Evidence map›Paper›PMID 40268817›Full record

ArticleTranslational stroke research2025

Proteomic and Demographic Comparisons of Recurrent Ischemic Stroke Patients.

Nicholas Meredith, Jordan Harp, Christopher J McLouth, Jacqueline A Frank, Will Cranford, Mais N Al-Kawaz, Shivani Pahwa, Amanda L Trout, Ann M Stowe, David L Dornbos and 2 more

Abstract readComparative Study
In one paragraph

Article in Translational stroke research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

12 authors.

Nicholas MeredithCollege of Medicine, University of Kentucky, Lexington, KY, USA.
Jordan HarpDepartment of Neurology, University of Kentucky, Lexington, KY, USA.
Christopher J McLouthDepartment of Neurology, University of Kentucky, Lexington, KY, USA.
Jacqueline A FrankDepartment of Neurosurgery, University of Kentucky, Lexington, KY, USA.
Will CranfordDepartment of Biostatistics, University of Kentucky, Lexington, KY, USA.
Mais N Al-KawazDepartment of Neurosurgery, University of Kentucky, Lexington, KY, USA.
Shivani PahwaDepartment of Neurosurgery, University of Kentucky, Lexington, KY, USA.
Amanda L TroutDepartment of Neurosurgery, University of Kentucky, Lexington, KY, USA.
Ann M StoweDepartment of Neurology, University of Kentucky, Lexington, KY, USA.
David L DornbosDepartment of Neurosurgery, University of Kentucky, Lexington, KY, USA.
Justin F FraserDepartment of Neurology, University of Kentucky, Lexington, KY, USA.
Keith R PennypackerDepartment of Neurology, University of Kentucky, Lexington, KY, USA. keith.pennypacker@uky.edu.

Funding

Predictors and Biomarkers for VCID versus Cognitive Recovery after Stroke Thrombectomy in Rural AppalachiaR01NS127974 · NINDS · UNIVERSITY OF KENTUCKY · PI Jordan Patrick Harp · 2023 to 2026
$2.4M
NINDS NIH HHS R01 NS127974NINDS NIH HHS R01NS127974
6 · The paper itself

Abstract

Rates of recurrent strokes have remained relatively unchanged over the past couple decades, highlighting a need for advancements in secondary prevention of stroke recurrence. This study utilizes the Blood And Clot Thrombectomy Registry And Collaboration (BACTRAC) tissue bank to identify proteomic and demographic differences in recurrent ischemic stroke patients. Blood samples were collected during mechanical thrombectomy of large-vessel occlusion ischemic strokes. Plasma levels for 184 inflammatory and cardiometabolic proteins were measured in systemic blood and intracranial blood from the infarction area. Differences between recurrent and first-stroke patients were analyzed using Fisher's Exact Test for categorical variables and Student's independent samples t tests or Welch's t tests for continuous variables. Proteins were divided into systemic and intracranial proteins, and independent samples t tests were performed with a False Discovery Rate of 5.0%. Significant variables were used in multiple logistic regression. There were 20 patients in the prior stroke group and 121 in the first stroke group. The prior stroke group had a significantly higher percentage of females (80.0% vs 50.4%, p = 0.016) and lower rate of hyperlipidemia comorbidity (10.5% vs 35.5%, p = 0.034). Two systemic proteins were significantly higher in those with a prior stroke: CCL14 and FGF-19. Multiple logistic regression found higher levels of CCL14 and FGF-19 to be predictive of a stroke being recurrent. Along with other demographics, these proteins could provide a predictive model to identify patients with risk of recurrent ischemic strokes. Serum CCL14 and FGF-19 levels are easily accessible biomarkers, making them possible therapeutic targets for recurrent stroke prevention.

Indexed as

Brain IschemiaIschemic StrokeProteomicsAgedAged, 80 and overBiomarkersDemographyFemaleHumansMaleMiddle AgedRecurrenceRegistriesBiomarkersCCL14 protein, humanCerebrovascular accidentFGF- 19 protein, humanIschemic strokeStrokeThrombectomy

Identifiers

PMID40268817
PMCPMC12596381

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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.