Exploration of the shared pathophysiological mechanisms of gestational diabetes and large for gestational age offspring.

Biomarkers Gestational diabetes mellitus Glucose Large for gestational age Lipids Metabolism

Journal

World journal of diabetes
ISSN: 1948-9358
Titre abrégé: World J Diabetes
Pays: United States
ID NLM: 101547524

Informations de publication

Date de publication:
15 Jun 2019
Historique:
received: 30 03 2019
revised: 13 05 2019
accepted: 23 05 2019
entrez: 25 6 2019
pubmed: 25 6 2019
medline: 25 6 2019
Statut: ppublish

Résumé

Gestational diabetes mellitus (GDM) and large for gestational age (LGA) offspring are two common pregnancy complications. Connections also exist between the two conditions, including mutual maternal risk factors for the conditions and an increased prevalence of LGA offspring amongst pregnancies affected by GDM. Thus, it is important to elucidate potential shared underlying mechanisms of both LGA and GDM. One potential mechanistic link relates to macronutrient metabolism. Indeed, derangement of carbohydrate and lipid metabolism is present in GDM, and maternal biomarkers of glucose and lipid control are associated with LGA neonates in such pregnancies. The aim of this paper is therefore to reflect on the existing nutritional guidelines for GDM in light of our understanding of the pathophysiological mechanisms of GDM and LGA offspring. Lifestyle modification is first line treatment for GDM, and while there is some promise that nutritional interventions may favourably impact outcomes, there is a lack of definitive evidence that changing the macronutrient composition of the diet reduces the incidence of either GDM or LGA offspring. The quality of the available evidence is a major issue, and rigorous trials are needed to inform evidence-based treatment guidelines.

Identifiants

pubmed: 31231456
doi: 10.4239/wjd.v10.i6.333
pmc: PMC6571486
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

333-340

Déclaration de conflit d'intérêts

Conflict-of-interest statement: The authors have no conflicts of interest to declare.

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Auteurs

Sofia Nahavandi (S)

The Royal Children's Hospital Melbourne, Parkville, VIC 3052, Australia. elif.ekinci@unimelb.edu.au.

Sarah Price (S)

Department of Endocrinology, Austin Health, Repatriation Campus Heidelberg West, Melbourne, VIC 3081, Australia.

Priya Sumithran (P)

Department of Endocrinology, Austin Health, Repatriation Campus Heidelberg West, Melbourne, VIC 3081, Australia.

Elif Ilhan Ekinci (EI)

Department of Endocrinology, Austin Health, Repatriation Campus Heidelberg West, Melbourne, VIC 3081, Australia.

Classifications MeSH