Assessment of population-based input functions for Patlak imaging of whole body dynamic 18F-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 AIFs...
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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. |
doi_str_mv | 10.1186/s40658-020-00330-x |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7683759</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2463606906</sourcerecordid><originalsourceid>FETCH-LOGICAL-c447t-f8460a15a5ba87566bfa28f44ecf6fbe6b4982623ebe92800b2b9c1093d9c3473</originalsourceid><addsrcrecordid>eNp9kU9P3DAQxa2KqiDKF-jJUi-9uPhfbOeChIAFJKRyoGfLduwlNLFTOwH229fLorb00NOMZn7vaUYPgE8EfyVEiePCsWgUwhQjjBnD6PkdOKCklUgywff-6vfBUSkPGGNCG0EJ_QD2GaNUNJQeAHdaii9l9HGGKcApTctg5j5FZE3xHezjtMwwLNFthwWGlOGtmQfzA_ajWfdxvZU93afBQ5u6Dew20Yy9g0St0Or8Et5e3H0E74MZij96rYfg--ri7uwK3Xy7vD47vUGOczmjoLjAhjSmsUbJRggbDFWBc--CCNYLy1tFBWXe-pYqjC21rSO4ZV3rGJfsEJzsfKfFjr5z9adsBj3lemne6GR6_XYT-3u9To9aCsVk01aDL68GOf1cfJn12Bfnh8FEn5aiKRdMYNFiUdHP_6APacmxvlcpyZjkpKGVojvK5VRK9uH3MQTrbYx6F6OuMeqXGPVzFbGdqFQ4rn3-Y_0f1S_KgZ7t</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2473374152</pqid></control><display><type>article</type><title>Assessment of population-based input functions for Patlak imaging of whole body dynamic 18F-FDG PET</title><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>SpringerLink Journals - AutoHoldings</source><source>PubMed Central Open Access</source><source>Springer Nature OA Free Journals</source><creator>Naganawa, Mika ; Gallezot, Jean-Dominique ; Shah, Vijay ; Mulnix, Tim ; Young, Colin ; Dias, Mark ; Chen, Ming-Kai ; Smith, Anne M. ; Carson, Richard E.</creator><creatorcontrib>Naganawa, Mika ; Gallezot, Jean-Dominique ; Shah, Vijay ; Mulnix, Tim ; Young, Colin ; Dias, Mark ; Chen, Ming-Kai ; Smith, Anne M. ; Carson, Richard E.</creatorcontrib><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.</description><identifier>ISSN: 2197-7364</identifier><identifier>EISSN: 2197-7364</identifier><identifier>DOI: 10.1186/s40658-020-00330-x</identifier><identifier>PMID: 33226522</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Aorta ; Applied and Technical Physics ; Blood ; Computational Mathematics and Numerical Analysis ; Engineering ; Fluorine isotopes ; Imaging ; Medicine ; Medicine & Public Health ; Nuclear Medicine ; Original Research ; Parameter estimation ; Positron emission ; Radiology ; Sampling ; Scaling ; Tomography ; Windows (intervals)</subject><ispartof>EJNMMI physics, 2020-11, Vol.7 (1), p.67-67, Article 67</ispartof><rights>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</rights><rights>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. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>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</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-f8460a15a5ba87566bfa28f44ecf6fbe6b4982623ebe92800b2b9c1093d9c3473</citedby><cites>FETCH-LOGICAL-c447t-f8460a15a5ba87566bfa28f44ecf6fbe6b4982623ebe92800b2b9c1093d9c3473</cites><orcidid>0000-0002-4408-2621</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683759/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683759/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,41464,42165,42533,51294,51551,53766,53768</link.rule.ids></links><search><creatorcontrib>Naganawa, Mika</creatorcontrib><creatorcontrib>Gallezot, Jean-Dominique</creatorcontrib><creatorcontrib>Shah, Vijay</creatorcontrib><creatorcontrib>Mulnix, Tim</creatorcontrib><creatorcontrib>Young, Colin</creatorcontrib><creatorcontrib>Dias, Mark</creatorcontrib><creatorcontrib>Chen, Ming-Kai</creatorcontrib><creatorcontrib>Smith, Anne M.</creatorcontrib><creatorcontrib>Carson, Richard E.</creatorcontrib><title>Assessment of population-based input functions for Patlak imaging of whole body dynamic 18F-FDG PET</title><title>EJNMMI physics</title><addtitle>EJNMMI Phys</addtitle><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.