## Abstract In vivo longitudinal relaxation times of __N__‐acetyl compounds (NA), choline‐containing substances (Cho), creatine (Cr), __myo__‐inositol (mI), and tissue water were measured at 1.5 and 3 T using a point‐resolved spectroscopy (PRESS) sequence with short echo time (TE). __T__~1~ values
Line scan imaging of brain metabolites with CPMG sequences at 1.5 tesla
✍ Scribed by Robert V. Mulkern; Jiqun Meng; Koichi Oshio; A. Aria Tzika
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 830 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1053-1807
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A line scan Carr‐Purcell‐Meiboom‐Gill (CPMG) spectroscopic imaging sequence has been implemented on a standard 1.5 T clinical scanner to map metabolite signals at multiple echo times from voxels along selected tissue columns through the brain. The CPMG multi‐echo spectroscopic image data sets are used to estimate brain metabolite T2 decay parameters in a group of healthy volunteers and in one tumor patient. Inherent trade‐offs between T2 decay, spectral resolution, and echo spacing prove to be important limiting factors. In particular, separate quantitation of choline and creatine resonances at 1.5 T was not achieved in the present implementation. However, the ability to collect data sets suitable for T2 decay analyses of combined choline and creatine resonances and N‐acetyl aspartate resonances in under 10 minutes may prove of clinical utility in the study of brain pathology.
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