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HERMES: Hadamard encoding and reconstruction of MEGA-edited spectroscopy
Kimberly L Chan1,2,3, Nicolaas A J Puts2,3, Michael Schär3
1Department of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
This study introduces HERMES, a novel Hadamard-encoded spectral editing technique for simultaneously quantifying N-acetyl aspartate (NAA) and N-acetyl aspartyl glutamate (NAAG) at 3 Tesla. The method demonstrated accurate and separable detection of these metabolites in vivo.
Area of Science:
- Magnetic Resonance Spectroscopy
- Neuroimaging
- Metabolomics
Background:
- Simultaneous quantification of N-acetyl aspartate (NAA) and N-acetyl aspartyl glutamate (NAAG) is challenging due to overlapping signals.
- Accurate measurement of NAA and NAAG is crucial for understanding brain metabolism and neurological conditions.
Purpose of the Study:
- To introduce and evaluate a novel Hadamard-encoded spectral editing scheme, HERMES (Hadamard Encoding and Reconstruction of MEGA-Edited Spectroscopy).
- To assess the performance of HERMES for simultaneous quantification of NAA and NAAG at 3 Tesla magnetic resonance imaging (MRI).
Main Methods:
- Utilized density-matrix simulations for optimizing the HERMES pulse sequence.
- Validated the method using phantom experiments at 3T.
- Acquired in vivo data from the centrum semiovale of 12 healthy subjects.
- Modeled in vivo data to determine the NAA:NAAG concentration ratio and assessed potential coediting.
Main Results:
- HERMES demonstrated excellent signal segregation for NAA and NAAG with minimal crosstalk in simulations and phantom studies.
- In vivo data showed good agreement with simulated multiplet patterns.
- The in vivo NAA:NAAG concentration ratio was determined to be 4.22:1, consistent with literature values.
- Simulations indicated minor coediting from aspartate and glutathione.
Conclusions:
- The HERMES technique enables simultaneous and separable detection of NAA and NAAG at 3T.
- This method offers a viable solution for quantifying otherwise overlapping metabolites in magnetic resonance spectroscopy.
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