Neuronal plasma biomarkers in acute ischemic stroke

Early imaging-based detection of acute ischemic stroke (AIS) has improved in the era of reperfusion therapy. Despite of this, prognosis of outcome after AIS remains a challenge. Therefore, parameters that support clinical decision making are sought. Blood-based biomarkers have the potential to provide valuable information in addition to the established prognostic factors. Neuronal biomarkers of acute or degenerative neuronal injury have shown to be reliably detected in plasma. These biomarkers are well-established in neurodegenerative pathology, such as Alzheimer's disease. In this study, we explored the association between stroke diameter and plasma biomarkers for neuronal injury and tau pathophysiology (brain-derived tau [BD-tau], phosphorylated-tau-217 [p-tau21] and neurofilament light [NfL]) in patients (n = 193) admitted to the acute ward, Akershus University Hospital. All patients received a final diagnosis of AIS, transient ischemic attack or stroke mimics. Blood samples were obtained the day after admission. We find that levels of BD-tau (p = .004) and NfL (p = .011) were higher after AIS than in patients with stroke mimics. The cortical stroke diameter correlated with BD-tau (tau-b = 0.64, p < .001) and p-tau217 (tau-b = 0.36, p = .003). Linear regression confirmed BD-tau to be the strongest variable associated with stroke diameter, pointing to the potential clinical value of plasma BD-tau in outcome prediction after AIS.

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Publication Details

Journal
Journal of Cerebral Blood Flow & Metabolism
Published
2024-10-25
DOI
https://doi.org/10.1177/0271678x241293537
Citations
11
Primary Topic
Acute Ischemic Stroke Management
Type
article
Field-Weighted Citation Impact
4.25

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article

Neuronal plasma biomarkers in acute ischemic stroke

Berglind Gísladóttir, Bjørn‐Eivind Kirsebom, Hlin Kvartsberg, Fernando González‐Ortiz et al.
11 citations
Journal of Cerebral Blood Flow & Metabolism
Acute Ischemic Stroke Management
4.25
article

Neuronal plasma biomarkers in acute ischemic stroke

Berglind Gísladóttir, Bjørn‐Eivind Kirsebom, Hlin Kvartsberg, Fernando González‐Ortiz, Thomas K. Karikari, Ole Morten Rønning, Tormod Fladby, Julia K. Gundersen, Katrin Mertes, Henrik Zetterberg, Kaj Blennow
article en
11 citations

Abstract

Early imaging-based detection of acute ischemic stroke (AIS) has improved in the era of reperfusion therapy. Despite of this, prognosis of outcome after AIS remains a challenge. Therefore, parameters that support clinical decision making are sought. Blood-based biomarkers have the potential to provide valuable information in addition to the established prognostic factors. Neuronal biomarkers of acute or degenerative neuronal injury have shown to be reliably detected in plasma. These biomarkers are well-established in neurodegenerative pathology, such as Alzheimer's disease. In this study, we explored the association between stroke diameter and plasma biomarkers for neuronal injury and tau pathophysiology (brain-derived tau [BD-tau], phosphorylated-tau-217 [p-tau21] and neurofilament light [NfL]) in patients (n = 193) admitted to the acute ward, Akershus University Hospital. All patients received a final diagnosis of AIS, transient ischemic attack or stroke mimics. Blood samples were obtained the day after admission. We find that levels of BD-tau (p = .004) and NfL (p = .011) were higher after AIS than in patients with stroke mimics. The cortical stroke diameter correlated with BD-tau (tau-b = 0.64, p < .001) and p-tau217 (tau-b = 0.36, p = .003). Linear regression confirmed BD-tau to be the strongest variable associated with stroke diameter, pointing to the potential clinical value of plasma BD-tau in outcome prediction after AIS.

Journal of Cerebral Blood Flow & MetabolismVol. 45(1)
University of Wisconsin–Madison (US), University of Freiburg (DE), University of Pittsburgh (US), University of Oslo (NO), Akershus University Hospital (NO), Sahlgrenska University Hospital (SE), UK Dementia Research Institute (GB), National Hospital for Neurology and Neurosurgery (GB), University College London (GB), University of Gothenburg (SE)
Alzheimer's Association, Alzheimer's Drug Discovery Foundation, BrightFocus Foundation, Familjen Erling-Perssons Stiftelse, Gun och Bertil Stohnes Stiftelse, EU Joint Programme – Neurodegenerative Disease Research, National Institute for Health and Care Research, University College London, European Commission, Vetenskapsrådet, Alzheimerfonden, International Society for Neurochemistry, UK Dementia Research Institute, Parkinsonfonden, HORIZON EUROPE Framework Programme
Openalex Percentile: Top 5%
Acute Ischemic Stroke Management
4.25
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