Intracranial VCAM1 at Time of Mechanical Thrombectomy Predicts Ischemic Stroke Severity
Overview
Authors
Affiliations
Background: Emergent large vessel occlusion (ELVO) strokes are devastating ischemic vascular events for which novel treatment options are needed. Using vascular cell adhesion molecule 1 (VCAM1) as a prototype, the objective of this study was to identify proteomic biomarkers and network signaling functions that are potential therapeutic targets for adjuvant treatment for mechanical thrombectomy.
Methods: The blood and clot thrombectomy and collaboration (BACTRAC) study is a continually enrolling tissue bank and registry from stroke patients undergoing mechanical thrombectomy. Plasma proteins from intracranial (distal to clot) and systemic arterial blood (carotid) were analyzed by Olink Proteomics for N=42 subjects. Statistical analysis of plasma proteomics used independent sample t tests, correlations, linear regression, and robust regression models to determine network signaling and predictors of clinical outcomes. Data and network analyses were performed using IBM SPSS Statistics, SAS v 9.4, and STRING V11.
Results: Increased systemic (p<0.001) and intracranial (p=0.013) levels of VCAM1 were associated with the presence of hypertension. Intracranial VCAM1 was positively correlated to both infarct volume (p=0.032; r=0.34) and edema volume (p=0.026; r=0.35). The %∆ in NIHSS from admittance to discharge was found to be significantly correlated to both systemic (p=0.013; r = -0.409) and intracranial (p=0.011; r = -0.421) VCAM1 levels indicating elevated levels of systemic and intracranial VCAM1 are associated with reduced improvement of stroke severity based on NIHSS from admittance to discharge. STRING-generated analyses identified biologic functional descriptions as well as function-associated proteins from the predictive models of infarct and edema volume.
Conclusions: The current study provides novel data on systemic and intracranial VCAM1 in relation to stroke comorbidities, stroke severity, functional outcomes, and the role VCAM1 plays in complex protein-protein signaling pathways. These data will allow future studies to develop predictive biomarkers and proteomic targets for drug development to improve our ability to treat a devastating pathology.
Kongbunkiat K, Thukham-Mee W, Tiamkao S, Kasemsap N, Vorasoot N, Wattanathorn J Nutrients. 2024; 16(22).
PMID: 39599732 PMC: 11597798. DOI: 10.3390/nu16223946.
Sands M, McLouth C, Frank J, Maglinger B, Millson N, Al-Kawaz M Int J Mol Sci. 2024; 25(18).
PMID: 39337456 PMC: 11432069. DOI: 10.3390/ijms25189968.
McLouth C, Maglinger B, Frank J, Hazelwood H, Harp J, Cranford W J Neuroinflammation. 2024; 21(1):205.
PMID: 39154085 PMC: 11330053. DOI: 10.1186/s12974-024-03201-9.
Blue light impairs cornea and corneal wound healing by downregulating VCAM1 partly.
Chen K, Jin L, Wen Y, Yang Q, Li X, Zhang L iScience. 2023; 26(12):108448.
PMID: 38034364 PMC: 10687337. DOI: 10.1016/j.isci.2023.108448.
Specific inflammatory profile of acute ischemic stroke patients with left atrial enlargement.
Fontaine J, Leboube S, Bochaton T, Thibault H, Amaz C, Cho T Front Cardiovasc Med. 2023; 10:1190857.
PMID: 37539088 PMC: 10394294. DOI: 10.3389/fcvm.2023.1190857.