Role of S100B protein in urine and serum as an early predictor of mortality after severe traumatic brain injury in adults
S100B is a calcium-binding protein released into the blood from astroglial cells due to brain injury. Some authors have described a correlation between S100B serum concentration and severity of brain damage. There is not much information about the accuracy of urinary S100B for predicting outcome aft...
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Veröffentlicht in: | Clinica chimica acta 2012-12, Vol.414, p.228-233 |
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Sprache: | eng |
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Zusammenfassung: | S100B is a calcium-binding protein released into the blood from astroglial cells due to brain injury. Some authors have described a correlation between S100B serum concentration and severity of brain damage. There is not much information about the accuracy of urinary S100B for predicting outcome after severe traumatic brain injury (TBI). 55 patients with severe TBI were included in the study. Blood and urine samples were drawn to determine S100B levels on admission and on the subsequent 24, 48, 72 and 96h. S100B concentrations (serum and urine) were significantly higher in patients who were dead a month after the accident compared to survivors. ROC-analysis showed that S100B at 24h post-severe TBI is a useful tool for predicting mortality (serum: AUC 0.958, urine: AUC 0.778). The best cut-offs for S100B were 0.461μg/L and 0.025μg/L (serum and urine respectively), with a sensitivity of 90% for both measurements and a specificity of 88.4% (serum) and 62.8% (urine). We can state that the determination of S100B levels both in urine and serum acts as a sensitive and an effective biomarker for the early prediction of mortality after severe TBI.
► Blood and urine samples were drawn on admission and every 24h up to 4days. ► Serum and urine S100B levels were higher in patients dead within a month of trauma. ► S100B in serum and urine at 24h post-severe TBI is useful for predicting mortality. ► S100B acts as a sensitive biomarker for the prediction of mortality after severe TBI. |
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ISSN: | 0009-8981 1873-3492 |
DOI: | 10.1016/j.cca.2012.09.025 |