Evidence map›Paper›PMID 40680598›Full record

ArticleThe Journal of surgical research2025

Inflammatory Cytokines Outperform Endotheliopathy Markers as Early Predictors of Mortality in Trauma.

Ellen R Becker, Adam D Price, Gregory C Wetmore, Robert C Shondel, Rebecca M Schuster, Maia P Smith, Timothy A Pritts, Michael D Goodman

Abstract readComparative Study
In one paragraph

Article in The Journal of surgical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Ellen R BeckerDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Adam D PriceDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Gregory C WetmoreDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Robert C ShondelDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Rebecca M SchusterDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Maia P SmithDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Timothy A PrittsDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio.
Michael D GoodmanDepartment of Surgery, University of Cincinnati, Cincinnati, Ohio. Electronic address: arndten@ucmail.uc.edu.

Funding

HOST RESPONSE TO TRAUMA RESEARCH TRAINING PROGRAMT32GM008478 · NIGMS · UNIVERSITY OF CINCINNATI · PI TIMOTHY A PRITTS, BASILIA ZINGARELLI · 1993 to 2026
$6.7M
Hemorrhage and hemorrheology – the critical interaction of the erythrocyte and the endothelium after injuryR35GM156315 · NIGMS · UNIVERSITY OF CINCINNATI · PI Michael Goodman · 2025 to 2026
$810k
NIGMS NIH HHS R35 GM156315NIGMS NIH HHS T32 GM008478
6 · The paper itself

Abstract

introductionTrauma induces cellular injury, coagulopathy, and a dysregulated physiologic response that results from endotheliopathy and the inflammatory response. This study aimed to compare early serum markers of endotheliopathy versus inflammatory cytokines to predict 30-day mortality in critically ill trauma patients.

methodsSerum samples were collected from 232 trauma patients on admission to the intensive care unit. Twelve endothelial markers were analyzed, including angiopoietin 1, E-selectin, P-selectin, syndecan-1, thrombomodulin, and vascular endothelial growth factors. Inflammatory cytokines analyzed included eotaxin, interleukin (IL) 1 receptor antagonist, IL-6, IL-8, IL-10, interferon-gamma inducible protein-10, and monocyte chemoattractant protein-. The primary outcome was 30-day mortality with subgroup analyses based on transfusion status at 6 hours.

resultsSubjects were 67% White, 67% male, with a median age of 58 years (34, 75). Injuries were 88% blunt with a median injury severity score of 21 (14, 30) and a 7.3% mortality rate. Mortality did not differ by transfusion status. No endothelial marker was associated with mortality, even for transfusion subgroups. By contrast, six inflammatory cytokines were associated with 30-day mortality (P < 0.05). Inflammatory markers remained associated with mortality in the no transfusion cohort for eotaxin (P = 0.04), IL-6 (P = 0.005), and IL-8 (P = 0.02), and the submassive transfusion cohort for IL-6 (P = 0.045), IL-8 (P = 0.04), and interferon-gamma inducible protein-10 (P = 0.02).

conclusionsPostinjury inflammatory markers collected at the time of intensive care unit admission offer potential 30-day mortality predictive value even in patients who do not undergo massive transfusion. In contrast, early markers of endotheliopathy may not predict mortality.

Indexed as

CytokinesEndothelium, VascularWounds and InjuriesAdultAgedBiomarkersCritical IllnessFemaleHumansInjury Severity ScoreMaleMiddle AgedPredictive Value of TestsPrognosisProspective StudiesBiomarkersCytokinesEndothelial injuryEndotheliopathyMortalityTrauma

Identifiers

PMID40680598
PMCPMC12710749

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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.