Pregnancy outcomes in women with booking HbA1c ≤ 40 mmol/mol compared with 41-49 mmol/mol in South Auckland, New Zealand.


Journal

The Australian & New Zealand journal of obstetrics & gynaecology
ISSN: 1479-828X
Titre abrégé: Aust N Z J Obstet Gynaecol
Pays: Australia
ID NLM: 0001027

Informations de publication

Date de publication:
10 2021
Historique:
revised: 19 02 2021
received: 05 10 2020
accepted: 22 03 2021
pubmed: 14 5 2021
medline: 3 11 2021
entrez: 13 5 2021
Statut: ppublish

Résumé

There are few data on pregnancy outcomes in women with pre-diabetes (HbA1c 41-49 mmol/mmol) at pregnancy booking. We aimed to (i) identify the proportion of women in Counties Manukau Health (CMH), South Auckland, New Zealand (NZ), with pre-diabetes at booking and (ii) compare outcomes between women with normal HbA1c and pre-diabetes. Using data from a multi-ethnic population of 10,869 singleton pregnancies, booked at <20 weeks from January 2017 to December 2018 in CMH, we compared outcomes between those with normal HbA1c (≤40 mmol/mol) and those with pre-diabetes (HbA1c 41-49 mmol/mol). The primary outcomes were gestational diabetes mellitus (GDM) by NZ criteria and large for gestational age (LGA) defined as birthweight >90th customised centile. Logistic regression determined the contribution of HbA1c 41-49 mmol/mol to the development of GDM. Among 10,869 participants, 193 (1.78%) had an HbA1c 41-49 mmol/mol at <20 weeks' gestation. Those with HbA1c 41-49 mmol/mol were 11 times more likely to develop GDM (59.6 vs 7.9%; adjusted odds ratio (aOR) 11.16 (7.59, 16.41)) and were more likely to have an LGA baby (47 (24.4%) vs 1436 (13.5%) aOR 1.63 (1.10, 2.41)) versus those with normal HbA1c. They also had significantly higher rates of pre-eclampsia, caesarean sections, preterm births and perinatal deaths. Nearly two-thirds of women with a booking HbA1c of 41-49 mmol/mmol developed GDM as well as multiple other perinatal complications compared to women with HbA1c ≤40. Trials to evaluate the impact of treatment in early pregnancy on the risk of late-pregnancy complications are required.

Identifiants

pubmed: 33984154
doi: 10.1111/ajo.13357
doi:

Substances chimiques

Glycated Hemoglobin A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

742-749

Informations de copyright

© 2021 The Royal Australian and New Zealand College of Obstetricians and Gynaecologists.

Références

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Auteurs

Yuxin Lim (Y)

Counties Manukau Health, Auckland, New Zealand.

Christin Coomarasamy (C)

Middlemore Hospital, Auckland, New Zealand.

Sharron Arrol (S)

Counties Manukau Health, Auckland, New Zealand.

Charlotte Oyston (C)

Counties Manukau Health, Auckland, New Zealand.
Department of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.

Karaponi Okesene-Gafa (K)

Counties Manukau Health, Auckland, New Zealand.
Department of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.

Lesley M E McCowan (LME)

Counties Manukau Health, Auckland, New Zealand.
Department of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.

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