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**-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release
PURPOSE: [S-methyl-(11)C]-L-methionine ([(11)C]MET) uptake in the pancreas might be a central indicator of beta cell function. Since gastric emptying was recently shown to influence glycemic control in subjects after pancreaticoduodenectomy (PD, the surgical treatment of neoplasms of the pancreas he...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591624/ https://www.ncbi.nlm.nih.gov/pubmed/27389029 http://dx.doi.org/10.1007/s00259-016-3451-0 |
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author | Steiner, Emanuel Kazianka, Lukas Breuer, Robert Hacker, Marcus Wadsak, Wolfgang Mitterhauser, Markus Stimpfl, Thomas Reiter, Birgit Karanikas, Georgios Miholic, Johannes |
author_facet | Steiner, Emanuel Kazianka, Lukas Breuer, Robert Hacker, Marcus Wadsak, Wolfgang Mitterhauser, Markus Stimpfl, Thomas Reiter, Birgit Karanikas, Georgios Miholic, Johannes |
author_sort | Steiner, Emanuel |
collection | PubMed |
description | PURPOSE: [S-methyl-(11)C]-L-methionine ([(11)C]MET) uptake in the pancreas might be a central indicator of beta cell function. Since gastric emptying was recently shown to influence glycemic control in subjects after pancreaticoduodenectomy (PD, the surgical treatment of neoplasms of the pancreas head), we looked for imaginable relationships between gastric emptying, pre- and postprandial insulin concentrations, and [(11)C]MET uptake. METHODS: Nineteen tumor-free survivors after PD (age mean ± SD: 61 ± 8.7 yrs.; 10 male, 9 female) and 10 healthy controls (age: 27 ± 8.7 yrs.; 7 male, 3 female) were given a mixed test meal. One gram of paracetamol was ingested with the meal to evaluate the speed of gastric emptying. Insulin, glucose, and paracetamol plasma concentrations were measured before and over 180 minutes after ingestion. Beta cell function was calculated from fasting glucose and insulin plasma concentrations. Simultaneously, 800 MBq of [(11)C]MET were administered and the activity (maximum tissue standardized uptake values [SUVmax]) over the pancreas was measured at 15, 30, and 60 minutes after injection. Total integrated SUVmax (area under the curve [AUC]) and incremental SUVmax were calculated. RESULTS: The uptake of [(11)C]MET in the pancreas was significantly higher (p < 0.0001) in controls compared to the PD group. Gastric emptying was significantly slower in controls compared to pancreatectomy subjects (p < 0.0001). Paracetamol AUC(30) correlated with the SUVmax increment between 15 and 30 minutes (R(2) = 0.27, p = 0.0263), suggesting a relationship between gastric emptying and the uptake of [(11)C]MET. Total integrated SUVmax correlated with insulin AUC(60) (R(2) = 0.66,p < 0.0001) in patients after PD. Multivariate regression analysis revealed insulin AUC(60) and beta cell function, calculated from the fasting insulin to glucose ratio, as independent predictors of (11)C-methionine uptake, i.e. total integrated SUVmax, in patients after PD (R(2) = 0.78, p < 0.0001). CONCLUSION: Postprandial [(11)C]MET uptake may represent basal and postprandial beta cell function. The findings suggest a possible usefulness of this imaging procedure for further studying beta cell function. |
format | Online Article Text |
id | pubmed-5591624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-55916242017-09-19 **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release Steiner, Emanuel Kazianka, Lukas Breuer, Robert Hacker, Marcus Wadsak, Wolfgang Mitterhauser, Markus Stimpfl, Thomas Reiter, Birgit Karanikas, Georgios Miholic, Johannes Eur J Nucl Med Mol Imaging Original Article PURPOSE: [S-methyl-(11)C]-L-methionine ([(11)C]MET) uptake in the pancreas might be a central indicator of beta cell function. Since gastric emptying was recently shown to influence glycemic control in subjects after pancreaticoduodenectomy (PD, the surgical treatment of neoplasms of the pancreas head), we looked for imaginable relationships between gastric emptying, pre- and postprandial insulin concentrations, and [(11)C]MET uptake. METHODS: Nineteen tumor-free survivors after PD (age mean ± SD: 61 ± 8.7 yrs.; 10 male, 9 female) and 10 healthy controls (age: 27 ± 8.7 yrs.; 7 male, 3 female) were given a mixed test meal. One gram of paracetamol was ingested with the meal to evaluate the speed of gastric emptying. Insulin, glucose, and paracetamol plasma concentrations were measured before and over 180 minutes after ingestion. Beta cell function was calculated from fasting glucose and insulin plasma concentrations. Simultaneously, 800 MBq of [(11)C]MET were administered and the activity (maximum tissue standardized uptake values [SUVmax]) over the pancreas was measured at 15, 30, and 60 minutes after injection. Total integrated SUVmax (area under the curve [AUC]) and incremental SUVmax were calculated. RESULTS: The uptake of [(11)C]MET in the pancreas was significantly higher (p < 0.0001) in controls compared to the PD group. Gastric emptying was significantly slower in controls compared to pancreatectomy subjects (p < 0.0001). Paracetamol AUC(30) correlated with the SUVmax increment between 15 and 30 minutes (R(2) = 0.27, p = 0.0263), suggesting a relationship between gastric emptying and the uptake of [(11)C]MET. Total integrated SUVmax correlated with insulin AUC(60) (R(2) = 0.66,p < 0.0001) in patients after PD. Multivariate regression analysis revealed insulin AUC(60) and beta cell function, calculated from the fasting insulin to glucose ratio, as independent predictors of (11)C-methionine uptake, i.e. total integrated SUVmax, in patients after PD (R(2) = 0.78, p < 0.0001). CONCLUSION: Postprandial [(11)C]MET uptake may represent basal and postprandial beta cell function. The findings suggest a possible usefulness of this imaging procedure for further studying beta cell function. Springer Berlin Heidelberg 2016-07-07 2017 /pmc/articles/PMC5591624/ /pubmed/27389029 http://dx.doi.org/10.1007/s00259-016-3451-0 Text en © The Author(s) 2016 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 | Original Article Steiner, Emanuel Kazianka, Lukas Breuer, Robert Hacker, Marcus Wadsak, Wolfgang Mitterhauser, Markus Stimpfl, Thomas Reiter, Birgit Karanikas, Georgios Miholic, Johannes **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
title | **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
title_full | **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
title_fullStr | **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
title_full_unstemmed | **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
title_short | **-Postprandial pancreatic [(11)C]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
title_sort | **-postprandial pancreatic [(11)c]methionine uptake after pancreaticoduodenectomy mirrors basal beta cell function and insulin release |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591624/ https://www.ncbi.nlm.nih.gov/pubmed/27389029 http://dx.doi.org/10.1007/s00259-016-3451-0 |
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