Aurelien Destruel1, Mingyan Li 1, Craig Engstrom2, Ewald Weber1, Jin Jin1,3,4, Rahel Heule5, Oliver Bieri6, Feng Liu1, and Stuart Crozier1
1School of Information Technology and Electrical Engineering, The University of Queensland, Brisbane, Australia, 2School of Human Movement and Nutrition Sciences, The University of Queensland, Brisbane, Australia, 3University of Southern California, Los Angeles, CA, United States, 4Siemens Healthcare Pty Ltd, Brisbane, Australia, 5High Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Tübingen, Germany, 6Division of Radiological Physics, Department of Radiology, University Hospital Basel, Basel, Switzerland
Synopsis
The double-echo steady-state (DESS) sequence has been used successfully
in 3T MRI imaging of the musculoskeletal system for segmentation of joint. However,
in 3D-DESS images acquired at 7T MRI, a reduction in the contrast between
tissues due to an increased diffusion sensitivity may complicate cartilage
segmentation. Typically, the signals acquired with DESS are averaged without
any pre-processing. However, these signals give different contrasts and have
different noise behaviours. In this work, we improve the contrast-to-noise
ratio (CNR) whilst preserving anatomical detail in high-resolution 7T DESS
images through a new approach combining L1-norm denoising and p-norm
combination of the echo signals.
Introduction
The clinical assessment of pathoanatomical conditions of hip
joint cartilages, such as osteoarthritis, can be enhanced by automated
segmentation and quantitative analyses of hip joint cartilages from magnetic
resonance imaging (MRI). High resolution 3D sequences such as double-echo
steady-state (DESS) are beneficial to facilitate the separation of the femoral
and acetabular cartilages, which are thin and highly curved, and a high contrast-to-noise
ratio (CNR) is required to reduce segmentation errors between joint cartilage,
ligamentous structures and synovial fluid1,2.
Ultra-high field (UHF) MRI has the capacity to provide high resolution images to
allow improved spatial segmentations of joint cartilage, however there is the
potential for better processing of current 3D-DESS images at 7T3.
Specifically, the two echoes acquired during the DESS sequence, PSIF (high
contrast, low signal-to-noise ratio (SNR)) and FISP (high SNR, low contrast)
are typically averaged without any pre-processing4, which does not use the full
potential of their individual features3.
In this work, we developed a new approach to improve the contrast in 7T hip
DESS images through combined application of L1-norm denoising and a p-norm
combination of the echo signals. Methods
Images of the hip joint were acquired on a 7T research
system (Siemens Healthcare, Erlangen, Germany) using a prototype radiofrequency
pTx hip coil modified from a previous work5. The eight-channel coil allowed
unilateral hip imaging, while B1-shimming6
and virtual observation points7 were used to improve the B1-field
and limit the 10g-average specific absorption rate (SAR10g)8, respectively. In line with
the UHF capabilities of 7T MRI, high-resolution 3D water-excited DESS (we-DESS)
images were obtained with an acquired resolution of 0.4x0.4x0.6mm3 (sequence
parameters given in Figure 2 caption). To mitigate the decrease in tissue contrast with high resolutions, a
modified DESS sequence was used to allow spoiler gradients in the slice
direction9.
Images were imported in Matlab (MathWorks, MA, USA) for
post-processing. The effect of denoising the PSIF and FISP images before combination
was investigated. L1-norm denoising was applied
due to its edge preserving and denoising features10, by converting images to the
wavelet domain and applying L1-norm minimisation with a total variation (TV)
and L1-norm penalty = 0.01 and 0.025, respectively.
In addition, different combinations of the PSIF and FISP
signals were analysed to optimize CNR between cartilage and synovial fluid (CNRC/F)
and CNR between bone and ligaments (CNRB/L):
Original: $$DESS = PSIF + FISP$$
Weight
optimisation: $$DESS_{WO} = w1 PSIF + (2 - w1) FISP$$
p-Norm
optimisation: $$DESS_{NO} = (PSIF^{w2} + FISP^{w2})^{1/w2}$$
where w1 and w2 are the optimized parameters. The signal
intensity (SI) was calculated by manually segmenting regions of the cartilage,
bone, ligament and synovial fluid in an axial slice directed through the
femoral head and acetabulum. The CNR between two tissues was calculated as the
difference between the average SI in each tissue divided by the standard
deviation of the background SI. A summary of the different signal processing
and combinations is given in Figure 1. Because the denoising and different
signal combinations affect the SI, all DESS images were normalized to have
identical average cartilage SI in the reference slice. Results
Figure 2 shows comparisons between PSIF, FISP and DESS before
and after L1-norm denoising. It can be seen that the noise was substantially reduced,
in particular for the PSIF image, while preserving tissue details and therefore
enhancing the contrast.
Figure 3 shows the evolution of the CNR and SI differences between
tissues when varying the parameters w1
and w2, with and without denoising.
The standard deviation of the background SI with and without denoising is also
shown, to identify the behaviours of the different CNR components with different
combination methods. It can be seen that denoising increases the CNR in all
cases, which is caused by a small increase in SI difference, and large decrease
in noise standard deviation. It can also be observed that CNRB/L and
CNRC/F have different optimal weightings and norm-values. For
example, decreasing w2 significantly
increases CNRC/F, but at the cost of lower CNRB/L and
larger noise.
Figure 4 shows DESSWO and DESSNO with
w1 and w2 ranging from 0 to 2. Although the PSIF image has the largest SI
difference between the cartilage and synovial fluid, it contributes substantially
to the amount of noise in the combined image and has poor contrast between bone
and ligaments.
A trade-off between noise amplification and contrast
improvement was chosen by using DESSNO using denoised data and with w2 = 0.7 (Figure 5). This resulted in an
increase of CNRC/F and CNRB/L of 104% and 70%,
respectively, compared to the original DESS image, and a reduction of the
standard deviation of the noise of 31%. Discussion and Conclusion
In this work, we have developed a new approach using L1-norm denoising and p-norm combination (p = 0.7) of the PSIF and FISP images
to improve the CNR between cartilage, synovial fluid, bone and ligaments in 7T
images of the hip joint. These improvements have the potential to significantly
improve the performance of automated hip segmentation, where errors often occur
due to poor contrast between certain tissues. The method used in this work can
be used at lower field MRI and for other applications than hip imaging. Acknowledgements
This work received funding from the ‘MR Hip Intervention and
Planning System to enhance clinical and surgical outcomes’ NHMRC Development
Grant.References
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