Wei-Ching Lo1, Nelson Gil2, Azadeh Tabari2, Dominik Nickel3, Min Lang2, Maryam Vedjani-Jahromi2, Bryan Clifford1, John Conklin2, and Susie Huang2
1Siemens Medical Solutions, Boston, MA, United States, 2Department of Radiology, Massachusetts General Hospital, Boston, MA, United States, 3Siemens Healthcare GmbH, Erlangen, Germany
Synopsis
Keywords: Other Neurodegeneration, MR Value, AI/ML Image Reconstruction, Brain, Translational studies, Neurodegeneration
Motivation: Deep-learning-accelerated MPRAGE holds potential to enhance image resolution, reduce acquisition times, and improve diagnostic precision. However, there is currently a lack of clinical validation regarding its performance in neuroimaging.
Goal(s): To optimize and assess the performance of deep-learning-accelerated MPRAGE in comparison to Wave-CAIPI MPRAGE for non-contrast T1-weighted volumetric brain imaging.
Approach: In this prospective clinical study, we systematically optimized and implemented a novel deep-learning-accelerated MPRAGE sequence and compared against Wave-CAIPI MPRAGE, a state-of-the-art acceleration method.
Results: Deep-learning-accelerated MPRAGE enhances resolution and grey-white matter differentiation compared to Wave-CAIPI MPRAGE, with equivalent volumetric estimation in most brain regions.
Impact: Deep-learning-accelerated
MPRAGE yields sharper, higher-resolution images while preserving equivalent
volumetric estimations. This technique holds significant potential for
deploying deep learning across various medical imaging disciplines, potentially
enabling faster and more precise disease characterization.
Introduction
The 3D T1-weighted
MPRAGE sequence has been widely used for assessing regional brain volume in patients
with neurodegenerative diseases. Recent advances in acquisition techniques such
as Wave-CAIPI have provided 2-3 fold acceleration for non-contrast1,2
while preserving diagnostic quality.
Deep
learning reconstruction has emerged as a powerful approach for accelerating image
acquisition and improving image quality in MRI3,4. The application of
these techniques in clinical settings especially for 3D sequences like MPRAGE remains
underexplored.
The goal of this
study was to optimize and evaluate a novel deep-learning-accelerated MPRAGE (DL-MPRAGE)
sequence for volumetric brain MRI relative to state-of-the-art Wave-CAIPI MPRAGE.Methods
Data
acquisition
This prospective study
was approved by the Mass General Brigham Institutional Review Board. A healthy
adult volunteer was scanned with non-contrast 3D-T1-MPRAGE for optimization of
DL settings. The optimized DL protocol was then implemented on three clinical 3T
MRI scanners (MAGNETOM Vida, Siemens Healthineers, Erlangen, Germany) and run alongside Wave-CAIPI MPRAGE in an
outpatient imaging facility. Adult patients undergoing brain MRI exams for
evaluation of memory loss were recruited during October 2023. Acquisition
parameters for Wave-CAIPI and DL-MPRAGE are provided in Table 1.
Image reconstruction
The research
application DL-MPRAGE uses a two-step
deep-learning-based image reconstruction (Figure 1). The first step, inspired by
variational networks5, reconstructed images from undersampled
k-space data and coil sensitivity maps. This process involved six iterations
alternating between data consistency updates and neural network evaluations.
Implementation in PyTorch and training with 5000 pairs of 500 fully sampled 3D
datasets from healthy volunteers was carried out on 1.5 and 3T scanners
(MAGNETOM scanners, Siemens Healthineers, Erlangen, Germany). The resulting
network was integrated into the scanner's reconstruction pipeline using ONNX
Runtime, processing a single volume in approximately 15 seconds. The second
step involved a super-resolution algorithm for further enhancement6,7.
Both steps were integrated into a research application for prospective use in
the scanner's reconstruction pipeline. The research application was tested in healthy adult volunteer data and retrospectively reconstructed with conventional
GRAPPA and DL-MPRAGE with mild, moderate, and strong denoising strength levels
(Figure 2).
Quantitative evaluation –
Non-contrast MPRAGE
Cortical volume and thickness
measurements were performed on non-contrast
DL and Wave-CAIPI MPRAGE images using the longitudinal FreeSurfer pipeline8,9. Differences in cortical volume between the two
sequences were quantified across patients using the absolute symmetrized
percent change (ASPC)8. Significance for all comparisons was
assessed using paired Wilcoxon rank sum tests with Bonferroni correction, with
a significance threshold set at p < 0.005. Results and Discussion
In the volunteer study, DL-MPRAGE
at different denoising levels showed better overall image quality and clearer
gray-white interface delineation as compared to conventional GRAPPA (Figure 2).
The optimized protocol with low denoising strength and super-resolution was
subsequently evaluated in a clinical setting.
Nine patients (4F/5M,
60±21 years old) undergoing evaluation for memory loss were
scanned with non-contrast
DL
and Wave-CAIPI MPRAGE.
Automated FreeSurfer segmentations were qualitatively similar for both sequences across all
subjects (Figure 3).
Cortical
volumes from DL and Wave-CAIPI MPRAGE showed no significant differences (p >
0.005), except in the occipital lobe where DL-MPRAGE demonstrated higher
volumes (Figure 4). ASPC values averaged around 2.5%, peaking at 5.1% in the
occipital lobe. Similarly, cortical thicknesses exhibited no significant
differences (p > 0.005), except in the occipital lobe and cingulate gyrus.
Here, DL-MPRAGE showed higher thicknesses in the occipital lobe and lower in
the cingulate gyrus. ASPC values for thicknesses were lower than for volumes,
with peak values at 1.6% and 1.7% in the occipital lobe and cingulate gyrus, respectively. The discrepancies observed in the occipital lobe and cingulate
gyrus may be due to sharper delineation of the gray-white interface on the DL-MPRAGE
images, which has been observed in other super-resolution reconstruction
methods10.Conclusion
The newly
developed and optimized DL-MPRAGE acquisition demonstrates superior resolution
and enhanced gray-white matter differentiation compared to state-of-the-art
Wave-CAIPI MPRAGE. This technique also maintains equivalent volumetric
measurements, indicating its potential to enable precise characterization of
regional brain volumes, ultimately benefiting a broad spectrum of patients undergoing
evaluation for neurodegenerative disorders. Separate studies are underway evaluating the diagnostic quality of
DL-MPRAGE for assessment of intracranial enhancing lesions11.Acknowledgements
No acknowledgement found.References
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