Renee Miller1,2, Arunark Kolipaka3, Martyn P Nash2,4, and Alistair A Young1,2
1Anatomy and Medical Imaging, University of Auckland, Auckland, New Zealand, 2Auckland Bioengineering Institute, University of Auckland, Auckland, New Zealand, 3The Ohio State University Wexner Medical Center, Ohio State University, Columbus, OH, United States, 4Department of Engineering Science, University of Auckland, Auckland, New Zealand
Synopsis
Despite the anisotropy of myocardium, previous cardiac MR
elastography studies have investigated isotropic stiffness of heart tissue. Anisotropic
material properties could provide a better understanding of structural changes
that occur in the heart due to pathologies such as diastolic heart failure. However,
optimal imaging parameters to measure anisotropic properties are yet unknown. This
study investigates the optimal loading frequency that accurately recovers
anisotropic stiffness measurements using simulations of cardiac MR elastography
experiments in the presence of Gaussian noise and known fibre orientations. The
optimised virtual fields method is used as an inversion method to translate
harmonic displacements to stiffness parameters.
Introduction
Myocardial
stiffness is an important determinant of cardiac function, and significant
increases in global stiffness are thought to be associated with some forms of
diastolic heart failure1. Although magnetic resonance elastography
(MRE) has been previously used to estimate isotropic stiffness in the heart,
myocardium has anisotropic material properties with greatest stiffness along
the fibre direction.
In addition to anisotropy, the heart provides significant challenges to MRE due
to thin-walled structure2. At loading frequencies below 60 Hz, not enough
wavelengths are present within the thin wall to accurately estimate material
properties since at least half of one wavelength is needed. Biological tissue,
including myocardium, is viscous and results in large wave attenuation at frequencies
greater than 200 Hz. Previous studies, estimating isotropic shear moduli within
myocardium, have used frequencies ranging from 80 Hz – 220 Hz. It is unknown,
however, the optimal loading frequencies for estimating anisotropic material
properties. Therefore, this study investigated the impact of loading frequency
on the estimation of transversely isotropic material properties in silico in a left ventricular (LV)
model with simulated harmonic displacements.Methods
The optimised virtual fields method2,3 (VFM) was
used to estimate homogeneous transversely isotropic material properties from
simulated harmonic displacements in a canine LV model with fibre orientations
measured from histology. Simulations of steady-state harmonic displacement were
run at loading frequencies ranging from 60 Hz – 200 Hz (Figure 1). A Monte
Carlo simulation was run at each frequency (n = 30) in which the five
independent properties of the elasticity matrix (C11, C33,
C13, C44 and C66), which fully describe a
transversely isotropic material, were estimated from reference displacements
with added Gaussian noise (σNoise = 15% · σDisp).
Material constants (G12, G13, E1, E3
and v31) were then calculated from the inverse of the elasticity
matrix. A similar Monte Carlo simulation was run estimating three parameters4,5
(G12, G13 and τ), which avoided estimation of the longitudinal
wavelength. The optimised VFM is an iterative method and the maximum number of
iterations was set to 30. Results
Without noise, the estimated values of the shear moduli and
Young's moduli varied over the frequency range but there was no clear
difference in parameter estimates with increasing frequency. In the Monte Carlo
simulations with Gaussian noise, the number of converged simulations (out of
30) for the five-parameter formulation increased as the frequency increased (Table
1). Conversely, no simulations converged for the three-parameter formulation at
160 Hz, 180 Hz and 200 Hz. Figures 2 and 3 show box plots of the resulting
estimated material parameters for the five- and three-parameter formulations,
respectively. With the five-parameter material formulation, G13 was
most accurately estimated and had the smallest variance at 200 Hz. However,
estimated values of E3 showed the most variation at 200 Hz. At 100 Hz
and 160 Hz, G12 and E1 were underestimated. Estimated
Poisson's ratios were centred at the true values yet varied widely. With the
three-parameter formulation, loading at 80 Hz resulted in the most accurate
estimation of all three parameters: G12, G13 and τ. Results
at 60 Hz showed the largest variance compared with resulting estimated
parameters at other frequencies.Discussion
When estimating five parameters, improved convergence at
higher frequencies did not correlate with a decrease in variance in all estimated
parameters. Variance in estimated values of G13 generally decreased
whereas the variance in E3 generally increased. Therefore, when
choosing the frequency of excitation, better convergence (at a higher
frequency) may not necessarily result in accurate parameter estimates. In the three-parameter
formulation, convergence did not improve at higher frequencies. Therefore, the
material model-formulation also had a large impact on the accuracy, variance
and convergence of anisotropic
parameter estimates.
Conclusions
Overall, frequency of excitation had a large impact on both
the convergence of the optimised VFM as well as variance and accuracy of
estimated transversely isotropic material properties. It was shown that
estimates were poor for both formulations at 60 Hz, due to not enough wavelengths
present in the myocardium. When identifying transversely isotropic material
properties from cardiac MRE, these results showed that frequencies between 80
Hz – 140 Hz should be used in order to obtain adequate convergence using the
optimised VFM as well as estimated parameters with minimal variance. Accurate
measurements of anisotropic parameters from cardiac MRE could improve the
understanding of diseases such as diastolic heart failure, which alters the
material properties of myocardium. Acknowledgements
This research was supported by awards from the National Heart Foundation of New Zealand, American Heart Association 13SDG14690027, NHLBI R01HL124096 and The Royal Society of New Zealand Marsden Fund. The authors wish to acknowledge NeSI high performance computing facilities (https://www.nesi.org.nz) for their support of this research. The canine LV geometric model was provided by Dr. Vicky Wang at the Auckland Bioengineering Institute.References
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