Evidence map›Paper›PMID 42544483›Full record

ArticleStroke2026

Persistence of Association of Blood Biomarkers With Risk of Recurrent Stroke on Long-Term Follow-Up: Population-Based Study.

Linxin Li, Annette I Burgess, Julia Duerden, Katherine Onions, Helen C Segal, Peter M Rothwell, Oxford Vascular Study

Abstract read
In one paragraph

Article in Stroke, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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.

Linxin LiNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.ORCID 0000-0002-3636-8355
Annette I BurgessNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.ORCID 0000-0003-3442-8083
Julia DuerdenNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.ORCID 0000-0003-3218-0731
Katherine OnionsNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.ORCID 0009-0003-0778-440X
Helen C SegalNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.
Peter M RothwellNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.ORCID 0000-0001-9739-9211
Oxford Vascular StudyNuffield Department of Clinical Neurosciences, Wolfson Centre For Prevention of Stroke and Dementia, John Radcliffe Hospital, University of Oxford, United Kingdom.

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundRaised inflammatory biomarkers predict an increased short-term risk of recurrent vascular events after stroke or transient ischemic attack, but it is uncertain whether the hazard is maintained thereafter. In the absence of previous population-based studies, we aimed to determine the predictive value of biomarkers for the long-term risk of recurrent stroke in intensively treated patients following transient ischemic attack or stroke.

methodsWe studied 12 blood biomarkers related to inflammation, neuronal cell damage, and thrombosis soon after transient ischemic attack or stroke in a population-based study (OXVASC [Oxford Vascular Study]; 2002-2011) with follow-up to 2025. We used Cox and negative binomial regressions to assess associations between each log-transformed biomarker (per SD increase) and recurrent stroke (first event and total number), adjusted for age, sex, and baseline vascular risk factors.

resultsOf 1292 consecutive patients (mean/SD age, 73.1/13.2 years; 47.8% male), 365 recurrent strokes occurred in 280 patients during 11 336 patient-years. All inflammatory biomarkers were associated with 10-year risk of recurrence, with little impact of adjustment for other risk factors (adjusted incidence rate ratio: IL-6 [interleukin-6], 1.21 [95% CI, 1.04-1.42]; CRP [C-reactive protein], 1.29 [95% CI, 1.11-1.49]; TNFR-1 [tumor necrosis factor receptor-1], 1.24 [95% CI, 1.05-1.46]; and NGAL [neutrophil gelatinase-associated lipocalin], 1.15 [95% CI, 0.99-1.33]). Moreover, number of elevated (top quartile) inflammatory markers was associated with higher burden of recurrence (incidence rate ratio, 1.31 [95% CI, 1.15-1.50];

conclusionsInflammatory biomarkers were more predictive of long-term recurrent stroke than neuronal or thrombotic biomarkers, particularly when several inflammatory markers were raised. Predictive value was independent of other vascular risk factors and did not diminish with duration of follow-up, supporting trials of anti-inflammatory strategies for long-term secondary prevention.

Indexed as

BiomarkersIschemic Attack, TransientStrokeAgedAged, 80 and overFemaleFollow-Up StudiesHumansMaleMiddle AgedRecurrenceRisk FactorsBiomarkersbiomarkerischemic attack, transientrisk assessmentsecondary preventionstroke

Identifiers

PMID42544483
PMCPMC13619134

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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.