Evidence map›Paper›PMID 39191173›Full record

Observational studyEBioMedicine2024

Association of early blood-based biomarkers and six-month functional outcomes in conventional severity categories of traumatic brain injury: capturing the continuous spectrum of injury.

Lindsay Wilson, Virginia F J Newcombe, Daniel P Whitehouse, Stefania Mondello, Andrew I R Maas, David K Menon, CENTER-TBI participants and investigators

Abstract readObservational Study
In one paragraph

Observational study in EBioMedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Review
  8. Update on traumatic brain injury in the ICU.Current opinion in anaesthesiology · 2025
    Review
  9. Article
  10. Observational
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

7 authors.

Lindsay WilsonDivision of Psychology, University of Stirling, Stirling, United Kingdom. Electronic address: l.wilson@stir.ac.uk.
Virginia F J NewcombeDivision of Anaesthesia and PACE, Department of Medicine, University of Cambridge, Cambridge, United Kingdom.
Daniel P WhitehouseDivision of Anaesthesia and PACE, Department of Medicine, University of Cambridge, Cambridge, United Kingdom.
Stefania MondelloDepartment of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.
Andrew I R MaasDepartment of Neurosurgery, Antwerp University Hospital, Edegem, Belgium; Department of Translational Neuroscience, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.
David K MenonDivision of Anaesthesia and PACE, Department of Medicine, University of Cambridge, Cambridge, United Kingdom.
CENTER-TBI participants and investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTraumatic brain injury is conventionally categorised as mild, moderate, or severe on the Glasgow Coma Scale (GCS). Recently developed biomarkers can provide more objective and nuanced measures of the extent of brain injury.

methodsExposure-response relationships were investigated in 2479 patients aged ≥16 enrolled in the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) prospective observational cohort study. Neurofilament protein-light (NFL), ubiquitin carboxy-terminal hydrolase L1 (UCH-L1), and glial fibrillary acidic protein (GFAP) were assayed from serum sampled in the first 24 h; concentrations were divided into quintiles within GCS severity groups. Relationships with the Glasgow Outcome Scale-Extended were examined using modified Poisson regression including age, sex, major extracranial injury, time to sample, and log biomarker concentration as covariates.

findingsWithin severity groups there were associations between biomarkers and outcomes after adjustment for covariates: GCS 13-15 and negative CT imaging (relative risks [RRs] from 1.28 to 3.72), GCS 13-15 and positive CT (1.21-2.81), GCS 9-12 (1.16-2.02), GCS 3-8 (1.09-1.94). RRs were associated with clinically important differences in expectations of prognosis. In patients with GCS 3 (RRs 1.51-1.80) percentages of unfavourable outcome were 37-51% in the lowest quintiles of biomarker levels and reached 90-94% in the highest quintiles. Similarly, for GCS 15 (RRs 1.83-3.79), the percentages were 2-4% and 19-28% in the lowest and highest biomarker quintiles, respectively.

interpretationConventional TBI severity classification is inadequate and underestimates heterogeneity of brain injury and associated outcomes. The adoption of circulating biomarkers can add to clinical assessment of injury severity.

fundingEuropean Union 7th Framework program (EC grant 602150), Hannelore Kohl Stiftung, One Mind, Integra LifeSciences, Neuro-Trauma Sciences, NIHR Rosetrees Trust.

Indexed as

BiomarkersBrain Injuries, TraumaticAdolescentAdultAgedFemaleGlasgow Coma ScaleGlial Fibrillary Acidic ProteinHumansMaleMiddle AgedNeurofilament ProteinsPrognosisProspective StudiesSeverity of Illness IndexUbiquitin ThiolesteraseBiomarkersGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament ProteinsUbiquitin ThiolesteraseUCHL1 protein, humanBlood biomarkersGFAPNFLOutcomesTraumatic brain injuryUCH-L1

Identifiers

PMID39191173
PMCPMC11400615

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Registered trials

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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.