Comparative fMRI correlates of PNFS and DBS for facial pain.

Poster No:

1882 

Submission Type:

Abstract Submission 

Authors:

Clement Chow1, Michelle Paff2, Can Sarica1, Brendan Santyr1, Sriranga Kashyap1, Aaron Loh1, Michael Colditz3, Kimia Pourhossein4, Asma Naheed1, Kâmil Uludağ1, Jürgen Germann1, Alexandre Boutet1, Andres Lozano1, Mojgan Hodaie1

Institutions:

1University Health Network, Toronto, ON, 2University of California Irvine Health, Orange County, CA, 3Royal Brisbane and Women's Hospital, Brisbane, VIC, 4University of Melbourne, Melbourne, VIC

First Author:

Clement Chow  
University Health Network
Toronto, ON

Co-Author(s):

Michelle Paff  
University of California Irvine Health
Orange County, CA
Can Sarica  
University Health Network
Toronto, ON
Brendan Santyr  
University Health Network
Toronto, ON
Sriranga Kashyap  
University Health Network
Toronto, ON
Aaron Loh  
University Health Network
Toronto, ON
Michael Colditz  
Royal Brisbane and Women's Hospital
Brisbane, VIC
Kimia Pourhossein  
University of Melbourne
Melbourne, VIC
Asma Naheed  
University Health Network
Toronto, ON
Kâmil Uludağ  
University Health Network
Toronto, ON
Jürgen Germann  
University Health Network
Toronto, ON
Alexandre Boutet  
University Health Network
Toronto, ON
Andres Lozano  
University Health Network
Toronto, ON
Mojgan Hodaie  
University Health Network
Toronto, ON

Introduction:

Neuromodulation involves the stimulation of pain pathways using implantable devices that deliver electrical currents to achieve reversible modifications in the nociceptive system. Melzack's "Pain Neuromatrix" theory highlights the interplay between sensory-motor, affective-motivational, and cognitive-evaluative components of chronic pain (Melzack, 1999). Peripheral nerve field stimulation (PNFS) is a minimally invasive treatment for refractory trigeminal neuropathic pain, yet its central nervous system responses require clarification (Machado et al., 2013). This study investigates stimulation-related functional responses during PNFS using task-based fMRI and compares them to resting-state functional connectivity (FC) patterns in patients with ventral caudal (Vc)/periventricular gray (PVG) deep brain stimulation (DBS) for chronic neuropathic pain.

Methods:

Two PNFS patients with trigeminal neuropathic pain were studied using a block design paradigm with 30-second ON/OFF stimulation cycles. High- (1 kHz) and low-frequency (30–40 Hz) PNFS settings were applied, and task-based BOLD response maps were generated. Additionally, three DBS patients with chronic neuropathic facial pain (following thalamic hemorrhage, brachial plexus injury, middle cerebral artery stroke) underwent resting-state fMRI during DBS-ON and DBS-OFF conditions. Functional connectivity of the volume of tissue activated (VTA) was analyzed for changes associated with different DBS settings.
Supporting Image: methods.png
 

Results:

In PNFS, high-frequency stimulation in a non-responder induced BOLD changes in the orbitofrontal cortex, posterior cingulate, and motor cortex, whereas low-frequency stimulation elicited no response. Conversely, in a responder, low-frequency stimulation induced BOLD changes in the anterior cingulate cortex, posterior cingulate cortex, prefrontal cortex, amygdala, nucleus accumbens, primary motor cortex, and primary somatosensory area corresponding to the facial region, while high-frequency stimulation had no changes.

For Vc/PVG DBS patients, the FC of VTAs demonstrated brain-wide differences between DBS-ON and DBS-OFF states. Acute Vc stimulation (Patient 1) resulted in reduced positive connectivity and increased negative connectivity in the medial prefrontal cortex and anterior cingulate cortex. Chronic Vc stimulation (Patients 2 and 3) revealed diminished positive FC with posterior cingulate cortex, precuneus, and medial motor cortices in the DBS-ON condition. PVG stimulation (Patient 2) demonstrated increased negative FC with the PCC, precuneus, and temporal lobes during DBS-ON.
Supporting Image: nonr-vs-resp.png
 

Conclusions:

Functional responses to PNFS vary based on stimulation efficacy and parameters. DBS impacts FC differently in acute and chronic stimulation states, emphasizing dynamic changes in brain connectivity. Further analyses including additional participants will be presented during the conference.

Brain Stimulation:

Deep Brain Stimulation
Invasive Stimulation Methods Other

Modeling and Analysis Methods:

fMRI Connectivity and Network Modeling

Novel Imaging Acquisition Methods:

BOLD fMRI 1

Perception, Attention and Motor Behavior:

Perception: Pain and Visceral 2

Keywords:

Limbic Systems
MRI
Neurological
Pain
Peripheral Nerve
Somatosensory
Thalamus
Other - Neuromodulation

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

Resting state
Task-activation

Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Patients

Was this research conducted in the United States?

No

Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

Yes

Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

Not applicable

Please indicate which methods were used in your research:

Functional MRI

For human MRI, what field strength scanner do you use?

1.5T
3.0T

Which processing packages did you use for your study?

AFNI
SPM
FSL

Provide references using APA citation style.

Machado, A. G., Baker, K. B., Plow, E., & Malone, D. A. (2013). Cerebral stimulation for the affective component of neuropathic pain. Neuromodulation: Technology at the Neural Interface, 16(6), 514-518.
Melzack, R. (1999). From the gate to the neuromatrix. Pain, 82, S121-S126.

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