Prognostic Utility of Serum Biomarkers in Intracerebral Hemorrhage: A Systematic Review

2021 ◽  
pp. 154596832110413
Author(s):  
Zachary Troiani ◽  
Luis Ascanio ◽  
Christina P. Rossitto ◽  
Muhammad Ali ◽  
Nicki Mohammadi ◽  
...  

Background. Intracerebral hemorrhage (ICH) accounts for 10–20% of all strokes and is associated with high morbidity and mortality. Recent studies have identified serum biomarkers as a means to improve outcome prognostication in poor grade ICH patients. Poor prognosis of ICH patients and complex pathophysiology of the disease necessitate prognostic serum biomarkers to help guide treatment recommendations. Objective. The objective is to systematically review all biomarkers used to predict long-term functional outcome in patients with spontaneous intracerebral hemorrhage. Results. We identified 36 studies investigating the predictive utility of 50 discrete biomarkers. Data from 4865 ICH patients were reviewed. Inflammatory biomarkers (11/50) were most often studied, followed by oxidative (8/50), then neuron and astrocyte-specific (7/50). S100 calcium binding protein B, white blood cell count, and copeptin were the most often studied individual biomarkers. The prognostic utility of 23 biomarkers was analyzed using receiver operating characteristic curves. Area under the curve (AUC) values for all available biomarkers except neutrophil/lymphocyte ratio were acceptable. Twenty of the 23 biomarkers were characterized by at least one excellent AUC value. Vascular endothelial growth factor, glial fibrillary astrocyte protein, and S100 calcium binding protein B were characterized by outstanding AUC. Conclusions. We identified the inflammatory and neuron and astrocyte-specific biomarker categories as having the greatest number of significant individual biomarker predictors of long-term outcome. Further investigation utilizing cross-validation of prediction models in a second independent group and blinded assessment of outcomes for the predictive utility of biomarkers in patients with ICH is warranted.

2020 ◽  
Vol 37 (17) ◽  
pp. 1864-1869
Author(s):  
Julie Linding Kjerulff ◽  
Sophie-Charlott Seidenfaden ◽  
Niels Juul ◽  
Mette Fogh Møller ◽  
Anna-Marie Bloch Munster ◽  
...  

2012 ◽  
Vol 42 (3) ◽  
pp. 199-204 ◽  
Author(s):  
S González-García ◽  
A González-Quevedo ◽  
M Peña-Sánchez ◽  
C Menéndez-Saínz ◽  
R Fernández-Carriera ◽  
...  

2020 ◽  
Vol 15 (6) ◽  
pp. 900-902
Author(s):  
Jan Schroeder ◽  
Franziska Erthel ◽  
Karsten Hollander

Purpose: Foot-strike patterns (FSP) in running are related to certain impact kinetics during ground contact. A rear-foot strike (RFS) has been associated with higher impact forces, whereas a forefoot strike (FFS) is assumed to minimize these impact forces. This study investigated the effects of running with RFS or FFS on impact-sensitive neuronal biomarkers S100 calcium-binding protein B (S100B), neuron-specific enolase (NSE), and lactate dehydrogenase (LDH). Methods: In this randomized crossover study, 18 healthy recreational runners (14 male, mean [SD] age 28.2 [4.7] y, body mass index 22.8 [1.9]) ran 2 separate 5-mile runs with RFS or FFS, respectively. Blood samples were taken before (pre), 30 min after (post 0), and 24 h after (post 24) the run. S100B, NSE, and LDH concentrations were determined and analyzed (3 × 2 data model). Results: S100B, NSE, and LDH concentrations increased from pre to post 0 and decreased within 24 h back to the baseline level, demonstrating a significant time effect (all P < .01, all ). No main effect for FSP or any significant interaction effect indicating FSP-specific differences between FFS or RFS was found (all P > .05, all ), except for LDH (P < .001, ). Conclusions: NSE, S100B, and LDH concentration increased in the short term after running and returned to normal in 24 h. FSP with varying impact forces does not influence the increase of these biomarkers. LDH findings favor peripheral origins, but mixed effects are possible. Thus, further research is needed to estimate the risk of mild traumatic encephalopathy.


2020 ◽  
Vol 41 (Supplement_1) ◽  
pp. S261-S262
Author(s):  
Jusong Song ◽  
Xiaofu Wang ◽  
Ryan M Huebinger ◽  
Ravi S Radhakrishnan ◽  
Steven E Wolf

Abstract Introduction Severe burn causes a dramatic metabolic response associated with multi-organ damage. Mononeuropathy is also associated to muscle wasting after injury. Schwann cells are the glial cells that support neurons in the nervous system. S100 calcium-binding protein B (S100B) and Myelin basic protein (MBP) are biomarkers of Schwann cells. We hypothesize that severe burn affects these biomarkers, and is related to burn induced nerve impairment. The purpose of the study was to investigate biomarkers related to neural damage in response to severe burn. Methods Thirty-five Sprague Dawley rats received 40% total body surface area scald burn. Serum was collected at 6 hours, 1, 3, 7 and 14 days after injury. Six underwent sham burn as controls. Serum was analyzed for S100B and myelin basic protein using ELISA. One way ANOVA was applied for statistical analysis. Results The baseline of S100B level was 45.01±3.58 pg/ml in the sham group. S100B significantly increased to 99.42±9.13 pg/ml with no significant change at other time points. MBP serum level is 4.12± 0.13 ng/ml at baseline. MBP level did not change significantly in burn compared to sham. Conclusions In summary, S100B serum increased markedly after burn and returned to baseline thereafter. Burn did not change MBP levels. The findings could lead to further efforts in elucidating changes in neural function after burn. Applicability of Research to Practice The current study implies a novel biomarker candidate in response to severe burn related to nerve damage.


2019 ◽  
Vol 110 ◽  
pp. 104414
Author(s):  
Angela Carlier ◽  
Kimberly Boers ◽  
Robert Veerhuis ◽  
Filip Bouckaert ◽  
Pascal Sienaert ◽  
...  

2015 ◽  
Vol 63 (10) ◽  
pp. 2212-2214 ◽  
Author(s):  
Sara J. Beishuizen ◽  
Rikie M. Scholtens ◽  
Annelies E. Vellekoop ◽  
Bart C. Vrouenraets ◽  
Dunja Westhoff ◽  
...  

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