2019
DOI: 10.1007/s11910-019-0961-8
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Neuroimaging Technological Advancements for Targeting in Functional Neurosurgery

Abstract: Purpose of review Ablations and particularly deep brain stimulation (DBS) of a variety of CNS targets are established therapeutic tool for movement disorders. Accurate targeting of the intended structure is crucial for optimal clinical outcomes. However, most targets used in functional neurosurgery are poorly visualized on routine MRI and indirect targeting methods are commonly used. This article reviews recent neuroimaging advancements for targeting in movement disorders. Recent findings Dedicated MRI sequenc… Show more

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Cited by 31 publications
(35 citation statements)
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References 104 publications
(137 reference statements)
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“…These studies have provided evidence of differential tract engagement between therapeutic and nontherapeutic DBS for depression and OCD 88,90,97,98 . In addition, several studies have applied large‐scale, publicly available normative resting state fMRI and dMRI datasets to DBS cohorts, permitting connectomic analysis of patients lacking native fMRI/dMRI scans 14 . Again, these analyses have demonstrated that the pattern of structural and functional networks engaged by DBS is predictive of clinical outcome in varied diseases including PD, dystonia, tremor, and OCD 19,50,51,99 .…”
Section: Discussionmentioning
confidence: 99%
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“…These studies have provided evidence of differential tract engagement between therapeutic and nontherapeutic DBS for depression and OCD 88,90,97,98 . In addition, several studies have applied large‐scale, publicly available normative resting state fMRI and dMRI datasets to DBS cohorts, permitting connectomic analysis of patients lacking native fMRI/dMRI scans 14 . Again, these analyses have demonstrated that the pattern of structural and functional networks engaged by DBS is predictive of clinical outcome in varied diseases including PD, dystonia, tremor, and OCD 19,50,51,99 .…”
Section: Discussionmentioning
confidence: 99%
“…To examine potential connectomic differences between these hotspots and routinely described contact coordinates, functional and structural network maps were computed using high‐quality normative connectomes in a manner similar to previous studies 19,64–68 . Although these data may not reflect the idiosyncrasies of patient‐ or pathology‐specific connectivity, they typically offer superior data quality to native imaging due to the specialized hardware and optimized acquisition parameters used by normative data initiatives 69–71 and the technical (eg, spatial resolution, signal‐to‐noise ratio, artifactual) concessions and hardware/technique inconsistencies that are associated with clinical scans 14 . First, VTAs associated with above‐mean clinical improvement (see Table 2) were employed as seeds for connectomic mapping within 2 large‐scale normative datasets: a 1,000‐subject resting state functional MRI (fMRI) dataset (Brain Genomics Superstruct Project; http://neuroinformatics.harvard.edu/gsp/) 70 and a 985‐subject multishell diffusion‐weighted MRI (dMRI) dataset (Human Connectome Project; http://www.humanconnectomeproject.org/) 72 assembled into a ∼12 million‐streamline, whole‐brain tractogram using generalized q‐sampling imaging (http://dsi-studio.labsolver.org) and Lead‐Connectome (http://www.lead-connectome.org).…”
Section: Methodsmentioning
confidence: 99%
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“…For targeting, there are two basic approaches: indirect targeting using coordinates derived from autopsy-based atlases, or direct visualization of target structures on magnetic resonance imaging (MRI). However, in contrast to the STN and GPi, in vivo segmentation of thalamic nuclei such as the VIM remains challenging, despite significant advances in neuroimaging technology [ 3 , 4 ]. Although some groups have reported VIM visualization on 3T proton density [ 5 ], fast gray matter T1 inversion recovery sequences [ 6 ], or ultra-high field MRI [ 4 ], it is not readily visible on conventional stereotactic MR imaging sequences.…”
Section: Introductionmentioning
confidence: 99%
“…However, in contrast to the STN and GPi, in vivo segmentation of thalamic nuclei such as the VIM remains challenging, despite significant advances in neuroimaging technology [ 3 , 4 ]. Although some groups have reported VIM visualization on 3T proton density [ 5 ], fast gray matter T1 inversion recovery sequences [ 6 ], or ultra-high field MRI [ 4 ], it is not readily visible on conventional stereotactic MR imaging sequences. Other recent advances include connectivity-based segmentation of the VIM using probabilistic tractography [ 2 ].…”
Section: Introductionmentioning
confidence: 99%