Effects of antiepileptic drug monotherapy on one-carbon metabolism and DNA methylation in patients with epilepsy

PLoS One. 2015 Apr 27;10(4):e0125656. doi: 10.1371/journal.pone.0125656. eCollection 2015.

Abstract

Purpose: The aim of this study was to compare the serum levels of one-carbon metabolism (OCM) nutrients (e.g., folate, homocysteine and vitamin B12) and peripheral blood DNA methylation in epileptic patients under treatment with antiepileptic drugs (AEDs) and in healthy controls.

Methods: In this cross-sectional study, 60 patients with epilepsy who were receiving valproate (VPA) (n = 30) or lamotrigine (LTG) (n = 30) monotherapy were enrolled. Thirty age and sex matched healthy subjects served as the controls. Serum concentrations of OCM nutrients and peripheral blood DNA methylation status were measured.

Results: Compared to the control group, the VPA group had higher serum levels of homocysteine (p<0.05). No difference in homocysteine concentration was observed in the LTG group. Patients receiving VPA or LTG had significantly lower serum folate levels in comparison with controls (p<0.001). The level of methylation of long interspersed nucleotide element-1 (LINE-1) in peripheral blood was not significantly different between the AED monotherapy group and healthy controls. A difference in the methylation levels of methylenetetrahydrofolate reductase (MTHFR) amplicon was observed between AED-treated patients with epilepsy and controls (p<0.01). A positive correlation between serum folate levels and peripheral blood MTHFR amplicon methylation status was also observed (r = 0.25, p = 0.023).

Conclusion: Our findings suggest that the effects of AED monotherapy on OCM may induce specific regions of DNA hypomethylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anticonvulsants / pharmacology*
  • Anticonvulsants / therapeutic use
  • Case-Control Studies
  • Cross-Sectional Studies
  • DNA Methylation / drug effects*
  • Epilepsy / blood
  • Epilepsy / drug therapy*
  • Epilepsy / genetics
  • Female
  • Folic Acid / blood
  • Heterocyclic Compounds / blood*
  • Homocysteine / blood*
  • Humans
  • Lamotrigine
  • Long Interspersed Nucleotide Elements
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Middle Aged
  • Triazines / pharmacology
  • Triazines / therapeutic use
  • Valproic Acid / pharmacology
  • Valproic Acid / therapeutic use
  • Vitamin B 12 / blood
  • Young Adult

Substances

  • Anticonvulsants
  • Heterocyclic Compounds
  • Triazines
  • Homocysteine
  • Valproic Acid
  • Folic Acid
  • MTHFR protein, human
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Vitamin B 12
  • Lamotrigine

Grants and funding

This work was funded by grants from the National Natural Science Foundation of China (81071050, http://isisn.nsfc.gov.cn) and the Natural Science Foundation of Guangdong Province (S2011020005483, http://gdsf.gdstc.gov.cn/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.