Abstract

BackgroundDirect measurement of disc biochemical content is impossible in vivo. Therefore, magnetic resonance imaging (MRI) is used to evaluate disc health. Unfortunately, current clinical imaging techniques do not adequately assess degeneration, especially in the early stage of cartilage endplate, and subchondral bone zone (CEPZ). Therefore, this study aimed to investigate the sensitivity of quantitative MRI methods, namely T2 relaxation time and Magnetic Transfer Ratio (MTR), to identify early disc degeneration, especially for the CEPZ, using an experimental canine model of intervertebral disc injury and to investigate their sensitivity in depicting biochemically and histologically controlled degenerative changes in the disc.MethodsSixteen juvenile dogs underwent iatrogenic annular disruption via stab incisions. The animals underwent repeated 3.0 T MR imaging, and were sacrificed 4, 8, and 12 weeks post-operatively. A continuous rectangle drawing method was used to select regions of interest for the intervertebral disc from the cephalic to caudal CEPZ including the vertebrae, nucleus pulposus (NP) and annulus fibrosus (AF), which resembled pixel measurement for imaging analysis. Presence of degenerative changes was controlled by biochemical and histological analyses. The correlations between histological score, biochemical content, and quantitative MRI signal intensities were also analyzed.ResultsBoth T2 relaxation time and MTR values changed for CEPZ, NP, and AF tissues within 12 weeks. T2 relaxation time values decreased significantly in the NP, AF, and CEPZ separately at pre-operation, 4, 8, and 12 weeks when compared each time (P < 0.05). MTR values showed no significant differences for the CEPZ between 8 and 4 weeks or 12 weeks, or compared to pre-operative values; there were significant differences for the AF. Biochemical and histological analysis showed changes consistent with quantitative MRI signal intensities for early stage degeneration.ConclusionsEarly traumatic or degenerative changes are detectable with both T2 and MTR. T2 changes were more sensitive to the differences in disc status, especially for the CEPZ. Since T2 and MTR reflect different disc properties, performing both imaging under the same conditions would be helpful in the evaluation of disc degeneration. The continuous rectangle drawing can be a sensitive method to detect the changes of CEPZ.Electronic supplementary materialThe online version of this article (doi:10.1186/s12891-015-0610-6) contains supplementary material, which is available to authorized users.

Highlights

  • Direct measurement of disc biochemical content is impossible in vivo

  • This study aimed to evaluate the correlation between biochemical changes in the intervertebral disc (IVD) and T2 relaxation times and Magnetic Transfer Ratio (MTR)

  • In this study, we demonstrated changes in T2 and MTR patterns that were related to IVD degeneration (IVDD) in a canine model

Read more

Summary

Introduction

Direct measurement of disc biochemical content is impossible in vivo. magnetic resonance imaging (MRI) is used to evaluate disc health. The etiological event or agent responsible for primary IVD degeneration (IVDD) has not been clearly identified, one major theory regarding the biomechanical failure of the CEP matrix, wherein structural damage to the collagen network (due to abnormal joint loading) reduces the restraining force capacity of the CEP [4]. This reduced restraint force of the CEP allows for increased swelling of the IVD by proteoglycans (PG), increased hydration, and, the loss of PGs and a corresponding loss of the functional integrity of the disc. The ability to detect changes in the biochemical composition of the CEP and subchondral bone could enhance our understanding of cartilage physiology and pathophysiology in IVDD and, potentially, our ability to diagnose, monitor, and treat IVDD diseases in the longer term

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call