Movement Disorders (revue)

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Clinicopathological Study in Progressive Supranuclear Palsy With Pedunculopontine Stimulation

Identifieur interne : 001166 ( Main/Exploration ); précédent : 001165; suivant : 001167

Clinicopathological Study in Progressive Supranuclear Palsy With Pedunculopontine Stimulation

Auteurs : Lili-Naz Hazrati [Canada] ; Janice C. Wong [Canada] ; Clement Hamani [Canada] ; Andres M. Lozano [Canada] ; Yu-Yan Poon [Canada] ; Jonathan O. Dostrovsky [Canada] ; William D. Hutchison [Canada] ; Cindy Zadikoff [Canada, États-Unis] ; Elena Moro [Canada]

Source :

RBID : Pascal:12-0369637

Descripteurs français

English descriptors

Abstract

Background: Pedunculopontine nucleus (PPN) DBS has emerged as a potential intervention for patients with gait and balance disorders. However, targeting this nucleus can be challenging. We report on the first neuropathological analyses after PPN-DBS surgery in advanced progressive supranuclear palsy (PSP). Methods: Two patients with PSP underwent unilateral PPN-DBS surgery and were clinically followed to autopsy. Both patients underwent postmortem neuropathological analysis, including choline acetyltransferase immunohistochemistry, to ascertain PPN boundaries and electrode location. Results: Both patients experienced partial improvement in some motor and nonmotor domains postintervention, but died shortly of other complications. Postmortem neuropathological analysis of each patient confirmed the electrode in a region of cholinergic neuronal loss corresponding to the PPN. Conclusions: We provide histopathological evidence for the validity of our stereotactic approach to target the PPN and correlate electrode location with clinical outcomes.


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Background: Pedunculopontine nucleus (PPN) DBS has emerged as a potential intervention for patients with gait and balance disorders. However, targeting this nucleus can be challenging. We report on the first neuropathological analyses after PPN-DBS surgery in advanced progressive supranuclear palsy (PSP). Methods: Two patients with PSP underwent unilateral PPN-DBS surgery and were clinically followed to autopsy. Both patients underwent postmortem neuropathological analysis, including choline acetyltransferase immunohistochemistry, to ascertain PPN boundaries and electrode location. Results: Both patients experienced partial improvement in some motor and nonmotor domains postintervention, but died shortly of other complications. Postmortem neuropathological analysis of each patient confirmed the electrode in a region of cholinergic neuronal loss corresponding to the PPN. Conclusions: We provide histopathological evidence for the validity of our stereotactic approach to target the PPN and correlate electrode location with clinical outcomes.</div>
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