Rapid 3D‐T1 mapping of cartilage with variable flip angle and parallel imaging at 3.0T

PURPOSE: To rapidly acquire T(1)-weighted images using a three-dimensional fast low angle shot (3D FLASH) sequence in combination with generalized autocalibrating partially parallel acquisitions (GRAPPA) and variable flip angle (VFA) method at 3.0T. MATERIALS AND METHODS: 3D T(1) maps of model systems (gadolinium [Gd] and agarose phantoms), bovine cartilage, and human subjects were constructed on a 3.0T clinical whole-body MR scanner. The T(1) values of model systems measured using the 2D inversion-recovery fast-spin-echo (IR-FSE) sequence were considered as a reference method to validate the rapid 3D method for comparison. RESULTS: The root mean square coefficient of variation percentage (RMS-CV%) of the median T(1) of agarose phantom across different acquisition methods was approximately 6.2%. The RMS-CV% of the median T(1) of bovine cartilage across different acquisition methods was approximately 4.1%. The RMS-CV% of median T(1) of the cartilages among the subjects was between approximately 7.3% to 11.1%. In our study, rapid 3D-T(1) mapping with VFA and parallel imaging with different acceleration factors (AFs) (AF = 1, 2, 3, and 4) seems to have no obvious influence on the T(1) mapping (before and after contrast agent administration). CONCLUSION: The preliminary results demonstrate that it is possible to quantify 3D-T(1) mapping of the whole knee joint (with 0.7 mm(3) isotropic resolution) under approximately five minutes with excellent in vivo reproducibility at 3.0T.