# 10-year clinical outcomes of subthalamic nucleus versus pallidal deep brain stimulation for Parkinson’s disease: VA/NINDS CSP #468F

**Authors:** Jill L. Ostrem, Ping Luo, Frances M. Weaver, Kenneth Follett, Johannes Rothlind, Nicholas B. Galifianakis, Eugene C. Lai, Jeff Bronstein, John Duda, Kathryn Holloway, Aliya Sarwar, Matthew Brodsky, Kathryn Chung, Meredith Spindler, Domenic Reda, Amanda Snodgrass, Claudia Moy, Grant Huang, Yongliang Wei, William J. Marks

PMC · DOI: 10.3389/fneur.2025.1728999 · Frontiers in Neurology · 2026-01-16

## TL;DR

This study compares long-term outcomes of two brain stimulation targets for Parkinson's disease over 10 years.

## Contribution

The study provides the longest follow-up to date comparing subthalamic nucleus and pallidal deep brain stimulation for Parkinson’s disease.

## Key findings

- Both GPi and STN DBS improved motor function over 10 years, with no significant difference between the two targets.
- Improvements in bradykinesia and quality of life declined over time, while non-motor symptoms worsened.
- Medication reductions and improvements in dyskinesia and motor fluctuations were sustained regardless of stimulation target.

## Abstract

This study aimed to examine the very long-term effects of globus pallidus interna (GPi) or subthalamic nucleus (STN) deep brain stimulation (DBS) on Parkinson’s disease (PD) in a subset of patients enrolled in the CSP468 VA/NINDS prospective randomized trial.

The primary outcome was the change in off-medication/on-stimulation Unified Parkinson’s Disease Rating Scale III score (UPDRS III) from baseline over time between the two targets at 2, 7, and 10 years. Many secondary outcomes were also explored.

A total of 156 patients were enrolled in this substudy, and data were available for 68 GPi/49 STN participants at 7 years and 49 GPi/28 STN participants at 10 years. There was no overall difference in the time trend between the two targets (p < 0.09). UPDRS III improvements from baseline in the GPi cohort at 2, 7, and 10 years were 39.9% (p < 0.001), 16.4%, (p < 0.001), and 22.3%, (p = 0.10), respectively, and in the STN cohort at 2, 7, and 10 years it was 34.9% (p < 0.001), 16.9%, (p < 0.001), and 32.8%, (p < 0.001), respectively. Tremor subscores showed the greatest reduction, followed by rigidity subscores. Initial improvements in bradykinesia and axial subscores were attenuated, and UPDRS I, II, and III on-medication/on-stimulation scores significantly declined. UPDRS IV scores and motor diaries showed significant long-term improvement, and medication reductions were seen regardless of the target. At 7 and 10 years, the PDQ-39 total score no longer showed improvement, and more severe cognitive impairment was seen in both targets.

DBS therapy has a significant beneficial effect on overall motor function, dyskinesia, and motor fluctuations over 10 years (regardless of target), though non-motor symptoms progressed. Bradykinesia, axial, and quality-of-life improvement were maintained at 2 years and then declined over time.

ClinicalTrials.gov, identifier NCT01022073, NCT00056563, NCT01076452.

## Linked entities

- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Diseases:** rigidity (MESH:D009127), Bradykinesia (MESH:D018476), Tremor (MESH:D014202), dyskinesia (MESH:D004409), PD (MESH:D010300), cognitive impairment (MESH:D003072)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12856926/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12856926/full.md

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Source: https://tomesphere.com/paper/PMC12856926