Quantitative magnetic resonance imaging in the assessment of degenerative disc disease

Magn Reson Med. 1998 Dec;40(6):900-7. doi: 10.1002/mrm.1910400616.

Abstract

Understanding degenerative intervertebral disc diseases hinges on the ability to objectively and noninvasively assess the disc matrix composition and integrity. The potential of quantitative magnetic resonance imaging to meet these demands was evaluated. Analyzing the T1 and T2 signal patterns in the nucleus pulposus with increasing Thompson morphological grade revealed a significant reduction related to grade. This significant decrease in T1 and T2 in the nucleus pulposus with grade 4 degeneration and the corresponding low correlation coefficients with respect to the content of individual matrix molecules suggest that matrix integrity plays an important and distinct role in determining T1 and T2 signal. Similarly, the significant increase in magnetization transfer in the nucleus pulposus observed in grade 4 degeneration did not correlate with the changes in molecular content in these highly degenerated discs. Again, this lack of correlation clearly indicates that the tissue integrity and matrix composition independently contribute to the magnetization transfer signal. This study presents the first clear evidence that quantitative magnetic resonance analysis reflects not only the disc matrix composition, but also the structural integrity of the matrix of the disc.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Analysis of Variance
  • Body Water / chemistry
  • Cadaver
  • Collagen / analysis
  • Glycosaminoglycans / analysis
  • Humans
  • Intervertebral Disc / chemistry
  • Intervertebral Disc / pathology*
  • Lumbar Vertebrae / chemistry
  • Lumbar Vertebrae / pathology*
  • Magnetic Resonance Imaging / instrumentation
  • Magnetic Resonance Imaging / methods*
  • Magnetic Resonance Imaging / statistics & numerical data
  • Middle Aged
  • Regression Analysis
  • Spinal Diseases / diagnosis*
  • Spinal Diseases / metabolism
  • Time Factors

Substances

  • Glycosaminoglycans
  • Collagen