Abstract

Background: High-frequency Deep Brain Stimulation (DBS) of the subcallosal cingulate (SCC) region is an emerging strategy for treatment-resistant depression (TRD). This study examined changes in SCC local field potentials (LFPs). The LFPs were recorded from the DBS leads following transient, unilateral stimulation at the neuroimaging-defined optimal electrode contact. The goal was identifying a putative electrophysiological measure of target engagement during implantation.Methods: Fourteen consecutive patients underwent bilateral SCC DBS lead implantation. LFP recordings were collected from all electrodes during randomized testing of stimulation on each DBS contact (eight total). Analyses evaluated changes in spectral power before and after 3 min of unilateral stimulation at the contacts that later facilitated antidepressant response, as a potential biomarker of optimal contact selection in each hemisphere.Results: Lateralized and asymmetric power spectral density changes were detected in the SCC with acute unilateral SCC stimulation at those contacts subsequently selected for chronic, therapeutic stimulation. Left stimulation induced broadband ipsilateral decreases in theta, alpha, beta and gamma bands. Right stimulation effects were restricted to ipsilateral beta and gamma decreases. These asymmetric effects contrasted with identical white matter stimulation maps used in each hemisphere. More variable ipsilateral decreases were seen with stimulation at the adjacent “suboptimal” contacts, but changes were not statistically different from the “optimal” contact in either hemisphere despite obvious differences in impacted white matter bundles. Change in theta power was, however, most robust and specific with left-sided optimal stimulation, which suggested a putative functional biomarker on the left with no such specificity inferred on the right.Conclusion: Hemisphere-specific oscillatory changes can be detected from the DBS lead with acute intraoperative testing at contacts that later engender antidepressant effects. Our approach defined potential target engagement signals for further investigation, particularly left-sided theta decreases following initial exposure to stimulation. More refined models combining tractography, bilateral SCC LFP, and cortical recordings may further improve the precision and specificity of these putative biomarkers. It may also optimize and standardize the lead implantation procedure and provide input signals for next generation closed-loop therapy and/or monitoring technologies for TRD.

Highlights

  • High-frequency, bilateral Deep Brain Stimulation (DBS) of the subcallosal cingulate (SCC) region is an emerging strategy for treatment-resistant depression (TRD)

  • With SCC DBS for TRD, recent refinements of DBS surgical targeting methods using diffusion tractography demonstrate that stimulation of 4 white matter bundles—the cingulum bundle (CB), uncinate fasciculus (UF), forceps minor (FM) and frontostriatal fibers (F-St)—converging at the anatomically defined SCC DBS target in each hemisphere is necessary for positive outcomes (Riva-Posse et al, 2014, 2017)

  • We examined changes in local field potentials (LFPs) within the SCC following transient, unilateral SCC stimulation at DBS contacts known to elicit both acute intraoperative behavioral effects and facilitate sustained chronic antidepressant response with bilateral stimulation (Holtzheimer et al, 2012; Choi et al, 2015; RivaPosse et al, 2017)

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Summary

Introduction

High-frequency, bilateral Deep Brain Stimulation (DBS) of the subcallosal cingulate (SCC) region is an emerging strategy for treatment-resistant depression (TRD). Confirmation of correct placement in each hemisphere while in the operating room is an important step Toward this goal, controlled experiments demonstrate that immediate and stereotypic self-reported behavioral changes can be elicited with short exposures to unilateral stimulation using therapeutic DBS parameters (Choi et al, 2015). Such observations provide important foundation to examine electrophysiological changes with unilateral stimulation as a more quantitative biomarker strategy to validate effective surgical targeting in each hemisphere. The goal was identifying a putative electrophysiological measure of target engagement during implantation

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