Evidence map›Paper›PMID 41963069›Full record

ArticleJournal of neurophysiology2026

Therapy-specific motoneuron activation with epidural and dorsal root ganglion stimulation in spinal cord injury.

Anders J Asp, Megan L Gill, K A Fernandez, Daniel D Veith, Margaux B Linde, Candee J Mills, Andrew R Thoreson, Jon M Hagedorn, Mark A Bendel, Rayyan A Iqbal and 4 more

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2026. 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.

No citing paper in PubMed yet.

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

14 authors.

Anders J AspAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-7793-9951
Megan L GillAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.
K A FernandezMayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-3231-9003
Daniel D VeithAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0001-8250-3848
Margaux B LindeAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0009-0007-4427-3501
Candee J MillsAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0009-0009-8015-8660
Andrew R ThoresonAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.
Jon M HagedornDepartment of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, United States.
Mark A BendelDepartment of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, United States.
Rayyan A IqbalDepartment of Chemistry, University of Illinois Urbana-Champagne, Urbana, Illinois, United States.ORCID 0009-0004-9544-9819
Dimitry G SayenkoDepartment of Neurosurgery, Houston Methodist, Houston, Texas, United States.ORCID 0000-0002-4154-6873
Ryan J SolinskyAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-7121-8678
Kristin D ZhaoAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.
Peter J GrahnAssistive and Restorative Technology Laboratory, Rehabilitation Medicine Research Center, Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-2976-814X

Funding

Elucidating spinal sensorimotor network components that underlie recovery of motor functions via lumbosacral epidural electrical stimulation in humans with spinal cord injuryR01NS115877 · NINDS · MAYO CLINIC ROCHESTER · PI GRAHN, PETER JONAS · 2020 to 2024
$3.0M
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS115877Mayo Foundation for Medical Education and Research (MFMER)Minnesota Office of Higher Education (OHE) 191542Minnesota Office of Higher Education (OHE) 214556NINDS NIH HHS R01 NS115877
6 · The paper itself

Abstract

Over the past decade, there has been a remarkable increase in the number of clinical trials using electrical spinal cord stimulation to alleviate sensorimotor dysfunctions caused by traumatic spinal cord injury (SCI). Interestingly, despite using different stimulation modalities across studies, such as epidural stimulation (ES) or dorsal root ganglia stimulation (DRGS), similar motor outcomes have been achieved, and in turn, strengthened momentum to translate spinal stimulation as a robust clinical tool for SCI rehabilitation. To investigate how spinal stimulation affects motor outcomes, surface electromyography is used to assess muscle activity in response to specific stimulation parameters (e.g., frequency, amplitude) and contact configurations. We characterized lower extremity evoked responses produced by ES and DRGS in 19 clinical trial participants with traumatic SCI. Our results showed that at threshold intensity, ES demonstrated bias for activating distal muscles whereas DRGS preferentially activated proximal muscles ipsilateral to the stimulation electrode. Following paired stimulation pulses spaced 50 ms apart, suppression of the second pulse response was observed in both modalities for all participants, while more pronounced suppression was observed with ES compared with DRGS. DRGS-evoked electromyography (EMG) response latencies were shorter compared with ES-evoked EMG response across proximal leg muscles. Altogether, these results demonstrate that ES and DRGS activate motoneurons projecting to lower extremity muscles through distinct yet overlapping mechanisms. These electrophysiological signatures are unique to each stimulation modality and may guide individually tailored therapies to improve task-specific lower extremity motor function.

Indexed as

Ganglia, SpinalMotor NeuronsSpinal Cord InjuriesSpinal Cord StimulationAdultElectromyographyEpidural SpaceFemaleHumansMaleMiddle AgedMuscle, Skeletaldorsal root ganglionepiduralneuromodulationspinal cord injuryspinal cord stimulation

Identifiers

PMID41963069
PMCPMC13178577

What Socratic 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 Socratic graph.