Abstract

In the clinical practice PET imaging provides semi-quantitative information about metabolic activities in human body, using the Standardized Uptake Value (SUV). The SUV scale, by itself, does not to establish thresholds between benign and malignant uptake in high-level analyses, such as pattern recognition. The objective of this work is to investigate in PET image volume with high-uptake regions, two additional descriptors, besides the SUV measurements: the amount of information given by the Hartley function ( I Hartley ) and its expected value, the Shannon entropy ( H ). To estimate these descriptors, two models of the probability distribution were obtained from a high-uptake region of interest (ROI): (i) the normalized grayscale histogram from SUV intensity levels ( P i ), which provides global I HG and H G ; and (ii) the normalized gray level co-occurrence matrix (GLCM) of these graylevels ( P g,k ) at the same range, which provides local I HL and H L . The beginning results have shown that for the ROI (12x12 pixels) and for mean SUV ranging of 6.6213±0. 5196 g/ml, with SUV Max = 14,7372 g/ml, the global entropy (2,3778±0,0364) has a higher average uncertainty that local entropy (2,2069±0,0758), with a confidence interval of 99.95% (p value < 0,05%). This can be explained by analysing the sample from the amount of information, I Hartley , noting that on average local P g,k provides up to 90,55±9,18% more information when compared to the amount of information given by global P i. Therefore, these initial results suggest that, for build algorithms for PET image segmentations using threshold based in entropy measures, it is more appropriate to use a distribution functions estimator which considers the local information of the pixels intensities. The main application of this approach will be for, among other things, to construct pathological phantoms from PET images for dosimetry applications.

Highlights

  • The Positron Emission Tomography (PET) is a method used to visualize physiological processes in living individuals, in the non-invasive way

  • The beginning results have shown that for the region of interest (ROI) (12x12 pixels) and for mean Standardized Uptake Value (SUV) ranging of 6.6213±0. 5196 g/ml, with SUVMax = 14,7372 g/ml, the global entropy (2,3778±0,0364) has a higher average uncertainty that local entropy (2,2069±0,0758), with a confidence interval of 99.95%. This can be explained by analysing the sample from the amount of information, IHartley, noting that on average local Pg,k provides up to 90,55±9,18% more information when compared to the amount of information given by global Pi. These initial results suggest that, for build algorithms for PET image segmentations using threshold based in entropy measures, it is more appropriate to use a distribution functions estimator which considers the local information of the pixels intensities

  • Two models of the probability distribution were obtained from a high-uptake region of interest (ROI), using: (i) the normalized grayscale histogram from SUV intensity levels (Pi), which provides global IHartley and HG; and (ii) the normalized gray level cooccurrence matrix (GLCM) of these graylevels (Pg,k) at the same range, which provides local IHartley and HL [12]

Read more

Summary

Introduction

The Positron Emission Tomography (PET) is a method used to visualize physiological processes in living individuals, in the non-invasive way. It is important to emphasize that the SUV indice is linearly related to a set of random variables such as the image intensity, specific parameters of patient and scanner, as well the kinetics of tracer [2]. Recent studies have sought to increase the characterization of the uptake pattern from radiotracer with goal of lesions analysis [4, 5, 6, 7]. Once PET image has modest spatial resolution [3] and the SUV scale, by itself, is not sufficient to establish thresholds between benign and malignant uptake in high-level analyses, such as pattern recognition, it is important to find other tools that provide more information about the heterogeneity uptake distribution within tumor regions

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call