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Journal Article

In vivo proton magnetic resonance spectroscopic imaging of the healthy human brain at 9.4 T: initial experience

MPS-Authors
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Chadzynski,  GL
Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Pohmann,  R
Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Shajan,  G
Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Scheffler,  K
Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Citation

Chadzynski, G., Pohmann, R., Shajan, G., Kolb, R., Bisdas, S., Klose, U., et al. (2015). In vivo proton magnetic resonance spectroscopic imaging of the healthy human brain at 9.4 T: initial experience. Magnetic Resonance Materials in Physics, Biology and Medicine, 28(3), 239-249. doi:10.1007/s10334-014-0460-5.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002A-463F-1
Abstract
Object
In this study, the feasibility of in vivo proton magnetic resonance spectroscopic imaging (1H MRSI) of the healthy human brain at a field strength of 9.4 T, using conventional acquisition techniques, is examined and the initial experience is summarized.
Materials and methods
MRSI measurements were performed on a 9.4 T MR scanner (Siemens, Erlangen, Germany) equipped with head-only gradient insert (AC84, Siemens) and custom-developed, 8-channel transmit/24-channel receive, and 16-channel transmit/31-channel receive coils. Spectra were acquired from the superior part of the human brain with a modified STEAM sequence. Spectral quantification was done with LCModel software.
Results
Reasonable quality and signal-to-noise ratio of the acquired spectra allowed reliable quantification of 12 metabolites (Cramer-Rao lower bounds < 20 ), some of which may be difficult to quantify at field strengths below 7 T due to overlapping resonances or low concentrations.
Conclusion
While further developments are necessary to minimize chemical shift displacement and homogeneity of the transmit field, it is demonstrated that in vivo 1H MRSI at a field strength of 9.4 T is possible. However, further studies applying up-to-date techniques to overcome high-field specific problems are needed in order to assess the potential gain in sensitivity that may be offered by MRSI at 9.4 T.