“…The remaining asymptomatic volunteers and symptomatic patients were scanned with the resultant optimized protocol: (i) DIR-UTE: TR/TI 1 /TI 2 = 1500/610/150 ms, TE = 0.032 ms, FA = 10 ° , N sp = 27, FOV = 28 × 28 × 4.32 cm 3 , matrix = 320 × 320 × 12, voxel size = 0.875 × 0.875 × 3.6 mm 3 , bandwidth = 125 kHz, and scan time = 10 min; (ii) IR-FS-UTE [ 19 ]: TR/TI = 1200/600 ms, TE = 0.032 ms, FA = 10 ° , N sp = 21, FOV = 28 × 28 × 4.32 cm 3 , matrix = 320 × 320 × 12, voxel size = 0.875 × 0.875 × 3.6 mm 3 , bandwidth = 125 kHz, and scan time = 10 min; (iii) T 1w -FS-UTE: TR = 120 ms, TE = 0.032 ms, FA = 15 ° , FOV = 28 × 28 × 4.32 cm 3 , matrix = 320 × 320 × 12, voxel size = 0.875 × 0.875 × 3.6 mm 3 , bandwidth = 125 kHz, and scan time = 2 min 20 s; (iv) FS-UTE: TR = 120 ms, TE = 0.032 ms, FA = 6 ° , FOV = 28 × 28 × 4.32 cm 3 , matrix = 320 × 320 × 12, voxel size = 0.875 × 0.875 × 3.6 mm 3 , bandwidth = 125 kHz, and scan time = 2 min 20 s. Clinical T 1w - and T 2w -FSE sequences were scanned for comparison. In addition, for the patient scan, a proton density weighted-UTE (PDw-UTE) sequence with an isotropic resolution (1.2 mm 3 ) was also employed for high contrast cortical bone imaging [ 29 ]. The sequence parameters used in the other UTE sequences were optimized in previous studies.…”