[18F]FNDP PET neuroimaging test–retest repeatability and whole-body dosimetry in humans

Purpose Soluble epoxide hydrolase (sEH) is an enzyme that shapes immune signaling through its role in maintaining the homeostasis of polyunsaturated fatty acids and their related byproducts. [ 18 F]FNDP is a radiotracer developed for use with positron emission tomography (PET) to image sEH, which ha...

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Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2023-10, Vol.50 (12), p.3659-3665
Hauptverfasser: Du, Yong, Coughlin, Jennifer M., Amindarolzarbi, Alireza, Sweeney, Shannon Eileen, Harrington, Courtney K., Brosnan, Mary Katherine, Zandi, Adeline, Shinehouse, Laura K., Sanchez, Alejandra N. Reyes, Abdallah, Rehab, Holt, Daniel P., Fan, Hong, Lesniak, Wojciech G., Nandi, Ayon, Rowe, Steven P., Solnes, Lilja B., Dannals, Robert F., Horti, Andrew G., Lodge, Martin A., Pomper, Martin G.
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container_end_page 3665
container_issue 12
container_start_page 3659
container_title European journal of nuclear medicine and molecular imaging
container_volume 50
creator Du, Yong
Coughlin, Jennifer M.
Amindarolzarbi, Alireza
Sweeney, Shannon Eileen
Harrington, Courtney K.
Brosnan, Mary Katherine
Zandi, Adeline
Shinehouse, Laura K.
Sanchez, Alejandra N. Reyes
Abdallah, Rehab
Holt, Daniel P.
Fan, Hong
Lesniak, Wojciech G.
Nandi, Ayon
Rowe, Steven P.
Solnes, Lilja B.
Dannals, Robert F.
Horti, Andrew G.
Lodge, Martin A.
Pomper, Martin G.
description Purpose Soluble epoxide hydrolase (sEH) is an enzyme that shapes immune signaling through its role in maintaining the homeostasis of polyunsaturated fatty acids and their related byproducts. [ 18 F]FNDP is a radiotracer developed for use with positron emission tomography (PET) to image sEH, which has been applied to imaging sEH in the brains of healthy individuals. Here, we report the test–retest repeatability of [ 18 F]FNDP brain PET binding and [ 18 F]FNDP whole-body dosimetry in healthy individuals. Methods Seven healthy adults (4 men, 3 women, ages 40.1 ± 4.6 years) completed [ 18 F]FNDP brain PET on two occasions within a period of 14 days in a test–retest study design. [ 18 F]FNDP regional total distribution volume (V T ) values were derived from modeling time-activity data with a metabolite-corrected arterial input function. Test–retest variability, mean absolute deviation, and intraclass correlation coefficient (ICC) were investigated. Six other healthy adults (3 men, 3 women, ages 46.0 ± 7.0 years) underwent [ 18 F]FNDP PET/CT for whole-body dosimetry, which was acquired over 4.5 h, starting immediately after radiotracer administration. Organ-absorbed doses and the effective dose were then estimated. Results The mean test–retest difference in regional V T (ΔV T ) was 0.82 ± 5.17%. The mean absolute difference in regional V T was 4.01 ± 3.33%. The ICC across different brain regions ranged from 0.92 to 0.99. The organs with the greatest radiation-absorbed doses included the gallbladder (0.081 ± 0.024 mSv/MBq), followed by liver (0.077 ± 0.018 mSv/MBq) and kidneys (0.063 ± 0.006 mSv/MBq). The effective dose was 0.020 ± 0.003 mSv/MBq. Conclusion These data support a favorable test–retest repeatability of [ 18 F]FNDP brain PET regional V T . The radiation dose to humans from each [ 18 F]FNDP PET scan is similar to that of other 18 F-based PET radiotracers.
