2022
DOI: 10.1177/23969873221145391
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Serum S-100B adds incremental value for the prediction of symptomatic intracranial hemorrhage and brain edema after acute ischemic stroke

Abstract: Background: Early identification of patients developing symptomatic intracranial hemorrhage and symptomatic brain edema after acute ischemic stroke is essential for clinical decision-making. Astroglial protein S-100B is a marker of blood-brain barrier disruption, which plays an important role in the formation of intracranial hemorrhage and brain edema. In this study, we assessed the prognostic value of serum S-100B for the development of these complications. Methods: Serum S-100B levels were measured within 24… Show more

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Cited by 6 publications
(1 citation statement)
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“…[ 26 ] Damage to the blood–brain barrier after stroke is associated with neuroinflammation. [ 27 ] Serum biomarkers of blood–brain barrier dysfunction, such as S-100B, [ 28 ] astrocytic endothelin-1, [ 29 ] matrix metalloproteinase-9 and cellular-fibronectin, [ 30 ] and serum inflammatory biomarkers, such as procalcitonin and neutrophil counts, [ 31 ] neutrophil-to-lymphocyte ratio, [ 32 ] E-selectin, [ 33 ] brain natriuretic peptide, [ 34 ] and NOD-like receptor protein 3, [ 35 ] were reported to be associated with the development of brain edema after stroke. A number of multivariable models have been developed for predicting malignant brain edema, containing a combination of clinical characteristics, imaging features, and serum biomarkers, with the most commonly included factors being NIHSS score, large infarction, and revascularization status.…”
Section: Prediction and Prevention Of Malignant Brain Edemamentioning
confidence: 99%
“…[ 26 ] Damage to the blood–brain barrier after stroke is associated with neuroinflammation. [ 27 ] Serum biomarkers of blood–brain barrier dysfunction, such as S-100B, [ 28 ] astrocytic endothelin-1, [ 29 ] matrix metalloproteinase-9 and cellular-fibronectin, [ 30 ] and serum inflammatory biomarkers, such as procalcitonin and neutrophil counts, [ 31 ] neutrophil-to-lymphocyte ratio, [ 32 ] E-selectin, [ 33 ] brain natriuretic peptide, [ 34 ] and NOD-like receptor protein 3, [ 35 ] were reported to be associated with the development of brain edema after stroke. A number of multivariable models have been developed for predicting malignant brain edema, containing a combination of clinical characteristics, imaging features, and serum biomarkers, with the most commonly included factors being NIHSS score, large infarction, and revascularization status.…”
Section: Prediction and Prevention Of Malignant Brain Edemamentioning
confidence: 99%