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Published online April 19, 2007
Diabetes Care 30:1920-1925, 2007
DOI: 10.2337/dc07-0278
© 2007 by the American Diabetes Association
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Review Article
Reviews/Commentaries/ADA Statements

Use of Maternal GHb Concentration to Estimate the Risk of Congenital Anomalies in the Offspring of Women with Prepregnancy Diabetes

Andrea Guerin, BSC1, Rosane Nisenbaum, PHD2 and Joel G. Ray, MD, MSC, FRCPC3

1 Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada
2 Center for Research on Inner City Health, St. Michael's Hospital, Toronto, Ontario, Canada
3 Departments of Medicine, Obstetrics and Gynecology and Health Policy Management and Evaluation, and the Divisions of General Internal Medicine and Endocrinology and Metabolism, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada

Address correspondence and reprint requests to Joel G. Ray, Department of Medicine, St. Michael's Hospital, 30 Bond St., Toronto, Ontario, M5B 1W8, Canada. E-mail: rayj{at}smh.toronto.on.ca

ABSTRACT

OBJECTIVE— We sought to determine the absolute risk of having a congenital anomaly in relation to periconceptional GHb concentration among women with prepregnancy diabetes.

RESEARCH DESIGN AND METHODS— Two reviewers independently retrieved all cohort studies through a systematic literature search between January 1985 and May 2006. For each study, the absolute risk of having a pregnancy affected by a major or minor structural anomaly (diagnosed either antenatally or up to 28 days after conception) was calculated according to the number of SDs of GHb above the mean for nondiabetic, nonpregnant control subjects. A multilevel logistic-normal model was used to pool the data, which were expressed in tabular and graphic formats.

RESULTS— In seven cohort studies, there were 117 anomalies among 1,977 pregnancies. At a periconceptional GHb concentration 0 SD above normal, the absolute risk of a pregnancy affected by a congenital anomaly was ~2% (95% CI 0.0–4.4). At 2 SD above normal, the risk was 3% (0.4–6.1), and at 8 SD it was ~10% (2.3–17.8). For each 1-SD unit increase in GHb, the associated risk of a congenital malformation increased by an odds ratio of 1.2 (95% CI 1.1–1.4). The risk in relation to A1C followed the same pattern.

CONCLUSIONS— Using data from a limited number of published studies, a practical aid was developed to optimize use of the GHb and A1C concentrations for estimating the absolute risk of a congenital anomaly in the offspring of women with prepregnancy diabetes.


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