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APRIL: Adaptive Regression-Based Two-Dimensional Quantitative Anisotropy Imaging Using Acoustic Radiation Force
Md Walid Hassan1, Kayla Crook2, Young Jin Gi
1Department of Electrical and Computer Engineering, University of Hawai'i at Manoa, Honolulu, HI 96822, USA.
Objective:
This study aims to develop and validate a quantitative, depth-resolved anisotropy imaging framework that extends ARFI-based focal degree-of-anisotropy (DoA) estimation into two-dimensional mapping by modeling the depth-dependent relationship between shear modulus ratio (SMR) and peak displacement ratio (PDR).
Methods:
We propose APRIL (Adaptive Polynomial Regression for anisotropy Imaging via ARFI-induced DispLacements), a framework for quantitative, depth-resolved DoA imaging that adaptively selects polynomial regression or shape-preserving spline interpolation based on excitation PSF asymmetry. Training data were generated using an LS-DYNA3D + Field II simulation pipeline in homogeneous transversely isotropic media (SMR 0.9-4.9). Testing included shifted SMRs under varied acoustic conditions and three heterogeneous inclusion configurations (anisotropic inclusion in isotropic background and vice versa). Experimental validation was performed in an in-vivo murine tumor model over the time, ex-vivo chicken breast, and tissue-mimicking gelatin phantoms, using a Verasonics system with an L11-5v transducer.
Results:
APRIL achieved depth-resolved SMR prediction errors below 9% over 10-30 mm, with highest accuracy in the focal region (MAE 2.3%, RMSE < 0.1) and stable performance across PSF transition zones. In heterogeneous phantoms, it reconstructed anisotropy maps with SSIM up to 86% and MPE below 7%, accurately delineating inclusion boundaries. Under acoustic parameter variations, mean absolute errors remained below 10%, demonstrating robustness to system and tissue heterogeneity.
Conclusion:
APRIL enables robust, two-dimensional anisotropy imaging beyond focal estimates.
Significance:
The method provides a physically grounded and generalizable framework for clinically viable anisotropy biomarkers in muscle, tendon, kidney, tumor and breast tissues.
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