Abstract
Purpose: Chemical exchange saturation transfer is used commonly to generate MRI contrast based on the chemical exchange effect. The spin-lock techniques can also be used to probe the chemical exchange and other molecular motion processes in tissues. The presence of fat can cause errors in spin-lock MRI. Signals from fat are typically suppressed based on spectral selectivity or T1 nulling approaches in spin-lock imaging. However, these methods cannot be used to suppress fat signals from multiple fat peaks. To address this problem, we report chemical-shift encoding–based water–fat separation approaches with multifrequency fat spectrum modeling. Methods: Both the conventional spin-lock and the adiabatic continuous-wave constant-amplitude spin lock (ACCSL) with multi-echo acquisitions are investigated for chemical-shift encoding–based water–fat separation in spin-lock imaging. A comparison is made of reconstructions based on 3 models: a single-peak fat spectrum model, a standard precalibrated proton density 6-peak fat spectrum model, and the self-calibrated relaxation-dependent 3-peak fat spectrum model. Comparisons were performed using Bloch simulations, phantom, and in vivo experiments at 3 T. Results: Conventional spin-lock acquisitions cannot be used for reliable water–fat separation with a multipeak fat spectrum model. Water–fat separation based on ACCSL acquisitions achieves superior performance compared with the use of conventional spin-lock acquisitions. The best result is achieved from ACCSL acquisition with self-calibrated relaxation-dependent multipeak fat spectrum modeling. Conclusion: The ACCSL acquisition can be used for chemical-shift encoding–based water–fat separation with multipeak fat spectrum modeling. This approach has the potential to improve quantitative analysis using spin-lock MRI for assessing the biochemical properties of tissues.
Originalsprache | Englisch |
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Seiten (von - bis) | 1608-1624 |
Seitenumfang | 17 |
Fachzeitschrift | Magnetic Resonance in Medicine |
Jahrgang | 83 |
Ausgabenummer | 5 |
DOIs | |
Publikationsstatus | Veröffentlicht - 1 Mai 2020 |