Investigating the Role of Brain Natriuretic Peptide (BNP) and N-Terminal-proBNP in Thrombosis and Acute Ischemic Stroke Etiology

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Institut Català de la Salut

[Rossi R] Department of Physiology and Galway Neuroscience Centre, School of Medicine, University of Galway, University Road, Galway, Ireland. CÚRAM–SFI Research Centre in Medical Devices, University of Galway, Galway, Ireland. Institut de Biotecnologia i Biomedicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Jabrah D, Prendergast J] Department of Physiology and Galway Neuroscience Centre, School of Medicine, University of Galway, University Road, Galway, Ireland. [Douglas A] Department of Physiology and Galway Neuroscience Centre, School of Medicine, University of Galway, University Road, Galway, Ireland. CÚRAM–SFI Research Centre in Medical Devices, University of Galway, Galway, Ireland. [Pandit A] CÚRAM–SFI Research Centre in Medical Devices, University of Galway, Galway, Ireland. [Gilvarry M] Cerenovus, Block 3, Corporate House, Ballybrit Business Park, Galway, Ireland. [Juega J] Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2024-03-19T13:15:24Z

2024-03-19T13:15:24Z

2024-03-05



Abstract

Acute ischemic stroke; Brain natriuretic peptide; Thrombus


Ictus isquèmic agut; Pèptid natriurètic cerebral; Trombe


Ictus isquémico agudo; Péptido natriurético cerebral; Trombo


The need for biomarkers for acute ischemic stroke (AIS) to understand the mechanisms implicated in pathological clot formation is critical. The levels of the brain natriuretic peptides known as brain natriuretic peptide (BNP) and NT-proBNP have been shown to be increased in patients suffering from heart failure and other heart conditions. We measured their expression in AIS clots of cardioembolic (CE) and large artery atherosclerosis (LAA) etiology, evaluating their location inside the clots, aiming to uncover their possible role in thrombosis. We analyzed 80 thrombi from 80 AIS patients in the RESTORE registry of AIS clots, 40 of which were of CE and 40 of LAA etiology. The localization of BNP and NT-BNP, quantified using immunohistochemistry and immunofluorescence, in AIS-associated white blood cell subtypes was also investigated. We found a statistically significant positive correlation between BNP and NT-proBNP expression levels (Spearman’s rho = 0.668 p < 0.0001 *). We did not observe any statistically significant difference between LAA and CE clots in BNP expression (0.66 [0.13–3.54]% vs. 0.53 [0.14–3.07]%, p = 0.923) or in NT-proBNP expression (0.29 [0.11–0.58]% vs. 0.18 [0.05–0.51]%, p = 0.119), although there was a trend of higher NT-proBNP expression in the LAA clots. It was noticeable that BNP was distributed throughout the thrombus and especially within platelet-rich regions. However, NT-proBNP colocalized with neutrophils, macrophages, and T-lymphocytes, suggesting its association with the thrombo-inflammatory process.


This publication has emanated from research conducted with the financial support of Science Foundation Ireland (SFI) and is co-funded by the European Regional Development Fund under Grant Number 13/RC/2073_2. Furthermore, it was supported by the industrial partner Cerenovus.

Document Type

Article


Published version

Language

English

Publisher

MDPI

Related items

International Journal of Molecular Sciences;25(5)

https://doi.org/10.3390/ijms25052999

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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