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Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate

Precision targeting of specific white matter bundles that traverse the subcallosal cingulate (SCC) has been linked to efficacy of deep brain stimulation (DBS) for treatment resistant depression (TRD). Methods to confirm optimal target engagement in this heterogenous region are now critical to establ...

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Autores principales: Smith, Ezra E., Choi, Ki Sueng, Veerakumar, Ashan, Obatusin, Mosadoluwa, Howell, Bryan, Smith, Andrew H., Tiruvadi, Vineet, Crowell, Andrea L., Riva-Posse, Patricio, Alagapan, Sankaraleengam, Rozell, Christopher J., Mayberg, Helen S., Waters, Allison C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433578/
https://www.ncbi.nlm.nih.gov/pubmed/36061500
http://dx.doi.org/10.3389/fnhum.2022.939258
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author Smith, Ezra E.
Choi, Ki Sueng
Veerakumar, Ashan
Obatusin, Mosadoluwa
Howell, Bryan
Smith, Andrew H.
Tiruvadi, Vineet
Crowell, Andrea L.
Riva-Posse, Patricio
Alagapan, Sankaraleengam
Rozell, Christopher J.
Mayberg, Helen S.
Waters, Allison C.
author_facet Smith, Ezra E.
Choi, Ki Sueng
Veerakumar, Ashan
Obatusin, Mosadoluwa
Howell, Bryan
Smith, Andrew H.
Tiruvadi, Vineet
Crowell, Andrea L.
Riva-Posse, Patricio
Alagapan, Sankaraleengam
Rozell, Christopher J.
Mayberg, Helen S.
Waters, Allison C.
author_sort Smith, Ezra E.
collection PubMed
description Precision targeting of specific white matter bundles that traverse the subcallosal cingulate (SCC) has been linked to efficacy of deep brain stimulation (DBS) for treatment resistant depression (TRD). Methods to confirm optimal target engagement in this heterogenous region are now critical to establish an objective treatment protocol. As yet unexamined are the time-frequency features of the SCC evoked potential (SCC-EP), including spectral power and phase-clustering. We examined these spectral features—evoked power and phase clustering—in a sample of TRD patients (n = 8) with implanted SCC stimulators. Electroencephalogram (EEG) was recorded during wakeful rest. Location of electrical stimulation in the SCC target region was the experimental manipulation. EEG was analyzed at the surface level with an average reference for a cluster of frontal sensors and at a time window identified by prior study (50–150 ms). Morlet wavelets generated indices of evoked power and inter-trial phase clustering. Enhanced phase clustering at theta frequency (4–7 Hz) was observed in every subject and was significantly correlated with SCC-EP magnitude, but only during left SCC stimulation. Stimulation to dorsal SCC evinced stronger phase clustering than ventral SCC. There was a weak correlation between phase clustering and white matter density. An increase in evoked delta power (2–4 Hz) was also coincident with SCC-EP, but was less consistent across participants. DBS evoked time-frequency features index mm-scale changes to the location of stimulation in the SCC target region and correlate with structural characteristics implicated in treatment optimization. Results also imply a shared generative mechanism (inter-trial phase clustering) between evoked potentials evinced by electrical stimulation and evoked potentials evinced by auditory/visual stimuli and behavioral tasks. Understanding how current injection impacts downstream cortical activity is essential to building new technologies that adapt treatment parameters to individual differences in neurophysiology.
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spelling pubmed-94335782022-09-02 Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate Smith, Ezra E. Choi, Ki Sueng Veerakumar, Ashan Obatusin, Mosadoluwa Howell, Bryan Smith, Andrew H. Tiruvadi, Vineet Crowell, Andrea L. Riva-Posse, Patricio Alagapan, Sankaraleengam Rozell, Christopher J. Mayberg, Helen S. Waters, Allison C. Front Hum Neurosci Neuroscience Precision targeting of specific white matter bundles that traverse the subcallosal cingulate (SCC) has been linked to efficacy of deep brain stimulation (DBS) for treatment resistant depression (TRD). Methods to confirm optimal target engagement in this heterogenous region are now critical to establish an objective treatment protocol. As yet unexamined are the time-frequency features of the SCC evoked potential (SCC-EP), including spectral power and phase-clustering. We examined these spectral features—evoked power and phase clustering—in a sample of TRD patients (n = 8) with implanted SCC stimulators. Electroencephalogram (EEG) was recorded during wakeful rest. Location of electrical stimulation in the SCC target region was the experimental manipulation. EEG was analyzed at the surface level with an average reference for a cluster of frontal sensors and at a time window identified by prior study (50–150 ms). Morlet wavelets generated indices of evoked power and inter-trial phase clustering. Enhanced phase clustering at theta frequency (4–7 Hz) was observed in every subject and was significantly correlated with SCC-EP magnitude, but only during left SCC stimulation. Stimulation to dorsal SCC evinced stronger phase clustering than ventral SCC. There was a weak correlation between phase clustering and white matter density. An increase in evoked delta power (2–4 Hz) was also coincident with SCC-EP, but was less consistent across participants. DBS evoked time-frequency features index mm-scale changes to the location of stimulation in the SCC target region and correlate with structural characteristics implicated in treatment optimization. Results also imply a shared generative mechanism (inter-trial phase clustering) between evoked potentials evinced by electrical stimulation and evoked potentials evinced by auditory/visual stimuli and behavioral tasks. Understanding how current injection impacts downstream cortical activity is essential to building new technologies that adapt treatment parameters to individual differences in neurophysiology. Frontiers Media S.A. 2022-08-18 /pmc/articles/PMC9433578/ /pubmed/36061500 http://dx.doi.org/10.3389/fnhum.2022.939258 Text en Copyright © 2022 Smith, Choi, Veerakumar, Obatusin, Howell, Smith, Tiruvadi, Crowell, Riva-Posse, Alagapan, Rozell, Mayberg and Waters. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Smith, Ezra E.
Choi, Ki Sueng
Veerakumar, Ashan
Obatusin, Mosadoluwa
Howell, Bryan
Smith, Andrew H.
Tiruvadi, Vineet
Crowell, Andrea L.
Riva-Posse, Patricio
Alagapan, Sankaraleengam
Rozell, Christopher J.
Mayberg, Helen S.
Waters, Allison C.
Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
title Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
title_full Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
title_fullStr Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
title_full_unstemmed Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
title_short Time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
title_sort time-frequency signatures evoked by single-pulse deep brain stimulation to the subcallosal cingulate
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433578/
https://www.ncbi.nlm.nih.gov/pubmed/36061500
http://dx.doi.org/10.3389/fnhum.2022.939258
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