Abstract

Applicability of intravoxel incoherent motion (IVIM) imaging in the clinical setting is hampered by the limited reliability in particular of the perfusion-related parameter estimates. To alleviate this problem, various advanced postprocessing methods have been introduced. However, the underlying algorithms are not readily available and generally suffer from an increased computational burden. Contrary, several computationally fast image denoising methods have recently been proposed which are accessible online and may improve reliability of IVIM parameter estimates. The objective of the present work is to investigate the impact of image denoising on accuracy and precision of IVIM parameter estimates using comprehensive in-silico and in-vivo experiments. Image denoising is performed with four different algorithms that work on magnitude data: two algorithms which are based on nonlocal means (NLM) filtering, one algorithm that relies on local principal component analysis (LPCA) of the diffusion-weighted images, and another algorithms that exploits joint rank and edge constraints (JREC). Accuracy and precision of IVIM parameter estimates is investigated in an in-silico brain phantom and an in-vivo ground truth as a function of the signal-to-noise ratio for spatially homogenous and inhomogenous levels of Rician noise. Moreover, precision is evaluated using bootstrap analysis of in-vivo measurements. In the experiments, IVIM parameters are computed a) by using a segmented fit method and b) by performing a biexponential fit of the entire attenuation curve based on nonlinear least squares estimates. Irrespective of the fit method, the results demonstrate that reliability of IVIM parameter estimates is substantially improved by image denoising. The experiments show that the LPCA and the JREC algorithms perform in a similar manner and outperform the NLM-related methods. Relative to noisy data, accuracy of the IVIM parameters in the in-silico phantom improves after image denoising by 76–79%, 79–81%, 84–99% and precision by 74–80%, 80–83%, 84–95% for the perfusion fraction, the diffusion coefficient, and the pseudodiffusion coefficient, respectively, when the segmented fit method is used. Beyond that, the simulations reveal that denoising performance is not impeded by spatially inhomogeneous levels of Rician noise in the image. Since all investigated algorithms are freely available and work on magnitude data they can be readily applied in the clinical setting which may foster transition of IVIM imaging into clinical practice.

Highlights

  • Using diffusion-weighted imaging (DWI), the apparent diffusion coefficient (ADC) can be calculated which is a measure of tissue diffusivity and has been shown to be a viable biomarker for various pathological conditions

  • The aim of the present study is to evaluate the impact of image denoising on accuracy and precision of intravoxel incoherent motion (IVIM) parameter estimates using comprehensive in-silico and in-vivo experiments

  • Denoising performance of the nonlocal means (NLM), the adaptive nonlocal means (ANLM), the local principal component analysis (LPCA), and the joint rank and edge constraints (JREC) algorithms was assessed with regard to accuracy and precision of the IVIM parameter estimates

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Summary

Introduction

Using diffusion-weighted imaging (DWI), the apparent diffusion coefficient (ADC) can be calculated which is a measure of tissue diffusivity and has been shown to be a viable biomarker for various pathological conditions. It has long been recognized that the ADC integrates the effects of diffusion and perfusion due to the pseudorandom organization of the capillary network at the voxel level [4, 5] For this reason, Le Bihan et al proposed the concept of intravoxel incoherent motion (IVIM) imaging. Le Bihan and Turner established a link between the product of the perfusion fraction and the pseudodiffusion coefficient and the relative perfusion or blood flow [6] In this manner, IVIM imaging permits separating the effects of diffusion and perfusion and may lead to a more comprehensive and differentiated understanding of the underlying tissue pathology and of alterations that occur in response to treatment

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