Affiliation:
1. Department of Biomedical Engineering University of Utah Salt Lake City Utah USA
2. Department of Radiology and Imaging Sciences University of Utah Salt Lake City Utah USA
3. 4D Surgical Salt Lake City Utah USA
Abstract
AbstractPurposeTo validate single reference variable flip angle (SR‐VFA) dynamic T1 mapping with and without T2* correction against inversion recovery (IR) T1 measurements.MethodsA custom cylindrical phantom with three concentric compartments was filled with variably doped agar to produce a smooth spatial gradient of the T1 relaxation rate as a function of angle across each compartment. IR T1, VFA T1, and B1+ measurements were made on the phantom before rotation, and multi‐echo stack‐of‐radial dynamic images were acquired during rotation via an MRI‐compatible motor. B1+‐corrected SR‐VFA and SR‐VFA‐T2* T1 maps were computed from the sliding window reconstructed images and compared against rotationally registered IR and VFA T1 maps to determine the percentage error.ResultsBoth VFA and SR‐VFA‐T2* T1 maps fell within 10% of IR T1 measurements for a low rotational speed, with a mean accuracy of 2.3% ± 2.6% and 2.8% ± 2.6%, respectively. Increasing rotational speed was found to decrease the accuracy due to increasing temporal smoothing over ranges where the T1 change had a nonconstant slope. SR‐VFA T1 mapping was found to have similar accuracy as the SR‐VFA‐T2* and VFA methods at low TEs (˜<2 ms), whereas accuracy degraded strongly with later TEs. T2* correction of the SR‐VFA T1 maps was found to consistently improve accuracy and precision, especially at later TEs.ConclusionSR‐VFA‐T2* dynamic T1 mapping was found to be accurate against reference IR T1 measurements within 10% in an agar phantom. Further validation is needed in mixed fat–water phantoms and in vivo.
Funder
National Institute of Biomedical Imaging and Bioengineering
NIH Office of the Director
Subject
Radiology, Nuclear Medicine and imaging