doi_str_mv 10.1007/s00259-023-06331-z
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Reyes ; Abdallah, Rehab ; Holt, Daniel P. ; Fan, Hong ; Lesniak, Wojciech G. ; Nandi, Ayon ; Rowe, Steven P. ; Solnes, Lilja B. ; Dannals, Robert F. ; Horti, Andrew G. ; Lodge, Martin A. ; Pomper, Martin G.</creator><creatorcontrib>Du, Yong ; Coughlin, Jennifer M. ; Amindarolzarbi, Alireza ; Sweeney, Shannon Eileen ; Harrington, Courtney K. ; Brosnan, Mary Katherine ; Zandi, Adeline ; Shinehouse, Laura K. ; Sanchez, Alejandra N. Reyes ; Abdallah, Rehab ; Holt, Daniel P. ; Fan, Hong ; Lesniak, Wojciech G. ; Nandi, Ayon ; Rowe, Steven P. ; Solnes, Lilja B. ; Dannals, Robert F. ; Horti, Andrew G. ; Lodge, Martin A. ; Pomper, Martin G.</creatorcontrib><description>Purpose Soluble epoxide hydrolase (sEH) is an enzyme that shapes immune signaling through its role in maintaining the homeostasis of polyunsaturated fatty acids and their related byproducts. [ 18 F]FNDP is a radiotracer developed for use with positron emission tomography (PET) to image sEH, which has been applied to imaging sEH in the brains of healthy individuals. Here, we report the test–retest repeatability of [ 18 F]FNDP brain PET binding and [ 18 F]FNDP whole-body dosimetry in healthy individuals. Methods Seven healthy adults (4 men, 3 women, ages 40.1 ± 4.6 years) completed [ 18 F]FNDP brain PET on two occasions within a period of 14 days in a test–retest study design. [ 18 F]FNDP regional total distribution volume (V T ) values were derived from modeling time-activity data with a metabolite-corrected arterial input function. Test–retest variability, mean absolute deviation, and intraclass correlation coefficient (ICC) were investigated. Six other healthy adults (3 men, 3 women, ages 46.0 ± 7.0 years) underwent [ 18 F]FNDP PET/CT for whole-body dosimetry, which was acquired over 4.5 h, starting immediately after radiotracer administration. Organ-absorbed doses and the effective dose were then estimated. Results The mean test–retest difference in regional V T (ΔV T ) was 0.82 ± 5.17%. The mean absolute difference in regional V T was 4.01 ± 3.33%. The ICC across different brain regions ranged from 0.92 to 0.99. The organs with the greatest radiation-absorbed doses included the gallbladder (0.081 ± 0.024 mSv/MBq), followed by liver (0.077 ± 0.018 mSv/MBq) and kidneys (0.063 ± 0.006 mSv/MBq). The effective dose was 0.020 ± 0.003 mSv/MBq. Conclusion These data support a favorable test–retest repeatability of [ 18 F]FNDP brain PET regional V T . The radiation dose to humans from each [ 18 F]FNDP PET scan is similar to that of other 18 F-based PET radiotracers.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-023-06331-z</identifier><identifier>PMID: 37458759</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adults ; Brain ; Cardiology ; Correlation coefficients ; Dosimeters ; Dosimetry ; Epoxide hydrolase ; Fatty acids ; Fluorine isotopes ; Gallbladder ; Homeostasis ; Imaging ; Medical imaging ; Medicine ; Medicine &amp; Public Health ; Men ; Metabolites ; Neuroimaging ; Nuclear Medicine ; Oncology ; Original Article ; Orthopedics ; Polyunsaturated fatty acids ; Positron emission ; Positron emission tomography ; Radiation ; Radiation dosage ; Radioactive tracers ; Radiology ; Reproducibility ; Staphylococcal enterotoxin H ; Women</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2023-10, Vol.50 (12), p.3659-3665</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. 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The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-75b3108bef19ecb4e38bb4bc1b935fc7906b8bd79c690a6e6df0bc1ea52b1b6e3</cites><orcidid>0000-0001-6753-3010</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00259-023-06331-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00259-023-06331-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27931,27932,41495,42564,51326</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37458759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Du, Yong</creatorcontrib><creatorcontrib>Coughlin, Jennifer M.</creatorcontrib><creatorcontrib>Amindarolzarbi, Alireza</creatorcontrib><creatorcontrib>Sweeney, Shannon Eileen</creatorcontrib><creatorcontrib>Harrington, Courtney K.</creatorcontrib><creatorcontrib>Brosnan, Mary Katherine</creatorcontrib><creatorcontrib>Zandi, Adeline</creatorcontrib><creatorcontrib>Shinehouse, Laura K.</creatorcontrib><creatorcontrib>Sanchez, Alejandra N. Reyes</creatorcontrib><creatorcontrib>Abdallah, Rehab</creatorcontrib><creatorcontrib>Holt, Daniel P.