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Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes
PURPOSE: The vesicular monoamine transporter, type 2 (VMAT2) is expressed by insulin producing β cells and was evaluated as a biomarker of β cell mass (BCM) by positron emission tomography (PET) with [(18)F]fluoropropyl-dihydrotetrabenazine ([(18)F]FP-(+)-DTBZ). PROCEDURES: We evaluated the feasibil...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783444/ https://www.ncbi.nlm.nih.gov/pubmed/26370678 http://dx.doi.org/10.1007/s11307-015-0888-7 |
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author | Freeby, Matthew J. Kringas, Patricia Goland, Robin S. Leibel, Rudolph L. Maffei, Antonella Divgi, Chaitan Ichise, Masanori Harris, Paul E. |
author_facet | Freeby, Matthew J. Kringas, Patricia Goland, Robin S. Leibel, Rudolph L. Maffei, Antonella Divgi, Chaitan Ichise, Masanori Harris, Paul E. |
author_sort | Freeby, Matthew J. |
collection | PubMed |
description | PURPOSE: The vesicular monoamine transporter, type 2 (VMAT2) is expressed by insulin producing β cells and was evaluated as a biomarker of β cell mass (BCM) by positron emission tomography (PET) with [(18)F]fluoropropyl-dihydrotetrabenazine ([(18)F]FP-(+)-DTBZ). PROCEDURES: We evaluated the feasibility of longitudinal pancreatic PET VMAT2 quantification in the pancreas in two studies of healthy controls and patients with type 1 or 2 diabetes. VMAT2 binding potential (BP(ND)) was estimated voxelwise using a reference tissue method in a cross-sectional study, followed by assessment of reproducibility using a test-retest paradigm. Metabolic function was evaluated by stimulated c-peptide measurements. RESULTS: Pancreatic BP(ND) was significantly decreased in patients with type 1 diabetes relative to controls and the test-retest variability was 9.4 %. CONCLUSIONS: Pancreatic VMAT2 content is significantly reduced in long-term diabetes patients relative to controls and repeat scans are sufficiently reproducible to suggest the feasibility clinically VMAT2 measurements in longitudinal studies of new onset diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11307-015-0888-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4783444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-47834442016-03-22 Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes Freeby, Matthew J. Kringas, Patricia Goland, Robin S. Leibel, Rudolph L. Maffei, Antonella Divgi, Chaitan Ichise, Masanori Harris, Paul E. Mol Imaging Biol Research Article PURPOSE: The vesicular monoamine transporter, type 2 (VMAT2) is expressed by insulin producing β cells and was evaluated as a biomarker of β cell mass (BCM) by positron emission tomography (PET) with [(18)F]fluoropropyl-dihydrotetrabenazine ([(18)F]FP-(+)-DTBZ). PROCEDURES: We evaluated the feasibility of longitudinal pancreatic PET VMAT2 quantification in the pancreas in two studies of healthy controls and patients with type 1 or 2 diabetes. VMAT2 binding potential (BP(ND)) was estimated voxelwise using a reference tissue method in a cross-sectional study, followed by assessment of reproducibility using a test-retest paradigm. Metabolic function was evaluated by stimulated c-peptide measurements. RESULTS: Pancreatic BP(ND) was significantly decreased in patients with type 1 diabetes relative to controls and the test-retest variability was 9.4 %. CONCLUSIONS: Pancreatic VMAT2 content is significantly reduced in long-term diabetes patients relative to controls and repeat scans are sufficiently reproducible to suggest the feasibility clinically VMAT2 measurements in longitudinal studies of new onset diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11307-015-0888-7) contains supplementary material, which is available to authorized users. Springer US 2015-09-14 2016 /pmc/articles/PMC4783444/ /pubmed/26370678 http://dx.doi.org/10.1007/s11307-015-0888-7 Text en © The Author(s) 2015 Open Access This 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 | Research Article Freeby, Matthew J. Kringas, Patricia Goland, Robin S. Leibel, Rudolph L. Maffei, Antonella Divgi, Chaitan Ichise, Masanori Harris, Paul E. Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes |
title | Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes |
title_full | Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes |
title_fullStr | Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes |
title_full_unstemmed | Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes |
title_short | Cross-sectional and Test-Retest Characterization of PET with [(18)F]FP-(+)-DTBZ for β Cell Mass Estimates in Diabetes |
title_sort | cross-sectional and test-retest characterization of pet with [(18)f]fp-(+)-dtbz for β cell mass estimates in diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783444/ https://www.ncbi.nlm.nih.gov/pubmed/26370678 http://dx.doi.org/10.1007/s11307-015-0888-7 |
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