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Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?

INTRODUCTION: The NMDA receptor radiotracer [(18)F]GE-179 has been used with 90-min scans and arterial plasma input functions. We explored whether (1) arterial blood sampling is avoidable and (2) shorter scans are feasible. METHODS: For 20 existing [(18)F]GE-179 datasets, we generated (1) standardis...

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Autores principales: McGinnity, Colm J., Riaño Barros, Daniela A., Trigg, William, Brooks, David J., Hinz, Rainer, Duncan, John S., Koepp, Matthias J., Hammers, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995767/
https://www.ncbi.nlm.nih.gov/pubmed/29892810
http://dx.doi.org/10.1186/s13550-018-0396-2
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author McGinnity, Colm J.
Riaño Barros, Daniela A.
Trigg, William
Brooks, David J.
Hinz, Rainer
Duncan, John S.
Koepp, Matthias J.
Hammers, Alexander
author_facet McGinnity, Colm J.
Riaño Barros, Daniela A.
Trigg, William
Brooks, David J.
Hinz, Rainer
Duncan, John S.
Koepp, Matthias J.
Hammers, Alexander
author_sort McGinnity, Colm J.
collection PubMed
description INTRODUCTION: The NMDA receptor radiotracer [(18)F]GE-179 has been used with 90-min scans and arterial plasma input functions. We explored whether (1) arterial blood sampling is avoidable and (2) shorter scans are feasible. METHODS: For 20 existing [(18)F]GE-179 datasets, we generated (1) standardised uptake values (SUVs) over eight intervals; (2) volume of distribution (V(T)) images using population-based input functions (PBIFs), scaled using one parent plasma sample; and (3) V(T) images using three shortened datasets, using the original parent plasma input functions (ppIFs). RESULTS: Correlations with the original ppIF-derived 90-min V(T)s increased for later interval SUVs (maximal ρ = 0.78; 80–90 min). They were strong for PBIF-derived V(T)s (ρ = 0.90), but between-subject coefficient of variation increased. Correlations were very strong for the 60/70/80-min original ppIF-derived V(T)s (ρ = 0.97–1.00), which suffered regionally variant negative bias. CONCLUSIONS: Where arterial blood sampling is available, reduction of scan duration to 60 min is feasible, but with negative bias. The performance of SUVs was more consistent across participants than PBIF-derived V(T)s. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13550-018-0396-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-59957672018-06-26 Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential? McGinnity, Colm J. Riaño Barros, Daniela A. Trigg, William Brooks, David J. Hinz, Rainer Duncan, John S. Koepp, Matthias J. Hammers, Alexander EJNMMI Res Short Communication INTRODUCTION: The NMDA receptor radiotracer [(18)F]GE-179 has been used with 90-min scans and arterial plasma input functions. We explored whether (1) arterial blood sampling is avoidable and (2) shorter scans are feasible. METHODS: For 20 existing [(18)F]GE-179 datasets, we generated (1) standardised uptake values (SUVs) over eight intervals; (2) volume of distribution (V(T)) images using population-based input functions (PBIFs), scaled using one parent plasma sample; and (3) V(T) images using three shortened datasets, using the original parent plasma input functions (ppIFs). RESULTS: Correlations with the original ppIF-derived 90-min V(T)s increased for later interval SUVs (maximal ρ = 0.78; 80–90 min). They were strong for PBIF-derived V(T)s (ρ = 0.90), but between-subject coefficient of variation increased. Correlations were very strong for the 60/70/80-min original ppIF-derived V(T)s (ρ = 0.97–1.00), which suffered regionally variant negative bias. CONCLUSIONS: Where arterial blood sampling is available, reduction of scan duration to 60 min is feasible, but with negative bias. The performance of SUVs was more consistent across participants than PBIF-derived V(T)s. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13550-018-0396-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-06-11 /pmc/articles/PMC5995767/ /pubmed/29892810 http://dx.doi.org/10.1186/s13550-018-0396-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Short Communication
McGinnity, Colm J.
Riaño Barros, Daniela A.
Trigg, William
Brooks, David J.
Hinz, Rainer
Duncan, John S.
Koepp, Matthias J.
Hammers, Alexander
Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?
title Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?
title_full Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?
title_fullStr Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?
title_full_unstemmed Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?
title_short Simplifying [(18)F]GE-179 PET: are both arterial blood sampling and 90-min acquisitions essential?
title_sort simplifying [(18)f]ge-179 pet: are both arterial blood sampling and 90-min acquisitions essential?
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995767/
https://www.ncbi.nlm.nih.gov/pubmed/29892810
http://dx.doi.org/10.1186/s13550-018-0396-2
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