Shraddha Pandey1, Manuel Taso2, Zhaoyang Fan3, Konstanze Guggenberger4, Alexia Tran5, Scott Raymond6, Shawn Lyo1, Marisa Sanchez1, Rob Sellers2, Julien Savatovsky5, Chengcheng Zhu7, Jae Song1, and M. Dylan Tisdall1
1Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States, 2Siemens Medical Solutions USA Inc, Malvern, PA, United States, 3Department of Radiology, Keck School of Medicine of USC, Los Angeles, CA, United States, 4Department of Radiology, University Hospital of Würzburg, Würzburg, Germany, 5Hôpital Fondation Adolphe de Rothschild, Paris, France, Metropolitan, 6Department of Radiology, The University of Vermont Medical Center, Burlington, VT, Canada, 7Department of Radiology, University of Washington, Medical Center, Seattle, WA, United States
Synopsis
Keywords: Blood Vessels, Blood vessels, Vessel Wall Imaging, Accelerated Acquisition, Compressed Sensing
Motivation: Clinical VWI scans demand high spatial resolutions, which lead to extended acquisition times, potentially causing limited field-of-view (FOV), motion artifacts, and patient burden.
Goal(s): We evaluated FDA-approved acceleration methods for 3D T1w SPACE to develop optimized protocols for clinical VWI studies.
Approach: Compressed Sensing (CS) and CAIPI acceleration techniques optimized to reduce scan times and provide whole-head coverage were compared against our current GRAPPA accelerated limited-FOV clinical protocol.
Results: The whole-head FOV combined with CS yielded image quality comparable to our current clinical protocol but with almost half the scan time, promising significant reductions in lengthy clinical VWI protocols and patient burden.
Impact: Compressed
Sensing enabled increased FOV imaging with substantially reduced scan times
without significant loss of image quality compared to CAIPI and
standard-of-care GRAPPA-accelerated techniques for a clinical T1-weighted
vessel wall imaging protocol.
Introduction
Magnetic Resonance Imaging (MRI) for
vessel wall assessment is crucial in diagnosing intracranial vasculopathies,
differentiating among various conditions. Vessel wall MR imaging (VWI) demands
high spatial resolutions with optimized tissue contrast, blood suppression, and
motion robustness. Our health system employs a GRAPPA-accelerated 3D
T1w-Sampling Perfection with Application optimized Contrasts using Different
Flip Angle Evolution (SPACE) [1] sequence for clinical VWI. However, achieving
the necessary submillimeter resolution necessitates extended acquisition times,
leading to trade-offs in FOV coverage, motion artifacts, and patient burden.
Previous studies using acceleration
methods like CAIPI [2] and CS [3,4,5] demonstrated substantial scan time
reductions. Nonetheless, these studies featured prototype sequences, limiting
their clinical applicability. In this research, we assess FDA-approved
acceleration methods for 3D T1w-SPACE, widely available in clinical scanners,
including GRAPPA, CAIPI, and CS. Our goal is to identify suitable accelerated
protocols for broader patient trials requiring clinical VWI exams.Method
We compared our standard clinical 3D
T1w-SPACE protocol, using standard FOV GRAPPA R=2 (SFGRAPPA), with matched
protocols that differed only in the use of CAIPI R=4 (SFCAIPI4, standard FOV
CAIPI4), and CS R=7 (SFCS7, standard FOV CS7) accelerations. To shorten scan
times, our standard clinical protocol incorporates a reduced FOV, truncating
the left-right and anterior-posterior dimensions, as depicted in Figure 1a.
This often leads to incomplete coverage of crucial cortical arteries for
assessing embolic strokes, insufficient imaging of scalp arteries for temporal
arteritis assessment, and the necessity of saturation pulses to reduce
aliasing. To address these challenges, we also introduced "Large FOV"
protocols with whole-head coverage and CS R=7 (LFCS7, large FOV CS7) and R=10
(LFCS10, large FOV CS10). Table 1 details the imaging parameters.
Five healthy subjects underwent
imaging with all five protocols using a 3.0 T MRI equipped with the
vendor-supplied 20-channel head/neck coil (MAGNETOM PrismaFit, Siemens
Healthineers). A 20-channel coil was chosen to replicate the hardware available
across our health system's clinical scanners.
Four neuroradiologists, experienced in
VWI, independently reviewed 25 randomly presented scans. They employed a
4-point Likert scale to assess Perceived Signal-to-Noise Ratio (SNR) and Image
Quality (1 = poor, 2 = fair, 3 = good, 4 = excellent). Vessel lumen and outer
wall diameters of the basilar artery (BA) , bilateral internal carotid (ICA,
supraclinoid segment), and middle cerebral arteries (MCA, M1 segment) were
manually measured by one neuroradiologist in all studies. The study received
approval from the local institutional review board.Results
Figure 1b displays BA, ICA, and MCA images from
healthy subjects. The SFCAIPI4 images exhibited low SNR towards the brain's
center, as expected with the 20-channel coil. Differences in SNR between
"standard" and "large" FOV CS-7 images were more pronounced
in subjects with larger head circumferences, resulting in increased wrap
artifacts in the "standard" FOV protocol.
Perceived SNR and Image Quality by the four
neuroradiologists are summarized in Table 2a and Figure 2. While none of the
tested accelerated protocols surpassed the SFGRAPPA based on qualitative
metrics, the LFCS7 protocol achieved the closest Perceived SNR and Image
Quality scores (Perceived SNR mean difference: 0.7, t: -3.77, one-sided paired
t-tests p=0.0006; Image Quality mean difference: 0.25, t: -1.39, one-sided
p=0.174). This was followed by the LFCS10 (Perceived SNR mean difference: 0.8,
t: -3.96, one-sided paired t-tests p=0.0003; Image Quality mean difference:
0.5, t: -2.5, one-sided p=0.017).
Quantitative vessel lumen and outer wall
diameter measurements are presented in Figure 3. Paired t-test analyses
compared diameter measurements between SFGRAPPA and each of the other protocols
(Table 2b). None of the compared protocols yielded statistically significant
p-values, suggesting no systematic detectable quantitative differences in
diameter measurements using these acceleration techniques.Discussion
All acceleration methods reduced scan time but displayed significant
variations in image quality. Large-FOV CS scans received the highest Image
Quality scores from neuroradiologists, closely matching our current clinical
SFGRAPPA protocol. Additionally, Large-FOV protocols exhibited reduced wrap
artifacts and provided extended coverage of brain/scalp tissue. This proves
beneficial when imaging patients with larger head circumferences and when
assessing intracranial cortical arteries in embolic stroke cases or scalp
arteries in systemic vasculitis/temporal arteritis patients. Consequently, the
Large-FOV CS protocol offers a 50% scan time reduction, enhancing clinical
utility for comprehensive vasculopathy assessment.Conclusion
This study assessed FDA-approved acceleration
methods for VWI using 3D T1w-SPACE. Qualitative and quantitative metrics from 5
healthy subjects' scans are evaluated from the acquired protocols. The findings
indicate that CS-accelerated protocols closely match clinical standard image
quality while significantly reducing scan time and enabling full-head coverage.
Subsequent research will involve evaluating large-FOV CS protocols in a broader
patient cohort to determine their efficacy in detecting vascular pathology.
Acknowledgements
Sources of Funding: The work is supported by the American Heart Association Career Development Awards (938082 to JWS) and Institute of Translational Medicine and Therapeutics (JWS).References
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