Longitudinal assessment of spinal cord injuries in nonhuman primates with quantitative magnetization transfer
Purpose This study aimed to evaluate the reproducibility and specificity of quantitative magnetization transfer (qMT) imaging for monitoring spinal cord injuries (SCIs). Methods MRI scans were performed in anesthetized monkeys at 9.4T, before and serially after a unilateral lesion of the cervical sp...
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Published in | Magnetic resonance in medicine Vol. 75; no. 4; pp. 1685 - 1696 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.04.2016
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Purpose
This study aimed to evaluate the reproducibility and specificity of quantitative magnetization transfer (qMT) imaging for monitoring spinal cord injuries (SCIs).
Methods
MRI scans were performed in anesthetized monkeys at 9.4T, before and serially after a unilateral lesion of the cervical spinal cord. A two‐pool fitting model was used to derive qMT parameters.
Results
qMT measures were reproducible across normal subjects, with an average pool size ratio (PSR) of 0.086 ± 0.003 (mean ± SD) for gray matter, and 0.120 ± 0.005 for white matter, respectively. Compared with normal gray matter, the PSR of abnormal tissues rostral and caudal to the injury site decreased by 19.5% (P < 0.05), while the PSR of the cyst‐like volume decreased drastically weeks after SCI. Strong correlations in cyst‐like regions were observed between PSR and other MRI measures including longitudinal relaxation rate (R1), apparent diffusion coefficient and fractional anisotropy (FA). Decreased PSR and FA values correlated well with demyelination in abnormal tissues.
Conclusion
The qMT parameters provide robust and specific information about the molecular and cellular changes produced by SCI. PSR detected demyelination and loss of macromolecules in abnormal tissue regions rostral and caudal to the cyst/lesion sites. Magn Reson Med 75:1685–1696, 2016. © 2015 Wiley Periodicals, Inc. |
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Bibliography: | NIH - No. NS069909-01; No. NS078680-01; No. CA184693; No. EB017767 ArticleID:MRM25725 istex:14DD8CD99E91B939ECF746F8A05A8D104867867F ark:/67375/WNG-N8BX7B45-F Dana foundation ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0740-3194 1522-2594 1522-2594 |
DOI: | 10.1002/mrm.25725 |