Decreased DNA methyltransferases expression is associated with coronary artery lesion formation in Kawasaki disease

Int J Med Sci. 2019 Apr 25;16(4):576-582. doi: 10.7150/ijms.32773. eCollection 2019.

Abstract

Background: Kawasaki disease (KD) is the most common acute coronary vasculitis to occur in children. Although we have uncovered global DNA hypomethylation in KD, its underlying cause remains uncertain. In this study, we performed a survey of transcript levels of DNA methyltransferases and demethylases in KD patients. Materials and Methods: We recruited 145 participants for this study. The chip studies consisted of 18 KD patients that were analyzed before undergoing intravenous immunoglobulin (IVIG) treatment and at least 3 weeks after IVIG treatment, as well as 36 control subjects, using Affymetrix GeneChip® Human Transcriptome Array 2.0. An additional study of 91 subjects was performed in order to validate real-time quantitative PCR. Results: In our microarray study, the mRNA levels of DNMT1 and DNMT3A were significantly lower while TET2 was higher in acute-stage KD patients compared to the healthy controls. Through PCR validation, we observed that the expression of DNMT1 and TET2 are consistent with the Transcriptome Array 2.0 results. Furthermore, we observed significantly lower DMNT1 mRNA levels following IVIG treatment between those who developed CAL and those who did not. Conclusion: Our findings provide an evidence of DNA methyltransferases and demethylases changes and are among the first report that transient DNA hypomethylation is induced during acute inflammatory phase of Kawasaki disease.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Coronary Artery Disease / complications
  • Coronary Artery Disease / genetics*
  • Coronary Artery Disease / pathology
  • Coronary Vessels / metabolism
  • Coronary Vessels / pathology
  • DNA (Cytosine-5-)-Methyltransferase 1 / genetics*
  • DNA (Cytosine-5-)-Methyltransferases / genetics*
  • DNA Methylation / genetics
  • DNA Methyltransferase 3A
  • DNA-Binding Proteins / genetics*
  • Dioxygenases
  • Female
  • Humans
  • Immunoglobulins, Intravenous / administration & dosage
  • Infant
  • Infant, Newborn
  • Inflammation / genetics
  • Inflammation / pathology
  • Male
  • Mucocutaneous Lymph Node Syndrome / complications
  • Mucocutaneous Lymph Node Syndrome / genetics*
  • Mucocutaneous Lymph Node Syndrome / pathology
  • Proto-Oncogene Proteins / genetics*
  • RNA, Messenger / genetics
  • Transcriptome / genetics

Substances

  • DNA-Binding Proteins
  • DNMT3A protein, human
  • Immunoglobulins, Intravenous
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Dioxygenases
  • TET2 protein, human
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases
  • DNA Methyltransferase 3A
  • DNMT1 protein, human