Susanne Schnell1, Maria Aristova1, Matthew B Potts2, Babak S Jahromi2, Liliana Ma1, Alireza Vali1, Amer A Syed1, Michael C Hurley3, Michael Markl1,4, and Sameer A Ansari5
1Radiology, Northwestern University, Chicago, IL, United States, 2Neurological Surgery, Northwestern University, Chicago, IL, United States, 3Radiology and Neurological Surgery, Northwestern University, Chicago, IL, United States, 4Biomedical Engineering, Northwestern University, Evanston, IL, United States, 5Radiology, Neurological Surgery and Neurology, Northwestern University, Chicago, IL, United States
Synopsis
We applied and investigated the benefits of using kt-GRAPPA
accelerated dual-venc 4D flow MRI in five
patients who presented with cerebral aneurysm between 4 and 12mm (smallest and
largest dimension). Velocity values were systematically compared with the high-venc-only part of the same acquisition
using correlation and histogram analysis. Blood flow was visualized with
streamlines and quality was visually assessed. Results show that dual-venc 4D flow MRI provides refined
information on slow flow and recirculating flow in cerebral aneurysms. Future
studies will assess the feasibility of advanced hemodynamic measures obtained
from dual-venc 4D flow MRI as
predictive imaging biomarkers.
Introduction
Cerebral aneurysms are life threatening
neurovascular lesions, with a significant prevalence of 3-6% in the general population1,2. Although the annual rupture rate is fairly low with < 1-2%3, it
is associated with high morbidity and mortality. Risk stratification is
currently based on empirical parameters (e.g. patient age, aneurysm size,
morphology, and location), or systemic risk factors (hypertension,
smoking/alcohol abuse etc.)4,5, but provide an incomplete assessment of this
complex disease. In addition, previous studies showed that aneurysm morphology,
flow characteristics, and vessel wall properties can be substantially different
for individual patients6. Hemodynamic parameters such as inflow jet patterns
and wall shear stress have been investigated in previous studies and constitute
potential new biomarkers for risk stratification and treatment planning.
However, blood flow velocities within aneurysms can differ
by an order of magnitude (high inflow jets with 150cm/s vs. slow flow
recirculation with 10cm/s versus). The detailed evaluation of complex neurovascular
flow occurring inside an aneurysm is thus challenging as it requires the
measurement of both slow and fast blood flow velocities within one acquisition.
The acquisition of cerebral aneurysmal hemodynamics with a single-venc 4D flow MRI acquisition is thus
difficult and would result in either substantial velocity aliasing for high inflow
into the aneurysm or high noise levels for low flow velocities in areas with vortex/helix
flow. The aim of this study was to perform dual-venc 4D Flow-MRI7 with inherently increased velocity dynamic
range in cerebral aneurysm patients and assess the ability to capture slow flow
regions as well as circulating flow areas.Methods
A fully integrated dual-venc sequence7 with a shared
reference scan (7-point encoding) was used in 5 cerebral aneurysm patients
(Table 1) on a 3T Skyra scanner (MAGNETOM, Siemens, Germany). kt-GRAPPA
acceleration with R=5 was applied8. A combined dual-venc data set was reconstructed using
the high-venc acquisition for
complete anti-aliasing of the low-venc
data while maintaining a favorable velocity to noise ratio (VNR) of the low-venc data7. Additionally,
the high-venc data set from the same
measurement (single-venc) was
processed for comparison purposes. All 4D flow data was corrected for phase
offsets and noise (independently for high-venc
and dual-venc), and a phase-contrast
angiogram (PC-MRA) was calculated. Based on the PC-MRA, the intracranial
vessels and aneurysms were manually segmented (MIMICS, Materialize, Belgium).
Segmentations and flow data were loaded into commercial software (ENSIGHT, CEI,
USA) for 3D visualization of blood flow through the intracranial vessels and aneurysms.
Single-venc (high-venc) and dual-venc scans from the same acquisitions were compared by using
velocity histograms and streamline visualization.Results
Dual-venc
and standard 2D PC-MRI data were successfully acquired (Figure 1) in all 5 patients. Figure 1 shows a comparison of dual-venc vs. single-venc 3D streamlines for visualizing blood flow through the
aneurysms. Especially in slow flow regions, dual-venc streamlines were less noisy and more collinear, resulting in
an improved depiction of flow patterns (increased streamline density, reduced
noise along individual traces) compared to the single-venc acquisition. Figure 2
shows histogram of blood flow velocities occurring in the aneurysms (all voxels
in 3D segmentation + time) for dual-venc
and single-venc 4D flow MRI, showing
a shift to more voxels with slower velocities in the dual-venc scan. Correlation between high-venc and low-venc
velocities within the aneurysm demonstrate excellent agreement (R= 0.93,
p<0.00001), though from the Bland-Altman plots it can be seen that the
higher the velocity value the larger the difference between the measurements (Figure 3).Discussion
Dual-venc
4D flow characterization of hemodynamics in cerebral aneurysms demonstrated less
noisy streamlines and more sensitivity to low velocities within the aneurysms,
providing a more complete evaluation of the occurring velocities of individual
aneurysms. Due to its ability to detect subtle hemodynamic changes for improved
aneurysm differentiation, dual-venc 4D
flow MRI may have the potential to improve risk stratification by associating Wall
Shear Stress differences and intra-aneurysmal 3D velocity distribution with
risk of rupture. This 7-point encoded dual-venc 4D flow MRI implementation is a 1.75x longer acquisition than standard single-venc, when acquired without advanced acceleration methods. We
acquired this data with k-t GRAPPA to overcome the lengthy acquisition time and
could show its advantage over a single-venc
acquisition.Conclusion
When applied to patients with cerebral aneurysms, dual-venc demonstrated higher sensitivity to
slower velocity values and provided less noisy data. Future longitudinal
studies and correlation with aneurysm risk factors or aneurysm growth/rupture are
required to evaluate the utility of hemodynamic markers for improved risk
assessment and therapy planning.Acknowledgements
Grant support by AHA Scientist Development Grant 16SDG30420005
and NIH R01HL115828References
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