Evidence map›Paper›PMID 33589720›Full record

ArticleScientific reports2021

Exploring the predictive value of lesion topology on motor function outcomes in a porcine ischemic stroke model.

Kelly M Scheulin, Brian J Jurgielewicz, Samantha E Spellicy, Elizabeth S Waters, Emily W Baker, Holly A Kinder, Gregory A Simchick, Sydney E Sneed, Janet A Grimes, Qun Zhao and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

12 authors.

Kelly M Scheulin *Regenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Brian J Jurgielewicz *Regenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Samantha E SpellicyRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Elizabeth S WatersRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Emily W BakerAruna Bio Inc, Athens, GA, USA.
Holly A KinderRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Gregory A SimchickRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Sydney E SneedRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Janet A GrimesDepartment of Small Animal Medicine and Surgery, College of Veterinary Medicine, University of Georgia, Athens, GA, USA.
Qun ZhaoRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Steven L SticeRegenerative Bioscience Center, University of Georgia, Athens, GA, USA.
Franklin D WestRegenerative Bioscience Center, University of Georgia, Athens, GA, USA. WestF@uga.edu.

Funding

Human Neural Cell Exosomes as a therapeutic treatment for strokeR43NS103596 · NINDS · ARUNA BIOMEDICAL, INC. · PI WEBB, ROBIN L · 2017 to 2017
$500k
NINDS NIH HHS R43 NS103596
6 · The paper itself

Abstract

Harnessing the maximum diagnostic potential of magnetic resonance imaging (MRI) by including stroke lesion location in relation to specific structures that are associated with particular functions will likely increase the potential to predict functional deficit type, severity, and recovery in stroke patients. This exploratory study aims to identify key structures lesioned by a middle cerebral artery occlusion (MCAO) that impact stroke recovery and to strengthen the predictive capacity of neuroimaging techniques that characterize stroke outcomes in a translational porcine model. Clinically relevant MRI measures showed significant lesion volumes, midline shifts, and decreased white matter integrity post-MCAO. Using a pig brain atlas, damaged brain structures included the insular cortex, somatosensory cortices, temporal gyri, claustrum, and visual cortices, among others. MCAO resulted in severely impaired spatiotemporal gait parameters, decreased voluntary movement in open field testing, and higher modified Rankin Scale scores at acute timepoints. Pearson correlation analyses at acute timepoints between standard MRI metrics (e.g., lesion volume) and functional outcomes displayed moderate R values to functional gait outcomes. Moreover, Pearson correlation analyses showed higher R values between functional gait deficits and increased lesioning of structures associated with motor function, such as the putamen, globus pallidus, and primary somatosensory cortex. This correlation analysis approach helped identify neuroanatomical structures predictive of stroke outcomes and may lead to the translation of this topological analysis approach from preclinical stroke assessment to a clinical biomarker.

Indexed as

AnimalsBrainBrain IschemiaDisease Models, AnimalGaitHumansInfarction, Middle Cerebral ArteryIschemic StrokeMagnetic Resonance ImagingMotor ActivityRecovery of FunctionSomatosensory CortexSwine

Identifiers

PMID33589720
PMCPMC7884696

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Registered trials

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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.