Abstract
In vivo MRS of the human brain at ultrahigh field allows for the identification of a large number of metabolites at higher spatial resolutions than currently possible in clinical practice. However, the in vivo localization of single-voxel spectroscopy has been shown to be challenging at ultrahigh field because of the low bandwidth of refocusing radiofrequency (RF) pulses. Thus far, the proposed methods for localized MRS at 7 T suffer from long TE, inherent signal loss and/or a large chemical shift displacement artifact that causes a spatial displacement between resonances, and results in a decreased efficiency in editing sequences. In this work, we show that, by driving a standard volume coil with two RF amplifiers, focusing the B 1+ field in a certain location and using high-bandwidth adiabatic refocusing pulses, a semi-LASER (semi-localized by adiabatic selective refocusing) localization is feasible at short TE in the human brain with full signal acquisition and a low chemical shift displacement artifact at 7 T.
Original language | English |
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Pages (from-to) | 1038-1046 |
Number of pages | 9 |
Journal | NMR in Biomedicine |
Volume | 24 |
Issue number | 9 |
DOIs | |
Publication status | Published - Nov 2011 |
Keywords
- 7 T
- Adiabatic refocusing
- Human brain
- Localized by adiabatic selective refocusing (LASER)
- Multi-transmit
- Signal-to-noise ratio
- Single-voxel MRS