TY - JOUR
T1 - Sensitivity and specificity of in vivo diffusion-weighted MRI in acute spinal cord injury
AU - Yin, Bo
AU - Tang, Yong
AU - Ye, Jichao
AU - Wu, Yanfeng
AU - Wang, Peng
AU - Huang, Lin
AU - Yang, Rui
AU - Shen, Huiyong
N1 - Funding Information:
This work was supported by grants from the Doctoral Fund of the Ministry of Education of China (2007, no. 20070558256 ), the Natural Science Foundation of Guangdong Province (2007, no. 7001603 ), the Guangzhou Science and Technology Project (2008, no. 2008A1-E4011-9 ), and the Science and Technology Social Development Project of Guangdong Province (2008, no. 2008B030301326 ).
PY - 2010/9
Y1 - 2010/9
N2 - The aim of this study was to test the sensitivity and specificity of diffusion-weighted MRI for the detection of acute spinal cord injury. Forty female New Zealand white rabbits were randomly divided into four groups: the mild, moderate and severe injury groups, and the control (sham operation) group. Contusion of the spinal cord was induced using a weight-drop impactor. All animals were imaged using T1-weighted, T2-weighted, and diffusion-weighted imaging (DWI) sequences at 30 minutes, 6 hours, and 24 hours after injury. One animal from each group was killed at each time point for histologic examination of the spinal cord. DWI had a sensitivity of 100% at all time points, whereas T2-weighted MRI had a sensitivity of 43.33% at 30 minutes after injury, 81.48% at 6 hours after injury, and 95.83% at 24 hours after injury. Conversely, the specificity of DWI was lower than that of T2-weighted MRI at all time points. One animal in the control group had a non-specific high signal on DWI. Significant systematic differences were seen between DWI and T2-weighted MRI at both 30 minutes and 6 hours after injury. The apparent diffusion coefficient values of the lesion were lower than those of adjacent unaffected regions in the mild and moderate injury groups, but higher than adjacent unaffected regions in the severe injury group. The histological findings were reliably correlated with the magnetic resonance findings. We found that DWI has a higher sensitivity, but a lower specificity, than conventional MRI for the detection of early pathological changes after contusive injury.
AB - The aim of this study was to test the sensitivity and specificity of diffusion-weighted MRI for the detection of acute spinal cord injury. Forty female New Zealand white rabbits were randomly divided into four groups: the mild, moderate and severe injury groups, and the control (sham operation) group. Contusion of the spinal cord was induced using a weight-drop impactor. All animals were imaged using T1-weighted, T2-weighted, and diffusion-weighted imaging (DWI) sequences at 30 minutes, 6 hours, and 24 hours after injury. One animal from each group was killed at each time point for histologic examination of the spinal cord. DWI had a sensitivity of 100% at all time points, whereas T2-weighted MRI had a sensitivity of 43.33% at 30 minutes after injury, 81.48% at 6 hours after injury, and 95.83% at 24 hours after injury. Conversely, the specificity of DWI was lower than that of T2-weighted MRI at all time points. One animal in the control group had a non-specific high signal on DWI. Significant systematic differences were seen between DWI and T2-weighted MRI at both 30 minutes and 6 hours after injury. The apparent diffusion coefficient values of the lesion were lower than those of adjacent unaffected regions in the mild and moderate injury groups, but higher than adjacent unaffected regions in the severe injury group. The histological findings were reliably correlated with the magnetic resonance findings. We found that DWI has a higher sensitivity, but a lower specificity, than conventional MRI for the detection of early pathological changes after contusive injury.
KW - Acute spinal cord injury
KW - Diffusion-weighted MRI
KW - Rabbits
KW - Sensitivity and specificity
UR - https://www.scopus.com/pages/publications/77955559550
U2 - 10.1016/j.jocn.2010.02.020
DO - 10.1016/j.jocn.2010.02.020
M3 - Article
C2 - 20541419
AN - SCOPUS:77955559550
SN - 0967-5868
VL - 17
SP - 1173
EP - 1179
JO - Journal of Clinical Neuroscience
JF - Journal of Clinical Neuroscience
IS - 9
ER -