## Abstract Echo‐planar spectroscopic imaging (EPSI) is one of the fastest spectroscopic imaging (SI) methods. It has been applied to ^1^H MR spectroscopy (MRS) studies of the human brain in vivo. However, to our knowledge, EPSI with detection of the ^31^P nucleus to monitor phosphorus‐containing n
High Speed 1H Spectroscopic Imaging in Human Brain by Echo Planar Spatial-Spectral Encoding
✍ Scribed by Stefan Posse; Gioacchino Tedeschi; Robert Risinger; Robert Ogg; Denis Le Bihan
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 969 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We introduce a fast and robust spatial‐spectral encoding method, which enables acquisition of high resolution short echo time (13 ms) proton spectroscopic images from human brain with acquisition times as short as 64 s when using surface coils. The encoding scheme, which was implemented on a clinical 1.5 Tesla whole body scanner, is a modification of an echo‐planar spectroscopic imaging method originally proposed by Mansfield Magn. Reson. Med. 1, 370–386 (1984), and utilizes a series of read‐out gradients to simultaneously encode spatial and spectral information. Superficial lipid signals are suppressed by a novel double outer volume suppression along the contours of the brain. The spectral resolution and the signal‐to‐noise per unit time and unit volume from resonances such as N‐acetyl aspartate, choline, creatine, and inositol are comparable with those obtained with conventional methods. The short encoding time of this technique enhances the flexibility of in vivo spectroscopic imaging by reducing motion artifacts and allowing acquisition of multiple data sets with different parameter settings.
📜 SIMILAR VOLUMES
## Abstract A new spectral bandwidth expansion technique for highspeed magnetic resonance spectroscopic imaging (MRSI) based on an echo‐planar technique is presented. This expansion can be achieved by spatial and chemical shift selective saturation without increasing the total measurement time. In