Congenital heart defects and biomarkers of methylation in children: a case–control study
Article first published online: 27 SEP 2010
© 2010 The Authors. European Journal of Clinical Investigation © 2010 Stichting European Society for Clinical Investigation Journal Foundation
European Journal of Clinical Investigation
Volume 41, Issue 2, pages 143–150, February 2011
How to Cite
Obermann-Borst, S. A., van Driel, L. M. J. W., Helbing, W. A., de Jonge, R., Wildhagen, M. F., Steegers, E. A. P. and Steegers-Theunissen, R. P. M. (2011), Congenital heart defects and biomarkers of methylation in children: a case–control study. European Journal of Clinical Investigation, 41: 143–150. doi: 10.1111/j.1365-2362.2010.02388.x
- Issue published online: 11 JAN 2011
- Article first published online: 27 SEP 2010
- Received 21 May 2010; accepted 26 August 2010
- congenital heart malformations;
Eur J Clin Invest 2011; 41 (2): 143–150
Background Derangements in the maternal methylation pathway, expressed by global hypomethylation and hyperhomocysteinemia, are associated with the risk of having a child with a congenital heart defect (CHD). It is not known whether periconception exposure to these metabolic derangements contributes to chromosome segregation and metabolic programming of this pathway in the foetus.
Design In a Dutch population-based case–control study of 143 children with CHD and 186 healthy children, we investigated S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), total homocysteine (tHcy), the vitamins folate and B12 and the functional single nucleotide polymorphisms in the folate gene MTHFR 677C>T and 1298A>C. Comparisons were made between cases and controls adjusting for age, medication, vitamin use and CHD family history.
Results In the overall CHD group, the median concentrations of SAM (P = 0·011), folate in serum (P = 0·021) and RBC (P = 0·030) were significantly higher than in the controls. Subgroup analysis showed that this was mainly attributable to complex CHD with higher SAM (P < 0·001), SAH (P = 0·012) and serum folate (P = 0·010) independent of carriership of MTHFR polymorphisms. Highest concentrations of SAM, SAH and folate RBC were observed in complex syndromic CHD. The subgroup of children with Down syndrome, however, showed significantly higher SAH (P = 0·037) and significantly lower SAM:SAH ratio (P = 0·034) compared with other complex CHD, suggesting a state of global hypomethylation.
Conclusion High concentrations of methylation biomarkers in very young children are associated with complex CHD. Down syndrome and CHD may be associated with a global hypomethylation status, which has to be confirmed in tissues and global DNA methylation in future studies.