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No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland

Studies of the association between maternal blood glucose measured by glycated haemoglobin (HbA1c) during pregnancy and the offspring’s birthweight have been heterogeneous. The aim of this study was to examine the association between maternal HbA1c level before gestational week 20 and the offspring’...

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Autores principales: Rasmussen, Katja Vedsted, Nielsen, Karoline Kragelund, Pedersen, Michael Lynge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913641/
https://www.ncbi.nlm.nih.gov/pubmed/31825748
http://dx.doi.org/10.1080/22423982.2019.1702798
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author Rasmussen, Katja Vedsted
Nielsen, Karoline Kragelund
Pedersen, Michael Lynge
author_facet Rasmussen, Katja Vedsted
Nielsen, Karoline Kragelund
Pedersen, Michael Lynge
author_sort Rasmussen, Katja Vedsted
collection PubMed
description Studies of the association between maternal blood glucose measured by glycated haemoglobin (HbA1c) during pregnancy and the offspring’s birthweight have been heterogeneous. The aim of this study was to examine the association between maternal HbA1c level before gestational week 20 and the offspring’s birthweight among predominantly indigenous women in Greenland. A retrospective cohort study including all women (n = 503) and their offspring delivered from September 2015 to September 2016 at Queen Ingrid’s Hospital in Nuuk was conducted. Data were obtained from the electronic medical record. Linear regression models were used to analyse the effect of maternal HbA1c on the offspring’s birthweight with adjustment and stratification for relevant confounders and effect modifiers. Birthweight increased with 3.3 g per mmol/mol increase in HbA1c. Yet, no significant association between maternal HbA1c and the offspring’s birthweight was found after adjustment for maternal age, ethnicity, residence, smoking, and parity (β = 0.058, p = 0.711). Among obese women, a borderline significant positive association (β = 0.657, p = 0.059) was found. For term newborns, this corresponded to an increase in birthweight of 31 g per mmol/mol increase in HbA1c. Based on the current study, the use of HbA1c during pregnancy to detect the risk of delivering a newborn with macrosomia is not recommended in Greenland. Abbreviation: HbA1c: glycosylated haemoglobin; GA: gestational age; SD: standard deviation; CI: confidence interval.
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spelling pubmed-69136412020-01-01 No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland Rasmussen, Katja Vedsted Nielsen, Karoline Kragelund Pedersen, Michael Lynge Int J Circumpolar Health Article Studies of the association between maternal blood glucose measured by glycated haemoglobin (HbA1c) during pregnancy and the offspring’s birthweight have been heterogeneous. The aim of this study was to examine the association between maternal HbA1c level before gestational week 20 and the offspring’s birthweight among predominantly indigenous women in Greenland. A retrospective cohort study including all women (n = 503) and their offspring delivered from September 2015 to September 2016 at Queen Ingrid’s Hospital in Nuuk was conducted. Data were obtained from the electronic medical record. Linear regression models were used to analyse the effect of maternal HbA1c on the offspring’s birthweight with adjustment and stratification for relevant confounders and effect modifiers. Birthweight increased with 3.3 g per mmol/mol increase in HbA1c. Yet, no significant association between maternal HbA1c and the offspring’s birthweight was found after adjustment for maternal age, ethnicity, residence, smoking, and parity (β = 0.058, p = 0.711). Among obese women, a borderline significant positive association (β = 0.657, p = 0.059) was found. For term newborns, this corresponded to an increase in birthweight of 31 g per mmol/mol increase in HbA1c. Based on the current study, the use of HbA1c during pregnancy to detect the risk of delivering a newborn with macrosomia is not recommended in Greenland. Abbreviation: HbA1c: glycosylated haemoglobin; GA: gestational age; SD: standard deviation; CI: confidence interval. Taylor & Francis 2019-12-11 /pmc/articles/PMC6913641/ /pubmed/31825748 http://dx.doi.org/10.1080/22423982.2019.1702798 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Rasmussen, Katja Vedsted
Nielsen, Karoline Kragelund
Pedersen, Michael Lynge
No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland
title No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland
title_full No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland
title_fullStr No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland
title_full_unstemmed No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland
title_short No association between early maternal HbA1c and offspring birthweight among women without pre-existing diabetes in Greenland
title_sort no association between early maternal hba1c and offspring birthweight among women without pre-existing diabetes in greenland
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913641/
https://www.ncbi.nlm.nih.gov/pubmed/31825748
http://dx.doi.org/10.1080/22423982.2019.1702798
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