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Importance of beta cell mass for glycaemic control in people with type 1 diabetes
AIMS/HYPOTHESIS: The role of beta cell mass in the balance of glucose control and hypoglycaemic burden in people with type 1 diabetes is unclear. We applied positron emission tomography (PET) imaging with radiolabelled exendin to compare beta cell mass among people with type 1 diabetes and either lo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669532/ https://www.ncbi.nlm.nih.gov/pubmed/36394644 http://dx.doi.org/10.1007/s00125-022-05830-2 |
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author | Jansen, Theodorus J. P. Brom, Maarten Boss, Marti Buitinga, Mijke Tack, Cees J. van Meijel, Lian A. de Galan, Bastiaan E. Gotthardt, Martin |
author_facet | Jansen, Theodorus J. P. Brom, Maarten Boss, Marti Buitinga, Mijke Tack, Cees J. van Meijel, Lian A. de Galan, Bastiaan E. Gotthardt, Martin |
author_sort | Jansen, Theodorus J. P. |
collection | PubMed |
description | AIMS/HYPOTHESIS: The role of beta cell mass in the balance of glucose control and hypoglycaemic burden in people with type 1 diabetes is unclear. We applied positron emission tomography (PET) imaging with radiolabelled exendin to compare beta cell mass among people with type 1 diabetes and either low glucose variability (LGV) or high glucose variability (HGV). METHODS: All participants with either LGV (n=9) or HGV (n=7) underwent a mixed-meal tolerance test to determine beta cell function and wore a blinded continuous glucose monitor for a week. After an i.v. injection with [(68)Ga]Ga-NODAGA-exendin-4, PET images were acquired for the quantification of pancreatic uptake of radiolabelled exendin. The mean standardised uptake value (SUVmean) of the pancreas was used to determine the amount of beta cell mass. RESULTS: Participants with LGV had lower HbA(1c) (46.0 mmol/mol [44.5–52.5] [6.4% (6.3–7)] vs 80 mmol/mol [69.0–110] [9.5% (8.5–12.2)], p=0.001) and higher time in range (TIR) (75.6% [73.5–90.3] vs 38.7% [25.1–48.5], p=0.002) than those with HGV. The SUVmean of the pancreas was higher for the LGV than for the HGV group (5.1 [3.6–5.6] vs 2.9 [2.1–3.4], p=0.008). The AUC(C-peptide):AUC(glucose) ratio was numerically, but not statistically, higher in the LGV compared with the HGV group (2.7×10(−2) [6.2×10(−4)–5.3×10(−2)] vs 9.3×10(−4) [4.7×10(−4)–5.2×10(−3)], p=0.21). SUVmean correlated with the AUC(C-peptide):AUC(glucose) ratio (Pearson r=0.64, p=0.01), as well as with the TIR (r=0.64, p=0.01) and the SD of interstitial glucose levels (r=−0.66, p=0.007). CONCLUSION/INTERPRETATION: Our data show higher beta cell mass in people with type 1 diabetes and LGV than in those with HGV, independent of beta cell function. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9669532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-96695322022-11-18 Importance of beta cell mass for glycaemic control in people with type 1 diabetes Jansen, Theodorus J. P. Brom, Maarten Boss, Marti Buitinga, Mijke Tack, Cees J. van Meijel, Lian A. de Galan, Bastiaan E. Gotthardt, Martin Diabetologia Article AIMS/HYPOTHESIS: The role of beta cell mass in the balance of glucose control and hypoglycaemic burden in people with type 1 diabetes is unclear. We applied positron emission tomography (PET) imaging with radiolabelled exendin to compare beta cell mass among people with type 1 diabetes and either low glucose variability (LGV) or high glucose variability (HGV). METHODS: All participants with either LGV (n=9) or HGV (n=7) underwent a mixed-meal tolerance test to determine beta cell function and wore a blinded continuous glucose monitor for a week. After an i.v. injection with [(68)Ga]Ga-NODAGA-exendin-4, PET images were acquired for the quantification of pancreatic uptake of radiolabelled exendin. The mean standardised uptake value (SUVmean) of the pancreas was used to determine the amount of beta cell mass. RESULTS: Participants with LGV had lower HbA(1c) (46.0 mmol/mol [44.5–52.5] [6.4% (6.3–7)] vs 80 mmol/mol [69.0–110] [9.5% (8.5–12.2)], p=0.001) and higher time in range (TIR) (75.6% [73.5–90.3] vs 38.7% [25.1–48.5], p=0.002) than those with HGV. The SUVmean of the pancreas was higher for the LGV than for the HGV group (5.1 [3.6–5.6] vs 2.9 [2.1–3.4], p=0.008). The AUC(C-peptide):AUC(glucose) ratio was numerically, but not statistically, higher in the LGV compared with the HGV group (2.7×10(−2) [6.2×10(−4)–5.3×10(−2)] vs 9.3×10(−4) [4.7×10(−4)–5.2×10(−3)], p=0.21). SUVmean correlated with the AUC(C-peptide):AUC(glucose) ratio (Pearson r=0.64, p=0.01), as well as with the TIR (r=0.64, p=0.01) and the SD of interstitial glucose levels (r=−0.66, p=0.007). CONCLUSION/INTERPRETATION: Our data show higher beta cell mass in people with type 1 diabetes and LGV than in those with HGV, independent of beta cell function. GRAPHICAL ABSTRACT: [Image: see text] Springer Berlin Heidelberg 2022-11-17 2023 /pmc/articles/PMC9669532/ /pubmed/36394644 http://dx.doi.org/10.1007/s00125-022-05830-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jansen, Theodorus J. P. Brom, Maarten Boss, Marti Buitinga, Mijke Tack, Cees J. van Meijel, Lian A. de Galan, Bastiaan E. Gotthardt, Martin Importance of beta cell mass for glycaemic control in people with type 1 diabetes |
title | Importance of beta cell mass for glycaemic control in people with type 1 diabetes |
title_full | Importance of beta cell mass for glycaemic control in people with type 1 diabetes |
title_fullStr | Importance of beta cell mass for glycaemic control in people with type 1 diabetes |
title_full_unstemmed | Importance of beta cell mass for glycaemic control in people with type 1 diabetes |
title_short | Importance of beta cell mass for glycaemic control in people with type 1 diabetes |
title_sort | importance of beta cell mass for glycaemic control in people with type 1 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669532/ https://www.ncbi.nlm.nih.gov/pubmed/36394644 http://dx.doi.org/10.1007/s00125-022-05830-2 |
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