Towards Precision Medicine in Gestational Diabetes: Pathophysiology and Glycemic Patterns in Pregnant Women With Obesity

Author:

White Sara L1ORCID,Koulman Albert23ORCID,Ozanne Susan E3ORCID,Furse Samuel23ORCID,Poston Lucilla1,Meek Claire L234ORCID

Affiliation:

1. Department of Women and Children’s Health, School of Life Course and Population Sciences, Faculty of Life Sciences and Medicine, King’s College London , London, SE1 7EH , UK

2. Core Metabolomics and Lipidomics Laboratory, Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Addenbrooke’s Treatment Centre , Cambridge, CB2 0QQ , UK

3. Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Addenbrooke’s Treatment Centre , Cambridge, CB2 0QQ , UK

4. Department of Clinical Biochemistry/Wolfson Diabetes & Endocrine Clinic, Cambridge University Hospitals NHS Foundation Trust , Cambridge, CB2 0QQ , UK

Abstract

Abstract Aims Precision medicine has revolutionized our understanding of type 1 diabetes and neonatal diabetes but has yet to improve insight into gestational diabetes mellitus (GDM), the most common obstetric complication and strongly linked to obesity. Here we explored if patterns of glycaemia (fasting, 1 hour, 2 hours) during the antenatal oral glucose tolerance test (OGTT), reflect distinct pathophysiological subtypes of GDM as defined by insulin secretion/sensitivity or lipid profiles. Methods 867 pregnant women with obesity (body mass index ≥ 30 kg/m2) from the UPBEAT trial (ISRCTN 89971375) were assessed for GDM at 28 weeks’ gestation (75 g oral glucose tolerance test OGTT; World Health Organization criteria). Lipid profiling of the fasting plasma OGTT sample was undertaken using direct infusion mass spectrometry and analyzed by logistic/linear regression, with and without adjustment for confounders. Insulin secretion and sensitivity were characterized by homeostatic model assessment 2b and 2s, respectively. Results In women who developed GDM (n = 241), patterns of glycaemia were associated with distinct clinical and biochemical characteristics and changes to lipid abundance in the circulation. Severity of glucose derangement, rather than pattern of postload glycaemia, was most strongly related to insulin action and lipid abundance/profile. Unexpectedly, women with isolated postload hyperglycemia had comparable insulin secretion and sensitivity to euglycemic women, potentially indicative of a novel mechanistic pathway. Conclusions Patterns of glycemia during the OGTT may contribute to a precision approach to GDM as assessed by differences in insulin resistance/secretion. Further research is indicated to determine if isolated postload hyperglycemia reflects a different mechanistic pathway for targeted management.

Funder

Biotechnology and Biological Sciences Research Council

Diabetes UK

Tommy's Charity

European Foundation for the Study of Diabetes—Novo Nordisk Foundation

National Institute of Health Research

Medical Research Council UK

Chief Scientist Office, Scottish Government Health Directorates

Biomedical Research Centre

Guys & St Thomas NHS Foundation Trust

King's College London

National Institute for Health Research Bristol Biomedical Research Centre

Tommy's Charity, UK

Cambridge Biomedical Research Centre

core biochemical assay laboratory

core metabolomic and lipidomic laboratory

Department of Health and Social Care

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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