Evidence map›Paper›PMID 36337080›Full record

ArticleNeurotrauma reports2022

Blood-Based Biomarkers of Repetitive, Subconcussive Blast Overpressure Exposure in the Training Environment: A Pilot Study.

Denes V Agoston, Jesse McCullough, Roxanne Aniceto, I-Hsuan Lin, Alaa Kamnaksh, Michael Eklund, Wallace M Graves, Cyrus Dunbar, James Engall, Eric B Schneider and 2 more

Open access · goldAbstract read
In one paragraph

Article in Neurotrauma reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Denes V AgostonDepartment of Anatomy, Physiology, and Genetics, Uniformed Services University, Bethesda, Maryland, USA.
Jesse McCulloughDepartment of Anatomy, Physiology, and Genetics, Uniformed Services University, Bethesda, Maryland, USA.
Roxanne AnicetoDepartment of Anatomy, Physiology, and Genetics, Uniformed Services University, Bethesda, Maryland, USA.
I-Hsuan LinDepartment of Anatomy, Physiology, and Genetics, Uniformed Services University, Bethesda, Maryland, USA.
Alaa KamnakshDepartment of Anatomy, Physiology, and Genetics, Uniformed Services University, Bethesda, Maryland, USA.
Michael EklundDepartment of Anatomy, Physiology, and Genetics, Uniformed Services University, Bethesda, Maryland, USA.
Wallace M GravesNeuroTactical Research Team, Marine Corps Base Camp Pendleton, Camp Pendleton, California, USA.
Cyrus DunbarNeuroTactical Research Team, Marine Corps Base Camp Pendleton, Camp Pendleton, California, USA.
James EngallNeuroTactical Research Team, Marine Corps Base Camp Pendleton, Camp Pendleton, California, USA.
Eric B SchneiderDepartment of Surgery, Yale School of Medicine, New Haven, Connecticut, USA.
Fabio LeonessaDepartment of Neurology, Uniformed Services University, Bethesda, Maryland, USA.
Josh L DuckworthNeuroTactical Research Team, Marine Corps Base Camp Pendleton, Camp Pendleton, California, USA.
Uniformed Services University of the Health Sciences · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because of their unknown long-term effects, repeated mild traumatic brain injuries (TBIs), including the low, subconcussive ones, represent a specific challenge to healthcare systems. It has been hypothesized that they can have a cumulative effect, and they may cause molecular changes that can lead to chronic degenerative processes. Military personnel are especially vulnerable to consequences of subconcussive TBIs because their training involves repeated exposures to mild explosive blasts. In this pilot study, we collected blood samples at baseline, 6 h, 24 h, 72 h, 2 weeks, and 3 months after heavy weapons training from students and instructors who were exposed to repeated subconcussive blasts. Samples were analyzed using the reverse and forward phase protein microarray platforms. We detected elevated serum levels of glial fibrillary acidic protein, ubiquitin C-terminal hydrolase L1 (UCH-L1), nicotinic alpha 7 subunit (CHRNA7), occludin (OCLN), claudin-5 (CLDN5), matrix metalloprotease 9 (MMP9), and intereukin-6 (IL-6). Importantly, serum levels of most of the tested protein biomarkers were the highest at 3 months after exposures. We also detected elevated autoantibody titers of proteins related to vascular and neuroglia-specific proteins at 3 months after exposures as compared to baseline levels. These findings suggest that repeated exposures to subconcussive blasts can induce molecular changes indicating not only neuron and glia damage, but also vascular changes and inflammation that are detectable for at least 3 months after exposures whereas elevated titers of autoantibodies against vascular and neuroglia-specific proteins can indicate an autoimmune process.

Indexed as

biomarkerbloodheavyproteintrainingweapons

Identifiers

PMID36337080
PMCPMC9634979
OpenAlexW4308023968

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.