The Ultrasonic Tissue Characterization (UTC) is primarily based on radio-frequency (RF) signals′analysis. The processing of these signals allowed the estimation of different quantitative ultrasonic parameters (backscattered coefficients-ICB-, velocity-SoS, etc). It is known that the RF contains information that can be used to noninvasively characterize the structural and mechanical properties of tissue. Scatterer diameter (or size) from ICB measurements have been already used to discriminate fibrosis from normal tissue. From these findings, our goal was to evaluate the scatterer diameter to test its potential in the discrimination of fibrosis groups (F0, F1, F2, F3, and F4, METAVIR scale) from 20 in-vitro human liver samples, explored at 20 MHz. The mean scatterer diameters (µm) measured were: 42.14±4.90 (F0), 40.18±10.51 (F1), 38.82±6.05 (F3) and 40.30±2.22 (F4). The Kolmogorov-Smirnov test has shown a non-significant level (p>0.05) indicating that the scatterer size estimation alone cannot differentiate between all fibrosis groups; an obvious overlap between groups appears. However, fr the two different combinations (ICB, Size) and (ICB, Size, SoS), the discriminant analysis has correctly classified 75% and 85%, respectively, of liver samples at a significant level (p<0.00005). The multiparametric study could play an important role to aid in the diagnostic of liver fibrosis.
Ultrasonic tissue characterization is primarily based on radio-frequency (RF) signals. Different studies have demonstrated that the RF signals are closely linked to tissue structures. The processing of these signals using spectral methods has shown the possibility of deriving quantitative parameters (attenuation and backscattered coefficients) and also of providing a means to estimate the elementary properties of tissue (scatterer size, concentration, periodicity) by evaluating spectral parameters (slope, intercept etc). We have estimated the spectral slope of the average backscattering curve to test its potential in the discrimination of fibrosis stages (F0, F1, F2, F3, and F4, METAVIR scale) from 20 in-vitro human liver samples, insonified at 20 MHz. The slope estimations were (dB/MHz): 0.95,0.24 (F0), 1.15,0.43 (F1), 1.20,0.26 (F3) and 1.07,0.33 (F4). The Kolmogorov-Smirnov test (p>0.05) indicated that the slope alone cannot discriminate all fibrosis groups (as well as the other mentioned parameters). When associated to integrated backscattered coefficient, discriminant analysis has correctly classified 80% of liver samples (p<0.0000). The misclassification resulted from some F0 samples grouped as F4 or vice-versa, which agrees with our previous results that suggested some parameter overlapping for normal and cirrhotic hepatic tissue. Nevertheless, combination of these parameters can help the diagnosis of liver fibrosis.
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