Association between hyperglycaemia in pregnancy and growth of offspring in early childhood: The PANDORA study.


Journal

Pediatric obesity
ISSN: 2047-6310
Titre abrégé: Pediatr Obes
Pays: England
ID NLM: 101572033

Informations de publication

Date de publication:
10 2022
Historique:
received: 16 12 2021
accepted: 09 05 2022
pubmed: 2 6 2022
medline: 11 9 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

Few studies have assessed whether children exposed to in utero hyperglycaemia experience different growth trajectories compared to unexposed children. To assess association of type 2 diabetes (T2D) and gestational diabetes mellitus (GDM) with early childhood weight, length/height and body mass index (BMI) trajectories, and with timing and magnitude of peak BMI in infancy. PANDORA is a birth cohort recruited from an Australian hyperglycaemia in pregnancy register, and women with normoglycaemia recruited from the community. Offspring growth measures were obtained from health records over a median follow-up of 3.0 years (interquartile range 1.9-4.0). This analysis included children born to Aboriginal mothers with in utero normoglycaemia (n = 95), GDM (n = 228) or T2D (n = 131). Growth trajectories (weight, length/height and BMI) were estimated using linear mixed models with cubic spline functions of child age. After adjustment for maternal factors (age, BMI, parity, smoking, and socioeconomic measures) and child factors (age, gestational age at birth, and sex), children born to mothers with T2D or GDM had lower weight, length/height and BMI trajectories in infancy than children born to mothers with normoglycaemia, but similar weight and BMI by completion of follow-up. Children exposed to T2D had lower mean peak BMI 17.6 kg/m Maternal hyperglycaemia was associated with differences in early childhood growth trajectories after adjustment for maternal BMI. Exploration of associations between in utero hyperglycaemia exposure and growth trajectories into later childhood is required.

Sections du résumé

BACKGROUND
Few studies have assessed whether children exposed to in utero hyperglycaemia experience different growth trajectories compared to unexposed children.
OBJECTIVES
To assess association of type 2 diabetes (T2D) and gestational diabetes mellitus (GDM) with early childhood weight, length/height and body mass index (BMI) trajectories, and with timing and magnitude of peak BMI in infancy.
METHODS
PANDORA is a birth cohort recruited from an Australian hyperglycaemia in pregnancy register, and women with normoglycaemia recruited from the community. Offspring growth measures were obtained from health records over a median follow-up of 3.0 years (interquartile range 1.9-4.0). This analysis included children born to Aboriginal mothers with in utero normoglycaemia (n = 95), GDM (n = 228) or T2D (n = 131). Growth trajectories (weight, length/height and BMI) were estimated using linear mixed models with cubic spline functions of child age.
RESULTS
After adjustment for maternal factors (age, BMI, parity, smoking, and socioeconomic measures) and child factors (age, gestational age at birth, and sex), children born to mothers with T2D or GDM had lower weight, length/height and BMI trajectories in infancy than children born to mothers with normoglycaemia, but similar weight and BMI by completion of follow-up. Children exposed to T2D had lower mean peak BMI 17.6 kg/m
CONCLUSIONS
Maternal hyperglycaemia was associated with differences in early childhood growth trajectories after adjustment for maternal BMI. Exploration of associations between in utero hyperglycaemia exposure and growth trajectories into later childhood is required.

Identifiants

pubmed: 35644889
doi: 10.1111/ijpo.12932
pmc: PMC9539556
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12932

Informations de copyright

© 2022 The Authors. Pediatric Obesity published by John Wiley & Sons Ltd on behalf of World Obesity Federation.

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Auteurs

Angela Titmuss (A)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Department of Paediatrics, Division of Women, Children and Youth, Royal Darwin Hospital, Darwin, Northern Territory, Australia.

Danielle K Longmore (DK)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.

Federica Barzi (F)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Poche Centre for Indigenous Health, University of Queensland, Brisbane, Queensland, Australia.

Elizabeth L M Barr (ELM)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Clinical and Population Health, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.

Vanya Webster (V)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.

Anna Wood (A)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Endocrinology Department, Division of Medicine, Royal Darwin Hospital, Darwin, Northern Territory, Australia.

Alison Simmonds (A)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.

Alex D H Brown (ADH)

Wardliparingga Aboriginal Research Unit, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Faculty of Health and Medical Science, University of Adelaide, Adelaide, South Australia, Australia.

Christine Connors (C)

Top End Health Service, Northern Territory Department of Health, Darwin, Northern Territory, Australia.

Jacqueline A Boyle (JA)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Monash Centre for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.

Jeremy Oats (J)

Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.

H David McIntyre (HD)

Faculty of Medicine, Mater Medical Research Institute, University of Queensland, Brisbane, Queensland, Australia.

Jonathan E Shaw (JE)

Clinical and Population Health, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.

Maria E Craig (ME)

School of Women and Children's Health, University of New South Wales, Sydney, New South Wales, Australia.

Louise J Maple-Brown (LJ)

Wellbeing and Preventable Chronic Diseases Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Endocrinology Department, Division of Medicine, Royal Darwin Hospital, Darwin, Northern Territory, Australia.

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