</description><subject>Aorta</subject><subject>Applied and Technical Physics</subject><subject>Blood</subject><subject>Computational Mathematics and Numerical Analysis</subject><subject>Engineering</subject><subject>Fluorine isotopes</subject><subject>Imaging</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nuclear Medicine</subject><subject>Original Research</subject><subject>Parameter estimation</subject><subject>Positron emission</subject><subject>Radiology</subject><subject>Sampling</subject><subject>Scaling</subject><subject>Tomography</subject><subject>Windows (intervals)</subject><issn>2197-7364</issn><issn>2197-7364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kU9P3DAQxa2KqiDKF-jJUi-9uPhfbOeChIAFJKRyoGfLduwlNLFTOwH229fLorb00NOMZn7vaUYPgE8EfyVEiePCsWgUwhQjjBnD6PkdOKCklUgywff-6vfBUSkPGGNCG0EJ_QD2GaNUNJQeAHdaii9l9HGGKcApTctg5j5FZE3xHezjtMwwLNFthwWGlOGtmQfzA_ajWfdxvZU93afBQ5u6Dew20Yy9g0St0Or8Et5e3H0E74MZij96rYfg--ri7uwK3Xy7vD47vUGOczmjoLjAhjSmsUbJRggbDFWBc--CCNYLy1tFBWXe-pYqjC21rSO4ZV3rGJfsEJzsfKfFjr5z9adsBj3lemne6GR6_XYT-3u9To9aCsVk01aDL68GOf1cfJn12Bfnh8FEn5aiKRdMYNFiUdHP_6APacmxvlcpyZjkpKGVojvK5VRK9uH3MQTrbYx6F6OuMeqXGPVzFbGdqFQ4rn3-Y_0f1S_KgZ7t</recordid><startdate>20201123</startdate><enddate>20201123</enddate><creator>Naganawa, Mika</creator><creator>Gallezot, Jean-Dominique</creator><creator>Shah, Vijay</creator><creator>Mulnix, Tim</creator><creator>Young, Colin</creator><creator>Dias, Mark</creator><creator>Chen, Ming-Kai</creator><creator>Smith, Anne M.</creator><creator>Carson, Richard E.</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>P5Z</scope><scope>P62</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4408-2621</orcidid></search><sort><creationdate>20201123</creationdate><title>Assessment of population-based input functions for Patlak imaging of whole body dynamic 18F-FDG PET</title><author>Naganawa, Mika ; Gallezot, Jean-Dominique ; Shah, Vijay ; Mulnix, Tim ; Young, Colin ; Dias, Mark ; Chen, Ming-Kai ; Smith, Anne M. ; Carson, Richard E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-f8460a15a5ba87566bfa28f44ecf6fbe6b4982623ebe92800b2b9c1093d9c3473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aorta</topic><topic>Applied and Technical Physics</topic><topic>Blood</topic><topic>Computational Mathematics and Numerical Analysis</topic><topic>Engineering</topic><topic>Fluorine isotopes</topic><topic>Imaging</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nuclear Medicine</topic><topic>Original Research</topic><topic>Parameter estimation</topic><topic>Positron emission</topic><topic>Radiology</topic><topic>Sampling</topic><topic>Scaling</topic><topic>Tomography</topic><topic>Windows (intervals)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Naganawa, Mika</creatorcontrib><creatorcontrib>Gallezot, Jean-Dominique</creatorcontrib><creatorcontrib>Shah, Vijay</creatorcontrib><creatorcontrib>Mulnix, Tim</creatorcontrib><creatorcontrib>Young, Colin</creatorcontrib><creatorcontrib>Dias, Mark</creatorcontrib><creatorcontrib>Chen, Ming-Kai</creatorcontrib><creatorcontrib>Smith, Anne M.</creatorcontrib><creatorcontrib>Carson, Richard E.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>EJNMMI physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Naganawa, Mika</au><au>Gallezot, Jean-Dominique</au><au>Shah, Vijay</au><au>Mulnix, Tim</au><au>Young, Colin</au><au>Dias, Mark</au><au>Chen, Ming-Kai</au><au>Smith, Anne M.</au><au>Carson, Richard E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of population-based input functions for Patlak imaging of whole body dynamic 18F-FDG PET</atitle><jtitle>EJNMMI physics</jtitle><stitle>EJNMMI Phys</stitle><date>2020-11-23</date><risdate>2020</risdate><volume>7</volume><issue>1</issue><spage>67</spage><epage>67</epage><pages>67-67</pages><artnum>67</artnum><issn>2197-7364</issn><eissn>2197-7364</eissn><abstract>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.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>33226522</pmid><doi>10.1186/s40658-020-00330-x</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4408-2621</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; SpringerLink Journals - AutoHoldings; PubMed Central Open Access; Springer Nature OA Free Journals |
subjects | Aorta Applied and Technical Physics Blood Computational Mathematics and Numerical Analysis Engineering Fluorine isotopes Imaging Medicine Medicine & Public Health Nuclear Medicine Original Research Parameter estimation Positron emission Radiology Sampling Scaling Tomography Windows (intervals) |
title | Assessment of population-based input functions for Patlak imaging of whole body dynamic 18F-FDG PET |
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