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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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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. |
format | Online Article Text |
id | pubmed-10008518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
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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