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Silent T2* and T2 encoding using ZTE combined with BURST
Rolf F Schulte1, Guido Buonincontri2, Mauro Costagli2
1GE Healthcare, Munich, Germany.
Magnetic Resonance in Medicine
|November 3, 2018
Summary
This study introduces a new silent 3D imaging technique combining zero-echo-time (ZTE) and BURST encoding. This method successfully acquires high-quality T2*-weighted and T2-weighted brain images, enabling quantitative mapping.
Area of Science:
- Magnetic Resonance Imaging
- Biomedical Engineering
Background:
- Traditional MRI sequences can be noisy, potentially causing patient discomfort and limiting scan quality.
- Quantitative imaging of T2* and T2 relaxation times, as well as magnetic susceptibility, is crucial for diagnosing various neurological conditions.
Purpose of the Study:
- To develop and validate a novel, silent 3D imaging method for acquiring T2*-weighted and T2-weighted images.
- To enable the generation of quantitative T2*, T2, and magnetic susceptibility maps.
- To combine zero-echo-time (ZTE) imaging with gradient- and spin-echo BURST encoding for silent MRI.
Main Methods:
- A novel silent 3D imaging approach was developed, integrating zero-echo-time (ZTE) with gradient- and spin-echo BURST encoding.
- The method involves ZTE encoding followed by reversed k-space traversal to recall gradient echoes (BURST).
- Spin echoes were generated using 180° pulses, allowing for T2-weighted imaging. Data was reconstructed via 3D gridding and Fourier transformation.
Main Results:
- High-quality, silent T2*-weighted and T2-weighted brain images were acquired in vivo.
- Quantitative T2* and magnetic susceptibility maps were successfully extracted from gradient-echo ZTE-BURST data.
- Quantitative T2 maps were obtained from the spin-echo version of the sequence.
Conclusions:
- The combination of ZTE and BURST encoding facilitates silent acquisition of T2*- and T2-weighted brain images with excellent quality.
- This novel technique offers a promising approach for advanced quantitative MRI without acoustic noise.
- The method allows for comprehensive tissue characterization through multiple quantitative maps derived from a single silent acquisition.
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