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Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET

BACKGROUND: Arterial blood sampling is the gold standard method to obtain the arterial input function (AIF) for quantification of whole body (WB) dynamic (18)F-FDG PET imaging. However, this procedure is invasive and not typically available in clinical environments. As an alternative, we compared AI...

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Autores principales: Naganawa, Mika, Gallezot, Jean-Dominique, Shah, Vijay, Mulnix, Tim, Young, Colin, Dias, Mark, Chen, Ming-Kai, Smith, Anne M., Carson, Richard E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683759/
https://www.ncbi.nlm.nih.gov/pubmed/33226522
http://dx.doi.org/10.1186/s40658-020-00330-x
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author Naganawa, Mika
Gallezot, Jean-Dominique
Shah, Vijay
Mulnix, Tim
Young, Colin
Dias, Mark
Chen, Ming-Kai
Smith, Anne M.
Carson, Richard E.
author_facet Naganawa, Mika
Gallezot, Jean-Dominique
Shah, Vijay
Mulnix, Tim
Young, Colin
Dias, Mark
Chen, Ming-Kai
Smith, Anne M.
Carson, Richard E.
author_sort Naganawa, Mika
collection PubMed
description BACKGROUND: Arterial blood sampling is the gold standard method to obtain the arterial input function (AIF) for quantification of whole body (WB) dynamic (18)F-FDG PET imaging. However, this procedure is invasive and not typically available in clinical environments. As an alternative, we compared AIFs to population-based input functions (PBIFs) using two normalization methods: area under the curve (AUC) and extrapolated initial plasma concentration (C(P)*(0)). To scale the PBIFs, we tested two methods: (1) the AUC of the image-derived input function (IDIF) and (2) the estimated C(P)*(0). The aim of this study was to validate IDIF and PBIF for FDG oncological WB PET studies by comparing to the gold standard arterial blood sampling. METHODS: The Feng (18)F-FDG plasma concentration model was applied to estimate AIF parameters (n = 23). AIF normalization used either AUC(0–60 min) or C(P)*(0), estimated from an exponential fit. C(P)*(0) is also described as the ratio of the injected dose (ID) to initial distribution volume (iDV). iDV was modeled using the subject height and weight, with coefficients that were estimated in 23 subjects. In 12 oncological patients, we computed IDIF (from the aorta) and PBIFs with scaling by the AUC of the IDIF from 4 time windows (15–45, 30–60, 45–75, 60–90 min) (PBIF(AUC)) and estimated C(P)*(0) (PBIF(iDV)). The IDIF and PBIFs were compared with the gold standard AIF, using AUC values and Patlak K(i) values. RESULTS: The IDIF underestimated the AIF at early times and overestimated it at later times. Thus, based on the AUC and K(i) comparison, 30–60 min was the most accurate time window for PBIF(AUC); later time windows for scaling underestimated K(i) (− 6 ± 8 to − 13 ± 9%). Correlations of AUC between AIF and IDIF, PBIF(AUC(30–60)), and PBIF(iDV) were 0.91, 0.94, and 0.90, respectively. The bias of K(i) was − 9 ± 10%, − 1 ± 8%, and 3 ± 9%, respectively. CONCLUSIONS: Both PBIF scaling methods provided good mean performance with moderate variation. Improved performance can be obtained by refining IDIF methods and by evaluating PBIFs with test-retest data.
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spelling pubmed-76837592020-11-27 Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET Naganawa, Mika Gallezot, Jean-Dominique Shah, Vijay Mulnix, Tim Young, Colin Dias, Mark Chen, Ming-Kai Smith, Anne M. Carson, Richard E. EJNMMI Phys Original Research BACKGROUND: Arterial blood sampling is the gold standard method to obtain the arterial input function (AIF) for quantification of whole body (WB) dynamic (18)F-FDG PET imaging. However, this procedure is invasive and not typically available in clinical environments. As an alternative, we compared AIFs to population-based input functions (PBIFs) using two normalization methods: area under the curve (AUC) and extrapolated initial plasma concentration (C(P)*(0)). To scale the PBIFs, we tested two methods: (1) the AUC of the image-derived input function (IDIF) and (2) the estimated C(P)*(0). The aim of this study was to validate IDIF and PBIF for FDG oncological WB PET studies by comparing to the gold standard arterial blood sampling. METHODS: The Feng (18)F-FDG plasma concentration model was applied to estimate AIF parameters (n = 23). AIF normalization used either AUC(0–60 min) or C(P)*(0), estimated from an exponential fit. C(P)*(0) is also described as the ratio of the injected dose (ID) to initial distribution volume (iDV). iDV was modeled using the subject height and weight, with coefficients that were estimated in 23 subjects. In 12 oncological patients, we computed IDIF (from the aorta) and PBIFs with scaling by the AUC of the IDIF from 4 time windows (15–45, 30–60, 45–75, 60–90 min) (PBIF(AUC)) and estimated C(P)*(0) (PBIF(iDV)). The IDIF and PBIFs were compared with the gold standard AIF, using AUC values and Patlak K(i) values. RESULTS: The IDIF underestimated the AIF at early times and overestimated it at later times. Thus, based on the AUC and K(i) comparison, 30–60 min was the most accurate time window for PBIF(AUC); later time windows for scaling underestimated K(i) (− 6 ± 8 to − 13 ± 9%). Correlations of AUC between AIF and IDIF, PBIF(AUC(30–60)), and PBIF(iDV) were 0.91, 0.94, and 0.90, respectively. The bias of K(i) was − 9 ± 10%, − 1 ± 8%, and 3 ± 9%, respectively. CONCLUSIONS: Both PBIF scaling methods provided good mean performance with moderate variation. Improved performance can be obtained by refining IDIF methods and by evaluating PBIFs with test-retest data. Springer International Publishing 2020-11-23 /pmc/articles/PMC7683759/ /pubmed/33226522 http://dx.doi.org/10.1186/s40658-020-00330-x Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020, This is a U.S. government work and not under copyright protection in the U.S; foreign copyright protection may apply 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to theoriginal author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images orother third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a creditline to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted bystatutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view acopy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Research
Naganawa, Mika
Gallezot, Jean-Dominique
Shah, Vijay
Mulnix, Tim
Young, Colin
Dias, Mark
Chen, Ming-Kai
Smith, Anne M.
Carson, Richard E.
Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET
title Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET
title_full Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET
title_fullStr Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET
title_full_unstemmed Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET
title_short Assessment of population-based input functions for Patlak imaging of whole body dynamic (18)F-FDG PET
title_sort assessment of population-based input functions for patlak imaging of whole body dynamic (18)f-fdg pet
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683759/
https://www.ncbi.nlm.nih.gov/pubmed/33226522
http://dx.doi.org/10.1186/s40658-020-00330-x
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