</creatorcontrib><creatorcontrib>Fan, Hong</creatorcontrib><creatorcontrib>Lesniak, Wojciech G.</creatorcontrib><creatorcontrib>Nandi, Ayon</creatorcontrib><creatorcontrib>Rowe, Steven P.</creatorcontrib><creatorcontrib>Solnes, Lilja B.</creatorcontrib><creatorcontrib>Dannals, Robert F.</creatorcontrib><creatorcontrib>Horti, Andrew G.</creatorcontrib><creatorcontrib>Lodge, Martin A.</creatorcontrib><creatorcontrib>Pomper, Martin G.</creatorcontrib><title>[18F]FNDP PET neuroimaging test–retest repeatability and whole-body dosimetry in humans</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Purpose Soluble epoxide hydrolase (sEH) is an enzyme that shapes immune signaling through its role in maintaining the homeostasis of polyunsaturated fatty acids and their related byproducts. [ 18 F]FNDP is a radiotracer developed for use with positron emission tomography (PET) to image sEH, which has been applied to imaging sEH in the brains of healthy individuals. Here, we report the test–retest repeatability of [ 18 F]FNDP brain PET binding and [ 18 F]FNDP whole-body dosimetry in healthy individuals. Methods Seven healthy adults (4 men, 3 women, ages 40.1 ± 4.6 years) completed [ 18 F]FNDP brain PET on two occasions within a period of 14 days in a test–retest study design. [ 18 F]FNDP regional total distribution volume (V T ) values were derived from modeling time-activity data with a metabolite-corrected arterial input function. Test–retest variability, mean absolute deviation, and intraclass correlation coefficient (ICC) were investigated. Six other healthy adults (3 men, 3 women, ages 46.0 ± 7.0 years) underwent [ 18 F]FNDP PET/CT for whole-body dosimetry, which was acquired over 4.5 h, starting immediately after radiotracer administration. Organ-absorbed doses and the effective dose were then estimated. Results The mean test–retest difference in regional V T (ΔV T ) was 0.82 ± 5.17%. The mean absolute difference in regional V T was 4.01 ± 3.33%. The ICC across different brain regions ranged from 0.92 to 0.99. The organs with the greatest radiation-absorbed doses included the gallbladder (0.081 ± 0.024 mSv/MBq), followed by liver (0.077 ± 0.018 mSv/MBq) and kidneys (0.063 ± 0.006 mSv/MBq). The effective dose was 0.020 ± 0.003 mSv/MBq. Conclusion These data support a favorable test–retest repeatability of [ 18 F]FNDP brain PET regional V T . The radiation dose to humans from each [ 18 F]FNDP PET scan is similar to that of other 18 F-based PET radiotracers.</description><subject>Adults</subject><subject>Brain</subject><subject>Cardiology</subject><subject>Correlation coefficients</subject><subject>Dosimeters</subject><subject>Dosimetry</subject><subject>Epoxide hydrolase</subject><subject>Fatty acids</subject><subject>Fluorine isotopes</subject><subject>Gallbladder</subject><subject>Homeostasis</subject><subject>Imaging</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Men</subject><subject>Metabolites</subject><subject>Neuroimaging</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Polyunsaturated fatty acids</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Radiation</subject><subject>Radiation dosage</subject><subject>Radioactive tracers</subject><subject>Radiology</subject><subject>Reproducibility</subject><subject>Staphylococcal enterotoxin H</subject><subject>Women</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kM1KxDAQx4Mofqy-gAcJePFSTZo2H0fRXRVEPehBRELSTtdKP9akRXZPvoNv6JOYdXUFD55mYH7zn-GH0C4lh5QQceQJiVMVkZhFhDNGo9kK2qScqkgQqVaXvSAbaMv7Z0KojKVaRxtMJKkUqdpE9w9Ujh5HV6c3-GZ4ixvoXVvWZlw2Y9yB7z7e3h3MG-xgAqYztqzKbopNk-PXp7aCyLb5FOetL2vo3BSXDX7qa9P4bbRWmMrDzncdoLvR8PbkPLq8Prs4Ob6MMhbzLhKpZZRICwVVkNkEmLQ2sRm1iqVFJhThVtpcqIwrYjjwvCBhCiaNLbUc2AAdLHInrn3pw6e6Ln0GVWUaaHuvY8lUnHDJk4Du_0Gf29414btACaoEE5IFKl5QmWu9d1DoiQtK3FRToufi9UK8DuL1l3g9C0t739G9rSFfrvyYDgBbAD6MmjG439v_xH4CTPSQHA</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Du, Yong</creator><creator>Coughlin, Jennifer M.</creator><creator>Amindarolzarbi, Alireza</creator><creator>Sweeney, Shannon Eileen</creator><creator>Harrington, Courtney K.</creator><creator>Brosnan, Mary Katherine</creator><creator>Zandi, Adeline</creator><creator>Shinehouse, Laura K.</creator><creator>Sanchez, Alejandra N. 