Radiological-Pathological Correlation of Diffusion Tensor and Magnetization Transfer Imaging in a Closed Head Traumatic Brain Injury Model

被引:78
作者
Tu, Tsang-Wei [1 ]
Williams, Rashida A. [1 ]
Lescher, Jacob D. [1 ]
Jikaria, Neekita [1 ]
Turtzo, L. Christine [1 ,2 ]
Frank, Joseph A. [1 ,3 ]
机构
[1] NIH, Frank Lab, Radiol & Imaging Sci, Ctr Clin, Bethesda, MD 20892 USA
[2] Uniformed Serv Univ Hlth Sci, Ctr Neurosci & Regenerat Med, Bethesda, MD 20814 USA
[3] Natl Inst Biomed Imaging & Bioengn, NIH, Bethesda, MD USA
关键词
FINITE-ELEMENT-ANALYSIS; AXONAL INJURY; MULTIPLE-SCLEROSIS; SPINAL-CORD; MOUSE MODEL; RAT-BRAIN; REMYELINATION; DEMYELINATION; ANISOTROPY; DISEASE;
D O I
10.1002/ana.24641
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Metrics of diffusion tensor imaging (DTI) and magnetization transfer imaging (MTI) can detect diffuse axonal injury in traumatic brain injury (TBI). The relationship between the changes in these imaging measures and the underlying pathologies is still relatively unknown. This study investigated the radiological-pathological correlation between these imaging techniques and immunohistochemistry using a closed head rat model of TBI. Methods: TBI was performed on female rats followed longitudinally by magnetic resonance imaging (MRI) out to 30 days postinjury, with a subset of animals selected for histopathological analyses. A MRI-based finite element analysis was generated to characterize the pattern of the mechanical insult and estimate the extent of brain injury to direct the pathological correlation with imaging findings. Results: DTI axial diffusivity and fractional anisotropy (FA) were sensitive to axonal integrity, whereas radial diffusivity showed significant correlation to the myelin compactness. FA was correlated with astrogliosis in the gray matter, whereas mean diffusivity was correlated with increased cellularity. Secondary inflammatory responses also partly affected the changes of these DTI metrics. The magnetization transfer ratio (MTR) at 3.5ppm demonstrated a strong correlation with both axon and myelin integrity. Decrease in MTR at 20ppm correlated with the extent of astrogliosis in both gray and white matter. Interpretation: Although conventional T2-weighted MRI did not detect abnormalities following TBI, DTI and MTI afforded complementary insight into the underlying pathologies reflecting varying injury states over time, and thus may substitute for histology to reveal diffusive axonal injury pathologies in vivo. This correlation of MRI and histology furthers understanding of the microscopic pathology underlying DTI and MTI changes in TBI.
引用
收藏
页码:907 / 920
页数:14
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