Background It is controversial whether maternal hyperglycemialess severe than that in diabetes mellitus is associated withincreased risks of adverse pregnancy outcomes.
Methods A total of 25,505 pregnant women at 15 centers in ninecountries underwent 75-g oral glucose-tolerance testing at 24to 32 weeks of gestation. Data remained blinded if the fastingplasma glucose level was 105 mg per deciliter (5.8 mmol perliter) or less and the 2-hour plasma glucose level was 200 mgper deciliter (11.1 mmol per liter) or less. Primary outcomeswere birth weight above the 90th percentile for gestationalage, primary cesarean delivery, clinically diagnosed neonatalhypoglycemia, and cord-blood serum C-peptide level above the90th percentile. Secondary outcomes were delivery before 37weeks of gestation, shoulder dystocia or birth injury, needfor intensive neonatal care, hyperbilirubinemia, and preeclampsia.
Results For the 23,316 participants with blinded data, we calculatedadjusted odds ratios for adverse pregnancy outcomes associatedwith an increase in the fasting plasma glucose level of 1 SD(6.9 mg per deciliter [0.4 mmol per liter]), an increase inthe 1-hour plasma glucose level of 1 SD (30.9 mg per deciliter[1.7 mmol per liter]), and an increase in the 2-hour plasmaglucose level of 1 SD (23.5 mg per deciliter [1.3 mmol per liter]).For birth weight above the 90th percentile, the odds ratioswere 1.38 (95% confidence interval [CI], 1.32 to 1.44), 1.46(1.39 to 1.53), and 1.38 (1.32 to 1.44), respectively; for cord-bloodserum C-peptide level above the 90th percentile, 1.55 (95% CI,1.47 to 1.64), 1.46 (1.38 to 1.54), and 1.37 (1.30 to 1.44);for primary cesarean delivery, 1.11 (95% CI, 1.06 to 1.15),1.10 (1.06 to 1.15), and 1.08 (1.03 to 1.12); and for neonatalhypoglycemia, 1.08 (95% CI, 0.98 to 1.19), 1.13 (1.03 to 1.26),and 1.10 (1.00 to 1.12). There were no obvious thresholds atwhich risks increased. Significant associations were also observedfor secondary outcomes, although these tended to be weaker.
Conclusions Our results indicate strong, continuous associationsof maternal glucose levels below those diagnostic of diabeteswith increased birth weight and increased cord-blood serum C-peptidelevels.
Source Information
The members of the Writing Group (Boyd E. Metzger, M.D., Lynn P. Lowe, Ph.D., Alan R. Dyer, Ph.D., Northwestern University Feinberg School of Medicine, Chicago; Elisabeth R. Trimble, M.D., Queen's University Belfast, Belfast, Northern Ireland; Udom Chaovarindr, M.D., Rajavithi Hospital, Bangkok, Thailand; Donald R. Coustan, M.D., Women and Infants' Hospital of Rhode Island–Brown University Medical School, Providence, RI; David R. Hadden, M.D., David R. McCance, M.D., Royal Jubilee Maternity Hospital, Belfast, Northern Ireland; Moshe Hod, M.D., Helen Schneider Hospital for Women, Rabin Medical Center–Sackler Faculty of Medicine, Tel-Aviv University, Petah-Tiqva, Israel; Harold David McIntyre, M.B., B.S., Jeremy J.N. Oats, M.D., Mater Misericordiae Mothers' Hospital–University of Queensland, Brisbane, Australia; Bengt Persson, M.D., Ph.D., Karolinska Institute, Stockholm, Sweden; Michael S. Rogers, M.D., Prince of Wales Hospital–Chinese University of Hong Kong, Hong Kong; and David A. Sacks, M.D., Kaiser Foundation Hospital, Bellflower, CA) of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cooperative Research Group assume responsibility for the overall content and integrity of the article.
Address reprint requests to Dr. Metzger at the Northwestern University Feinberg School of Medicine, Endocrinology, 645 N. Michigan Ave., Suite 530-22, Chicago, IL 60611, or at bem{at}northwestern.edu.
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