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Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28
BACKGROUND: The aim of this study was to test seven previously published image-input methods in state-of-the-art high resolution PET brain images. Images were obtained with a High Resolution Research Tomograph plus a resolution-recovery reconstruction algorithm using two different radioligands with...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045425/ https://www.ncbi.nlm.nih.gov/pubmed/21364880 http://dx.doi.org/10.1371/journal.pone.0017056 |
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author | Zanotti-Fregonara, Paolo Liow, Jeih-San Fujita, Masahiro Dusch, Elodie Zoghbi, Sami S. Luong, Elise Boellaard, Ronald Pike, Victor W. Comtat, Claude Innis, Robert B. |
author_facet | Zanotti-Fregonara, Paolo Liow, Jeih-San Fujita, Masahiro Dusch, Elodie Zoghbi, Sami S. Luong, Elise Boellaard, Ronald Pike, Victor W. Comtat, Claude Innis, Robert B. |
author_sort | Zanotti-Fregonara, Paolo |
collection | PubMed |
description | BACKGROUND: The aim of this study was to test seven previously published image-input methods in state-of-the-art high resolution PET brain images. Images were obtained with a High Resolution Research Tomograph plus a resolution-recovery reconstruction algorithm using two different radioligands with different radiometabolite fractions. Three of the methods required arterial blood samples to scale the image-input, and four were blood-free methods. METHODS: All seven methods were tested on twelve scans with [(11)C](R)-rolipram, which has a low radiometabolite fraction, and on nineteen scans with [(11)C]PBR28 (high radiometabolite fraction). Logan V (T) values for both blood and image inputs were calculated using the metabolite-corrected input functions. The agreement of image-derived Logan V (T) values with the reference blood-derived Logan V (T) values was quantified using a scoring system. Using the image input methods that gave the most accurate results with Logan analysis, we also performed kinetic modelling with a two-tissue compartment model. RESULTS: For both radioligands the highest scores were obtained with two blood-based methods, while the blood-free methods generally performed poorly. All methods gave higher scores with [(11)C](R)-rolipram, which has a lower metabolite fraction. Compartment modeling gave less reliable results, especially for the estimation of individual rate constants. CONCLUSION: Our study shows that: 1) Image input methods that are validated for a specific tracer and a specific machine may not perform equally well in a different setting; 2) despite the use of high resolution PET images, blood samples are still necessary to obtain a reliable image input function; 3) the accuracy of image input may also vary between radioligands depending on the magnitude of the radiometabolite fraction: the higher the metabolite fraction of a given tracer (e.g., [(11)C]PBR28), the more difficult it is to obtain a reliable image-derived input function; and 4) in association with image inputs, graphical analyses should be preferred over compartmental modelling. |
format | Text |
id | pubmed-3045425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30454252011-03-01 Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 Zanotti-Fregonara, Paolo Liow, Jeih-San Fujita, Masahiro Dusch, Elodie Zoghbi, Sami S. Luong, Elise Boellaard, Ronald Pike, Victor W. Comtat, Claude Innis, Robert B. PLoS One Research Article BACKGROUND: The aim of this study was to test seven previously published image-input methods in state-of-the-art high resolution PET brain images. Images were obtained with a High Resolution Research Tomograph plus a resolution-recovery reconstruction algorithm using two different radioligands with different radiometabolite fractions. Three of the methods required arterial blood samples to scale the image-input, and four were blood-free methods. METHODS: All seven methods were tested on twelve scans with [(11)C](R)-rolipram, which has a low radiometabolite fraction, and on nineteen scans with [(11)C]PBR28 (high radiometabolite fraction). Logan V (T) values for both blood and image inputs were calculated using the metabolite-corrected input functions. The agreement of image-derived Logan V (T) values with the reference blood-derived Logan V (T) values was quantified using a scoring system. Using the image input methods that gave the most accurate results with Logan analysis, we also performed kinetic modelling with a two-tissue compartment model. RESULTS: For both radioligands the highest scores were obtained with two blood-based methods, while the blood-free methods generally performed poorly. All methods gave higher scores with [(11)C](R)-rolipram, which has a lower metabolite fraction. Compartment modeling gave less reliable results, especially for the estimation of individual rate constants. CONCLUSION: Our study shows that: 1) Image input methods that are validated for a specific tracer and a specific machine may not perform equally well in a different setting; 2) despite the use of high resolution PET images, blood samples are still necessary to obtain a reliable image input function; 3) the accuracy of image input may also vary between radioligands depending on the magnitude of the radiometabolite fraction: the higher the metabolite fraction of a given tracer (e.g., [(11)C]PBR28), the more difficult it is to obtain a reliable image-derived input function; and 4) in association with image inputs, graphical analyses should be preferred over compartmental modelling. Public Library of Science 2011-02-25 /pmc/articles/PMC3045425/ /pubmed/21364880 http://dx.doi.org/10.1371/journal.pone.0017056 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Zanotti-Fregonara, Paolo Liow, Jeih-San Fujita, Masahiro Dusch, Elodie Zoghbi, Sami S. Luong, Elise Boellaard, Ronald Pike, Victor W. Comtat, Claude Innis, Robert B. Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 |
title | Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 |
title_full | Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 |
title_fullStr | Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 |
title_full_unstemmed | Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 |
title_short | Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28 |
title_sort | image-derived input function for human brain using high resolution pet imaging with [(11)c](r)-rolipram and [(11)c]pbr28 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045425/ https://www.ncbi.nlm.nih.gov/pubmed/21364880 http://dx.doi.org/10.1371/journal.pone.0017056 |
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