The purpose of this paper is a quantification of displacement parameters used in the imaging of brain tissue endogenous motion using ultrasonic radiofrequency (RF) signals. In a preclinical study, an ultrasonic diagnostic system with RF output was equipped with dedicated signal processing software and subject head–ultrasonic transducer stabilization. This allowed the use of RF scanning frames for the calculation of micrometer-range displacements, excluding sonographer-induced motions. Analysis of quantitative displacement estimates in dynamical phantom experiments showed that displacements of 55 µm down to 2 µm were quantified as confident according to Pearson correlation between signal fragments (minimum p ≤ 0.001). The same algorithm and scanning hardware were used in experiments and clinical imaging which allows translating phantom results to Alzheimer’s disease patients and healthy elderly subjects as examples. The confident quantitative displacement waveforms of six in vivo heart-cycle episodes ranged from 8 µm up to 263 µm (Pearson correlation p ≤ 0.01). Displacement time sequences showed promising possibilities to evaluate the morphology of endogenous displacement signals at each point of the scanning plane, while displacement maps—regional distribution of displacement parameters—were essential for tissue characterization.
Ultrasound echoscopy technologies are continuously evolving towards new modalities including quantitative parameter imaging, elastography, 3D scanning, and others. The development and analysis of new methods and algorithms require an adequate digital simulation of radiofrequency (RF) signal transformations. The purpose of this paper is the quantitative evaluation of RF signal simulation uncertainties in resolution and contrast reproduction with the model of a phased array transducer. The method is based on three types of standard physical phantoms. Digital 3D models of those phantoms are composed of point scatterers representing the weak backscattering of the background material and stronger backscattering from inclusions. The simulation results of echoscopy with sector scanning transducer by Field II software are compared with the RF output of the Ultrasonix scanner after scanning standard phantoms with 2.5 MHz phased array. The quantitative comparison of axial, lateral, and elevation resolutions have shown uncertainties from 9 to 22% correspondingly. The echoscopy simulation with two densities of scatterers is compared with contrast phantom imaging on the backscattered RF signals and B-scan reconstructed image, showing that the main sources of uncertainties limiting the echoscopy RF signal simulation adequacy are an insufficient knowledge of the scanner and phantom’s parameters. The attempt made for the quantitative evaluation of simulation uncertainties shows both problems and the potential of echoscopy simulation in imaging technology developments. The analysis presented could be interesting for researchers developing quantitative ultrasound imaging and elastography technologies looking for simulated raw RF signals comparable to those obtained from real ultrasonic scanning.
We aim to estimate brain tissue displacements in the medial temporal lobe (MTL) using backscattered ultrasound radiofrequency (US RF) signals, and to assess the diagnostic ability of brain tissue displacement parameters for the differentiation of patients with Alzheimer’s disease (AD) from healthy controls (HC). Standard neuropsychological evaluation and transcranial sonography (TCS) for endogenous brain tissue motion data collection are performed for 20 patients with AD and for 20 age- and sex-matched HC in a prospective manner. Essential modifications of our previous method in US waveform parametrization, raising the confidence of micrometer-range displacement signals in the presence of noise, are done. Four logistic regression models are constructed, and receiver operating characteristic (ROC) curve analyses are applied. All models have cut-offs from 61.0 to 68.5% and separate AD patients from HC with a sensitivity of 89.5% and a specificity of 100%. The area under a ROC curve of predicted probability in all models is excellent (from 95.2 to 95.7%). According to our models, AD patients can be differentiated from HC by a sharper morphology of some individual MTL spatial point displacements (i.e., by spreading the spectrum of displacements to the high-end frequencies with higher variability across spatial points within a region), by lower displacement amplitude differences between adjacent spatial points (i.e., lower strain), and by a higher interaction of these attributes.
Arterial stiffness is an independent predictor of cardiovascular events. The motion of arterial tissues during the cardiac cycle is important as a mechanical deformation representing vessel elasticity and is related to arterial stiffness. In addition, arterial pulsation is the main source of endogenous tissue micro-motions currently being studied for tissue elastography. Methods based on artery motion detection are not applied in clinical practice these days, because they must be carefully investigated in silico and in vitro before wide usage in vivo. The purpose of this paper is to propose a dynamic 3D artery model capable of reproducing the biomechanical behavior of human blood vessels surrounded by elastic tissue for endogenous deformation elastography developments and feasibility studies. The framework is based on a 3D model of a pulsating artery surrounded by tissue and simulation of linear scanning by Field II software to generate realistic dynamic RF signals and B-mode ultrasound image sequential data. The model is defined by a spatial distribution of motions, having patient-specific slopes of radial and longitudinal motion components of the artery wall and surrounding tissues. It allows for simulating the quantified mechanical micro-motions in the volume of the model. Acceptable simulation errors calculated between modeled motion patterns and those estimated from simulated RF signals and B-scan images show that this approach is suitable for the development and validation of elastography algorithms based on motion detection.
Tissue pulsatility imaging is introduced as non-invasive ultrasonic (US) technique used to access endogenous motion of human brain. Increasing evidence suggests that brain tissue pulsatility have a potential to be used for diagnosis of neurodegenerative diseases. In this work, we aimed to assess quantitatively the brain tissue displacements with presented radiofrequency (RF) ultrasonic method. The obtained maps of intra-subject repeatable brain displacements enable spatial differentiation of dynamic structures from relatively static. Averaged displacement waveform in brain region were noticed to be intra-subject repeatable. The brain movement strength and mean frequency in mid-brain and hippocampus are explored in pilot groups of healthy volunteers and Alzheimer patients.