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Brain-Derived Microparticles in Patients with Severe Isolated TBI
M Nekludov1, B-M Bellander2, D Gryth1
1a Karolinska Institutet, Department of Physiology and Pharmacology, section for Anesthesiology and Intensive Care , Karolinska University Hospital Solna , Stockholm , Sweden.
Patients with severe traumatic brain injury (TBI) exhibit elevated levels of circulating brain-derived microparticles (MPs). These findings suggest MPs may serve as biomarkers for TBI, though further research is needed for specific markers.
Area of Science:
- Neuroscience
- Biomarkers
- Trauma Research
Background:
- Traumatic brain injury (TBI) is a significant cause of mortality and disability.
- Identifying reliable biomarkers for TBI is crucial for diagnosis and management.
- Circulating microparticles (MPs) are emerging as potential indicators of cellular damage.
Purpose of the Study:
- To investigate the presence and concentration of brain-derived microparticles (MPs) in patients with severe TBI.
- To assess MPs expressing glial fibrillary acidic protein (GFAP), neuron-specific enolase (NSE), and aquaporin-4 (AQP4) in systemic and cerebrovenous blood.
- To compare MP levels in TBI patients with healthy controls.
Main Methods:
- Prospective observational study involving 15 patients with severe isolated TBI.
- Repeated measurements of MP concentrations in arterial and cerebrovenous blood.
- MP analysis included markers GFAP, NSE, and AQP4 at baseline and up to 72 hours post-injury.
Main Results:
- Significantly higher concentrations of GFAP- and AQP4-expressing MPs were found in TBI patients compared to controls.
- NSE-expressing MP levels were also elevated in the TBI group.
- No significant transcranial gradients were observed for these MPs.
Conclusions:
- Patients with severe TBI demonstrate increased levels of circulating brain-derived MPs.
- These findings highlight the potential of MPs as biomarkers for brain injury.
- Further research is required to identify specific and sensitive MP markers for TBI.
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