Michael Carl1, Yajun Ma2, Ricardo Mello2, Jiang Du2, and Eric Y Chang2,3
1General Electric, Global MR Applications & Workflow, San Diego, CA, United States, 2UCSD, San Diego, CA, United States, 3VA San Diego Healthcare System, San Diego, CA, United States
Synopsis
We compared different center-out 3D radial trajectories (ZTE and UTE) and
assessed their advantages and disadvantages for bone imaging. We found that
while ZTE and UTE show similar results at the same read BW, the higher BWs
available with UTE can help reduce undesired background signals in the final
bone images.
Introduction:
Direct MR imaging of
tissues such as tendons, or ligaments, which have short transverse relaxation
times (T2s) has become possible using ultrashort echo time
(UTE) sequences [1-4]. There are several excitation RF and k-space trajectories
available for UTE imaging. In this work, we compare two different research prototype center-out 3D
radial trajectories and assess their advantages and disadvantages for MR bone
imaging.Theory:
The pulse sequences are shown in Fig.1. UTE employs the RF pulses while
the read gradients are ramped down, while in ZTE the read gradients are already ramped-up during excitation. Some consequences are:
1) The flip angle in ZTE is limited due to the need to keep the RF
excitation pulse very short.
2) The read BW in ZTE is limited to minimize the missing k-space data at
the center.
3) UTE can apply a slice-selection gradient, which allows application of
slab selection.
4) UTE acquires data during partially time-varying read gradients, while
ZTE uses an already fully ramped read gradient which means that ZTE does not
suffer from gradient delay errors.
The bone reconstruction algorithm in this work follows closely the
process used in PET-MR attenuation correction [5]. The main steps include performance
of a coil-bias correction algorithm followed by a simple contrast inversion. An
image mask is then used to remove any non-tissue signals (e.g. air,
coil-elements). The contrast inversion works best if the soft tissues have a uniform
signal intensity (PD contrast), meaning that one strives to minimize T2 and T1
contrast. The T1 contrast is readily minimized by using a low excitation flip
angle. To minimize T2 contrast requires the use of an ultrashort TE time, and
maximum possible read BW.Materials and Methods:
To experimentally study the
T2* blurring and contrast characteristics, we scanned a
plastic doll made of soft rubber (short T2* of about 400𝜇s).
Both UTE and ZTE scans were performed with BW of 31.25kHz, 62.5kHz, and 125kHz.
For the bone scans we imaged a shoulder specimen with an isotopic 0.8 mm
acquisition using a 1° flip angle. The ZTE acquisition was obtained at 62.5 kHz
BW, while the UTE scan was obtained at both 62.5 kHz and 125 kHz.Results:
The images of the
short T2 doll-phantom are shown in Fig.2. For either sequence there is
significant short T2 blurring for the 31.25kHz BW scans, while the best result
is obtained with UTE using BW=125kHz. The original shoulder images are shown in
Fig.3. As expected, both 62.5 kHz acquisition show similar image
features/contrast. The 125 kHz BW UTE images on the other hand show visibly
less T2 contrast. This in turn facilitates the contrast inversion (shown in the top
panel of Fig.4), which shows less background signals in the soft tissues
surrounding the bone. Finally, the bottom panel of Fig.4 shows the 3D
rendered bone images of the 62.5 kHz BW ZTE scans and the 125 kHz BW UTE scans.
These are displayed at their natural image window level and without any manual cleaning,
and show less confounding background signals in the soft tissues in the 125 kHz
UTE image.Conclusion:
We have examined two
similar ultrashort TE pulse sequences for their performance in bone image
capability. We found that for the same read BW, similar bone contrast images
can be obtained using either sequence, but that the overall results benefit
from using the highest available BW.Acknowledgements
The authors acknowledge support from GE Healthcare, VA Clinical Science and Rehabilitation R&D Awards (I01CX001388 and I01RX002604), and the NIH (1R21AR073496, R01AR068987).References
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Imag 2011:29:470–482
[3] Weiger et al, NMR Biomed. 2015 28(2):247-54
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[5] Wiesinger et al. Magn Reson Med. 2018 Oct;80(4):1440-1451