HbA1c at the time of testing for gestational diabetes identifies women at risk for pregnancy complications.


Journal

Diabetes & metabolism
ISSN: 1878-1780
Titre abrégé: Diabetes Metab
Pays: France
ID NLM: 9607599

Informations de publication

Date de publication:
05 2022
Historique:
received: 12 10 2021
revised: 19 11 2021
accepted: 23 11 2021
pubmed: 22 12 2021
medline: 20 5 2022
entrez: 21 12 2021
Statut: ppublish

Résumé

It is unclear whether glycated haemoglobin (HbA1c) has utility in predicting adverse outcomes in gestational diabetes mellitus (GDM). The aims of the study were to examine the predictive value of HbA1c at GDM diagnosis with adverse pregnancy outcomes. This was a cohort study of 4,383 women with GDM between 2011 and 2018. We assessed the association of HbA1c with pregnancy outcomes using logistic regression models before and after adjustment for predefined risk factors of GDM. We examined these associations considering HbA1c as categorical variables using five pre-specified HbA1c classes: and as a continuous variable. An HbA1c ≥ 5.6% (38 mmol/mol) identified women with at greater risk for macrosomia: odds ratio (OR) [95% confidence interval] = 2.12 [1.29; 3.46] for HbA1c = 5.6-5.9% and 2.06 [1.14; 3.70] for HbA1c > 5.9% versus HbA1c ≤ 4.5% (26 mmol/mol). Similarly, HbA1c ≥ 5.6% (38 mmol/mol) was associated with greater risk for caesarean: 1.64 [1.06; 2.53] for HbA1c = 5.6-5.9% and 1.58 [0.93; 2.7] for HbA1c > 5.9% (41 mmol/mol) versus HbA1c ≤ 4.5% (26 mmol/mol). Using HbA1c ≤ 4.5% (26 mmol/mol) as reference category, HbA1c > 5.9% (41 mmol/mol) increased the OR of preterm delivery to 3.33 [1.27; 8.71]. HbA1c remained significant for Adverse Pregnancy Outcome Composite after adjustment (P < 0.0001). Our finding suggests that a single HbA1c reading may be a useful pragmatic tool to identify women at risk. Such identification may be a useful guide for identifying and applying preventative treatment for women at increased risk.

Identifiants

pubmed: 34933118
pii: S1262-3636(21)00096-3
doi: 10.1016/j.diabet.2021.101313
pii:
doi:

Substances chimiques

Glycated Hemoglobin A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101313

Informations de copyright

Copyright © 2021. Published by Elsevier Masson SAS.

Déclaration de conflit d'intérêts

Declaration of Competing Interest No potential conflicts of interest relevant to this article were reported.

Auteurs

Floriane Barbry (F)

CHU Lille, Department of Diabetology, Endocrinology, Metabolism and, Nutrition Lille University Hospital, F-59000 Lille, France.

Madleen Lemaitre (M)

CHU Lille, Department of Diabetology, Endocrinology, Metabolism and, Nutrition Lille University Hospital, F-59000 Lille, France; University of Lille, F-59000 Lille, France.

Camille Ternynck (C)

University of Lille, CHU Lille, ULR 2694 - METRICS: évaluation des technologies de santé et des pratiques médicales, F-59000 Lille, France; CHU Lille, Department of Biostatistics, F-59000 Lille, France.

Helene Wallet (H)

CHU Lille, Department of Diabetology, Endocrinology, Metabolism and, Nutrition Lille University Hospital, F-59000 Lille, France.

Marie Cazaubiel (M)

CHU Lille, Department of Gynaecology and Obstetrics, Lille University Hospital, F-59000 Lille, France.

Julien Labreuche (J)

CHU Lille, Department of Biostatistics, F-59000 Lille, France.

Damien Subtil (D)

University of Lille, CHU Lille, ULR 2694 - METRICS: évaluation des technologies de santé et des pratiques médicales, F-59000 Lille, France; University of Lille, F-59000 Lille, France; CHU Lille, Department of Gynaecology and Obstetrics, Lille University Hospital, F-59000 Lille, France.

Anne Vambergue (A)

CHU Lille, Department of Diabetology, Endocrinology, Metabolism and, Nutrition Lille University Hospital, F-59000 Lille, France; University of Lille, F-59000 Lille, France; European Genomic Institute for Diabetes, University School of Medicine, F-59000 Lille, France. Electronic address: anne.vambergue@chru-lille.fr.

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