Background Chronic pain is a major healthcare problem associated with maladaptive brain circuit changes - many patients are unresponsive to all available therapies. Deep brain stimulation (DBS) is a promising treatment, but traditional targets have not proven consistently effective. DBS for pain may be improved by individualizing location and timing of stimulation based on real time brain measurements and patient reports.
Methods To optimize personalized stimulation targets, we first performed a double blind, sham-controlled, intracranial EEG brain mapping trial spanning 10 hospital days, in six participants with refractory neuropathic pain syndromes. Five participants with clinically meaningful pain relief were then implanted with permanent devices capable of brain stimulation and recording. We used ambulatory electrical brain recordings to derive bespoke pain biomarkers using machine learning. Pain biomarkers were used in closedloop DBS algorithms for personalized therapy. After an open-label period, we tested the feasibility and efficacy of closed-loop DBS for pain relief against sham in a double-blind, cross-over trial.
Results Trial intracranial testing revealed multiple brain targets among cortico-striatal-thalamocortical pathways that produced rapid pain relief across participants. We predicted individual pain metrics from both inpatient and ambulatory brain activity with high accuracy; pain biomarkers were incorporated into closed-loop DBS algorithms that also responded to sleep-wake cycles. Personalized, closed-loop DBS was superior to sham, with durability up to 3.5 years.
Conclusions Precision-medicine DBS, with individually optimized brain stimulation targets and closed-loop delivery of stimulation in response to pain biomarkers, is a feasible strategy to treat refractory chronic pain syndromes.
Trial Registration NCT04144972
Competing Interest StatementPS, PAS and EC were involved in the design of the clinical study. All authors were involved in the collection, analysis, and interpretation of the data and the writing of the manuscript. Medtronic Inc. donated the Summit RC+S device hardware for the permanent implants, but did not have any role in data collection, analysis, interpretation or writing of the manuscript. All authors vouch for the accuracy, ethical conduct, and completeness of the data collection and for the fidelity of the study to the protocol. Informed consent was obtained from all participants before study enrollment. PS, PAS and EC have obtained a patent related to the use of closed-loop DBS to treat chronic pain.
Clinical TrialNCT04144972
Funding StatementThis study was funded by the NIH BRAIN (UH3NS109556) and HEAL Initiatives (UH3NS115631).
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
IRB of University of California, San Francisco gave ethical approval for this work.
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Data AvailabilityAll data produced will be available online at the OpenScience Foundation (https://osf.io/) and Github.
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