Nonsyndromic orofacial clefts: association with maternal hyperhomocysteinemia
TeratologyPublished 1 November 1999
Wai Yee Wong, T.K.A.B. Eskes, Anne Marie Kuijpers‐Jagtman, Paul H.M. Spauwen, Eric A.P. Steegers, Chris M.G. Thomas
Citations138
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TL;DR
Evidence is offered that maternal hyperhomocysteinemia may be a risk factor for having nonsyndromic orofacial cleft offspring and vitamin B6 concentrations appeared to be significantly lower in cases compared with controls.
Abstract
Maternal folic acid supplementation has been suggested to play a role in the prevention of nonsyndromic orofacial clefts, i.e., cleft lip +/- cleft palate. Using a case-control design, we investigated vitamin-dependent homocysteine metabolism in 35 mothers with nonsyndromic orofacial cleft offspring and 56 control mothers with nonmalformed offspring. A standardized oral methionine loading test was performed, in which fasting and afterload plasma total homocysteine, serum and red-cell folate, serum vitamin B12, and whole-blood vitamin B6 levels were determined. We found that both fasting (P < 0.01) as well as afterload (P < 0.05) homocysteine concentrations were significantly higher in cases compared to controls. Hyperhomocysteinemia, defined by a fasting and/or afterload homocysteine concentration above the 97.5th percentile, was present in 15.6% of the cases and in 3.6% of controls (odds ratio, 5.3 (1.1-24.2)). The median concentrations of serum (P < 0. 01) and red-cell (P < 0.05) folate were significantly higher, and vitamin B6 concentrations appeared to be significantly lower (P < 0. 05), in cases compared with controls. No significant difference was observed between groups for vitamin B12. These preliminary data offer evidence that maternal hyperhomocysteinemia may be a risk factor for having nonsyndromic orofacial cleft offspring.
Keywords
MedicineBiochemistry, Genetics and Molecular Biology
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