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PET imaging during hypoglycaemia to study adipose tissue metabolism
BACKGROUND: Disturbances in adipose tissue glucose uptake may play a role in the pathogenesis of type 2 diabetes, yet its examination by 2‐deoxy‐2‐[(18)F]fluorodeoxyglucose ([(18)F]FDG) PET/CT is challenged by relatively low uptake kinetics. We tested the hypothesis that performing [(18)F]FDG PET/CT...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618104/ https://www.ncbi.nlm.nih.gov/pubmed/31002171 http://dx.doi.org/10.1111/eci.13120 |
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author | Boss, Marti Rooijackers, Hanne M. M. Buitinga, Mijke Janssen, Marcel J. R. Arens, Anne I. J. de Geus‐Oei, Lioe‐Fee Salm, Liesbeth P. de Galan, Bastiaan E. Gotthardt, Martin |
author_facet | Boss, Marti Rooijackers, Hanne M. M. Buitinga, Mijke Janssen, Marcel J. R. Arens, Anne I. J. de Geus‐Oei, Lioe‐Fee Salm, Liesbeth P. de Galan, Bastiaan E. Gotthardt, Martin |
author_sort | Boss, Marti |
collection | PubMed |
description | BACKGROUND: Disturbances in adipose tissue glucose uptake may play a role in the pathogenesis of type 2 diabetes, yet its examination by 2‐deoxy‐2‐[(18)F]fluorodeoxyglucose ([(18)F]FDG) PET/CT is challenged by relatively low uptake kinetics. We tested the hypothesis that performing [(18)F]FDG PET/CT during a hypoglycaemic clamp would improve adipose tissue tracer uptake to allow specific comparison of adipose tissue glucose handling between people with or without type 2 diabetes. DESIGN: We enrolled participants with or without diabetes who were at least overweight, to undergo a hyperinsulinaemic hypoglycaemic clamp or a hyperinsulinaemic euglycaemic clamp (n = 5 per group). Tracer uptake was quantified using [(18)F]FDG PET/CT. RESULTS: Hypoglycaemic clamping increased [(18)F]FDG uptake in visceral adipose tissue of healthy participants (P = 0.002). During hypoglycaemia, glucose uptake in visceral adipose tissue of type 2 diabetic participants was lower as compared to healthy participants (P < 0.0005). No significant differences were observed in skeletal muscle, liver or pancreas. CONCLUSIONS: The present findings indicate that [(18)F]FDG PET/CT during a hypoglycaemic clamp provides a promising new research tool to evaluate adipose tissue glucose metabolism. Using this method, we observed a specific impairment in visceral adipose tissue [(18)F]FDG uptake in type 2 diabetes, suggesting a previously underestimated role for adipose tissue glucose handling in type 2 diabetes. |
format | Online Article Text |
id | pubmed-6618104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66181042019-07-22 PET imaging during hypoglycaemia to study adipose tissue metabolism Boss, Marti Rooijackers, Hanne M. M. Buitinga, Mijke Janssen, Marcel J. R. Arens, Anne I. J. de Geus‐Oei, Lioe‐Fee Salm, Liesbeth P. de Galan, Bastiaan E. Gotthardt, Martin Eur J Clin Invest Original Articles BACKGROUND: Disturbances in adipose tissue glucose uptake may play a role in the pathogenesis of type 2 diabetes, yet its examination by 2‐deoxy‐2‐[(18)F]fluorodeoxyglucose ([(18)F]FDG) PET/CT is challenged by relatively low uptake kinetics. We tested the hypothesis that performing [(18)F]FDG PET/CT during a hypoglycaemic clamp would improve adipose tissue tracer uptake to allow specific comparison of adipose tissue glucose handling between people with or without type 2 diabetes. DESIGN: We enrolled participants with or without diabetes who were at least overweight, to undergo a hyperinsulinaemic hypoglycaemic clamp or a hyperinsulinaemic euglycaemic clamp (n = 5 per group). Tracer uptake was quantified using [(18)F]FDG PET/CT. RESULTS: Hypoglycaemic clamping increased [(18)F]FDG uptake in visceral adipose tissue of healthy participants (P = 0.002). During hypoglycaemia, glucose uptake in visceral adipose tissue of type 2 diabetic participants was lower as compared to healthy participants (P < 0.0005). No significant differences were observed in skeletal muscle, liver or pancreas. CONCLUSIONS: The present findings indicate that [(18)F]FDG PET/CT during a hypoglycaemic clamp provides a promising new research tool to evaluate adipose tissue glucose metabolism. Using this method, we observed a specific impairment in visceral adipose tissue [(18)F]FDG uptake in type 2 diabetes, suggesting a previously underestimated role for adipose tissue glucose handling in type 2 diabetes. John Wiley and Sons Inc. 2019-04-29 2019-07 /pmc/articles/PMC6618104/ /pubmed/31002171 http://dx.doi.org/10.1111/eci.13120 Text en © 2019 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Boss, Marti Rooijackers, Hanne M. M. Buitinga, Mijke Janssen, Marcel J. R. Arens, Anne I. J. de Geus‐Oei, Lioe‐Fee Salm, Liesbeth P. de Galan, Bastiaan E. Gotthardt, Martin PET imaging during hypoglycaemia to study adipose tissue metabolism |
title | PET imaging during hypoglycaemia to study adipose tissue metabolism |
title_full | PET imaging during hypoglycaemia to study adipose tissue metabolism |
title_fullStr | PET imaging during hypoglycaemia to study adipose tissue metabolism |
title_full_unstemmed | PET imaging during hypoglycaemia to study adipose tissue metabolism |
title_short | PET imaging during hypoglycaemia to study adipose tissue metabolism |
title_sort | pet imaging during hypoglycaemia to study adipose tissue metabolism |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618104/ https://www.ncbi.nlm.nih.gov/pubmed/31002171 http://dx.doi.org/10.1111/eci.13120 |
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