Computational analysis reveals increased blood deposition following repeated mild traumatic brain injury

Autor: Monica J. Carson, Anthony Bianchi, Andre Obenaus, Bir Bhanu, Virginia Donovan, Richard E. Hartman
Rok vydání: 2012
Předmět:
Pathology
computer.software_genre
0302 clinical medicine
Injury - Trauma - (Head and Spine)
Voxel
Cortex (anatomy)
Edema
2.1 Biological and endogenous factors
Computational analysis
FA
fractional anisotropy

Aetiology
0303 health sciences
T2
medicine.diagnostic_test
diffusion tensor imaging
Hemorrhagic progression
medicine.anatomical_structure
Neurology
DTI
HPC
Neurological
mean diffusivity
Biomedical Imaging
medicine.symptom
fractional anisotropy
medicine.medical_specialty
FA
Traumatic brain injury
Cognitive Neuroscience
HPC
hemorrhagic progression of the contusion

Neuropathology
Article
Lesion
03 medical and health sciences
medicine
Radiology
Nuclear Medicine and imaging

Quantitative magnetic resonance imaging
030304 developmental biology
MD
mean diffusivity

Histogram
business.industry
MD
Neurosciences
Magnetic resonance imaging
medicine.disease
Brain Disorders
hemorrhagic progression of the contusion
Injury (total) Accidents/Adverse Effects
Neurology (clinical)
DTI
diffusion tensor imaging

business
Injury - Traumatic brain injury
computer
030217 neurology & neurosurgery
Zdroj: NeuroImage. Clinical, vol 1, iss 1
NeuroImage : Clinical
ISSN: 2213-1582
DOI: 10.1016/j.nicl.2012.08.001
Popis: Mild traumatic brain injury (mTBI) has become an increasing public health concern as subsequent injuries can exacerbate existing neuropathology and result in neurological deficits. This study investigated the temporal development of cortical lesions using magnetic resonance imaging (MRI) to assess two mTBIs delivered to opposite cortical hemispheres. The controlled cortical impact model was used to produce an initial mTBI on the right cortex followed by a second injury induced on the left cortex at 3 (rmTBI 3d) or 7 (rmTBI 7d) days later. Histogram analysis was combined with a novel semi-automated computational approach to perform a voxel-wise examination of extravascular blood and edema volumes within the lesion. Examination of lesion volume 1d post last injury revealed increased tissue abnormalities within rmTBI 7d animals compared to other groups, particularly at the site of the second impact. Histogram analysis of lesion T2 values suggested increased edematous tissue within the rmTBI 3d group and elevated blood deposition in the rm TBI 7d animals. Further quantification of lesion composition for blood and edema containing voxels supported our histogram findings, with increased edema at the site of second impact in rmTBI 3d animals and elevated blood deposition in the rmTBI 7d group at the site of the first injury. Histological measurements revealed spatial overlap of regions containing blood deposition and microglial activation within the cortices of all animals. In conclusion, our findings suggest that there is a window of tissue vulnerability where a second distant mTBI, induced 7d after an initial injury, exacerbates tissue abnormalities consistent with hemorrhagic progression.
Highlights ► rmTBI 7d apart resulted in an increased total lesion volume 1d post last injury. ► Lesion volume was increased at the distant second injury site in rmTBI 7d animals. ► Increased edema was seen at the distant second injury site in rmTBI 3d animals. ► Voxel-wise analysis detected hemorrhagic progression in rmTBI 7d animals. ► Increased microglia were observed in the rmTBI 7d animals.
Databáze: OpenAIRE