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).
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).
Authors: Elizabeth A Maher; Isaac Marin-Valencia; Robert M Bachoo; Tomoyuki Mashimo; Jack Raisanen; Kimmo J Hatanpaa; Ashish Jindal; F Mark Jeffrey; Changho Choi; Christopher Madden; Dana Mathews; Juan M Pascual; Bruce E Mickey; Craig R Malloy; Ralph J DeBerardinis Journal: NMR Biomed Date: 2012-03-15 Impact factor: 4.044
Authors: Torill E Sjøbakk; Riyas Vettukattil; Michel Gulati; Sasha Gulati; Steinar Lundgren; Ingrid S Gribbestad; Sverre H Torp; Tone F Bathen Journal: Int J Mol Sci Date: 2013-01-22 Impact factor: 5.923