Evidence map›Paper›PMID 37509599›Full record

ArticleBiomedicines2023

Persistence of Hyper-Ramified Microglia in Porcine Cortical Gray Matter after Mild Traumatic Brain Injury.

Michael R Grovola, Alan Jinich, Nicholas Paleologos, Edgardo J Arroyo, Kevin D Browne, Randel L Swanson, John E Duda, D Kacy Cullen

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Quantifying microglial morphology: an insight into function.Clinical and experimental immunology · 2024
    Review
  6. 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

8 authors at 1 institution in 1 country.

Michael R GrovolaCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0003-4125-9329
Alan JinichCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0009-0001-9139-3756
Nicholas PaleologosCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0002-5110-9378
Edgardo J ArroyoCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.
Kevin D BrowneCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0002-5604-3021
Randel L SwansonCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0002-2707-2333
John E DudaCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0002-7282-2201
D Kacy CullenCenter for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0002-5355-5216
Philadelphia VA Medical Center · US

Funding

Tissue Engineered Rostral Migratory Stream for Directed Neuronal ReplacementR01NS117757 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI CULLEN, DANIEL KACY · 2021 to 2025
$2.9M
Chronic Neurodegenerative Sequelae Driven by Neuroinflammation After Mild TBIR03NS116301 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI CULLEN, DANIEL KACY · 2020 to 2020
$162k
SDR: Genomic analysis of blast tube induced TBI in miceI01BX005017 · VA · PHILADELPHIA VA MEDICAL CENTER · PI CULLEN, DANIEL KACY · 2020 to 2024
–
Chronic neurodegenerative and neurophysiological sequela of closed-head TBII01RX001097 · VA · PHILADELPHIA VA MEDICAL CENTER · PI DUDA, JOHN ERIC · 2015 to 2018
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Traumatic and Treatable Vascular Pathology in the Outcome of TBIIK2RX003651 · VA · PHILADELPHIA VA MEDICAL CENTER · PI SWANSON, RANDEL L · 2022 to 2025
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BLRD VA I01 BX005017NIH HHS NINDS R01-NS117757NIH HHS NINDS R03-NS116301NINDS NIH HHS R01 NS117757NINDS NIH HHS R03 NS116301RRD VA I01 RX001097RRD VA IK2 RX003651
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a major contributor to morbidity and mortality in the United States as several million people visit the emergency department every year due to TBI exposures. Unfortunately, there is still no consensus on the pathology underlying mild TBI, the most common severity sub-type of TBI. Previous preclinical and post-mortem human studies have detailed the presence of diffuse axonal injury following TBI, suggesting that white matter pathology is the predominant pathology of diffuse brain injury. However, the inertial loading produced by TBI results in strain fields in both gray and white matter. In order to further characterize gray matter pathology in mild TBI, our lab used a pig model (n = 25) of closed-head rotational acceleration-induced TBI to evaluate blood-brain barrier disruptions, neurodegeneration, astrogliosis, and microglial reactivity in the cerebral cortex out to 1 year post-injury. Immunohistochemical staining revealed the presence of a hyper-ramified microglial phenotype-more branches, junctions, endpoints, and longer summed process length-at 30 days post injury (DPI) out to 1 year post injury in the cingulate gyrus (

Indexed as

fibrinogenlarge animal modelsmicrogliamild TBIneuroinflammation

Identifiers

PMID37509599
PMCPMC10377269
OpenAlexW4384068127

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.