Evidence map›Paper›PMID 40656637›Full record

ArticleBrain, behavior, & immunity - health2025

Systemic S100A8/A9 in patients with moderate to severe acute ischemic stroke: Exploratory analysis of inflammation and functional outcome.

Christoph Vollmuth, Felipe A Montellano, Cornelia Fiessler, Fabian Essig, Christian Hametner, Alexander M Kollikowski, Vivian Vogt, Mirko Pham, Peter U Heuschmann, Karl Georg Haeusler and 3 more

Abstract read
In one paragraph

Article in Brain, behavior, & immunity - health, 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. Review
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

13 authors.

Christoph VollmuthUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.
Felipe A MontellanoUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.
Cornelia FiesslerUniversity of Würzburg, Institute for Clinical Epidemiology and Biometry, Würzburg, Germany.
Fabian EssigUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.
Christian HametnerUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.
Alexander M KollikowskiUniversity Hospital Würzburg (UKW), Department of Neuroradiology, Würzburg, Germany.
Vivian VogtUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.
Mirko PhamUniversity Hospital Würzburg (UKW), Department of Neuroradiology, Würzburg, Germany.
Peter U HeuschmannUniversity of Würzburg, Institute for Clinical Epidemiology and Biometry, Würzburg, Germany.
Karl Georg HaeuslerUniversity Hospital Ulm, Department of Neurology, Ulm, Germany.
Guido StollInstitute of Experimental Biomedicine I, University Hospital Würzburg, Germany.
Hermann NeugebauerUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.
Michael K SchuhmannUniversity Hospital Würzburg (UKW), Department of Neurology, Würzburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: S100A8/A9, a danger-associated molecular pattern (DAMP), is released from leukocytes, mainly neutrophils, and augments inflammation and tissue damage. The role of systemic plasma levels of S100A8/A9 in stroke-related inflammation and its association with clinical outcome lacks sufficient data. Methods: Prospective, monocentric, observational study including patients with moderate to severe acute ischemic anterior circulation stroke [National Institutes of Health Stroke Scale (NIHSS) score ≥6 points and/or mechanical recanalization)]. We assessed functional outcome by telephone interview 3 months (±14 days) after stroke using the 7-point modified Rankin Scale (mRS). Poor outcome was defined as mRS ≥3. Systemic plasma levels of S100A8/A9 were determined by ELISA <48 h after onset of symptoms, alongside a differential blood count. Univariable and multivariable logistic regression were performed to investigate the association between systemic plasma levels of S100A8/A9 and functional outcome. Results: Between June 2020 and September 2022, a total of 272 patients were enrolled [52 % female, median age 79 years (IQR: 66-84), median NIHSS score on admission 13 (IQR: 8-17), median ASPECTS 8 (IQR: 6-9)]. Of these, 220 patients (81 %) underwent mechanical recanalization, and 118 (43 %) received systemic thrombolytic therapy. There was a significant correlation between systemic plasma levels of S100A8/A9 and neutrophil counts at baseline [p < 0.0001; r = 0.33 (95 % confidence interval: 0.22; 0.44)]. At 3 months, 192 of 272 (71 %) patients had poor functional outcome, who had significantly higher systemic plasma levels of S100A8/A9 at baseline [median: 525 ng/ml (IQR: 342-897)] than those with good functional outcome [397 ng/ml (IQR: 232-580); p = 0.001]. Furthermore, systemic plasma levels of S100A8/A9 at baseline were associated with poor outcome [unadjusted odds ratio (OR): 2.01 (95 %CI: 1.04-3.96)], however this association was attenuated and no longer significant when adjusting for age, sex, NIHSS Score on admission, ASPECT Score on admission and recanalization therapy (yes/no) [adjusted OR: 1.92 (95 %CI: 0.86-4.34)]. Conclusions: Systemic plasma levels of S100A8/A9 were associated with poor outcome in patients with moderate to severe ischemic stroke. The observed correlation with neutrophil counts at baseline might underscore an important pathophysiological link between patients' prognosis and stroke-related inflammation. Study registration: DRKS00022064.

Indexed as

Blood-based biomarkerCalprotectinDanger-associated molecular patternsInflammationPrognosisS100A8/A9

Identifiers

PMID40656637
PMCPMC12246696

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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.