Abstract |
Mild traumatic brain injury (MTBI) is a major public health problem in the United States. A significant subset of MTBI patients develop persistent and distressing neurological, cognitive, and behavioral symptoms, known as the post-concussion syndrome (PCS). To date, multiple studies have assessed the relationship between brain-related proteins found in the serum at the time of injury, and the development of PCS. We conducted a systematic review of prospective cohort studies that assessed the ability of serum biochemical markers to predict PCS after MTBI. A total of 11 studies assessing three different potential biochemical markers of PCS--S100 proteins, neuron-specific enolase (NSE), and cleaved Tau protein ( CTP)--met selection criteria. Of these markers, S100 appeared to be the best researched. We conclude that no biomarker has consistently demonstrated the ability to predict PCS after MTBI. A combination of clinical factors in conjunction with biochemical markers may be necessary to develop a comprehensive decision rule that more accurately predicts PCS after MTBI.
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Authors | Tomer Begaz, Demetrios N Kyriacou, Jordana Segal, Jeffrey J Bazarian |
Journal | Journal of neurotrauma
(J Neurotrauma)
Vol. 23
Issue 8
Pg. 1201-10
(Aug 2006)
ISSN: 0897-7151 [Print] United States |
PMID | 16928178
(Publication Type: Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't, Review, Systematic Review)
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Chemical References |
- Biomarkers
- S100 Proteins
- tau Proteins
- Phosphopyruvate Hydratase
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Topics |
- Animals
- Biomarkers
(analysis)
- Brain Injuries
(diagnosis, metabolism)
- Humans
- Phosphopyruvate Hydratase
(analysis, metabolism)
- Post-Concussion Syndrome
(metabolism)
- S100 Proteins
(analysis, metabolism)
- tau Proteins
(analysis, metabolism)
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