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Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes

INTRODUCTION: Glycated albumin (GA), a biomarker reflecting short‐term glycaemia, may be useful to assess glycaemic control in pregnancy. We examined the association between GA and continuous glucose monitoring (CGM) metrics across gestation. METHODS: In this prospective cohort study including 40 wo...

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Autores principales: Toft, Johanne Holm, Dalen, Ingvild, Skadberg, Øyvind, Gøransson, Lasse Gunnar, Økland, Inger, Bleskestad, Inger Hjørdis
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/PMC9659665/
https://www.ncbi.nlm.nih.gov/pubmed/36121204
http://dx.doi.org/10.1002/edm2.376
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author Toft, Johanne Holm
Dalen, Ingvild
Skadberg, Øyvind
Gøransson, Lasse Gunnar
Økland, Inger
Bleskestad, Inger Hjørdis
author_facet Toft, Johanne Holm
Dalen, Ingvild
Skadberg, Øyvind
Gøransson, Lasse Gunnar
Økland, Inger
Bleskestad, Inger Hjørdis
author_sort Toft, Johanne Holm
collection PubMed
description INTRODUCTION: Glycated albumin (GA), a biomarker reflecting short‐term glycaemia, may be useful to assess glycaemic control in pregnancy. We examined the association between GA and continuous glucose monitoring (CGM) metrics across gestation. METHODS: In this prospective cohort study including 40 women with pre‐gestational diabetes, blood samples for analysis of GA and glycated haemoglobin A1c (HbA1c) were collected at pregnancy week 12, 20, 24, 28, 32 and 36. In the CGM‐group (n = 19), CGM data were collected from first trimester until pregnancy week 36. Receiver operating characteristic (ROC) curves were used to assess the accuracy of GA and HbA1c to detect poor glycaemic control, using CGM metrics as the reference standard. This study was conducted at Stavanger University Hospital, Norway, in 2016–2018. RESULTS: Glycaemic control improved across gestation with more time spent in target range, coinciding with decreased glycaemic variability and lower mean GA level. There was statistically significant correlation between GA and most CGM metrics. The area under the ROC curves (AUC) for detecting time in range <70% and time above range >25% for the pregnancy glucose target 63–140 mg/dl (3.5–7.8 mmol/L) were 0.78 and 0.82 for GA, whereas AUCs of 0.60 and 0.72 were found for HbA1c, respectively. CONCLUSIONS: Higher GA levels were associated with less time spent in target range, more time spent in the above range area and increased glycaemic variability. GA was more accurate than HbA1c to detect time above range >25% and time in range <70%.
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spelling pubmed-96596652022-11-14 Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes Toft, Johanne Holm Dalen, Ingvild Skadberg, Øyvind Gøransson, Lasse Gunnar Økland, Inger Bleskestad, Inger Hjørdis Endocrinol Diabetes Metab Research Articles INTRODUCTION: Glycated albumin (GA), a biomarker reflecting short‐term glycaemia, may be useful to assess glycaemic control in pregnancy. We examined the association between GA and continuous glucose monitoring (CGM) metrics across gestation. METHODS: In this prospective cohort study including 40 women with pre‐gestational diabetes, blood samples for analysis of GA and glycated haemoglobin A1c (HbA1c) were collected at pregnancy week 12, 20, 24, 28, 32 and 36. In the CGM‐group (n = 19), CGM data were collected from first trimester until pregnancy week 36. Receiver operating characteristic (ROC) curves were used to assess the accuracy of GA and HbA1c to detect poor glycaemic control, using CGM metrics as the reference standard. This study was conducted at Stavanger University Hospital, Norway, in 2016–2018. RESULTS: Glycaemic control improved across gestation with more time spent in target range, coinciding with decreased glycaemic variability and lower mean GA level. There was statistically significant correlation between GA and most CGM metrics. The area under the ROC curves (AUC) for detecting time in range <70% and time above range >25% for the pregnancy glucose target 63–140 mg/dl (3.5–7.8 mmol/L) were 0.78 and 0.82 for GA, whereas AUCs of 0.60 and 0.72 were found for HbA1c, respectively. CONCLUSIONS: Higher GA levels were associated with less time spent in target range, more time spent in the above range area and increased glycaemic variability. GA was more accurate than HbA1c to detect time above range >25% and time in range <70%. John Wiley and Sons Inc. 2022-09-19 /pmc/articles/PMC9659665/ /pubmed/36121204 http://dx.doi.org/10.1002/edm2.376 Text en © 2022 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Toft, Johanne Holm
Dalen, Ingvild
Skadberg, Øyvind
Gøransson, Lasse Gunnar
Økland, Inger
Bleskestad, Inger Hjørdis
Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
title Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
title_full Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
title_fullStr Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
title_full_unstemmed Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
title_short Glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
title_sort glycated albumin and continuous glucose monitoring metrics across pregnancy in women with pre‐gestational diabetes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659665/
https://www.ncbi.nlm.nih.gov/pubmed/36121204
http://dx.doi.org/10.1002/edm2.376
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