Proton‐decoupled 31P chemical shift imaging of the human brain in normal volunteers

Proton‐decoupled, 31P three‐dimensional (3‐D) chemical shift imaging (CSI) spectra have been acquired from the entire human brain using a new dual tuned resonator. The resonator operates in quadrature mode to provide improved sensitivity, excellent B1 homogeneity, and reduced power deposition at both frequencies. Proton‐decoupled and fully NOE enhanced, 31P spectra were acquired from normal volunteers using Waltz‐4 proton decoupling with continuous wave bi‐level excitation applied through a second radio frequency channel. Well resolved peaks in the phosphomonoester (PME) and phosphodiester regions were obtained from non‐localized FIDs and spectra localized with 3‐D CSI without processing for resolution enhancement. pH measurements made over large regions of the brain using the Pi resonance show no significant variations (6.9±0.02) for a single individual. The improved spectral resolution and sensitivity of the PME resonances results in more well defined metabolite images of the PME peak region.

[1]  T R Brown,et al.  Two configurations of the four-ring birdcage coil for 1H imaging and 1H-decoupled 31P spectroscopy of the human head. , 1994, Journal of magnetic resonance. Series B.

[2]  T. Brown,et al.  A multislice sequence for 31P in Vivo Spectroscopy. 1D chemical-shift imaging with an adiabatic half-passage pulse , 1989 .

[3]  H C Charles,et al.  Human in vivo phosphate metabolite imaging with 31P NMR , 1988, Magnetic resonance in medicine.

[4]  I J Lowe,et al.  A fast recovery probe and receiver for pulsed nuclear magnetic resonance spectroscopy. , 1968, Journal of scientific instruments.

[5]  J S Taylor,et al.  Chemical shift imaging of human brain: axial, sagittal, and coronal P-31 metabolite images. , 1990, Radiology.

[6]  J S Taylor,et al.  Metabolite images of the human arm: Changes in spatial and temporal distribution of high energy phosphates during exercise , 1991, NMR in biomedicine.

[7]  A. J. Shaka,et al.  Evaluation of a new broadband decoupling sequence: WALTZ-16 , 1983 .

[8]  B. Chance,et al.  31P nuclear magnetic resonance spectroscopic investigation of human neuroblastoma in situ. , 1985, The New England journal of medicine.

[9]  M. Crowley,et al.  Bone and soft-tissue lesions: diagnosis with combined H-1 MR imaging and P-31 MR spectroscopy. , 1989, Radiology.

[10]  Truman R. Brown,et al.  A method for automatic quantification of one-dimensional spectra with low signal-to-noise ratio , 1987 .

[11]  B. Ross,et al.  Metabolic Response of Glioblastoma to Adoptive Immunotherapy: Detection by Phosphorus MR Spectroscopy , 1989, Journal of computer assisted tomography.

[12]  W. J. Lorenz,et al.  In vivo nuclear overhauser effect in 31P‐ {1H} double‐resonance experiments in a 1.5‐T whole‐body MR system , 1990, Magnetic resonance in medicine.

[13]  W. Perman,et al.  Spatially resolved high resolution spectroscopy by “four-dimensional” NMR , 1983 .

[14]  G B Matson,et al.  Spin echo 31P spectroscopic imaging in the human brain , 1990, Magnetic resonance in medicine.

[15]  Truman R. Brown,et al.  The accuracy of quantification from 1D NMR spectra using the PIQABLE algorithm , 1989 .

[16]  D. Gadian,et al.  Phosphodiesters in the Liver: The Effect of Field Strength on the 31P Signal , 1989, Magnetic resonance in medicine.

[17]  P R Luyten,et al.  Broadband proton decoupling in human 31p NMR spectroscopy , 1989, NMR in biomedicine.

[18]  S. Naruse,et al.  Brain edema studied by magnetic resonance. , 1986, Seminars in neurology.

[19]  J. H. Noggle The nuclear Overhauser effect , 1971 .

[20]  J. Frahm,et al.  Localized 31P NMR spectroscopy of the amt human brain in vivo using stimulated-echo (STEAM) sequences , 1990 .

[21]  J. Evelhoch,et al.  Response-specific adriamycin sensitivity markers provided by in vivo 31P nuclear magnetic resonance spectroscopy in murine mammary adenocarcinomas. , 1987, Cancer research.

[22]  D. Gadian,et al.  31P magnetic resonance spectroscopy of the normal human brain: approaches using four dimensional chemical shift imaging and phase mapping techniques , 1989, NMR in biomedicine.