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3D Cones acquisition for human extremities using a 1.5 T compact superconducting magnet and unshielded gradient coil
Ayana Setoi1 and Katsumi Kose1

1University of Tsukuba, Tsukuba, Japan

Synopsis

We developed 3D Cones sequences for human extremities on a 1.5 T MRI system using a compact superconducting magnet (280 mm bore) equipped with an unshielded gradient coil. Linear eddy fields were measured using a spherical phantom and eddy current effects on the 3D Cones sequences were evaluated using a 3D water phantom. As a result, effects of higher-order eddy fields proportional to z2x and z2y spatial distributions were clearly observed. The 3D Cones sequences were applied to UTE imaging of a porcine hoof sample and a human forearm, which demonstrated their promise in UTE imaging.

Introduction

3D Cones acquisition is an attractive sequence for ultrashort TE (UTE) imaging because the image acquisition time can be shorten comparing with the radial acquisition. However, the design and implementation of the 3D Cones sequence for a customized MRI system are not straightforward because the sequence is sensitive to gradient system imperfections and eddy current effects. In this study, we implemented the 3D Cones UTE sequences for human extremity imaging on a home-built MRI system equipped with an unshielded gradient coil and evaluated the sequence using a 3D phantom, a biological sample, and a human forearm.

Materials and Methods

Figure 1(a) shows an overview of the home-built compact MRI system using a 1.5T horizontal bore (280 mm) superconducting magnet (JASTEC, Kobe, Japan) used in this study. This system is controlled by a fully-digital MRI console (DTRX6, MRTechnology, Tsukuba, Japan). Figure 1(b) shows an unshielded gradient coil set (inner diameter = 160mm). 3D Cones sequence was designed after Glover [1]. Figure 1(c) shows a 3D water phantom used for evaluation of the 3D Cones sequence.

Linear eddy fields caused by switching of the gradient coil currents were measured using spherical CuSO4 aqueous solution stored in a plastic sphere (inner diameter=23.5 mm). The linear eddy fields were analyzed by temporal shifts of the gradient-echo peak measured for gradient pulses with variable delay times (delay time = 0.01 to 100 ms) applied before the RF excitation pulse. The 3D Cones imaging was performed for the 3D water phantom, porcine hoof sample, and human forearm. For comparison, conventional gradient-echo imaging was performed for these objects.

Results

The linear eddy fields observed for the various delay times were decomposed to two exponentially decaying components with different amplitudes and time constants. The combination of the relative amplitudes (induced linear eddy field / applied gradient field) and the time constants of the linear eddy fields caused by Gx were (6.4%, 0.077ms) and (0.57%, 23.4ms), and those by Gy were (19%, 0.046ms) and (0.60%, 23.4ms), respectively. Figure 2(a) and (b) show estimated gradient fields with (orange) and without (blue) the linear eddy fields for (a) Gx and (b) Gy gradients. These figures demonstrate that the gradient waveforms are slightly delayed by the linear eddy fields.

Figure 3(a) and (b) shows axial cross-sections selected from 3D image datasets of the 3D water phantom acquired with (a) the 3D Cones and (b) the conventional 3D gradient-echo sequences. Figure 3(c) shows the inclination angle of the central line of the acrylic rods in the axial images plotted against the z for the 3D Cones and the conventional gradient-echo sequences. These graphs clearly show that the axial images acquired with the 3D Cones rotate proportional to (z-z0)2, where z0 is the central coordinate along the axial position.

Figure 4(a) shows a coronal cross-section of the porcine hoof sample acquired with a conventional gradient-echo sequence (TR=200ms, TE=4.6ms). Figure 4(b) shows axial cross-sections at the yellow line shown in Fig.4(a) acquired with 3D Cones (TE=0.4ms and 1.0ms) and conventional 3D gradient-echo (TE=2.3ms and 4.6ms) sequences. Image intensities lost in the 3D GRE image (TE=4.6ms) at deep flexor tendons recovered in the 3D Cones image (TE=0.4ms) as shown by the yellow arrows.

