Jeremiah J Hess1, Catherine J Moran1, Jana Vincent2, Fraser Robb2, Patricia Lan2, Arnaud Guidon2, Jessica McKay-Nault1, Bruce L Daniel1, and Brian A Hargreaves1
1Stanford University, Stanford, CA, United States, 2GE Healthcare, Chicago, IL, United States
Synopsis
Keywords: Breast, Breast
Motivation: Breast MRI typically is performed with a patient in the prone position. Imaging supine would dramatically improve patient comfort and possibly reduce setup and positioning times.
Goal(s): Compare image quality in breast MRI between the supine and prone positions with specialized coils using signal-to-noise ratio.
Approach: To account for tissue deformation between supine and prone positions, we compare “tissue-independent” relative SNR, which uses the body coil SNR as a reference, in the breast tissue between prone and supine.
Results: In multiple patients, the supine position consistently showed an improvement in SNR over the prone position.
Impact: Improvements
in motion correction approaches and development of flexible coils may enable
supine breast imaging, which is much more comfortable for the patient than
prone imaging. Using a careful
comparison, we demonstrate substantially higher SNR in supine imaging.
Introduction
Breast MRI is typically performed with the patient in a
prone position to mitigate respiration artifacts. However, co-localization of
these images with surgery, which is performed in the supine position, is
difficult. Additionally, the prone setup tends to be exceedingly uncomfortable
for patients, affecting patient movement and positioning during the scan.
Recent efforts have focused on developing supine breast imaging methods1-2
and coils to improve signal-to-noise ratio (SNR) and mitigate respiratory
motion.
Evaluating
potential SNR differences between supine and prone setups is exceedingly
difficult due to the large deformations, and thus tissue compositions seen by
coils, in the breast between the two positions. In this work, we present a novel SNR-based metric
that is independent of signal to allow for a tissue-independent SNR comparison
between supine and prone breast coils.Methods
Theory
To
evaluate SNR differences between the two positions, we propose a relative SNR
metric: $$$SNR_{rel} = \frac{SNR_{ext}}{SNR_{body}}$$$, where $$$SNR_{ext}$$$ refers to the SNR of the external coil and $$$SNR_{body}$$$ refers to the SNR of the the body coil. Assuming
the MR signal in each voxel does not change (gains constant at each position), we
get that $$$SNR_{rel} = \frac{\sigma_{body}}{\sigma_{ext}}$$$, where $$$\sigma$$$ represents the standard deviation of the noise
normalized by the signal sensitivity at each pixel, implying independence from
underlying signal variation.
Methods
Phantom
experiments were performed on a breast phantom to validate the
signal-independence of the relative SNR metric. Data was acquired using 3D
T1-weighted SPGR and 3D T2-weighted CUBE sequences on a 3T Premier (GE
Healthcare) using the 60-channel breast coil prototype3 and the body
coil.
Three
patients and two volunteers were recruited for a research breast MRI exam.
Recruitment followed IRB polices and all subjects provided written informed
consent. Volunteers and patients were scanned on a 3T Signa Premier System (GE
HealthCare) in both the supine (60-channel breast-specific flexible AIR coil3)
and prone (16-channel Sentinelle breast coil) positions. In each position, a low-resolution
(~3.5mm in-plane, 5mm slice thickness) 3D T1-weighted SPGR sequence was
acquired for the breast coil and body coil, with transmit gains and receiver
gains kept constant.
Images
were reconstructed using a standard SENSE reconstruction, and SNR maps were
computed using the pseudo-multiple replica method4 with 500
iterations. Coil sensitivity maps were estimated by lowpass filtering the fully
sampled k-space data.
Relative
SNR was measured in
breast tissue on 20 central slices for each acquisition. Segmentation of breast
tissue was performed to measure relative change in the tissue of interest. For
each set of in vivo data, a left-tailed Wilcoxon rank sum test was
performed to determine whether the median relative SNR for supine was greater
than for prone.Results
Phantom images demonstrating the metric’s signal
independence are shown in Figure 1. The spatial distributions of the relative
SNR are similar despite differences in the underlying MR signal, and the ratios
of the relative SNR metric is close to 1 across the phantom.
Sample
images of the relative SNR distributions for two patients overlaid on low-resolution
anatomical images are shown in Figure 2. The regional variation in relative SNR
can easily be seen between the prone and supine images.
Histograms
of the relative SNR distribution for all in vivo cases are shown in
Figure 3. The Wilcoxon rank sum test states that for all cases except 3, the median
relative SNR of supine is statistically higher than prone.Discussion
The phantom results indicate that relative SNR is a function
of coil performance and overall geometric position and is invariant to the
underlying voxel MR signal. The spread of the distribution is most likely due
to the Monte Carlo-based method used in calculating the SNR maps. In breast
MRI, where tissue composition can vary widely between patients and across the
breast, relative SNR can provide
a tissue-independent metric for SNR comparison.
While 4/5 datasets in this
initial method validation demonstrated higher SNR with the supine versus prone
coil, further investigation of the SNR performance of the supine coils is
necessary. SNR will vary from region to region based on the size and composition
of the breast tissue in an individual with both prone and supine coils. Refined
tissue segmentation and regional assessment of the SNR will help to inform
supine versus prone coil performance.Conclusion
Relative SNR is a signal-invariant
metric for analyzing the image quality between supine and prone breast MRI. In
a small number of subjects, these results indicate that supine positioning and flexible coils increase SNR
versus prone coils.Acknowledgements
We gratefully acknowledge the research support of GE Healthcare and the following funding sources: NIH R01-EB009055 and NIH R01-CA249893.References
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