Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data
[18F]fluoro-2-deoxy-D-glucose (FDG) is one of the most utilized tracers for positron emission tomography (PET) applications in oncology. FDG-PET relies on higher glycolytic activity in tumors compared to normal structures as the basis of image contrast. As a glucose analog, FDG is transported into m...
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doaj-b6f96982c5cc4b3aa6c430c640c5c6f82020-11-24T23:20:21ZengHindawi LimitedComputational and Mathematical Methods in Medicine1748-670X1748-67182013-01-01201310.1155/2013/793142793142Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine DataSara Garbarino0Giacomo Caviglia1Massimo Brignone2Michela Massollo3Gianmario Sambuceti4Michele Piana5Dipartimento di Matematica, Università di Genova, Via Dodecaneso 35, 16146 Genova, ItalyDipartimento di Matematica, Università di Genova, Via Dodecaneso 35, 16146 Genova, ItalyDipartimento di Ingegneria Navale, Elettrica, Elettronica e delle Telecomunicazioni, Università di Genova, Via Opera Pia 11, 16145 Genova, ItalyIRCCS San Martino IST, Largo Rosanna Benzi 10, 16132 Genova, ItalyDipartimento di Scienze della Salute, Università di Genova, Largo Rosanna Benzi 10, 16132 Genova, ItalyDipartimento di Matematica, Università di Genova, Via Dodecaneso 35, 16146 Genova, Italy[18F]fluoro-2-deoxy-D-glucose (FDG) is one of the most utilized tracers for positron emission tomography (PET) applications in oncology. FDG-PET relies on higher glycolytic activity in tumors compared to normal structures as the basis of image contrast. As a glucose analog, FDG is transported into malignant cells which typically exhibit an increased radioactivity. However, different from glucose, FDG is not reabsorbed by the renal system and is excreted to the bladder. The present paper describes a novel computational method for the quantitative assessment of this excretion process. The method is based on a compartmental analysis of FDG-PET data in which the excretion process is explicitly accounted for by the bladder compartment and on the application of an ant colony optimization (ACO) algorithm for the determination of the tracer coefficients describing the FDG transport effectiveness. The validation of this approach is performed by means of both synthetic data and real measurements acquired by a PET device for small animals (micro-PET). Possible oncological applications of the results are discussed in the final section.http://dx.doi.org/10.1155/2013/793142 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sara Garbarino Giacomo Caviglia Massimo Brignone Michela Massollo Gianmario Sambuceti Michele Piana |
spellingShingle |
Sara Garbarino Giacomo Caviglia Massimo Brignone Michela Massollo Gianmario Sambuceti Michele Piana Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data Computational and Mathematical Methods in Medicine |
author_facet |
Sara Garbarino Giacomo Caviglia Massimo Brignone Michela Massollo Gianmario Sambuceti Michele Piana |
author_sort |
Sara Garbarino |
title |
Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data |
title_short |
Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data |
title_full |
Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data |
title_fullStr |
Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data |
title_full_unstemmed |
Estimate of FDG Excretion by means of Compartmental Analysis and Ant Colony Optimization of Nuclear Medicine Data |
title_sort |
estimate of fdg excretion by means of compartmental analysis and ant colony optimization of nuclear medicine data |
publisher |
Hindawi Limited |
series |
Computational and Mathematical Methods in Medicine |
issn |
1748-670X 1748-6718 |
publishDate |
2013-01-01 |
description |
[18F]fluoro-2-deoxy-D-glucose (FDG) is one of the most utilized tracers for positron emission tomography (PET) applications in oncology. FDG-PET relies on higher glycolytic activity in tumors compared to normal structures as the basis of image contrast. As a glucose analog, FDG is transported into malignant cells which typically exhibit an increased radioactivity. However, different from glucose, FDG is not reabsorbed by the renal system and is excreted to the
bladder. The present paper describes a novel computational method
for the quantitative assessment of this excretion process. The method is based on a compartmental analysis of FDG-PET data in which the
excretion process is explicitly accounted for by the bladder compartment and on the application of an ant colony optimization (ACO)
algorithm for the determination of the tracer coefficients describing
the FDG transport effectiveness. The validation of this approach is
performed by means of both synthetic data and real measurements
acquired by a PET device for small animals (micro-PET). Possible
oncological applications of the results are discussed in the final section. |
url |
http://dx.doi.org/10.1155/2013/793142 |
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