Evidence map›Paper›PMID 27288907›Full record

ArticleJournal of neuropathology and experimental neurology2016

Delayed Hypoxemia Following Traumatic Brain Injury Exacerbates White Matter Injury.

Umang Parikh, Melissa Williams, Addison Jacobs, Jose A Pineda, David L Brody, Stuart H Friess

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Recombinant Erythropoietin Induces Oligodendrocyte Progenitor Cell Proliferation After Traumatic Brain Injury and Delayed Hypoxemia.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
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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

6 authors at 1 institution in 1 country.

Umang ParikhFrom the Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri (UP, MW, AJ, JAP, SHF)Department of Neurology, Washington University School of Medicine, St. Louis, Missouri (DLB).
Melissa WilliamsFrom the Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri (UP, MW, AJ, JAP, SHF)Department of Neurology, Washington University School of Medicine, St. Louis, Missouri (DLB).
Addison JacobsFrom the Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri (UP, MW, AJ, JAP, SHF)Department of Neurology, Washington University School of Medicine, St. Louis, Missouri (DLB).
Jose A PinedaFrom the Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri (UP, MW, AJ, JAP, SHF)Department of Neurology, Washington University School of Medicine, St. Louis, Missouri (DLB).
David L BrodyFrom the Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri (UP, MW, AJ, JAP, SHF)Department of Neurology, Washington University School of Medicine, St. Louis, Missouri (DLB).
Stuart H FriessFrom the Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri (UP, MW, AJ, JAP, SHF)Department of Neurology, Washington University School of Medicine, St. Louis, Missouri (DLB). Friess_S@kids.wustl.edu.
Washington University in St. Louis · US

Funding

Mechanisms Underlying Tauopathy Following Traumatic Brain InjuryR01NS065069 · NINDS · WASHINGTON UNIVERSITY · PI BRODY, DAVID L · 2009 to 2017
$3.3M
Modulating Secondary Damage Following Traumatic Brain Injury in the ChildK08NS064051 · NINDS · WASHINGTON UNIVERSITY · PI FRIESS, STUART H · 2010 to 2014
$820k
WHOLE SLIDE IMAGING SYSTEM FOR TRANSLATIONAL NEUROSCIENCES10RR027552 · NCRR · WASHINGTON UNIVERSITY · PI LEE, JIN-MOO · 2010 to 2010
$275k
NCRR NIH HHS S10 RR027552NINDS NIH HHS K08 NS064051NINDS NIH HHS R01 NS065069
6 · The paper itself

Abstract

Hypoxemia immediately following traumatic brain injury (TBI) has been observed to exacerbate injury. However, it remains unclear whether delayed hypoxemia beyond the immediate postinjury period influences white matter injury. In a retrospective clinical cohort of children aged 4-16 years admitted with severe TBI, 28/74 (35%) patients were found to experience delayed normocarbic hypoxemia within 7 days of admission. Based on these clinical findings, we developed a clinically relevant mouse model of TBI with delayed hypoxemia by exposing 5-week old (adolescent) mice to hypoxic conditions for 30 minutes starting 24 hours after moderate controlled cortical impact (CCI). Injured mice with hypoxemia had increased axonal injury using both β-amyloid precursor protein and NF200 immunostaining in peri-contusional white matter compared with CCI alone. Furthermore, we detected increased peri-contusional white matter tissue hypoxia with pimonidazole and augmented astrogliosis with anti-glial fibrillary acidic protein staining in CCI + delayed hypoxemia compared with CCI alone or sham surgery + delayed hypoxemia. Microglial activation as evidenced by Iba1 staining was not significantly altered by delayed hypoxemia. These clinical and experimental data indicate the prevention or amelioration of delayed hypoxemia effects following TBI may provide a unique opportunity for the development of therapeutic interventions to reduce axonal injury and improve clinical outcomes.

Indexed as

Axonal injuryBrain hypoxiaControlled cortical impactDelayed hypoxemiaSecondary injuryTraumatic brain injury

Identifiers

PMID27288907
PMCPMC7299434
OpenAlexW2412925914

What OpenQuestion holds

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LicenceCC BY-NC
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.