Diffusion tensor imaging reliably detects experimental traumatic axonal injury and indicates approximate time of injury

被引:346
|
作者
Mac Donald, Christine L.
Dikranian, Krikor
Bayly, Philip
Holtzman, David
Brody, David
机构
[1] Washington Univ, Dept Neurol, St Louis, MO 63110 USA
[2] Washington Univ, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[3] Washington Univ, Dept Mol Biol, St Louis, MO 63110 USA
[4] Washington Univ, Hope Ctr Neurol Disorders, St Louis, MO 63110 USA
[5] Washington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
[6] Washington Univ, Dept Mech Engn, St Louis, MO 63130 USA
来源
JOURNAL OF NEUROSCIENCE | 2007年 / 27卷 / 44期
关键词
magnetic resonance imaging; diffusion tensor imaging; traumatic brain injury; axonal injury; white matter injury; forensic imaging;
D O I
10.1523/JNEUROSCI.3647-07.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Traumatic axonal injury (TAI) may contribute greatly to neurological impairments after traumatic brain injury, but it is difficult to assess with conventional imaging. We quantitatively compared diffusion tensor imaging (DTI) signal abnormalities with histological and electron microscopic characteristics of pericontusional TAI in a mouse model. Two DTI parameters, relative anisotropy and axial diffusivity, were significantly reduced 6 h to 4 d after trauma, corresponding to relatively isolated axonal injury. One to 4 weeks after trauma, relative anisotropy remained decreased, whereas axial diffusivity "pseudo-normalized" and radial diffusivity increased. These changes corresponded to demyelination, edema, and persistent axonal injury. At every time point, DTI was more sensitive to injury than conventional magnetic resonance imaging, and relative anisotropy distinguished injured from control mice with no overlap between groups. Remarkably, DTI changes strongly predicted the approximate time since trauma. These results provide an important validation of DTI for pericontusional TAI and suggest novel clinical and forensic applications.
引用
收藏
页码:11869 / 11876
页数:8
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