Update on the role of S100B in traumatic brain injury in pediatric population: a meta-analysis

Alberto Morello1, Irene Schiavetti2, Enrico Lo Bue3

  • 1Neurosurgery Unit, Department of Neuroscience, "Rita Levi Montalcini", "Città Della Salute E Della Scienza" University Hospital, University of Turin, 10124, Turin, Italy. alberto.morello@unito.it.

Insights

Serum S100B measurement shows high sensitivity and negative predictive value for pediatric traumatic brain injury (TBI). This biomarker may help reduce CT scans in children, but further research is needed for regular clinical use.

Area of Science:

  • Pediatric Traumatic Brain Injury (TBI)
  • Biomarker Discovery
  • Radiology and Imaging

Background:

  • Cranial computed tomography (CT) is standard for diagnosing intracranial lesions in pediatric TBI.
  • Radiation exposure from CT scans in children increases risks of hematological and brain cancers.
  • Serum biomarkers, like S100B, are emerging as potential tools to aid TBI management.

Purpose of the Study:

  • To systematically review the utility of serum S100B as a biomarker for intracranial lesions in pediatric TBI.
  • To evaluate the diagnostic accuracy of S100B in predicting the need for CT scans in children with TBI.
  • To assess the potential of S100B to reduce CT scan utilization in pediatric TBI cases.

Main Methods:

  • Systematic review conducted following PRISMA protocol.
  • Inclusion of studies reporting serum S100B measurements and CT scans in pediatric TBI patients.
  • Meta-analysis of pooled sensitivity, specificity, negative predictive value (NPV), and positive predictive value (PPV).

Main Results:

  • 10 studies involving 1325 patients with mild TBI were included.
  • Pooled sensitivity was 98% and specificity was 45%.
  • High pooled NPV (99%) and low PPV (41%) were observed, with an AUC of 76%.

Conclusions:

  • Serum S100B measurement can aid decision-making in pediatric TBI, potentially reducing CT scan use.
  • High sensitivity and NPV suggest S100B is a promising biomarker in pediatric TBI.
  • Further studies are required to establish pediatric-specific cut-off levels and address high study heterogeneity before regular clinical adoption.
Abstract