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Localized 2D correlation spectroscopy in human brain at 3 T.
Anne Ziegler1, Brigitte Gillet, Jean-Claude Beloeil
1Unité mixte INSERM, Université J. Fourier U438 'RMN Bioclinique', LRC CEA, CHU pavillon B, BP 217, 38043 Cedex 9, Grenoble, France. anne.ziegler@ujf-grenoble.fr
Magma (New York, N.Y.)
|February 14, 2002
Summary
This study demonstrates a new method for acquiring localized 2D 1H correlation spectra quickly. This advance in magnetic resonance spectroscopy (MRS) is suitable for clinical applications.
Area of Science:
- Magnetic Resonance Spectroscopy (MRS)
- Biomedical Imaging
- Nuclear Magnetic Resonance (NMR)
Background:
- Localized 2D 1H correlation spectroscopy provides detailed metabolic information.
- Acquiring these spectra within clinically relevant timeframes has been a challenge.
- Previous methods were often too time-consuming for routine clinical use.
Purpose of the Study:
- To develop a method for obtaining localized 2D 1H correlation spectra.
- To achieve this within a small volume of interest and a clinically feasible experiment time.
- To assess the feasibility of this technique for clinical applications.
Main Methods:
- A modified Pulse-acquire, Echo-train, SpectroscopY (PRESS) technique was employed.
- The final 180-degree pulse in the PRESS sequence was modified to a 90-degree pulse.
- This modification facilitated both refocusing and coherence transfer.
- 2D correlation spectroscopy was performed on healthy volunteers using a 3 T clinical magnet.
Main Results:
- Localized 2D 1H correlation spectra were successfully acquired.
- The experiment was completed within 34 minutes.
- A voxel size of 27 cm³ was achieved.
- The technique demonstrated compatibility with clinical settings.
Conclusions:
- The developed method enables rapid acquisition of localized 2D 1H correlation spectra.
- The achieved speed and resolution are compatible with clinical magnetic resonance spectroscopy applications.
- This technique holds promise for future clinical metabolic profiling.