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Diabetes Care 24:1151-1155, 2001
© 2001 by the American Diabetes Association, Inc.


Epidemiology/Health Services/Psychosocial Research
Original Article

Gestational Diabetes Mellitus Diagnosed With a 2-h 75-g Oral Glucose Tolerance Test and Adverse Pregnancy Outcomes

Maria I. Schmidt, MD, PHD1, Bruce B. Duncan, MD, PHD1, Angela J. Reichelt, MD, PHD2, Leandro Branchtein, MD, PHD2, Maria C. Matos, MD, PHD2, Adriana Costa e Forti, MD, PHD3, Ethel R. Spichler, MD, PHD4, Judith M.D.C. Pousada, MD, PHD5, Margareth M. Teixeira, MD, MS6, Tsuyoshi Yamashita, MD7 and For the Brazilian Gestational Diabetes Study Group

1 Department of Social Medicine, School of Medicine, Federal University of Rio Grande do Sul, Porto Alegre
2 Postgraduate Program in Clinical Medicine, Federal University of Rio Grande do Sul, Porto Alegre
3 Department of Clinical Medicine, School of Medicine, Federal University of Ceará, Fortaleza, Ceará
4 Department of Obstetrics and Gynecology, Instituto Fernandes Figueira–Oswaldo Cruz Foundation, Rio de Janeiro
5 Department of Medicine, Medical School, Federal University of Bahia, Salvador, Bahia
6 Department of Medicine, Federal University of Amazonas, Manaus, Amazonas
7 Hospital dos Servidores Públicos do Estado de São Paulo, São Paulo, Brazil

OBJECTIVE—To evaluate American Diabetes Association (ADA) and World Health Organization (WHO) diagnostic criteria for gestational diabetes mellitus (GDM) against pregnancy outcomes.

RESEARCH DESIGN AND METHODS—This cohort study consecutively enrolled Brazilian adult women attending general prenatal clinics. All women were requested to undertake a standardized 2-h 75-g oral glucose tolerance test (OGTT) between their estimated 24th and 28th gestational weeks and were then followed to delivery. New ADA criteria for GDM require two plasma glucose values >=5.3 mmol/l (fasting), >=10 mmol/l (1 h), and >=8.6 mmol/l (2 h). WHO criteria require a plasma glucose >=7.0 mmol/l (fasting) or >=7.8 mmol/l (2 h). Individuals with hyperglycemia indicative of diabetes outside of pregnancy were excluded.

RESULTS—Among the 4,977 women studied, 2.4% (95% CI 2.0–2.9) presented with GDM by ADA criteria and 7.2% (6.5–7.9) by WHO criteria. After adjustment for the effects of age, obesity, and other risk factors, GDM by ADA criteria predicted an increased risk of macrosomia (RR 1.29, 95% CI 0.73–2.18), preeclampsia (2.28, 1.22–4.16), and perinatal death (3.10, 1.42–6.47). Similarly, GDM by WHO criteria predicted increased risk for macrosomia (1.45, 1.06–1.95), preeclampsia (1.94, 1.22–3.03), and perinatal death (1.59, 0.86–2.90). Of women positive by WHO criteria, 260 (73%) were negative by ADA criteria. Conversely, 22 (18%) women positive by ADA criteria were negative by WHO criteria.

CONCLUSIONS—GDM based on a 2-h 75-g OGTT defined by either WHO or ADA criteria predicts adverse pregnancy outcomes.

Abbreviations: ADA, American Diabetes Association • GDM, gestational diabetes mellitus • OGTT, oral glucose tolerance test • RR, relative risk • WHO, World Health Organization


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