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Updated: Aug 9, 2026

Magnetic Resonance Imaging of Multiple Sclerosis at 7.0 Tesla
Published on: February 19, 2021
Fast CT-PRESS-based spiral chemical shift imaging at 3 Tesla
Dirk Mayer1, Dong-Hyun Kim, Elfar Adalsteinsson
1Richard M. Lucas Center for Magnetic Resonance Spectroscopy and Imaging, Department of Radiology, Stanford University, Stanford, California 94305-5488, USA. dirk.mayer@stanford.edu
This study introduces a novel magnetic resonance imaging (MRI) technique, combining constant-time point-resolved spectroscopy (CT-PRESS) and fast spiral chemical shift imaging. This method enables rapid, high-resolution multivoxel spectroscopy for improved metabolite detection in vivo.
Area of Science:
- Magnetic Resonance Imaging
- Spectroscopy
- Neuroimaging
Background:
- Multivoxel magnetic resonance spectroscopy (MRS) is crucial for non-invasive metabolite quantification in the brain.
- Existing techniques often face challenges with acquisition time, resolution, and spectral quality.
- Advanced pulse sequences are needed to overcome these limitations for clinical applications.
Purpose of the Study:
- To develop and validate a novel MRS sequence combining CT-PRESS and fast spiral chemical shift imaging.
- To achieve rapid acquisition of multivoxel spectra with high in-plane resolution and minimal line splitting.
- To assess the feasibility of detecting key brain metabolites within a clinically relevant timeframe.
Main Methods:
- Implementation of a novel sequence integrating constant-time point-resolved spectroscopy (CT-PRESS) with fast spiral chemical shift imaging.
- Acquisition of multivoxel spectra with a minimum total measurement time under 5 minutes.
- In-plane resolution of 1.5x1.5 cm2 within a 24 cm field of view.
- Utilized 17 CS encoding steps in t1 (Δt1=12.8 ms) and an average echo time of 151 ms.
Main Results:
- Successful acquisition of multivoxel spectra with minimal line splitting and baseline distortions.
- Detection of key metabolites including N-acetyl-aspartate, total creatine, choline-containing compounds (Cho), glutamate (Glu), and myo-inositol (mI).
- Demonstrated feasibility in a healthy volunteer within 14 minutes on a 3 T MR scanner.
Conclusions:
- The novel CT-PRESS and fast spiral sequence enables rapid, high-quality multivoxel MRS.
- This technique shows promise for efficient in vivo brain metabolite analysis.
- Further validation may lead to improved diagnostic capabilities in neurological conditions.
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