Evidence map›Paper›PMID 41614521›Full record

ArticleEuropean stroke journal2026

Circulating cytokine levels and 5-year vascular recurrence after stroke: A multicenter prospective cohort study.

Lanyue Zhang, Mohamad Ali Antabi, Jana Mattar, Omar El Bounkari, Rong Fang, Karin Waegemann, Felix J Bode, Sebastian Stösser, Peter Hermann, Thomas G Liman and 8 more

Erratum issuedAbstract readMulticenter Study
In one paragraph

Article in European stroke journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Lanyue ZhangInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0002-6798-1320
Mohamad Ali AntabiInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.
Jana MattarInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.
Omar El BounkariInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.
Rong FangInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0002-5663-9407
Karin WaegemannInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.
Felix J BodeGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.ORCID 0000-0003-4498-186X
Sebastian StösserGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Peter HermannDepartment of Neurology, University Medical Center Göttingen, Göttingen, Germany.
Thomas G LimanCenter for Stroke Research Berlin (CSB), Charité - Universitätsmedizin Berlin, Berlin, Germany.
Christian H NolteGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.ORCID 0000-0001-5577-1775
Benno IkenbergDepartment of Neurology, Klinikum rechts der Isar, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Kathleen BernkopfDepartment of Neurology, Klinikum rechts der Isar, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Gabor C PetzoldGerman Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Jürgen BernhagenInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.
Martin DichgansInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0002-0654-387X
Marios K GeorgakisInstitute for Stroke and Dementia Research (ISD), LMU University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0003-3507-3659
DEMDAS Investigators

Funding

FöFoLe program of LMU Munich FöFoLe-Forschungsprojekt Reg.-Nr. 1120the Fritz-Thyssen Foundation 10.22.2.024MNthe German Research Foundation DFG; Emmy Noether grant GZ: GE 3461/2-1, ID 512461the German Research Foundation Munich Cluster for Systems Neurology EXC 2145 SyNethe German Research Foundation (DFG) as part of the Munich Cluster for Systems Neurology EXC 2145 SyNergy - ID 390857198the German Research Foundation DFG under Germany's Excellence Strategy EXC-2049 - 390688087the German Research Foundation DFG under Germany's Excellence Strategy KFO-5023 project 2the Hertie Foundation ID P1230035
6 · The paper itself

Abstract

BACKGROUND AND

objectivesAnti-inflammatory therapies are tested in randomized trials for secondary stroke prevention. Detecting inflammatory biomarkers that predict vascular recurrence could optimize patient selection for these trials.

methodsIn a multicenter prospective cohort study, we measured plasma levels of 22 inflammatory cytokines in 486 acute stroke patients (474 ischemic strokes and 12 intracerebral hemorrhages; median age 68 years, 34% female, median 3 days post-stroke onset). Patients were followed for over 5 years through telephone and in-person interviews to record the occurrence of the following outcomes: (1) recurrent stroke or transient ischemic attack (TIA; primary outcome); (2) a composite of recurrent vascular events (stroke, TIA, acute coronary syndrome, hospital admission due to heart failure, and death; secondary outcome). Associations between cytokine levels and these outcomes were analyzed using Cox proportional hazards models adjusted for demographic and vascular risk factors.

resultsDuring the 5-year follow-up period, 59 patients (12.1%) experienced recurrent stroke or TIA, and 118 (24.3%) experienced recurrent vascular events. After adjustments for demographic and vascular risk factors, and correction for multiple comparisons, higher plasma levels of CD62E (adjusted Hazard Ratio (aHR)/SD increment: 1.63, 95%CI 1.22-2.20) and MIF (aHR: 1.56, 95%CI 1.18-2.06) in the acute phase after stroke were statistically significantly associated with increased risk of recurrent stroke or TIA. The associations followed a dose-response pattern across quartiles of CD62E and MIF levels. Adding baseline CD62E and MIF levels to models including age, sex, vascular risk factors, and baseline C-reactive protein (CRP) levels led to significant improvements in the prediction of 5-year risk of recurrent stroke or TIA (ΔC-index 0.030-0.050).

conclusionAmong stroke patients, higher baseline levels of CD62E and MIF improved prediction of 5-year risk of recurrent stroke or TIA on top of vascular risk factors and CRP levels. Whether assessment of these cytokines could improve patient selection for secondary prevention trials of anti-inflammatory treatments, should be explored in future studies.

Indexed as

CytokinesIschemic Attack, TransientStrokeAgedBiomarkersFemaleHumansIschemic StrokeMaleMiddle AgedProspective StudiesRecurrenceRisk FactorsBiomarkersCytokinescytokinesinflammationrecurrencerisk predictionStroke

Identifiers

PMID41614521
PMCPMC12866279

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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.