3.8 Article

Deep brain stimulation of the Cuneiform nucleus for levodopa-resistant freezing of gait in Parkinson's disease: study protocol for a prospective, pilot trial

Journal

PILOT AND FEASIBILITY STUDIES
Volume 7, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s40814-021-00855-7

Keywords

Freezing of gait (FOG); Gait dysfunction; Parkinson's disease; Mesencephalic locomotor region (MLR); Cuneiform nucleus (CnF); Pedunculopontine nucleus (PPN)

Funding

  1. Boston Scientific Investigator Sponsored Research Award [ISRNMB0018]
  2. University of Miami Scientific Awards Committee Pilot Study Grant [ITS 001003]

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This study introduces a pilot study exploring a novel deep brain stimulation target for treating gait dysfunction, assessing the feasibility and safety of CnF nucleus in treating refractory FOG. The results of this study will help support future larger scale clinical trials.
Background Freezing of gait (FOG) is a particularly debilitating motor deficit seen in a subset of Parkinson's disease (PD) patients that is poorly responsive to standard levodopa therapy or deep brain stimulation (DBS) of established PD targets such as the subthalamic nucleus and the globus pallidus interna. The proposal of a DBS target in the midbrain, known as the pedunculopontine nucleus (PPN) to address FOG, was based on its observed pathology in PD and its hypothesized involvement in locomotor control as a part of the mesencephalic locomotor region, a functionally defined area of the midbrain that elicits locomotion in both intact animals and decerebrate animal preparations with electrical stimulation. Initial reports of PPN DBS were met with much enthusiasm; however, subsequent studies produced mixed results, and recent meta-analysis results have been far less convincing than initially expected. A closer review of the extensive mesencephalic locomotor region (MLR) preclinical literature, including recent optogenetics studies, strongly suggests that the closely related cuneiform nucleus (CnF), just dorsal to the PPN, may be a superior target to promote gait initiation. Methods We will conduct a prospective, open-label, single-arm pilot study to assess safety and feasibility of CnF DBS in PD patients with levodopa-refractory FOG. Four patients will receive CnF DBS and have gait assessments with and without DBS during a 6-month follow-up. Discussion This paper presents the study design and rationale for a pilot study investigating a novel DBS target for gait dysfunction, including targeting considerations. This pilot study is intended to support future larger scale clinical trials investigating this target.

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