Measurement of N-acetylaspartylglutamate in the human frontal brain by 1H-MRS at 7 T
✍ Scribed by Changho Choi; Subroto Ghose; Jinsoo Uh; Aditya Patel; Ivan E. Dimitrov; Hanzhang Lu; Deborah Douglas; Sandeep Ganji
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 262 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
N‐Acetylaspartylglutamate in human brain has been measured with difference editing at 7 T. The CH~2~ proton resonances (∼2.5 ppm) of the aspartyl groups of N‐acetylaspartylglutamate and N‐acetylaspartate were difference edited (MEGA) using 20‐msec gaussian radiofrequency pulses for selective 180° rotations of the coupling partners at 4.61 and 4.38 ppm, respectively. The echo time of the editing sequence, 108 msec, was obtained in phantom tests. Single‐voxel localized in vivo measurements were conducted in the medial prefrontal and right frontal cortices of five healthy volunteers. The gray and white matter fractions within the voxels were obtained from T~1~‐weighted image segmentation. Using linear regression of the metabolite concentration vs. fractional white matter contents within the voxels, the N‐acetylaspartylglutamate‐to‐N‐acetylaspartate concentration ratios in gray and white matter were estimated to be 0.13 and 0.28 by difference editing (95% confidence intervals 0.07–0.19 and 0.22–0.34), respectively, assuming identical relaxation effects between the metabolites. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract A new ^1^H‐MRS filtering strategy for selective measurement of glycine (Gly) in human brain in vivo at 3.0T is proposed. Investigation of multiple refocusing following a 90° excitation pulse indicated that triple refocusing is most effective for suppression of the strongly coupled reson
## Abstract In vivo ^1^H NMR spectra from the human brain were measured at 7 T. Ultrashort echo‐time STEAM was used to minimize J‐modulation and signal attenuation caused by the shorter __T__~2~ of metabolites. Precise adjustment of higher‐order shims, which was achieved with FASTMAP, was crucial t
## Abstract A single‐voxel proton magnetic resonance spectroscopy (^1^H‐MRS) filtering strategy for in vivo detection of serine (Ser) in human brain at 7T is proposed. Spectral difference of coupled resonances arising from different subecho times of triple refocusing at a constant total echo time (
## Abstract ^1^H‐MRS at high field has been increasingly utilized to study brain metabolism in healthy and pathological states. The aim of this work was to determine the effects of physiological motion on the results of this exam in the presence of the increased susceptibility differences at high f