Evidence map›Paper›PMID 35320026›Full record

ArticleJournal of neurophysiology2022

Subthalamic deep brain stimulation of an anatomically detailed model of the human hyperdirect pathway.

Clayton S Bingham, Cameron C McIntyre

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Prospective Connectomic-Based Deep Brain Stimulation Programming for Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  6. A survey on integral equations for bioelectric modeling.Physics in medicine and biology · 2024
    Review
  7. Article
  8. Coupled Activation of the Hyperdirect and Cerebellothalamic Pathways with Zona Incerta Deep Brain Stimulation.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Clayton S BinghamDepartment of Biomedical Engineering, Duke University, Durham, North Carolina.ORCID 0000-0001-5850-1308
Cameron C McIntyreDepartment of Biomedical Engineering, Duke University, Durham, North Carolina.ORCID 0000-0003-0932-854X

Funding

Augmented Reality Platform for Deep Brain StimulationR01NS105690 · NINDS · DUKE UNIVERSITY · PI MCINTYRE, CAMERON · 2018 to 2022
$2.2M
Biophysical Characterization of Subthalamic Local Field Potentials in Parkinson's DiseaseR01NS119520 · NINDS · DUKE UNIVERSITY · PI MCINTYRE, CAMERON · 2021 to 2024
$1.9M
NINDS NIH HHS R01 NS105690NINDS NIH HHS R01 NS119520
6 · The paper itself

Abstract

The motor hyperdirect pathway (HDP) is considered a key target in the treatment of Parkinson's disease with subthalamic deep brain stimulation (DBS). This hypothesis is partially derived from the association of HDP activation with evoked potentials (EPs) generated in the motor cortex and subthalamic nucleus (STN) after a DBS pulse. However, the biophysical details of how and when DBS-induced action potentials (APs) in HDP neurons reach their terminations in the cortex or STN remain unclear. Therefore, we used an anatomically detailed representation of the motor HDP, as well as the internal capsule (IC), in a model of human subthalamic DBS to explore AP activation and transmission in the HDP and IC. Our results show that small diameter HDP axons exhibited AP initiation in their subthalamic terminal arbor, which resulted in relatively long transmission latencies to cortex (∼3.5-8 ms). Alternatively, large diameter HDP axons were most likely to be directly activated in the capsular region, which resulted in short transmission times to the cortex (∼1-3 ms). However, those large diameter HDP antidromic APs would be indistinguishable from any other IC axons that were also activated by the stimulus. Conversely, DBS-induced APs in both small and large diameter HDP axons reached their synaptic boutons in the STN with similar timings, but both spanned a wide temporal range (∼0.5-5 ms). We also found that using anodic or bipolar stimulation helped to bias activation of the HDP over the IC. These computational results provide useful information for linking HDP activation with EP recordings in clinical experiments.

Indexed as

Deep Brain StimulationMotor CortexParkinson DiseaseSubthalamic NucleusAction PotentialsHumansaxonbasal gangliadeep brain stimulationmotor cortexsubthalamic nucleus

Identifiers

PMID35320026
PMCPMC9054256

What OpenQuestion holds

Textmetadata
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.