Reinsertion of autogenous nucleus pulposus, an innovative method to delay further disc degeneration, has been proved with an experimental animal model. This study examined whether coculture of nucleus pulposus cells with annulus fibrosus cells (a) activates annulus fibrosus cells and (b) retards dis
In vivo quantification of delayed gadolinium enhancement in the nucleus pulposus of human intervertebral disc
✍ Scribed by Jaakko L. Niinimäki; Outi Parviainen; Jyrki Ruohonen; Risto O. Ojala; Mauno Kurunlahti; Jaro Karppinen; Osmo Tervonen; Miika T. Nieminen
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 220 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1053-1807
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Purpose
To quantify the delayed contrast agent enhancement in the nucleus pulposus of the intervertebral disc by means by T1 relaxation time measurements, and to correlate the enhancement with visual grading of disc degeneration. Diffusion of nutrients through the endplate is a key factor in tissue viability in the intervertebral disc. It can be simulated in vivo using magnetic resonance imaging (MRI) by measuring delayed gadolinium (Gd) enhancement of the disc.
Materials and Methods
Twenty male volunteers underwent a lumbar spine examination at 1.5T. T2‐weighted sagittal images were used to score disc degeneration. T1 relaxation times were measured before and 90 minutes after intravenous administration of Gd‐DTPA‐BMA by applying a series of sagittal single‐slice inversion‐recovery fast spin‐echo (IR‐FSE) scans.
Results
A total of 93 discs were analyzed. A statistically significant decrease in the T1 relaxation time of the nucleus pulposus was observed as a result of contrast‐agent intake. The percentage change in the T1 relaxation rate for individual discs was up to 126%. A positive trend was observed between the change in the T1 relaxation rate and the grading of disc degeneration.
Conclusion
Quantification of delayed enhancement of the intervertebral disc may provide a new means of studying alterations in degenerative disc disease (DDD) that explain the variation in diffusion into the intervertebral disc. J. Magn. Reson. Imaging 2006;. © 2006 Wiley‐Liss, Inc.
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