Abstract
Diffusion weighted imaging (DWI) and intravoxel incoherent motion (IVIM) have been explored to assess liver tumors and diffused liver diseases. IVIM reflects the microscopic translational motions that occur in voxels in magnetic resonance (MR) DWI. In biologic tissues, molecular diffusion of water and microcirculation of blood in the capillary network can be assessed using IVIM DWI. The most commonly applied model to describe the DWI signal is a bi-exponential model, with a slow compartment of diffusion linked to pure molecular diffusion (represented by the coefficient Dslow), and a fast compartment of diffusion, related to microperfusion (represented by the coefficient Dfast). However, high variance in Dfast estimates has been consistently shown in literature for liver IVIM, restricting its application in clinical practice. This variation could be explained by the presence of another very fast compartment of diffusion in the liver. Therefore, a tri-exponential model would be more suitable to describe the DWI signal. This article reviews the published evidence of the existence of this additional very fast diffusion compartment and discusses the performance and limitations of the tri-exponential model for liver IVIM in current clinical settings.
Highlights
Diffusion weighted imaging (DWI) sequence has shown high-performance for the detection of malignant liver tumors, liver metastases from solid cancer [1,2,3,4]
Since flowing or moving spins are present in these compartments, which are directly or indirectly connected together, it can be hypothesized that more than two compartments of diffusion exist in the liver and could be analyzed through the recorded DWI signal decay
With a DWI protocol including 16 b-values (0, 2, 4, 8, 12, 18, 24, 32, 40, 50, 75, 110, 200, 300, 450, 600 s/mm2) and a group of eight healthy volunteers that were scanned at baseline and during three increasing doses of continuous intravenous Angiotensin II infusion, this study demonstrated that tri-exponential analysis was able to detect changes in renal perfusion during pharmacologically induced renal perfusion modulation
Summary
Diffusion weighted imaging (DWI) sequence has shown high-performance for the detection of malignant liver tumors, liver metastases from solid cancer [1,2,3,4]. Numerous studies aiming to assess diffused liver diseases using this two-compartment model have been published [7,9,19]. High variance in Dfast estimates has been consistently shown in literature, restricting its application in clinical practice [9]. This variance could be due to an additional perfusion component [20]. The aim of this article is to review and discuss the published evidence of a tri-exponential decay behavior of the DWI signal, and the technical requirements and the limitations of the tri-exponential IVIM model in current clinical settings
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