Evidence map›Paper›PMID 34827575›Full record

ArticleBiomolecules2021

Assessing Protein Biomarkers to Detect Lethal Acute Traumatic Brain Injuries in Cerebrospinal Fluid.

Johann Zwirner, Simone Bohnert, Heike Franke, Jack Garland, Niels Hammer, Dustin Möbius, Rexson Tse, Benjamin Ondruschka

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  4. The polychromatism of postmortem cerebrospinal fluid.Forensic science, medicine, and pathology · 2025
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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

8 authors at 6 institutions in 4 countries.

Johann ZwirnerDepartment of Anatomy, University of Otago, Dunedin 9016, New Zealand.
Simone BohnertInstitute of Forensic Medicine, University of Wuerzburg, 97078 Wuerzburg, Germany.
Heike FrankeRudolf Boehm Institute of Pharmacology and Toxicology, University of Leipzig, 04107 Leipzig, Germany.ORCID 0000-0001-7126-6146
Jack GarlandForensic and Analytical Science Service, NSW Health Pathology, Lidcombe 2141, Australia.
Niels HammerInstitute of Macroscopic and Clinical Anatomy, University of Graz, 8010 Graz, Austria.ORCID 0000-0001-8230-9383
Dustin MöbiusInstitute of Legal Medicine, University Medical Center Hamburg-Eppendorf, 22529 Hamburg, Germany.
Rexson TseDepartment of Forensic Pathology, LabPLUS, Auckland City Hospital, Auckland 1148, New Zealand.
Benjamin OndruschkaInstitute of Legal Medicine, University Medical Center Hamburg-Eppendorf, 22529 Hamburg, Germany.
Universität Hamburg · DEAuckland City Hospital · NZLeipzig University · DENew South Wales Department of Health · AUUniversity of Graz · ATUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diagnosing traumatic brain injury (TBI) from body fluids in cases where there are no obvious external signs of impact would be useful for emergency physicians and forensic pathologists alike. None of the previous attempts has so far succeeded in establishing a single biomarker to reliably detect TBI with regards to the sensitivity: specificity ratio in a post mortem setting. This study investigated a combination of body fluid biomarkers (obtained post mortem), which may be a step towards increasing the accuracy of biochemical TBI detection. In this study, serum and cerebrospinal fluid (CSF) samples from 30 acute lethal TBI cases and 70 controls without a TBI-related cause of death were evaluated for the following eight TBI-related biomarkers: brain-derived neurotrophic factor (BDNF), ferritin, glial fibrillary acidic protein (GFAP), interleukin 6 (IL-6), lactate dehydrogenase, neutrophil gelatinase-associated lipocalin (NGAL), neuron-specific enolase and S100 calcium-binding protein B. Correlations among the individual TBI biomarkers were assessed, and a specificity-accentuated threshold value analysis was conducted for all biomarkers. Based on these values, a decision tree modelling approach was performed to assess the most accurate biomarker combination to detect acute lethal TBIs. The results showed that 92.45% of acute lethal TBIs were able to be diagnosed using a combination of IL-6 and GFAP in CSF. The probability of detecting an acute lethal TBI was moderately increased by GFAP alone and considerably increased by the remaining biomarkers. BDNF and NGAL were almost perfectly correlated (

Indexed as

BiomarkersBrain-Derived Neurotrophic FactorBrain Injuries, TraumaticGlial Fibrillary Acidic ProteinLipocalin-2AdultAgedCase-Control StudiesFemaleFerritinsHumansInterleukin-6L-Lactate DehydrogenaseMaleMiddle AgedPhosphopyruvate HydrataseBDNF protein, humanBiomarkersBrain-Derived Neurotrophic FactorENO2 protein, humanFerritinsGFAP protein, humanGlial Fibrillary Acidic ProteinIL6 protein, humanInterleukin-6LCN2 protein, humanLipocalin-2L-Lactate DehydrogenasePhosphopyruvate HydrataseS100 Calcium Binding Protein beta Subunitbiomarker combinationglial fibrillary acidic proteininterleukin-6post mortem biochemistrytraumatic brain injury

Identifiers

PMID34827575
PMCPMC8615532
OpenAlexW3208364149

What OpenQuestion holds

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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.