Evidence map›Paper›PMID 34223546›Full record

ArticleNeurotrauma reports2021

Spatial Distribution of Neuropathology and Neuroinflammation Elucidate the Biomechanics of Fluid Percussion Injury.

Joshua A Beitchman, Jonathan Lifshitz, Neil G Harris, Theresa Currier Thomas, Audrey D Lafrenaye, Anders Hånell, C Edward Dixon, John T Povlishock, Rachel K Rowe

Open access · goldAbstract read
In one paragraph

Article in Neurotrauma reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
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  8. Review
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

9 authors at 6 institutions in 2 countries.

Joshua A BeitchmanBARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
Jonathan LifshitzBARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
Neil G HarrisUCLA Brain Injury Research Center, Department of Neurosurgery, and Intellectual Development and Disabilities Research Center, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, USA.
Theresa Currier ThomasBARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
Audrey D LafrenayeVirginia Commonwealth University, Richmond, Virginia, USA.
Anders HånellVirginia Commonwealth University, Richmond, Virginia, USA.
C Edward DixonUniversity of Pittsburgh, Pittsburgh, Pennsylvania, USA.
John T PovlishockVirginia Commonwealth University, Richmond, Virginia, USA.
Rachel K RoweBARROW Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.
Barrow Neurological Institute · USVirginia Commonwealth University · USMidwestern University · USUniversity of California, Los Angeles · USUniversity of Pittsburgh · USUppsala University Hospital · SE

Funding

RRD VA I01 RX002472RRD VA I01 RX002691
6 · The paper itself

Abstract

Diffuse brain injury is better described as multi-focal, where pathology can be found adjacent to seemingly uninjured neural tissue. In experimental diffuse brain injury, pathology and pathophysiology have been reported far more lateral than predicted by the impact site. We hypothesized that local thickening of the rodent skull at the temporal ridges serves to focus the intracranial mechanical forces experienced during brain injury and generate predictable pathology. We demonstrated local thickening of the skull at the temporal ridges using contour analysis on magnetic resonance imaging. After diffuse brain injury induced by midline fluid percussion injury (mFPI), pathological foci along the anterior-posterior length of cortex under the temporal ridges were evident acutely (1, 2, and 7 days) and chronically (28 days) post-injury by deposition of argyophilic reaction product. Area CA3 of the hippocampus and lateral nuclei of the thalamus showed pathological change, suggesting that mechanical forces to or from the temporal ridges shear subcortical regions. A proposed model of mFPI biomechanics suggests that injury force vectors reflect off the skull base and radiate toward the temporal ridge, thereby injuring ventral thalamus, dorsolateral hippocampus, and sensorimotor cortex. Surgically thinning the temporal ridge before injury reduced injury-induced inflammation in the sensorimotor cortex. These data build evidence for temporal ridges of the rodent skull to contribute to the observed pathology, whether by focusing extracranial forces to enter the cranium or intracranial forces to escape the cranium. Pre-clinical investigations can take advantage of the predicted pathology to explore injury mechanisms and treatment efficacy.

Indexed as

biomechanicsFPIhistopathologytemporal ridge

Identifiers

PMID34223546
PMCPMC8240834
OpenAlexW3127927697

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.