Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study

OBJECTIVE— To examine associations of neonatal adiposity with maternal glucose levels and cord serum C-peptide in a multicenter multinational study, the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study, thereby assessing the Ped- erson hypothesis linking maternal glycemia and fetal hyperinsulinemia to neonatal adiposity. RESEARCH DESIGN AND METHODS— Eligible pregnant women underwent a standard 75-g oral glucose tolerance test between 24 and 32 weeks gestation (as close to 28 weeks as possible). Neonatal anthropometrics and cord serum C-peptide were measured. Associations of maternal glucose and cord serum C-peptide with neonatal adiposity (sum of skin folds (cid:1) 90th percentile or percent body fat (cid:1) 90th percentile) were assessed using multiple logistic regression analyses, with adjust- ment for potential confounders, including maternal age, parity, BMI, mean arterial pressure, height, gestational age at delivery, and the baby’s sex. RESULTS— Among 23,316 HAPO Study participants with glucose levels blinded to caregivers, cord serum C-peptide results were available for 19,885 babies and skin fold measurements for 19,389. For measures of neonatal adiposity, there were strong statistically significant gradients across increasing levels of maternal glucose and cord serum C-peptide, which persisted after adjustment for potential confounders. In fully adjusted continuous variable models, odds ratios ranged from 1.35 to 1.44 for the two measures of adiposity for fasting, 1-h, and 2-h plasma glucose higher by 1 SD. CONCLUSIONS— These findings confirm the link between maternal glucose and neonatal adiposity and suggest that the relationship is mediated by fetal insulin production and that the Pedersen hypothesis describes a basic biological relationship influencing fetal growth. Diabetes 58:453–459, 2009

[1]  Sigridur Sia Jonsdottir,et al.  Hyperglycemia and Adverse Pregnancy Outcomes , 2009 .

[2]  A. Dyer,et al.  Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study , 2008, Diabetes.

[3]  P. Catalano,et al.  Management of obesity in pregnancy , 2022, The Australian & New Zealand journal of obstetrics & gynaecology.

[4]  G. S. Nesbitt,et al.  Integration of local and central laboratory functions in a worldwide multicentre study: Experience from the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study , 2006, Clinical trials.

[5]  S. Del Prato,et al.  Maternal triglyceride levels and newborn weight in pregnant women with normal glucose tolerance , 2005, Diabetic medicine : a journal of the British Diabetic Association.

[6]  S. O’Rahilly,et al.  Haemolysis affects insulin but not C-peptide immunoassay , 1987, Diabetologia.

[7]  S. Amini,et al.  Anthropometric estimation of neonatal body composition. , 1995, American journal of obstetrics and gynecology.

[8]  S. Amini,et al.  Factors affecting fetal growth and body composition. , 1995, American journal of obstetrics and gynecology.

[9]  E. K. Murthy,et al.  Diabetes and Pregnancy , 1949, Diabete & metabolisme.

[10]  J. Susa,et al.  Effects of Hyperinsulinemia in the Primate Fetus , 1985, Diabetes.

[11]  N. Freinkel,et al.  Banting Lecture 1980: of Pregnancy and Progeny , 1980, Diabetes.

[12]  A. Whitelaw SUBCUTANEOUS FAT IN NEWBORN INFANTS OF DIABETIC MOTHERS: AN INDICATION OF QUALITY OF DIABETIC CONTROL , 1977, The Lancet.

[13]  A. Banks Pregnancy and progeny. , 1968, International journal of fertility.

[14]  H. Wolf [Blood sugar in newborn infants]. , 1960, Klinische Wochenschrift.

[15]  H. C. Miller Diabetes and pregnancy: Blood sugar of newborn infants , 1953 .