Serum levels of gFaP and S100b predict outcomes in Tbi
investigators from the netherlands GFaP (1.5 g/l) and s100B (1.13 g/l) outcome scale extended [Gose] score have validated the predictive worth of in patients with severe tBi could predict 14) compared with individuals showing two biochemical markers for traumatic death and unfavorable outcomes with favorable outcomes (Gose score 28). brain injury (tBi). we showed that good sensitivity but poor specificity. the logistical regression analysis showed that glial fibrillary acid protein (GFaP) and new investigation aimed to validate models including the serum biomarkers s100B levels in serum are adjuncts to the the prognostic capabilities of these serum (at cut-off values determined in the assessment of brain damage following tBi biomarkers in people with either moderate previous study), mass lesion and pupillary and, when combined with clinical variables, (Glasgow Coma scale [GCs] 912) or reaction most accurately predicted may enhance our ability to provide accurate severe (GCs 38) tBi. patient outcomes. prognoses for patients, says the studys the researchers recorded various vos and his colleagues hypothesize lead researcher Pieter vos, of the radboud patient characteristics and collected that in the case of tBi, cut-off values for university nijmegen medical Centre. serum samples on hospital admission. GFaP and s100B can be determined that in patients with tBi, treatment GFaP and s100B levels were subsequently are associated with a small false-positive decisions may be guided by neurological measured, and patient outcomes were then rate of death or unfavorable outcomes. prognoses. Current prognostic models determined at 6 months after injury. to achieve this, says vos, we would for tBi, which include various patient among the 79 patients who met the need to conduct a larger, multicenter characteristics and brain damage indices, studys inclusion criteria, those who died study, involving hundreds rather than do not exhibit sufficiently high sensitivity within the follow-up period exhibited tens of patients with this serious and or specificity to accurately predict 33.4-fold and 2.1-fold higher median levels heterogeneous disorder. outcomes in individual patients. it is of serum GFaP and s100B, respectively, Darran Yates broadly felt among experts in the field that than those who were still alive at 6 months. the need exists to enlarge knowledge on median serum levels of GFaP and biochemical markers of injury, says vos. s100B were also increased (19.8-fold Original article Vos, P. E. et al. GFAP and S100B are in a previous study, vos and his and 2.1-fold, respectively) in patients biomarkers of traumatic brain injury: an observational cohort study. Neurology 75, 17861793 (2010) colleagues showed that serum levels of exhibiting unfavorable outcomes (Glasgow