Julio Garcia1, Roel L.F. van der Palen2, Alex J. Barker1, Jeremy D. Collins1, James C. Carr1, Joshua Robinson3, Cynthia Rigsby3, and Michael Markl1,4
1Radiology, Northwestern University, Chicago, IL, United States, 2Pediatric Cardiology, Leiden University Medical Center, Leiden, Netherlands, 3Department of Medical Imaging, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL, United States, 4Biomedical Engineering, Northwestern University, Evanston, IL, United States
Synopsis
The
systematic characterization of effects in aortic disease patients and healthy
controls is important to improve disease diagnosis. 4D flow MRI can be applied for the analysis of altered hemodynamics in cardiovascular disease.
However, data analysis can be time consuming and often data are not fully utilized by analysis based on 2D
planes. This
study aimed to systematically apply flow
distribution analysis in the entire volume of the aorta to establish
normative reference values across a wide age range from pediatric to adult subjects.Purpose:
The ability to
systematically characterize effects in aortic disease patients and healthy
controls is important to improve disease diagnosis. Time-resolved 3D PC-MRI
with three-directional velocity encoding (4D flow MRI) has been successfully
applied for the analysis of altered hemodynamics in cardiovascular disease
1.
However, data analysis can be time consuming and the inherent volumetric 3D coverage
provided by 4D flow MRI is often not fully utilized by analysis based on 2D
planes. Recently, a number of studies have demonstrated that velocity
distribution analysis can overcome these limitations by providing an efficient
data analysis workflow that exploits the full volumetric coverage and can detect
changes in vascular hemodynamics
2, 3. However, it is important to evaluate
altered hemodynamics in aortic disease relative to normal blood flow dynamics
which are known to be influenced by age and gender. It was thus the aim of this
study to systematically apply flow distribution
analysis in the entire volume of the aorta to establish
normative reference values across a wide age range from pediatric to adult subjects.
Methods:
101 control subjects (age=39±17
years, age range=9-78, female=42) were identified via an IRB-approved retrospective
chart review. 4D flow MRI was performed at 1.5T and 3T with full 3D coverage of
the thoracic aorta (spatial resolution=2.5×2.1×3.2 mm3; temporal
resolution=40-50 ms) using prospective ECG and respiratory navigator gating.
Pulse sequence parameters were as follows: 1.5 T scan parameters
ranged from TE/TR=2.3–3.4/4.8–6.6 ms, flip angle α=7–15° and a field of view of 340–400×200–300 mm; 3T scans used TE/TR
=2.5/5.1 ms, flip angle α=7–15°, and a field of view
of 400×308 mm. 3D PC-MR angiograms (3D PC-MRA) were computed and
segmented to obtain a 3D volume of the aorta (Mimics, Materialise, Leuven,
Belgium) which was used to compute a masked 4D velocity field (3
spatial dimensions + time). The masked aorta velocity field was used to
generate a maximum intensity projection (MIP) in an oblique sagittal plane
using the three peak systolic velocity phases to extract the aortic peak
velocity. The velocities from all voxels within the first 8 time steps in
systole, determinate optimal by a sensitivity analysis between groups
2,
inside an aorta segmentation were plotted in histogram form and normalized by
the total number of voxels in order to be compared across subjects and cohorts (Matlab, Natick, MA, USA). In addition, mean, median, standard deviation, skewness,
kurtosis, and the normalized number of voxels >1m/s (incidence) were
calculated for each case. Aortic diameter was extracted using a volume
centerline of the 3D PC-MRA in the ascending aorta
4. Each subject was classified into four groups of
age (group 1: <20 years, group 2: 20-39 years; group 3: 40-59 years; group 4:
>60 years) and gender (female and male). Association between computed
parameters was assessed by regressions analysis and comparison between groups
by ANOVA (P-value<0.05 was considered significant).
Results:
Table 1 summarizes subject
demographics by group. Examples of velocity MIPs in figure 1A illustrate visual
differences in the aortic velocity patterns and distribution. The velocity distribution
analysis for one subject is shown in figure 1C. Spider plots summarized for each
cohort are shown in figure 1D providing a visual impression of the flow
characteristics. Notice that peak velocity, aortic diameter, skewness, and
kurtosis were able to differentiate significant changes between groups (P<0.05
using ANOVA) whereas mean velocities did not. Significant correlations with age
are listed in Table 2, the three highest correlations plotted in figure 2. Notice
that a quadratic fit was also found for age and aortic diameter. Significant
inter-group analysis from spider plots for age and gender are presented in figure
3.
Discussion:
The volumetric velocity distribution
analysis presented here has demonstrated: 1) 3D blood flow velocity
distributions can identify hemodynamic differences in healthy subjects across age
and genders via basic statistical descriptors; 2) peak velocity, aortic
diameter, skewness, and kurtosis enabled better identification of hemodynamic
changes due to age and gender than mean and standard deviation. Our results indicate
which blood flow parameters are best to establish normative values to assess
flow disturbances in the thoracic aorta.
Conclusion:
Systematic velocity
distribution analysis of 4D flow velocity data may identify and differentiate
hemodynamic characteristics due to age, gender, and aortic peak velocity.
Further studies are needed to evaluate the association of velocity distribution
derived descriptors with patient prognosis.
Acknowledgements
Grant support by NIH R01HL115828, 5K25HL119608-02
and AHA 14POST18350019.References
1. Markl M, Harloff A, Bley TA, et al. Time-resolved 3D MR velocity mapping at 3T: improved navigator-gated assessment of vascular anatomy and blood flow. J
Magn Res Imaging 2007; 25:824-31.
2. Garcia J, Barker AJ, van Ooij P, et al. Assessment of altered three-dimensional blood characteristics in aortic disease by velocity distribution analysis. Magn Res Med 2015;
74:817-825.
3. Schnell S, Ansari SA, Vakil P, et al. Three-dimensional hemodynamics in intracranial aneurysms: influence of size and morphology. J Mag Reson Imaging 2014; 39 :120-131.
4. Garcia J, Barker AJ, Murphy I,
et al. Four-dimensional flow magnetic resonance imaging-based
characterization of aortic morphometry and haemodynamics: impact of age,
aortic diameter, and valve morphology. Eur Heart J Cardiovasc Imaging 2015. doi:10.1093/ehjci/jev228.