The discovery that aberrant synchronization of rhythmic neuronal activity recorded in PD patients is suppressed by DBS has advanced the concept that measures associated with pathological activity may be used as biomarkers to control the delivery of DBS therapy. Pilot studies of aDBS in PD have reported promising clinical results from triggering DBS stimulation when the signal recorded from the DBS electrode showed a high level of oscillatory power in the beta frequency range (13 ? 35 Hz). That approach, however, has important limitations. Most importantly, beta power recorded from the DBS lead is suppressed by movement including PD tremor, its detection is highly dependent on lead location and the recording montage needed to record during stimulation is incompatible with directional current steering, a recent innovation employing segmented stimulation contacts. The inherent complexity of the increased parameter space through DBS innovations also overwhelms standard programming techniques. Finally, use of additional biomarker signals (e.g., recorded from cortex) is likely to improve the ability to adaptively control DBS for disorders marked by complex multidimensional symptomatologies such as PD. The current proposal will establish methods for overcoming these limitations by developing techniques for multi-feature classification from ECoG recordings, using advanced machine learning algorithms. The proposed research builds upon the extensive and unique experiences with multi-day, extra-operative recording from DBS leads in patients at Charit Hospital and intraoperative ECoG and DBS recording from patients at the University of Pittsburgh, in order to develop computational methods to advance closed-loop, adaptive DBS (aDBS) strategies for movement disorders.

Public Health Relevance

This research seeks to improve computational methods for interpreting brain signals recorded from patients undergoing deep brain stimulation for Parkinson?s disease. The results may inform the design of novel strategies for biomarker-responsive brain stimulation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
7R01NS110424-02
Application #
10021999
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Kukke, Sahana Nalini
Project Start
2019-09-30
Project End
2021-08-31
Budget Start
2019-09-30
Budget End
2020-08-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114