Apparent T(2) relaxation times of lipid and macromolecules: a study of high-grade tumor spectra

J Magn Reson Imaging. 2008 Jan;27(1):178-84. doi: 10.1002/jmri.21223.

Abstract

Purpose: To determine T(2) relaxation times of lipid and macromolecules (Lip/MMs) observed by (1)H magnetic resonance spectroscopy ((1)H MRS) of metastases (MET) and glioblastomas (GBM), so that they may be better characterized.

Materials and methods: (1)H spectra were acquired at multiple echo times from brain lesions using point-resolved spectroscopy sequence (PRESS) at TE = 30 msec either with metabolite-nulling (six GBM and 11 MET), or without metabolite-nulling (four MET and one mucocele). All lesions were previously untreated and had subsequent histopathological classification.

Results: The T(2) of the 1.3-ppm Lip/MM peak was concentration-dependent, but at high concentrations it was significantly different (P = 0.015) between GBM (42 +/- 6 msec) and MET (63 +/- 18 msec). The broad 2.05-ppm and 0.09-ppm Lip/MM peaks had similar T(2)s in MET and GBM. The T(2) of the narrow 2.05-ppm Lip/MM peak sometimes observed had a T(2) of 100 +/- 17 msec in MET and 75 msec in the mucocele.

Conclusion: We observed significantly higher T(2) of the 1.3-ppm Lip/MM peak in MET compared with GBM at high 1.3-ppm proton concentrations, in agreement with a higher 1.3/0.9-ppm peak ratio found in MET. The relatively long T(2) of the 2.05-ppm Lip/MM peak sometimes observed in MET may cause it to be confused with N-acetyl aspartate (NAA).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / metabolism*
  • Fat Emulsions, Intravenous
  • Female
  • Glioblastoma / metabolism*
  • Humans
  • Lipid Metabolism*
  • Macromolecular Substances / metabolism*
  • Magnetic Resonance Spectroscopy / methods*
  • Male
  • Phantoms, Imaging
  • Statistics, Nonparametric

Substances

  • Fat Emulsions, Intravenous
  • Macromolecular Substances