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Rapid B1-Insensitive MR Fingerprinting for Quantitative Kidney Imaging.
Christina J MacAskill1, Michael Markley1, Susan Farr1
1From the Departments of Radiology (C.J.M., S.F., J.R.P., N.P., M.A.G., D.M., C.A.F., Y.C.), Genetics and Genome Sciences (M.L.D.), Pediatrics (M.L.D., K.M.D., C.A.F.), and Biomedical Engineering (M.A.G., D.M., C.A.F.), Case Western Reserve University, 11100 Euclid Ave, Bowell Building, Room B131, Cleveland, OH 44106; Departments of Radiology (M.M.) and Pediatrics (K.M., K.K.), University Hospitals Cleveland Medical Center, Cleveland, Ohio; and Center for Pediatric Nephrology, Cleveland Clinic Children's Hospital, Cleveland, Ohio (A.P., K.M.D.).
This study presents a fast kidney Magnetic Resonance Fingerprinting (MRF) technique for simultaneous T1 and T2 mapping. The rapid MRF method achieves precise in vivo kidney parameter quantification in a single breath hold.
Area of Science:
- Medical Imaging
- Biophysics
- Radiology
Background:
- Magnetic Resonance Fingerprinting (MRF) enables rapid, simultaneous tissue parameter quantification.
- Kidney imaging requires efficient techniques for accurate T1 and T2 mapping.
Purpose of the Study:
- To evaluate a rapid kidney MRF technique at 3.0 T.
- Assess the technique's performance in phantoms, healthy volunteers, and patients.
Main Methods:
- Developed a 15-second kidney MRF acquisition with low flip angles and spiral trajectory.
- Validated in vitro with phantoms and in vivo with 10 healthy volunteers and 3 pediatric ARPKD patients.
- Utilized multiple magnetization preparation schemes including T1, T2, and fat suppression.
Main Results:
- Excellent agreement between MRF and spin-echo T1/T2 values in phantoms (R² > 0.99).
- Precise in vivo T1 and T2 maps in healthy volunteers, consistent with literature values.
- Good reproducibility in ARPKD patients (<3% difference) and insensitivity to B1 field inhomogeneities.
Conclusions:
- A novel kidney MRF method provides accurate in vivo T1 and T2 maps at 3.0 T.
- The technique allows for single breath-hold acquisition with improved precision.
- No B1 correction is required, simplifying clinical application.
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