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Continuous glucose monitoring to assess glucose variability in type 3c diabetes

AIM: The effectiveness of continuous glucose monitoring (CGM) in maintaining glycaemic control in type 1 diabetes mellitus and type 2 diabetes mellitus has been well demonstrated. However, the degree of glycaemic variability (GV) in people with type 3c diabetes mellitus has not been fully explored u...

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Autores principales: Lee, Victoria T. Y., Poynten, Ann, Depczynski, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545045/
https://www.ncbi.nlm.nih.gov/pubmed/35569007
http://dx.doi.org/10.1111/dme.14882
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author Lee, Victoria T. Y.
Poynten, Ann
Depczynski, Barbara
author_facet Lee, Victoria T. Y.
Poynten, Ann
Depczynski, Barbara
author_sort Lee, Victoria T. Y.
collection PubMed
description AIM: The effectiveness of continuous glucose monitoring (CGM) in maintaining glycaemic control in type 1 diabetes mellitus and type 2 diabetes mellitus has been well demonstrated. However, the degree of glycaemic variability (GV) in people with type 3c diabetes mellitus has not been fully explored using CGM. This study aims to evaluate GV in type 3c diabetes mellitus participants and compare it to type 1 diabetes mellitus and type 2 diabetes mellitus. METHODS: Participants were grouped according to type of diabetes. GV, defined as percentage coefficient of variation (%CV), and other glycaemic indices were obtained using CGM (FreeStyle Libre, Abbott, Australia) from 82 participants across all three cohorts over a 14‐day period. Comparison of baseline characteristics and GV were performed across all groups. Correlation of GV with C‐peptide values, and whether pancreatic supplementation had an effect on GV were also assessed in the type 3c diabetes mellitus cohort. RESULTS: GV of type 3c diabetes mellitus participants was within the recommended target of less than %CV 36% (p = 0.004). Type 3c diabetes mellitus participants had the lowest GV among the three groups (p = 0.001). There was a trend for lower C‐peptide levels to be associated with higher GV in type 3c diabetes mellitus participants (p = 0.22). Pancreatic enzyme supplementation in type 3c diabetes mellitus participants did not have an effect on GV (p = 0.664). CONCLUSIONS: Although type 3c diabetes mellitus participants were the least variable, they had the highest mean glucose levels and estimated HbA(1c), which suggests that the concept of ‘brittle’ diabetes in type 3c diabetes mellitus is not supported by the results of CGM in this study and may be leading to poorer glycaemic control.
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spelling pubmed-95450452022-10-14 Continuous glucose monitoring to assess glucose variability in type 3c diabetes Lee, Victoria T. Y. Poynten, Ann Depczynski, Barbara Diabet Med Research: Care Delivery AIM: The effectiveness of continuous glucose monitoring (CGM) in maintaining glycaemic control in type 1 diabetes mellitus and type 2 diabetes mellitus has been well demonstrated. However, the degree of glycaemic variability (GV) in people with type 3c diabetes mellitus has not been fully explored using CGM. This study aims to evaluate GV in type 3c diabetes mellitus participants and compare it to type 1 diabetes mellitus and type 2 diabetes mellitus. METHODS: Participants were grouped according to type of diabetes. GV, defined as percentage coefficient of variation (%CV), and other glycaemic indices were obtained using CGM (FreeStyle Libre, Abbott, Australia) from 82 participants across all three cohorts over a 14‐day period. Comparison of baseline characteristics and GV were performed across all groups. Correlation of GV with C‐peptide values, and whether pancreatic supplementation had an effect on GV were also assessed in the type 3c diabetes mellitus cohort. RESULTS: GV of type 3c diabetes mellitus participants was within the recommended target of less than %CV 36% (p = 0.004). Type 3c diabetes mellitus participants had the lowest GV among the three groups (p = 0.001). There was a trend for lower C‐peptide levels to be associated with higher GV in type 3c diabetes mellitus participants (p = 0.22). Pancreatic enzyme supplementation in type 3c diabetes mellitus participants did not have an effect on GV (p = 0.664). CONCLUSIONS: Although type 3c diabetes mellitus participants were the least variable, they had the highest mean glucose levels and estimated HbA(1c), which suggests that the concept of ‘brittle’ diabetes in type 3c diabetes mellitus is not supported by the results of CGM in this study and may be leading to poorer glycaemic control. John Wiley and Sons Inc. 2022-05-23 2022-08 /pmc/articles/PMC9545045/ /pubmed/35569007 http://dx.doi.org/10.1111/dme.14882 Text en © 2022 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research: Care Delivery
Lee, Victoria T. Y.
Poynten, Ann
Depczynski, Barbara
Continuous glucose monitoring to assess glucose variability in type 3c diabetes
title Continuous glucose monitoring to assess glucose variability in type 3c diabetes
title_full Continuous glucose monitoring to assess glucose variability in type 3c diabetes
title_fullStr Continuous glucose monitoring to assess glucose variability in type 3c diabetes
title_full_unstemmed Continuous glucose monitoring to assess glucose variability in type 3c diabetes
title_short Continuous glucose monitoring to assess glucose variability in type 3c diabetes
title_sort continuous glucose monitoring to assess glucose variability in type 3c diabetes
topic Research: Care Delivery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545045/
https://www.ncbi.nlm.nih.gov/pubmed/35569007
http://dx.doi.org/10.1111/dme.14882
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