Short echo 1 H in-vivo brain MR spectra are difficult to quantify for several reasons: low signal to noise ratio, the severe overlap of spectral lines, the presence of macromolecule resonances beneath the resonances of interest, and the effect of resonances adjacent to the spectral region of interes
The use of a priori knowledge to quantify short echo in vivo1h mr spectra
✍ Scribed by Jeff A. Stanley; Dick J. Drost; Peter C. Williamson; R. Terry Thompson
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 805 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
In vivo ^1^H MR spectra of the prefrontal cortex acquired with the stimulated echo acquisition mode (STEAM) TE = 20 ms sequence were quantified to determine relative levels of cerebral metabolites. A priori knowledge of spectra from individual metabolites in aqueous solution was incorporated into a frequency domain quantification technique. The accuracy and precision of modeling these metabolites were investigated with simulated spectra of varying signal‐to‐noise ratios (SNRs) and relative metabolite levels. The efficacy of modeling in vivo data was tested by quantifying 10 repeated measures of two consecutively acquired in vivo spectra (an 8−cm^3^ volume of interest (VOI) and a 4−cm^3^ VOI positioned within the 8−cm^3^ VOI) on the same normal subject. The differences in levels of glutamate (Glu), phosphocreatine plus creatine (PCr+Cr) and choline‐containing compounds (Cho~1~ between spectra from the 8− and 4−cm^3^ VOIs corresponded with the expected differences observed in the proportions of gray matter within the VOIs (estimated from ^1^H images). Correcting for the T~1~ and T~2~ relaxation, the estimated concentrations of N‐acetylaspartate, PCr+Cr, Cho~1~, Glu, and glutamine were consistent with previous in vivo and in vitro reports.
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