RSNA 2011 

Abstract Archives of the RSNA, 2011


SSA17-07

Q-Space Diffusion Analysis of the Spinal Cord in Patients with Cervical Spondylotic Myelopathy in an Early Clinical Stage

Scientific Formal (Paper) Presentations

Presented on November 27, 2011
Presented as part of SSA17: Neuroradiology (Spine Imaging I)

Participants

Masaaki Hori MD, Presenter: Nothing to Disclose
Shigeki Aoki, Abstract Co-Author: Nothing to Disclose
Atsushi Nakanishi MD, PhD, Abstract Co-Author: Nothing to Disclose
Keigo Shimoji MD, Abstract Co-Author: Nothing to Disclose
Issei Fukunaga, Abstract Co-Author: Nothing to Disclose
Yuriko Suzuki BS, Abstract Co-Author: Nothing to Disclose
Koji Kamagata, Abstract Co-Author: Nothing to Disclose
Kouichi Asahi MD, Abstract Co-Author: Nothing to Disclose
Nozomi Hamasaki, Abstract Co-Author: Nothing to Disclose
Ryohei Kuwatsuru MD, Abstract Co-Author: Nothing to Disclose
Yoshitaka Masutani PhD, Abstract Co-Author: Nothing to Disclose

PURPOSE

Prospective investigation of the findings in the spinal cord in patients with cervical spondylotic myelopathy in an early clinical stage by using q-space diffusion analysis.

METHOD AND MATERIALS

Forty-seven patients with clinical symptoms of cervical myelopathy underwent MRI at a 3.0T MR system. Our implementation of q-space diffusion imaging acquired data with six b values (form 0 to 2500 sec/mm2 by 500 sec/mm2) and used diffusion encoding in six directions for every b value. Diffusional metric maps of fractional anisotropy (FA), apparent diffusion coefficient (ADC), full width at half maximum (FWHM) and mean diffusional kurtosis (MDK) were calculated by using the free software dTV II FZR (Image Computing and Analysis Laboratory, Department of Radiology, The University of Tokyo Hospital, Japan). The regions of interest (ROIs) were placed on the compressed and uncompressed spinal cords and compared.

RESULTS

In 14 patients, diffusion images were not successfully obtained, due to susceptibility and motion artifacts. Uncompressed spinal cords were measured on 27 ROIs in 15 patients, values for FA, ADC (10–3 mm2/sec), FWHM (μm) and MDK were 0.655±0.041, 0.940±0.034, 19.495±0.226 and 0.907±0.094, respectively (mean±SD). Compressed spinal cords were measured on 20 ROIs in 18 patients. Because Anderson–Darling test revealed the data are not normally distributed, Mann-Whitney U tests with the Bonferroni correction was performed for statistical analysis. Compared to the uncompressed area, FA (0.606±0.075) and MDK (0.802±0.095) decreased and FWHM (19.872±0.633) increased significantly (P < 0.05) on compressed spinal cord. Increased ADC (0.977±0.134) was also observed but statically analysis revealed no significant change.

CONCLUSION

These values may show promise as biomarkers of early microstructural changes in the compressed spinal cord. MDK and FWHM measurements are also sensitive method for evaluating spinal cord pathology in an early clinical stage cervical spondylosis and may provide additional information in vivo.

CLINICAL RELEVANCE/APPLICATION

In addition to conventional diffusion metrics, q-space diffusion analysis shows promising method for evaluating spinal cord pathology in patients with cervical spondylosis in an early clinical stage.

Cite This Abstract

Hori, M, Aoki, S, Nakanishi, A, Shimoji, K, Fukunaga, I, Suzuki, Y, Kamagata, K, Asahi, K, Hamasaki, N, Kuwatsuru, R, Masutani, Y, Q-Space Diffusion Analysis of the Spinal Cord in Patients with Cervical Spondylotic Myelopathy in an Early Clinical Stage.  Radiological Society of North America 2011 Scientific Assembly and Annual Meeting, November 26 - December 2, 2011 ,Chicago IL. http://archive.rsna.org/2011/11005934.html