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Open AccessResearch article

Metabolic Syndrome features and risk of neural tube defects

Joel G Ray1 email, Miles D Thompson2 email, Marian J Vermeulen3 email, Chris Meier4 email, Philip R Wyatt5 email, Pui-Yuen Wong2 email, Anne M Summers4 email, Sandra A Farrell6 email and David EC Cole7 email

1Departments of Medicine, Obstetrics and Gynecology and Health Policy Management and Evaluation, St. Michael's Hospital, University of Toronto, 30 Bond Street, Toronto, Ontario, M5B 1W8, Canada

2Department of Clinical Biochemistry, University of Toronto, Toronto, Ontario, Canada

3Institute for Clinical Evaluative Sciences, University of Toronto, Toronto, Ontario, Canada

4Department of Genetics, North York General Hospital, Toronto, Ontario, Canada

5Department of Genetics, York Central Hospital, Richmond Hill, Ontario, Canada

6Regional Genetics Program, The Credit Valley Hospital, Mississauga, Ontario, Canada

7Department of Laboratory Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada

author email corresponding author email

BMC Pregnancy and Childbirth 2007, 7:21doi:10.1186/1471-2393-7-21

Published: 19 September 2007

Abstract

Background

Maternal obesity and pre-pregnancy diabetes mellitus, features of the metabolic syndrome (MetSyn), are individual risk factors for neural tube defects (NTD). Whether they, in combination with additional features of MetSyn, alter this risk is not known. We evaluated the risk of NTD in association with maternal features of the MetSyn.

Methods

We used a population-based case-control study design in the province of Ontario, Canada. Cases and controls were derived from women who underwent antenatal maternal screening (MSS) at 15 to 20 weeks' gestation. There were 89 maternal cases with, and 434 controls without, an NTD-affected singleton pregnancy. Maternal features of MetSyn were defined by the presence of pre-pregnancy diabetes mellitus, body weight ≥ 90th centile among controls, non-white ethnicity and/or serum highly sensitive C-reactive protein (hsCRP) ≥ 75th centile of controls. Since hsCRP naturally increases in pregnancy, analyses were performed with, and without, the inclusion of hsCRP in the model.

Results

Mean hsCRP concentrations were exceptionally high among study cases and controls (6.1 and 6.4 mg/L, respectively). When hsCRP was excluded from the model, the adjusted odds ratios for NTD were 1.9 (95% confidence interval 1.1–3.4) in the presence 1 feature of MetSyn, and 6.1 (1.1–32.9) in the presence of 2 or more features. When hsCRP was included, the respective risk estimates were attenuated to 1.6 (0.88–2.8) and 3.1 (1.2–8.3).

Conclusion

We found about 2-fold and 6-fold higher risk for NTD in the presence 1, and 2 or more features, of the metabolic syndrome, respectively. It is not clear whether this risk is altered by the presence of a high serum hsCRP concentration.


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