Table 1.
Biomarkers and their applications.
Biomarker | Key features | References |
---|---|---|
S100B | Serum concentrations >0.48 μg/L in <6 hours predictive of Glasgow Outcome Scale Extended (GOSE) scores of <5 (severe disability) at 1 month post injury Extracerebral injuries have significant impact on predictive ability of S100B |
[7, 11, 12] |
| ||
GAL3 | High plasma levels associated with GCS and in-hospital mortality | [8, 21] |
| ||
Copeptin | Independent predictor of progressive haemorrhagic injury and acute traumatic coagulopathy and outcome at 1 year after injury | [23, 26] |
| ||
NSE | >10 μg/L in <6 hours associated with headaches at 6 months Elevated levels indicator of mortality |
[7, 13, 14] |
| ||
UCH-L1 | Plasma and CSF levels shown to be elevated for several days and associated with diffuse injuries | [9, 22, 27] |
| ||
GFAP | Elevations primarily found in patients with a focal mass lesion (V to Marshall VI) When Marshall is combined with GFAP, it produces superior sensitivity and specificity for TBI |
[10, 22] |
| ||
MMP9 | Elevated levels up to 8 hours after TBI; smaller increase maintained at 24 hours | [8] |
| ||
MBP | Serum concentrations peak 48–72 hours after injury and can remain elevated for 2 weeks Potential biomarker of intracranial haemorrhage and axonal injury |
[7, 15, 16, 18] |
| ||
MAG | Strong predictors of functional outcome in mild TBI | [17] |
| ||
Tau | Raised CSF levels associated with poor clinical outcome | [24] |