Inflammation biomarkers in the intracranial blood are associated with outcome in patients with ischemic stroke.

Angiography Brain Inflammation Stroke Thrombectomy

Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
21 Mar 2024
Historique:
received: 11 12 2023
accepted: 18 02 2024
medline: 22 3 2024
pubmed: 22 3 2024
entrez: 21 3 2024
Statut: aheadofprint

Résumé

Performing endovascular treatment (EVT) in patients with acute ischemic stroke (AIS) allows a port of entry for intracranial biological sampling. To test the hypothesis that specific immune players are molecular contributors to disease, outcome biomarkers, and potential targets for modifying AIS. We examined 75 subjects presenting with large vessel occlusion of the anterior circulation and undergoing EVT. Intracranial blood samples were obtained by microcatheter aspiration, as positioned for stent deployment. Peripheral blood samples were collected from the femoral artery. Plasma samples were quality controlled by electrophoresis and analyzed using a Mesoscale multiplex for targeted inflammatory and vascular factors. We measured 37 protein biomarkers in our sample cohort. Through multivariate analysis, adjusted for age, intravenous thrombolysis, pretreatment National Institutes of Health Stroke Scale and Alberta Stroke Program Early CT scores, we found that post-clot blood levels of interleukin-6 (IL-6) were significantly correlated (adjusted P value <0.05) with disability assessed by the modified Rankin Scale (mRS) score at 90 days, with medium effect size. Chemokine (C-C) ligand 17 CCL17/TARC levels were inversely correlated with the mRS score. Examination of peripheral blood showed that these correlations did not reach statistical significance after correction. Intracranial biomarker IL-6 level was specifically associated with a lower likelihood of favorable outcome, defined as a mRS score of 0-2. Our findings show a signature of blood inflammatory factors at the cerebrovascular occlusion site. The correlations between these acute-stage biomarkers and mRS score outcome support an avenue for add-on and localized immune modulatory strategies in AIS.

Sections du résumé

BACKGROUND BACKGROUND
Performing endovascular treatment (EVT) in patients with acute ischemic stroke (AIS) allows a port of entry for intracranial biological sampling.
OBJECTIVE OBJECTIVE
To test the hypothesis that specific immune players are molecular contributors to disease, outcome biomarkers, and potential targets for modifying AIS.
METHODS METHODS
We examined 75 subjects presenting with large vessel occlusion of the anterior circulation and undergoing EVT. Intracranial blood samples were obtained by microcatheter aspiration, as positioned for stent deployment. Peripheral blood samples were collected from the femoral artery. Plasma samples were quality controlled by electrophoresis and analyzed using a Mesoscale multiplex for targeted inflammatory and vascular factors.
RESULTS RESULTS
We measured 37 protein biomarkers in our sample cohort. Through multivariate analysis, adjusted for age, intravenous thrombolysis, pretreatment National Institutes of Health Stroke Scale and Alberta Stroke Program Early CT scores, we found that post-clot blood levels of interleukin-6 (IL-6) were significantly correlated (adjusted P value <0.05) with disability assessed by the modified Rankin Scale (mRS) score at 90 days, with medium effect size. Chemokine (C-C) ligand 17 CCL17/TARC levels were inversely correlated with the mRS score. Examination of peripheral blood showed that these correlations did not reach statistical significance after correction. Intracranial biomarker IL-6 level was specifically associated with a lower likelihood of favorable outcome, defined as a mRS score of 0-2.
CONCLUSIONS CONCLUSIONS
Our findings show a signature of blood inflammatory factors at the cerebrovascular occlusion site. The correlations between these acute-stage biomarkers and mRS score outcome support an avenue for add-on and localized immune modulatory strategies in AIS.

Identifiants

pubmed: 38514190
pii: jnis-2023-021365
doi: 10.1136/jnis-2023-021365
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Cyril Dargazanli (C)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France c-dargazanli@chu-montpellier.fr Nicola.Marchi@igf.cnrs.fr v-costalat@chu-montpellier.fr.
Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.

Marine Blaquière (M)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.

Marinette Moynier (M)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France.

Frédéric de Bock (F)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.

Julien Labreuche (J)

Unité Statistique, Évaluation Économique, Data-management, Centre Hospitalier Universitaire de Lille, Lille, France.

Adrien Ter Schiphorst (A)

Department of Neurology, CHRU Gui de Chauliac, University Hospital Centre Montpellier, Montpellier, France.

Imad Derraz (I)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France.

Răzvan Alexandru Radu (RA)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France.

Gregory Gascou (G)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France.

Pierre Henri Lefevre (PH)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France.

Francesca Rapido (F)

Department of Anesthesiology and Critical Care Medicine, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier, France.

Julien Fendeleur (J)

Department of Anesthesiology and Critical Care Medicine, Gui de Chauliac Hospital, Montpellier University Medical Center, Montpellier, France.

Caroline Arquizan (C)

Department of Neurology, CHRU Gui de Chauliac, University Hospital Centre Montpellier, Montpellier, France.

Romain Bourcier (R)

Department of Neuroradiology, Université de Nantes, Nantes, France.

Philippe Marin (P)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.

Paolo Machi (P)

Department of Neuroradiology, Geneva University Hospitals, Geneve, Switzerland.

Federico Cagnazzo (F)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France.
Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.

Christophe Hirtz (C)

Plateforme Protéomique Clinique, Montpellier, France.

Vincent Costalat (V)

Department of Neuroradiology, University Hospital Centre Montpellier, Montpellier, France c-dargazanli@chu-montpellier.fr Nicola.Marchi@igf.cnrs.fr v-costalat@chu-montpellier.fr.
Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.

Nicola Marchi (N)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France c-dargazanli@chu-montpellier.fr Nicola.Marchi@igf.cnrs.fr v-costalat@chu-montpellier.fr.

Classifications MeSH