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Reyes ; Abdallah, Rehab ; Holt, Daniel P. ; Fan, Hong ; Lesniak, Wojciech G. ; Nandi, Ayon ; Rowe, Steven P. ; Solnes, Lilja B. ; Dannals, Robert F. ; Horti, Andrew G. ; Lodge, Martin A. ; Pomper, Martin G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-75b3108bef19ecb4e38bb4bc1b935fc7906b8bd79c690a6e6df0bc1ea52b1b6e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adults</topic><topic>Brain</topic><topic>Cardiology</topic><topic>Correlation coefficients</topic><topic>Dosimeters</topic><topic>Dosimetry</topic><topic>Epoxide hydrolase</topic><topic>Fatty acids</topic><topic>Fluorine isotopes</topic><topic>Gallbladder</topic><topic>Homeostasis</topic><topic>Imaging</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Men</topic><topic>Metabolites</topic><topic>Neuroimaging</topic><topic>Nuclear Medicine</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Polyunsaturated fatty acids</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Radiation</topic><topic>Radiation dosage</topic><topic>Radioactive tracers</topic><topic>Radiology</topic><topic>Reproducibility</topic><topic>Staphylococcal enterotoxin H</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Du, Yong</creatorcontrib><creatorcontrib>Coughlin, Jennifer M.</creatorcontrib><creatorcontrib>Amindarolzarbi, Alireza</creatorcontrib><creatorcontrib>Sweeney, Shannon Eileen</creatorcontrib><creatorcontrib>Harrington, Courtney K.</creatorcontrib><creatorcontrib>Brosnan, Mary Katherine</creatorcontrib><creatorcontrib>Zandi, Adeline</creatorcontrib><creatorcontrib>Shinehouse, Laura K.</creatorcontrib><creatorcontrib>Sanchez, Alejandra N. 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Reyes</au><au>Abdallah, Rehab</au><au>Holt, Daniel P.</au><au>Fan, Hong</au><au>Lesniak, Wojciech G.</au><au>Nandi, Ayon</au><au>Rowe, Steven P.</au><au>Solnes, Lilja B.</au><au>Dannals, Robert F.</au><au>Horti, Andrew G.</au><au>Lodge, Martin A.</au><au>Pomper, Martin G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>[18F]FNDP PET neuroimaging test–retest repeatability and whole-body dosimetry in humans</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><stitle>Eur J Nucl Med Mol Imaging</stitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>50</volume><issue>12</issue><spage>3659</spage><epage>3665</epage><pages>3659-3665</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>Purpose Soluble epoxide hydrolase (sEH) is an enzyme that shapes immune signaling through its role in maintaining the homeostasis of polyunsaturated fatty acids and their related byproducts. [ 18 F]FNDP is a radiotracer developed for use with positron emission tomography (PET) to image sEH, which has been applied to imaging sEH in the brains of healthy individuals. Here, we report the test–retest repeatability of [ 18 F]FNDP brain PET binding and [ 18 F]FNDP whole-body dosimetry in healthy individuals. Methods Seven healthy adults (4 men, 3 women, ages 40.1 ± 4.6 years) completed [ 18 F]FNDP brain PET on two occasions within a period of 14 days in a test–retest study design. [ 18 F]FNDP regional total distribution volume (V T ) values were derived from modeling time-activity data with a metabolite-corrected arterial input function. Test–retest variability, mean absolute deviation, and intraclass correlation coefficient (ICC) were investigated. Six other healthy adults (3 men, 3 women, ages 46.0 ± 7.0 years) underwent [ 18 F]FNDP PET/CT for whole-body dosimetry, which was acquired over 4.5 h, starting immediately after radiotracer administration. Organ-absorbed doses and the effective dose were then estimated. Results The mean test–retest difference in regional V T (ΔV T ) was 0.82 ± 5.17%. The mean absolute difference in regional V T was 4.01 ± 3.33%. The ICC across different brain regions ranged from 0.92 to 0.99. The organs with the greatest radiation-absorbed doses included the gallbladder (0.081 ± 0.024 mSv/MBq), followed by liver (0.077 ± 0.018 mSv/MBq) and kidneys (0.063 ± 0.006 mSv/MBq). The effective dose was 0.020 ± 0.003 mSv/MBq. Conclusion These data support a favorable test–retest repeatability of [ 18 F]FNDP brain PET regional V T . The radiation dose to humans from each [ 18 F]FNDP PET scan is similar to that of other 18 F-based PET radiotracers.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37458759</pmid><doi>10.1007/s00259-023-06331-z</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6753-3010</orcidid></addata></record>
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subjects Adults
Brain
Cardiology
Correlation coefficients
Dosimeters
Dosimetry
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title [18F]FNDP PET neuroimaging test–retest repeatability and whole-body dosimetry in humans
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