Metabolic dysfunction in pregnancy: Fingerprinting the maternal metabolome using proton nuclear magnetic resonance spectroscopy.

APrON study biomarker body mass index gestational diabetes mellitus maternal health metabolomics nmr spectroscopy nuclear magnetic resonance obesity pathway analysis personalized medicine pregnancy preterm birth urine

Journal

Endocrinology, diabetes & metabolism
ISSN: 2398-9238
Titre abrégé: Endocrinol Diabetes Metab
Pays: England
ID NLM: 101732442

Informations de publication

Date de publication:
01 2021
Historique:
received: 20 06 2020
revised: 30 09 2020
accepted: 24 10 2020
entrez: 3 2 2021
pubmed: 4 2 2021
medline: 4 2 2021
Statut: epublish

Résumé

Maternal metabolic disorders place the mother at risk for negative pregnancy outcomes with potentially long-term health impacts for the child. Metabolic syndrome, a cluster of features associated with increased risk of metabolic disorders, such as cardiovascular disease, diabetes and stroke, affects roughly one in five Canadians. Metabolomics is a relatively new technique that may be a useful tool to identify women at risk of metabolic disorders. This study set out to characterize urinary metabolic biomarkers of pregnant women with obesity and of pregnant women who later developed gestational diabetes mellitus (pre-GDM), compared to controls. Second trimester urine samples were collected through the Alberta Pregnancy Outcomes and Nutrition (APrON) cohort and examined with Obesity and pre-GDM metabolomes were distinct from controls and from each other. In each comparison, the glycine, serine and threonine pathways were the most impacted. Pantothenate, formic acid and glycine were downregulated by obesity, while formic acid, dimethylamine and galactose were downregulated in pre-GDM. The three most impacted metabolites for the comparison of obesity versus pre-GDM groups were upregulated creatine/caffeine, downregulated sarcosine/dimethylamine and upregulated maltose/sucrose in individuals who later developed GDM. These findings suggest a role for urinary metabolomics in the prediction of GDM and metabolic marker identification for potential diagnostics and prognostics in women at risk.

Identifiants

pubmed: 33532625
doi: 10.1002/edm2.201
pii: EDM2201
pmc: PMC7831222
doi:

Types de publication

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

Langues

eng

Pagination

e00201

Informations de copyright

© 2020 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

The authors have no conflicts or competing interests to declare.

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Auteurs

Hannah D Scott (HD)

Canadian Centre for Behavioural Neuroscience Department of Neuroscience University of Lethbridge Lethbridge AB Canada.

Marrissa Buchan (M)

Canadian Centre for Behavioural Neuroscience Department of Neuroscience University of Lethbridge Lethbridge AB Canada.
Department of Chemistry and Biochemistry University of Lethbridge Lethbridge AB Canada.

Caylin Chadwick (C)

Canadian Centre for Behavioural Neuroscience Department of Neuroscience University of Lethbridge Lethbridge AB Canada.

Catherine J Field (CJ)

Department of Agriculture, Food and Nutritional Science University of Alberta Edmonton AB Canada.

Nicole Letourneau (N)

Faculty of Nursing and Cumming School of Medicine University of Calgary Calgary AB Canada.

Tony Montina (T)

Department of Chemistry and Biochemistry University of Lethbridge Lethbridge AB Canada.
Southern Alberta Genome Sciences Centre University of Lethbridge Lethbridge AB Canada.

Brenda M Y Leung (BMY)

Public Health Program Faculty of Health Sciences University of Lethbridge Lethbridge AB Canada.

Gerlinde A S Metz (GAS)

Canadian Centre for Behavioural Neuroscience Department of Neuroscience University of Lethbridge Lethbridge AB Canada.
Southern Alberta Genome Sciences Centre University of Lethbridge Lethbridge AB Canada.

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Classifications MeSH