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Published on: February 15, 2014
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Modulation of limbic resting-state networks by subthalamic nucleus deep brain stimulation
John Eraifej1, Joana Cabral2,3,4, Henrique M Fernandes4
1Oxford Functional Neurosurgery Group, Nuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom.
Network Neuroscience (Cambridge, Mass.)
|July 3, 2023
Summary
Subthalamic nucleus deep brain stimulation (STN-DBS) in Parkinson's disease modulates limbic networks, particularly the orbitofrontal cortex. This suggests STN-DBS rebalances limbic network activity, impacting non-motor symptoms.
Area of Science:
- Neuroscience
- Neurology
- Medical Imaging
Background:
- Subthalamic nucleus deep brain stimulation (STN-DBS) is established for Parkinson's disease motor symptoms.
- Its impact on non-motor symptoms and broader brain networks is less understood.
- Disseminated network modulation by STN-DBS requires quantitative evaluation.
Purpose of the Study:
- To quantitatively evaluate network-specific modulation induced by STN-DBS using Leading Eigenvector Dynamics Analysis (LEiDA).
- To assess the impact of STN-DBS on resting-state network (RSN) occupancy in Parkinson's disease patients.
- To compare RSN activity between STN-DBS ON and OFF conditions and with healthy controls.
Main Methods:
- Functional MRI data from 10 Parkinson's disease patients with STN-DBS were analyzed.
- Leading Eigenvector Dynamics Analysis (LEiDA) was employed to calculate RSN occupancy.
- Statistical comparisons were made between STN-DBS ON and OFF states, and against 49 age-matched healthy controls.
Main Results:
- STN-DBS significantly increased the occupancy of an orbitofrontal limbic subsystem compared to both DBS OFF and healthy controls (p < 0.006).
- A diffuse limbic RSN showed increased occupancy in patients OFF STN-DBS versus controls (p = 0.021), normalizing when STN-DBS was ON, indicating network rebalancing.
- These findings highlight STN-DBS's specific modulation of limbic system components, including the orbitofrontal cortex.
Conclusions:
- STN-DBS specifically modulates limbic RSNs, notably affecting the orbitofrontal cortex involved in reward processing.
- Quantitative LEiDA analysis provides valuable biomarkers for assessing the widespread effects of brain stimulation.
- These insights support personalized therapeutic strategies for Parkinson's disease by understanding network-level STN-DBS impacts.

