The potential neuromodulatory impact of subthalamic nucleus deep brain stimulation on Parkinson's disease progression

J Clin Neurosci. 2020 Mar:73:150-154. doi: 10.1016/j.jocn.2019.12.059. Epub 2020 Jan 27.

Abstract

Introduction: STN-DBS has been claimed to change progressionsymptomsin animal models of PD, but information is lacking about the possible neuromodulatory role of STN-DBS in humans. The aim of this prospective controlled study was to evaluate the long-term impact of STN-DBS on motor disabilities and cognitive impairment in PD patients in comparison to Best-Medical-Therapy (BMT) and Long-term-Post-Operative (POP) groups.

Material and methods: Patients were divided into 3 groups: the BMT-group consisted of 20 patients treated only with pharmacotherapy, the DBS-group consisted of 20 PD patients who underwent bilateral STN-DBS (examined pre- and postoperatively) and the POP-group consisted of 14 long-term postoperative patients in median 30 month-time after DBS. UPDRS III scale was measured during 3 visits in 9 ± 2 months periods (V1, V2, V3) in total-OFF phase. Cognitive assessment was performed during each visit in total-ON phase.

Results: The comparable UPDRS III OFF gain was observed in both BMT-group and POP-group evaluations (p < 0.05). UPDRS III OFF results in DBS-group revealed significant UPDRS III OFF increase in ΔV2-V1 assessment (p < 0.05) with no significant UPDRS III OFF alteration in ΔV3-V2 DBS-group evaluation (p > 0.05). Cognitive assessment revealed significant alterations between DBS-group and BMT-group in working memory, executive functions and learning abilities (p < 0.05).

Conclusions: The impact of STN-DBS on UPDRS III OFF score and cognitive alterations suggest its neuromodulatory role, mainly during the first 9-18 months after surgery.

Keywords: DBS; Deep brain stimulation; Neuromodulatory; Neuroprotection; Parkinson’s disease.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Antiparkinson Agents / therapeutic use
  • Cognitive Dysfunction* / epidemiology
  • Cognitive Dysfunction* / etiology
  • Deep Brain Stimulation / methods*
  • Disease Progression
  • Female
  • Humans
  • Male
  • Middle Aged
  • Motor Disorders* / epidemiology
  • Motor Disorders* / etiology
  • Parkinson Disease / complications*
  • Parkinson Disease / therapy*
  • Prospective Studies
  • Subthalamic Nucleus / physiology
  • Treatment Outcome

Substances

  • Antiparkinson Agents