Hyperglycemia and Adverse Pregnancy Outcome Study: Neonatal Glycemia

Author:

Metzger Boyd E.1,Persson Bengt2,Lowe Lynn P.3,Dyer Alan R.3,Cruickshank J. Kennedy4,Deerochanawong Chaicharn5,Halliday Henry L.6,Hennis Anselm J.7,Liley Helen8,Ng Pak C.9,Coustan Donald R.10,Hadden David R.11,Hod Moshe12,Oats Jeremy J. N.13,Trimble Elisabeth R.14,

Affiliation:

1. Departments of Medicine and

2. Department of Pediatrics, Karolinska Institute, Stockholm, Sweden;

3. Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois;

4. Department of Medicine, Central Manchester University Hospitals and St Mary's Hospital, University of Manchester, Manchester, United Kingdom;

5. Department of Endocrinology, Rajavithi Hospital, Bangkok, Thailand;

6. Departments of Child Health and

7. Chronic Disease Research Centre, University of the West Indies, Bridgetown, Barbados;

8. Department of Pediatrics, Mater Misericordiae Mothers' Hospital, University of Queensland, Brisbane, Australia;

9. Department of Pediatrics, Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong;

10. Department of Obstetrics and Gynecology, Women and Infants Hospital of Rhode Island and Warren Alpert Medical School, Brown University, Providence, Rhode Island;

11. Department of Endocrinology, Royal Victoria Hospital, Belfast, United Kingdom;

12. Department of Obstetrics and Gynecology, Helen Schneider Hospital for Women, Rabin Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; and

13. Department of Obstetrics and Gynecology, Royal Women's Hospital, University of Melbourne, Melbourne, Australia

14. Endocrinology, Queen's University, Belfast, United Kingdom;

Abstract

OBJECTIVE: The goal was to describe the temporal pattern of neonatal plasma glucose levels and associations with maternal glucose levels, cord serum C-peptide levels, and neonatal size and adiposity. METHODS: A total of 17 094 mothers and infants were included in the Hyperglycemia and Adverse Pregnancy Outcome Study (15 centers in 9 countries). Mothers underwent a 75-g, 2-hour, oral glucose tolerance test (OGTT) at 24 to 32 weeks of gestation. Cord blood and neonatal blood samples were collected. Biochemical neonatal hypoglycemia was defined as glucose levels of <10th percentile (2.2 mmol/L). Clinically identified hypoglycemia was ascertained through medical record review and associations were assessed. RESULTS: Plasma glucose concentrations were stable during the first 5 hours after birth. Maternal glucose levels were weakly positively associated with biochemical neonatal hypoglycemia (odds ratios: 1.07–1.14 for 1-SD higher OGTT glucose levels). Frequency of neonatal hypoglycemia was higher with higher cord C-peptide levels (odds ratio: 11.6 for highest versus lowest C-peptide category). Larger and/or fatter infants were more likely to have hypoglycemia (P < .001), and infants with hypoglycemia tended to have a higher frequency of cord C-peptide levels of >90th percentile. CONCLUSIONS: Mean neonatal plasma glucose concentrations varied little in the first 5 hours after birth, which suggests normal postnatal adjustment. Biochemical and clinical hypoglycemia were weakly related to maternal OGTT glucose measurements but were strongly associated with elevated cord serum C-peptide levels. Larger and/or fatter infants were more likely to develop hypoglycemia and hyperinsulinemia. These relationships suggest physiologic relationships between maternal glycemia and fetal insulin production.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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