Alba Iruela Sanchez1, Valentin H. Prevost2, Alicia Palomar Garcia1, Wolter de Graaf3, and Bruno Triaire2
1Canon Medical Systems Spain and Portugal, Barcelona, Spain, 2Canon Medical Systems Corporation, Tochigi, Japan, 3Canon Medical Systems Europe, Zoetermeer, Netherlands
Synopsis
This study evaluates the feasibility of
different approaches for the visualization of endolymphatic content in inner
ear structures on 1.5T MR systems without the need of contrast injection. The
results show that using an optimized high-resolution 3D T2w sequence combined
with DLR-based denoising tools it is possible to visualize the utricle and
saccule structures on healthy volunteers. The next step will be testing this
technique on patients with endolymphatic hydrops.
INTRODUCTION
Various techniques have been
developed over the last years to observe endolymphatic hydrops through MRI.
Most of them require the injection of contrast agent with subsequent waiting
times in order to enhance the contrast difference between endolymph and
perilymph [1][2]. Some other studies have developed protocols that did not
require contrast injection, but they all have been performed using a 3T system
due to the exigent requirements in terms of image resolution and tissue
contrast [3][4]. The aim of this study was to optimize on healthy volunteers an
MR technique for saccule and utricle visualization on a 1.5T system without the
need of contrast injection, by benefiting from advanced tools such as denoising
based on Deep Learning Reconstruction (DLR). METHODS
Six healthy volunteers were
scanned on a Vantage 1.5T Orian XGO 1.5T MR system (Canon Medical Systems
Corporation, Tochigi, Japan) using a 16ch head and neck coil. For the MR
protocol optimization, two different approaches were tested. The first one
consisted in finding the optimal inversion time (TI) for endolymph and
perilymph differentiation on a 3D FLAIR sequence, reproducing some previous
work that was done on a 3T system [3]. Acquisitions with 15 increasing TI
values between 208 and 3000ms were performed, and the resulting images were
evaluated to determine the point with the optimal visualization of the
endolymph. The second approach consisted in building a high-resolution (HR) 3D
T2-weighted (T2w) sequence and evaluating the endolymph visualization. A DLR-based
denoising solution [5] was applied and adjusted in order to improve SNR. 3D
FLAIR sequence was performed with the following parameters: FASE3D, TR=7000ms,
TE=475.2ms, TI=3000ms, recon. resolution=isotropic 0.45mm, acquisition
time=7min. For HR 3D T2w the parameters were the following: FASE3D, TR=5000ms,
TE=400ms, recon. resolution=isotropic 0.25mm, acquisition time=7:20min. Image
evaluation was performed by visual inspection in order to assess vestibular
endolymph depiction. The focus was especially on saccule and utricle
visualization for the corresponding MPRs, while comparing the images with and
without DLR. Signal profile plots in axial planes were used to evaluate the
structures differentiation. RESULTS
The 3D T2w sequence allowed
visualizing the endolymphatic content, as it presented a lower signal that the
perilymph surrounding it (Figure 1). After applying DLR, the vestibular
endolymphatic content was clearly identifiable for all the cases after
reconstructing the image in the adequate axial plane, independently for each
ear. On profile plots (Figure 2) saccule and utricle differentiation was
confirmed in 83.3% of the cases (10 out of 12). For the same acquisitions without
DLR, visualization of endolymphatic content was still possible in most cases,
but the capacity to differentiate the saccule and the utricle was reduced due
to the noise (Figure 3).
On the
contrary, the 3D FLAIR approach resulted in images with poor
endolymph-to-perilymph contrast in comparison with the 3D T2w acquisitions. Endolymph
was not identified in most cases (Figure 4). DISCUSSION
The 3D T2w approach outperformed
the 3D FLAIR one both in resolution and in contrast between endolymph and perilymph. The Inversion
Recovery (IR) pulse from the FLAIR sequence caused a significant signal
decrease, limiting the acceptable resolution that can be achieved. FLAIR only
allowed scanning with a 44% lower resolution while only being 4.5% faster. For
all the TI values that were tested, the images showed low contrast between
endolymph and perilymph, preventing to reproduce the previous study at 3T [3] and
to find a TI value that clearly differentiates the two structures. One hypothesis
for this low contrast could be linked to the impossibility to use T2Prep values
higher than 200ms, while in the 3T study they required a value of 400ms to
obtain optimal results [3].
While 3D T2w used a higher
resolution and could suffer from higher noise, DLR denoising allowed to recover
a SNR high enough to clearly identify the endolymphatic structures. For the images
processed without DLR, structures’ delineation was more challenging, or even
not possible in some cases. CONCLUSION
This study concludes that it is
possible to visualize endolymphatic structures at 1.5T, without the need of
contrast agent injection, when using 3D T2w images in combination with denoising
tools based on deep learning. Future studies will perform this 3D T2w sequence
on patients suffering from inner ear disorders such as endolymphatic hydrops and
will evaluate how these are visualized. Acknowledgements
No acknowledgement found.References
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