z-logo
open-access-imgOpen Access
Serum Levels of Biochemical Markers of Traumatic Brain Injury
Author(s) -
Keith Borg,
Jordan Bonomo,
Edward C. Jauch,
Peter Kupchak,
Eric Stanton,
Bruce Sawadsky
Publication year - 2012
Publication title -
isrn emergency medicine
Language(s) - English
Resource type - Journals
eISSN - 2090-5637
pISSN - 2090-5629
DOI - 10.5402/2012/417313
Subject(s) - glasgow coma scale , traumatic brain injury , medicine , algorithm , enolase , mathematics , surgery , psychiatry , immunohistochemistry
Background. A biomarker would be valuable in the diagnosis, risk stratification and prognosis of patients with traumatic brain injury (TBI). Methods. We measured serum levels of S-100 β, neuron specific enolase (NSE) and myelin basic protein (MBP) in 50 TBI subjects, and 50 age and gender matched controls. Patients were recruited within 6 hours of the initial injury, they had an initial Glasgow Coma Scale (GCS) score of 14 or less, or a GCS score of 15 with witnessed loss of consciousness (LOC) or amnesia. Results. S-100 β, NSE and MBP levels were significantly higher in TBI subjects than in control subjects ( 0 . 0 0 1 for S-100 β and NSE; = 0 . 0 0 9 for MBP). Initial S-100 β levels were significantly higher in TBI subjects who had not retuned to normal activities 2 weeks following their injury than in TBI subjects who had retuned to normal activities ( = 0 . 0 2 2 ). MBP levels were higher in TBI subjects with positive findings on the baseline CT scan than in CT-negative subjects ( = 0 . 0 0 7 ). Conclusions. S-100 β, NSE and MBP may be present in the sera of TBI subjects in elevated quantities relative to controls. S-100 β may aid in predicting short-term outcome in TBI subjects.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom