## Abstract Localized ^31^P‐STEAM experiments were performed at 3 T to estimate relaxation times of phosphorus‐containing metabolites in the human calf muscle in vivo. __T__~1~ and __T__~2~ times of PCr, P~i~, and NTPs were measured in the resting calf muscle of healthy subjects by varying TR and T
Relaxation times of skeletal muscle metabolites at 7T
✍ Scribed by Ligong Wang; Nouha Salibi; Yan Wu; Mark E. Schweitzer; Ravinder R. Regatte
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 577 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1053-1807
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✦ Synopsis
Abstract
Purpose
To demonstrate the feasibility of quantitatively evaluating and measuring T~1~ and T~2~ relaxation times of human tibialis anterior (TA) muscles metabolites in vivo at 7T and to compare these results with those of 3T.
Materials and Methods
A model lipid phantom (corn oil) and healthy volunteers (n = 4, mean ± SD age 35.6 ± 5.6 years) were scanned on 3T and 7T whole‐body MR scanners. A voxel of 10 × 10 × 10 mm^3^ was positioned on the lipid phantom and right calf TA muscles using the single‐voxel stimulated echo acquisition mode (STEAM) pulse sequence. All magnetic resonance spectroscopy (MRS) data were processed with Java‐based Magnetic Resonance User Interface (JMRUI) using Hankel Lanczos Singular Value Decomposition (HLSVD) filtering to remove the residual water signal.
Results
T~1~ shows a steady increase while T~2~ shows a slight decrease with B~0~ and the spectra show larger spectral resolution at 7T than at 3T in the lipid phantom. T~1~ values of all the metabolites are higher, while T~2~ values are slightly lower at 7T than those of 3T compared to reported results in TA. The maximum percentage of increase in T~1~ is about ≈488%, the maximum percentage of decrease in T~2~ is about ≈65%.
Conclusion
The preliminary results can potentially be used for calculating relaxation correction factors required for absolute quantitation of skeletal muscle metabolite concentrations and for further protocol and sequence optimization. J. Magn. Reson. Imaging 2009;29:1457–1464. © 2009 Wiley‐Liss, Inc.
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