The Role of Early Pregnancy Maternal pGCD59 Levels in Predicting Neonatal Hypoglycemia—Subanalysis of the DALI Study

Author:

Bogdanet Delia1ORCID,Luque-Fernandez Miguel Angel23,Toth-Castillo Michelle4,Desoye Gernot5,O’Shea Paula M16,Dunne Fidelma P1,Halperin Jose A4

Affiliation:

1. College of Medicine, Nursing and Health Sciences, School of Medicine, National University of Ireland , Galway H91TK33 , Ireland

2. Department of Epidemiology, Harvard T. H. Chan School of Public Health , Boston, MA 02115 , USA

3. Department of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine , London KT12EE , UK

4. Division of Hematology, Brigham & Women’s Hospital, Harvard Medical School , Boston, MA 02115 , USA

5. Department of Obstetrics and Gynecology, Medizinische Universitaet Graz , Graz A8036 , Austria

6. Department of Clinical Biochemistry, Saolta University Health Care Group (SUHCG), Galway University Hospitals , Galway H91YR71 , Ireland

Abstract

Abstract Context Neonatal hypoglycaemia (NH) is the most common metabolic problem in infants born of mothers with gestational diabetes. Plasma glycated CD59 (pGCD59) is an emerging biomarker that has shown potential in identifying women at risk of developing gestational diabetes. The aim of this study was to assess the association between early maternal levels of pGCD59 and NH. Objective The aim of this study was to assess the association between early pregnancy maternal levels of plasma glycated CD59 (pGCD59) and neonatal hypoglycemia (NH). Methods This is an observational study of pregnant women with a prepregnancy body mass index (BMI) greater than or equal to 29 screened for eligibility to participate in the Vitamin D and Lifestyle Intervention for Gestational Diabetes (DALI) trial. This analysis included 399 pregnancies. Levels of pGCD59 were measured in fasting maternal samples taken at the time of a 75-g, 2-hour oral glucose tolerance test performed in early pregnancy (< 20 weeks). NH, the study outcome, was defined as a heel-prick capillary glucose level of less than 2.6 mmol/L within 48 hours of delivery. Results We identified 30 infants with NH. Maternal levels of pGCD59 in early pregnancy were positively associated with the prevalence of NH (one-way analysis of variance, P < .001). The odds of NH were higher in infants from mothers in tertile 3 of pGCD59 levels compared to those from mothers in tertile 1 (odds ratio [OR]: 2.41; 95% CI, 1.03-5.63). However, this was attenuated when adjusted for maternal BMI (OR: 2.28; 95% CI, 0.96-5.43). The cross-validated area under the curve (AUC) was 0.64 (95% CI, 0.54-0.74), and adjusted for maternal BMI, age, and ethnicity, the AUC was 0.70 (95% CI, 0.56-0.78). Conclusion Although pGCD59 levels in early pregnancy in women with BMI greater than or equal to 29 are associated with NH, our results indicate that this biomarker by itself is only a fair predictor of NH.

Funder

National Institutes of Health

European Community’s Seventh Framework Programme

Publisher

The Endocrine Society

Subject

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

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