Ischemic stroke is a leading cause of mortality and morbidity globally. Prompt intervention is essential for arresting disease progression and minimizing central nervous system damage. Although imaging studies play a significant role in diagnosing ischemic stroke, their high costs and limited sensitivity often result in diagnostic and treatment delays. Blood biomarkers have shown considerable promise in the diagnosis and prognosis of ischemic stroke. Serum markers, closely associated with stroke pathophysiology, aid in diagnosis, subtype identification, prediction of disease progression, early neurological deterioration, and recurrence. Their advantages are particularly pronounced due to their low cost and rapid results. Despite the identification of numerous candidate blood biomarkers, their clinical application requires rigorous research and thorough validation. This review focuses on various blood biomarkers related to ischemic stroke, including coagulation and fibrinolysis-related factors, endothelial dysfunction markers, inflammatory biomarkers, neuronal and axonal injury markers, exosomes with their circular RNAs and other relevant molecules. It also summarizes the latest methods and techniques for stroke biomarker detection, aiming to provide critical references for the clinical application of key stroke biomarkers.
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http://dx.doi.org/10.3389/fneur.2025.1488726 | DOI Listing |
Front Neurol
February 2025
Center for Clinical Laboratory, General Hospital of the Yangtze River Shipping, Wuhan Brain Hospital, Wuhan, Hubei, China.
Ischemic stroke is a leading cause of mortality and morbidity globally. Prompt intervention is essential for arresting disease progression and minimizing central nervous system damage. Although imaging studies play a significant role in diagnosing ischemic stroke, their high costs and limited sensitivity often result in diagnostic and treatment delays.
View Article and Find Full Text PDFFront Neurol
February 2025
Department of Neurosurgery, University of Rochester Medical Center, Rochester, NY, United States.
Objectives: COVID-19 is an independent risk factor for ischemic stroke. Studies from early in the pandemic show increased rates of unfavorable recanalization, poor outcomes, and mortality in patients who were COVID-19 positive at the time of mechanical thrombectomy. However, there are currently no studies examining these parameters during the later pandemic when circulating variants were less virulent.
View Article and Find Full Text PDFCureus
February 2025
Emergency Medicine, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Background Hypertension is a risk factor for developing stroke after transient ischemic attack (TIA), yet it is unknown if stroke risk is altered by emergency department (ED) antihypertensive therapy. We aimed to investigate stroke rate in a population of TIA patients presenting with elevated blood pressure in the ED, comparing those who received antihypertensive medication in the ED to those who received no treatment. Secondarily, we aimed to assess the association between ED antihypertensive therapy and intensive care unit (ICU) admit rates, hospital length of stay (LOS), and discharge disposition setting in this population.
View Article and Find Full Text PDFThromb J
March 2025
Department of Neurology, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, 518035, P. R. China.
Intravenous thrombolysis (IVT) with recombinant tissue plasminogen activator (rt-PA) is the preferred treatment for acute ischemic stroke (AIS). Nevertheless, only approximately half of patients undergoing IVT experience positive outcomes. The objective of the study was to examine the clinical characteristics of patients with AIS and identify predictors for unfavorable clinical outcomes at 3 months after IVT.
View Article and Find Full Text PDFCardiovasc Diabetol
March 2025
School of Public Health and Emergency Management, Southern University of Science and Technology, Shenzhen, Guangdong Province, China.
Background: Although existing studies have reported associations between blood group A and cardiometabolic diseases (CMD), most have focused on dominant inheritance models. However, genome-wide association studies have mostly been based on additive genotypes. This study aims to investigate the association between the blood group A allele and 15 CMD using recessive, dominant, and additive models and identify potential mediators.
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