Ultra short echo time (UTE) techniques have been used to image cortical bone. However, imaging cortical bone in hip has been challenging due to limited signal-to-noise ratio (SNR), robust long T2 suppression, and long scan time. UTE sequences with TEs down to 32μs are able to acquire signal from both short and long T2* tissue. To suppress long T2* tissue, the combination of inversion recovery (IR) and UTE imaging can be used. In this report, we applied three-dimensional adiabatic inversion recovery prepared UTE with Cones trajectories (3D IR-UTE-Cones) to suppress long T2 tissue and to directly quantify cortical bone in the hip in vivo at 3T.
Method
The 3D IR-UTE-Cones sequence employing a short pulse excitation followed by spiral sampling with conical view ordering was implemented on a 3T scanner (Signa HDx, GE Healthcare, Milwaukee, WI) (6). The sequence has a minimal TE of 32 µs and allows anisotropic field of view and spatial resolution for fast volumetric imaging. An adiabatic inversion pulse (duration = 8.64ms) was used for robust inversion and suppression of the longitudinal magnetizations of long T2 water and fat. Two healthy volunteers (30 and 34 years old, male) were scanned by using a Torso phased-array coil. The following scan parameters were used: TR = 116.7ms, TI = 50ms, four TEs (0.032, 0.2, 0.4, and 0.8ms), BW = 250kHz, FOV = 340 x 340mm2, slice thickness = 3mm, matrix = 128×128, flip angle = 18°, acquired voxel size = 2.6×2.6×3mm3, and scan time = 4.5 minutes for each dataset. T2* was quantified with a single-component decay fitting of IR-UTE-Cones images.Results
Figure 1 shows a representative slice of the hip of a 31-year-old male healthy volunteer imaged with the 3D IR-UTE-Cones sequence. Cortical bone in the femoral midshaft, femoral head and neck as well as greater trochanter is depicted with excellent image contrast. Muscle and marrow fat in the hip, which typically have far higher signals than that of cortical bone, are efficiently suppressed by the adiabatic inversion pulse. SNR for cortical bone in the femoral head is relatively low due to the thin structure and limited coil sensitivity from the clinical torso phased array coil. Four ROIs were drawn in the hip for T2* analysis, including the greater trochanter (ROI 1), the femoral neck (ROI 2), the femoral head (ROI 3), and the lesser trochanter (ROI4). A representative T2* decay curve using single component fitting is shown in Figure 2. Excellent single component decay was observed for all ROIs, consistent with pore water being suppressed by the IR pulse and only collagen bound water being detected by the IR-UTE-Cones sequence. Table 1 summarizes the mean and standard deviation for T2* values for the greater trochanter, the femoral neck, the femoral head, and the lesser trochanter, respectively, between the two volunteers. The average T2* values ranged from 0.34 ms to 0.4 ms, largely consistent with previously reported T2* values of bound water in the tibial midshaft.Discussion and Conclusion
Preliminary results from this study show that cortical bone in the hip can be imaged with relatively high spatial resolution using the 3D IR-UTE-Cones sequence. The adiabatic inversion pulse provides robust suppression of long T2 water and marrow fat, creating very high contrast for cortical bone. T2* can be reliably estimated via single-component fitting of 3D IR-UTE-Cones acquisitions with a series TEs. Further optimization of the imaging protocol, including in-plane resolution, slice thickness and scan time will be performed in future studies. The 3D UTE-Cones and IR-UTE-Cones sequences can potentially evaluate cortical porosity (pore water content) and organic matrix (bound water content) in the hip (7-9). These techniques may provide more comprehensive evaluation of cortical bone quality, and thus may serve as predictors for risk of future hip fractures.1. Reichert ILH, Robson MD, Gatehouse PD, He T, Chappell KE, Holmes J, Girgis S, Bydder GM. Magnetic resonance imaging of cortical bone with ultrashort TE (UTE) pulse sequences. Magn Reson Imaging 2005; 23:611-618.
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