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Rosette Cardiac MR Fingerprinting for Simultaneous T1, T2, T 2 * , and Fat Fraction Mapping Using a Multi-Echo Deep
Evan Cummings1,2, Gastao Cruz1, Jacob Richardson1
1Radiology, University of Michigan, Ann Arbor, Michigan, USA.
This study introduces a new method combining multi-echo cardiac Magnetic Resonance Fingerprinting (cMRF) with deep image prior (DIP) reconstruction. This approach accurately quantifies multiple cardiac tissue properties simultaneously, showing reduced variance in healthy subjects.
Area of Science:
- Cardiovascular Imaging
- Medical Physics
- Biomedical Engineering
Background:
- Quantitative mapping of cardiac tissue properties is crucial for diagnosing and monitoring various heart conditions.
- Cardiac Magnetic Resonance Fingerprinting (cMRF) offers rapid, simultaneous multi-parameter quantification from a single scan.
Purpose of the Study:
- To develop and validate a multi-echo cMRF acquisition combined with a deep image prior (DIP) framework.
- To reconstruct simultaneous cardiac T1, T2, T2*, and fat fraction maps.
Main Methods:
- A 2D, single-breathhold, ECG-gated rosette trajectory cMRF sequence was used.
- Data were processed using a DIP reconstruction trained with the cMRF encoding model.
- T1, T2, T2*, and fat fraction maps were generated via curve fitting and pattern matching.
Main Results:
- The technique showed good agreement with gold-standard measurements in phantoms.
- In healthy subjects, DIP reconstruction measurements aligned with clinical cardiac measurements.
- DIP reconstruction demonstrated lower voxel-level variance compared to other methods in healthy subjects.
Conclusions:
- Multi-echo cMRF with DIP reconstruction enables simultaneous quantification of key cardiac parameters (T1, T2, T2*, fat).
- The method shows good agreement with conventional mapping techniques in phantom and in vivo studies.
- DIP reconstruction offers improved accuracy and reduced variance over direct gridding and iterative low-rank methods.
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