Figure 5 shows cross-sectional images selected from a 3D image dataset of a human forearm acquired with (a) a conventional 3D gradient-echo sequence (TE=4.6ms) and (b) the 3D Cones sequence (TE=0.4ms). Image intensities lost in the 3D GRE image at tendons slightly recovered in the 3D Cones image.

Discussion

The change of the inclination angle along the z direction observed for the GRE axial images (Fig.3(c)) includes imperfections of the 3D water phantom and the gradient coil, and errors in the phantom setting. On the other hand, the change of the inclination angle observed for the 3D Cones axial images shows a clear parabolic change, which suggests presence of eddy fields proportional to z2x or z2y. This is because linear eddy fields cause delay of the gradient waveform as shown in Fig.2. Because the angular velocity of the k-trajectory of the 3D Cones sequence (64 shot) is about 2π/1.4ms or about 1.3 degree/(5 µs), about 4 degree difference between the central and the end of the axial images corresponds to about 15 µs delay of the gradient waveform at the end of the axial plane. Therefore, the axial image rotation of the 3D Cones image should be corrected to obtain geometrically correct MR images.

In conclusion, 3D Cones sequences were successfully implemented on our compact 1.5T MRI system and demonstrated their usefulness for the 3D UTE imaging.

Acknowledgements

No acknowledgement found.

References

[1] Gary H. Glover, Simple Analytic Spiral K-space Algorithm, Magnetic Resonance in Medicine, 1999; 42: 412–415.

Figures

Fig.1. (a) Overview of the MRI system using a 1.5 T compact superconducting magnet. The room temperature bore of the magnet is 280 mm and its homogeneity is about 50 ppm over the 160 mm diameter spherical volume. (b) Unshielded gradient coil. Inner diameter is 160 mm and efficiencies of the gradient coil are 0.200, 0.193, and 0.251 G/cm/A. (c) 3D water phantom. An acrylic regular square pyramid (40 × 40 × 80 mm) and 14 acrylic circular rods (diameter = 8mm) were fixed inside an acrylic cylindrical container (diameter: 82mm, length: 108mm) filled with CuSO4 water solution.

Fig.2. Waveforms of the gradient field estimated with (orange) and without (blue) the linear eddy fields calculated for (a) Gx and (b) Gy gradient coils. The waveforms were calculated for one of 64 shots of the cone of the 3D Cones sequence.

Fig.3. Cross-sectional images selected from 3D image datasets of the 3D water phantom acquired with (a) the 3D cones sequence (TR=200ms, TE=0.4ms, number of cones = 128, number of shots = 64, FOV = (128 mm)3) and (b) the conventional 3D gradient-echo sequence (TR=200ms, TE=4.6ms, image matrix = 128×128×256, FOV = (128 mm)3). (c) Inclination angle measured in the axial plane plotted against z direction for the image acquired with the 3D Cones sequence and the conventional 3D gradient-echo sequence.

Fig.4. (a) Coronal cross-sectional image selected from a 3D image datasets of a porcine hoof sample acquired with a conventional 3D gradient-echo sequence (TR=200ms, TE=4.6ms, image matrix=128×128×256). (b) Axial cross-sections acquired with the 3D Cones (TE=0.4ms), 3D Cones (TE=1.0ms), 3D GRE (TE=2.3ms), and 3D GRE (TE=4.6ms) sequences are shown from the left to the right. The location of the axial cross-sections is shown in (a) by the yellow line. The deep flexor tendons are shown bright in the image acquired with the 3D cones (TE=0.4ms) but lost their signal intensity in the image acquired with the 3D GRE sequence (TE=4.6ms).

Fig.5. (a) Axial cross-section selected from a 3D image dataset of a human forearm acquired with a conventional 3D gradient-echo sequence (TR=100ms, TE=4.6ms, image matrix = 256×128×64). The image acquisition time was 13 min 40 s. (b) Axial cross-section selected from a 3D image dataset of a human forearm acquired with the 3D Cones sequence (TR=100ms, TE=0.4ms, number of cones = 64, number of shots = 64). The image acquisition time was 6 min 49 s.

Proc. Intl. Soc. Mag. Reson. Med. 26 (2018)
2705