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Patient-adaptive Population-based Modeling of Arterial Input Functions

Kinetic modeling of dynamic PET data requires knowledge of tracer concentration in blood plasma, described by the arterial input function (AIF). Arterial blood sampling is the gold standard for AIF measurement, but is invasive and labour intensive. A number of methods have been proposed to accuratel...

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Autores principales: Xiu, Zhaoyan, Muzi, Mark, Huang, Jian, Wolsztynski, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008518/
https://www.ncbi.nlm.nih.gov/pubmed/36094987
http://dx.doi.org/10.1109/TMI.2022.3205940
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author Xiu, Zhaoyan
Muzi, Mark
Huang, Jian
Wolsztynski, Eric
author_facet Xiu, Zhaoyan
Muzi, Mark
Huang, Jian
Wolsztynski, Eric
author_sort Xiu, Zhaoyan
collection PubMed
description Kinetic modeling of dynamic PET data requires knowledge of tracer concentration in blood plasma, described by the arterial input function (AIF). Arterial blood sampling is the gold standard for AIF measurement, but is invasive and labour intensive. A number of methods have been proposed to accurately estimate the AIF directly from blood sampling and/or imaging data. Here we consider fitting a patient-adaptive mixture of historical population time course profiles to estimate individual AIFs. Travel time of a tracer atom from the injection site to the right ventricle of the heart is modeled as a realization from a Gamma distribution, and the time this atom spends in circulation before being sampled is represented by a subject-specific linear mixture of population profiles. These functions are estimated from independent population data. Individual AIFs are obtained by projection onto this basis of population profile components. The model incorporates knowledge of injection duration into the fit, allowing for varying injection protocols. Analyses of arterial sampling data from (18)F-FDG, (15)O-H(2)O and (18)F-FLT clinical studies show that the proposed model can outperform reference techniques. The statistically significant gain achieved by using population data to train the basis components, instead of fitting these from the single individual sampling data, is measured on the FDG cohort. Kinetic analyses of simulated data demonstrate the reliability and potential benefit of this approach in estimating physiological parameters. These results are further supported by numerical simulations that demonstrate convergence and stability of the proposed technique under varying training population sizes and noise levels.
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spelling pubmed-100085182023-04-05 Patient-adaptive Population-based Modeling of Arterial Input Functions Xiu, Zhaoyan Muzi, Mark Huang, Jian Wolsztynski, Eric IEEE Trans Med Imaging Article Kinetic modeling of dynamic PET data requires knowledge of tracer concentration in blood plasma, described by the arterial input function (AIF). Arterial blood sampling is the gold standard for AIF measurement, but is invasive and labour intensive. A number of methods have been proposed to accurately estimate the AIF directly from blood sampling and/or imaging data. Here we consider fitting a patient-adaptive mixture of historical population time course profiles to estimate individual AIFs. Travel time of a tracer atom from the injection site to the right ventricle of the heart is modeled as a realization from a Gamma distribution, and the time this atom spends in circulation before being sampled is represented by a subject-specific linear mixture of population profiles. These functions are estimated from independent population data. Individual AIFs are obtained by projection onto this basis of population profile components. The model incorporates knowledge of injection duration into the fit, allowing for varying injection protocols. Analyses of arterial sampling data from (18)F-FDG, (15)O-H(2)O and (18)F-FLT clinical studies show that the proposed model can outperform reference techniques. The statistically significant gain achieved by using population data to train the basis components, instead of fitting these from the single individual sampling data, is measured on the FDG cohort. Kinetic analyses of simulated data demonstrate the reliability and potential benefit of this approach in estimating physiological parameters. These results are further supported by numerical simulations that demonstrate convergence and stability of the proposed technique under varying training population sizes and noise levels. 2023-01 2022-12-29 /pmc/articles/PMC10008518/ /pubmed/36094987 http://dx.doi.org/10.1109/TMI.2022.3205940 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 License. For more information, see https://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Xiu, Zhaoyan
Muzi, Mark
Huang, Jian
Wolsztynski, Eric
Patient-adaptive Population-based Modeling of Arterial Input Functions
title Patient-adaptive Population-based Modeling of Arterial Input Functions
title_full Patient-adaptive Population-based Modeling of Arterial Input Functions
title_fullStr Patient-adaptive Population-based Modeling of Arterial Input Functions
title_full_unstemmed Patient-adaptive Population-based Modeling of Arterial Input Functions
title_short Patient-adaptive Population-based Modeling of Arterial Input Functions
title_sort patient-adaptive population-based modeling of arterial input functions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008518/
https://www.ncbi.nlm.nih.gov/pubmed/36094987
http://dx.doi.org/10.1109/TMI.2022.3205940
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