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Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables

AIMS: To identify clinically useful associations between HbA(1c) levels and various continuous glucose monitoring‐derived metrics. METHODS: We retrospectively analysed end‐of‐study HbA(1c) levels and >2 weeks of continuous glucose monitoring data collected from 530 adults with Type 1 diabetes or...

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Autores principales: Hirsch, I. B., Welsh, J. B., Calhoun, P., Puhr, S., Walker, T. C., Price, D. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899839/
https://www.ncbi.nlm.nih.gov/pubmed/31267573
http://dx.doi.org/10.1111/dme.14065
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author Hirsch, I. B.
Welsh, J. B.
Calhoun, P.
Puhr, S.
Walker, T. C.
Price, D. A.
author_facet Hirsch, I. B.
Welsh, J. B.
Calhoun, P.
Puhr, S.
Walker, T. C.
Price, D. A.
author_sort Hirsch, I. B.
collection PubMed
description AIMS: To identify clinically useful associations between HbA(1c) levels and various continuous glucose monitoring‐derived metrics. METHODS: We retrospectively analysed end‐of‐study HbA(1c) levels and >2 weeks of continuous glucose monitoring data collected from 530 adults with Type 1 diabetes or insulin‐requiring Type 2 diabetes during four randomized trials. Each trial lasted ≥24 weeks and provided central laboratory end‐of‐study HbA(1c) levels and continuous glucose monitoring data from the preceding 3 months. Participants were assigned to groups based on either HbA(1c) levels or continuous glucose monitoring‐derived glucose values. RESULTS: HbA(1c) was strongly correlated with mean glucose value (r=0.80), time spent with glucose values in the 3.9–10.0 mmol/l range (time in range; r=–0.75) and percentage of glucose values >13.9 mmol/l (r=0.72), but was weakly correlated with the percentage of glucose values <3.9 mmol/l (r=–0.39) or <3.0 mmol/l (r=–0.21). The median percentage of glucose values <3.0 mmol/l was <1.2% (<20 min/day) for all HbA(1c)‐based groups, but the median percentage of values >13.9 mmol/l varied from 2.5% (0.6 h/day) to 27.8% (6.7 h/day) in the lowest and highest HbA(1c) groups, respectively. More than 90% of participants with either <2% of glucose values >13.9 mmol/l, mean glucose <7.8 mmol/l, or time in range >80% had HbA(1c) levels ≤53 mmol/mol (≤7.0%). For participants with HbA(1c) ≥64 mmol/mol (≥8.0%), the median time in range was 44%, with 90% of participants having a time in range of <59%. CONCLUSIONS: The associations shown in the present study suggest that continuous glucose monitoring‐derived metrics may help guide diabetes therapy intensification efforts in an HbA(1c)‐independent manner.
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spelling pubmed-68998392019-12-19 Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables Hirsch, I. B. Welsh, J. B. Calhoun, P. Puhr, S. Walker, T. C. Price, D. A. Diabet Med Research Articles AIMS: To identify clinically useful associations between HbA(1c) levels and various continuous glucose monitoring‐derived metrics. METHODS: We retrospectively analysed end‐of‐study HbA(1c) levels and >2 weeks of continuous glucose monitoring data collected from 530 adults with Type 1 diabetes or insulin‐requiring Type 2 diabetes during four randomized trials. Each trial lasted ≥24 weeks and provided central laboratory end‐of‐study HbA(1c) levels and continuous glucose monitoring data from the preceding 3 months. Participants were assigned to groups based on either HbA(1c) levels or continuous glucose monitoring‐derived glucose values. RESULTS: HbA(1c) was strongly correlated with mean glucose value (r=0.80), time spent with glucose values in the 3.9–10.0 mmol/l range (time in range; r=–0.75) and percentage of glucose values >13.9 mmol/l (r=0.72), but was weakly correlated with the percentage of glucose values <3.9 mmol/l (r=–0.39) or <3.0 mmol/l (r=–0.21). The median percentage of glucose values <3.0 mmol/l was <1.2% (<20 min/day) for all HbA(1c)‐based groups, but the median percentage of values >13.9 mmol/l varied from 2.5% (0.6 h/day) to 27.8% (6.7 h/day) in the lowest and highest HbA(1c) groups, respectively. More than 90% of participants with either <2% of glucose values >13.9 mmol/l, mean glucose <7.8 mmol/l, or time in range >80% had HbA(1c) levels ≤53 mmol/mol (≤7.0%). For participants with HbA(1c) ≥64 mmol/mol (≥8.0%), the median time in range was 44%, with 90% of participants having a time in range of <59%. CONCLUSIONS: The associations shown in the present study suggest that continuous glucose monitoring‐derived metrics may help guide diabetes therapy intensification efforts in an HbA(1c)‐independent manner. John Wiley and Sons Inc. 2019-07-17 2019-12 /pmc/articles/PMC6899839/ /pubmed/31267573 http://dx.doi.org/10.1111/dme.14065 Text en © 2019 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK 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 Research Articles
Hirsch, I. B.
Welsh, J. B.
Calhoun, P.
Puhr, S.
Walker, T. C.
Price, D. A.
Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables
title Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables
title_full Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables
title_fullStr Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables
title_full_unstemmed Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables
title_short Associations between HbA(1c) and continuous glucose monitoring‐derived glycaemic variables
title_sort associations between hba(1c) and continuous glucose monitoring‐derived glycaemic variables
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899839/
https://www.ncbi.nlm.nih.gov/pubmed/31267573
http://dx.doi.org/10.1111/dme.14065
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