Evidence map›Paper›PMID 36945412›Full record

ArticlebioRxiv : the preprint server for biology2023

Characterization of spatiotemporal dynamics of binary and graded tonic pain in humans using intracranial recordings.

Rose M Caston, Elliot H Smith, Tyler S Davis, Hargunbir Singh, Shervin Rahimpour, John D Rolston

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Rose M CastonDepartment of Biomedical Engineering, University of Utah, 84112.
Elliot H SmithDepartment of Neurosurgery, University of Utah, 84112.
Tyler S DavisDepartment of Neurosurgery, University of Utah, 84112.
Hargunbir SinghDepartment of Neurosurgery, Brigham & Women's Hospital, Harvard Medical School, 02115.
Shervin RahimpourDepartment of Biomedical Engineering, University of Utah, 84112.
John D RolstonDepartment of Biomedical Engineering, University of Utah, 84112.
University of Utah · USBrigham and Women's Hospital · US

Funding

Training in the Development of Novel Interventions for the Treatment of Neurological and Neurobehavioral DisordersT32NS115723 · NINDS · UNIVERSITY OF UTAH · PI KEEFE, KRISTEN A · 2020 to 2024
$1.1M
Patient-Specific Modeling and Network Perturbation to Enhance the Predictability of Direct Cortical Stimulation for EpilepsyK23NS114178 · NINDS · UNIVERSITY OF UTAH · PI ROLSTON, JOHN D · 2019 to 2023
$961k
Propagation patterns of microelectrode-recorded human interictal dischargesR21NS113031 · NINDS · UNIVERSITY OF UTAH · PI ROLSTON, JOHN D · 2019 to 2019
$427k
NINDS NIH HHS K23 NS114178NINDS NIH HHS R21 NS113031NINDS NIH HHS T32 NS115723
6 · The paper itself

Abstract

Pain is a complex experience involving sensory, emotional, and cognitive aspects, and multiple networks manage its processing in the brain. Examining how pain transforms into a behavioral response can shed light on the networks' relationships and facilitate interventions to treat chronic pain. However, studies using high spatial and temporal resolution methods to investigate the neural encoding of pain and its psychophysical correlates have been limited. We recorded from intracranial stereo-EEG (sEEG) electrodes implanted in sixteen different brain regions of twenty patients who underwent psychophysical pain testing consisting of a tonic thermal stimulus to the hand. Broadband high-frequency local field potential amplitude (HFA; 70-150 Hz) was isolated to investigate the relationship between the ongoing neural activity and the resulting psychophysical pain evaluations. Two different generalized linear mixed-effects models (GLME) were employed to assess the neural representations underlying binary and graded pain psychophysics. The first model examined the relationship between HFA and whether the patient responded "yes" or "no" to whether the trial was painful. The second model investigated the relationship between HFA and how painful the stimulus was rated on a visual analog scale. GLMEs revealed that HFA in the inferior temporal gyrus (ITG), superior frontal gyrus (SFG), and superior temporal gyrus (STG) predicted painful responses at stimulus onset. An increase in HFA in the orbitofrontal cortex (OFC), SFG, and striatum predicted pain responses at stimulus offset. Numerous regions including the anterior cingulate cortex, hippocampus, IFG, MTG, OFC, and striatum, predicted the pain rating at stimulus onset. However, only the amygdala and fusiform gyrus predicted increased pain ratings at stimulus offset. We characterized the spatiotemporal representations of binary and graded painful responses during tonic pain stimuli. Our study provides evidence from intracranial recordings that the neural encoding of psychophysical pain changes over time during a tonic thermal stimulus, with different brain regions being predictive of pain at the beginning and end of the stimulus.

Identifiers

PMID36945412
PMCPMC10028876
OpenAlexW4323818566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.