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Multi-parametric liver tissue characterization using MR fingerprinting: Simultaneous T1 , T2 , T2 *, and fat fraction
Olivier Jaubert1, Cristobal Arrieta2, Gastão Cruz1
1School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Magnetic Resonance in Medicine
|May 15, 2020
Summary
This study introduces a novel extended MR fingerprinting (MRF) method for simultaneous liver quantitative T1, T2, T2*, and fat fraction mapping. This technique enables comprehensive liver assessment in a single, rapid ~14-second breath-hold scan.
Area of Science:
- Magnetic Resonance Imaging
- Medical Physics
- Hepatology
Background:
- Quantitative imaging biomarkers like T1, T2, T2*, and fat fraction (FF) are crucial for assessing liver disease.
- Current methods often require sequential scans, increasing acquisition time and patient burden.
Purpose of the Study:
- To develop and evaluate an extended MR fingerprinting (MRF) framework for simultaneous quantitative mapping of liver T1, T2, T2*, and FF.
- To enable multi-parametric liver tissue characterization within a single, short breath-hold scan (~14 seconds).
Main Methods:
- A gradient echo (GRE) liver MRF sequence with nine readouts, low flip angles, and golden angle radial trajectory was implemented at 1.5T.
- A low-rank tensor constrained reconstruction was used for nine-echo time-series analysis.
- Dictionary matching and M0 map analysis were employed for water- and fat-specific parameter estimation, including FF.
Main Results:
- Phantom studies demonstrated high accuracy (r² > 0.97) for T1, T2, T2*, and FF mapping compared to reference methods.
- In vivo measurements in 12 subjects showed comparable results to conventional techniques with minimal bias.
- Preliminary feasibility was demonstrated in four patients.
Conclusions:
- The proposed nine-echo liver MRF sequence allows for efficient, quantitative multi-parametric liver tissue characterization.
- This technique offers a promising approach for liver disease assessment, with future validation in patient cohorts planned.
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