Mood Stabilizers and the Influence on Global Leukocyte DNA Methylation in Bipolar Disorder
Author(s) -
Lena Backlund,
Ya Bin Wei,
Lina Martinsson,
Philippe A. Melas,
Jia Jia Liu,
Ninni Mu,
ClaesGöran Östenson,
Tomas J. Ekström,
Martin Schalling,
Catharina Lavebratt
Publication year - 2015
Publication title -
complex psychiatry
Language(s) - English
Resource type - Journals
eISSN - 2673-3005
pISSN - 2673-298X
DOI - 10.1159/000430867
Subject(s) - dna methylation , lithium (medication) , methylation , bipolar disorder , mood stabilizer , mood , medicine , oncology , dna , psychiatry , biology , genetics , gene , gene expression
Little is known about the relationship between treatments for bipolar disorder (BD), their therapeutic responses and the DNA methylation status. We investigated whether global DNA methylation levels differ between healthy controls and bipolar patients under different treatments. Global DNA methylation was measured in leukocyte DNA from bipolar patients under lithium monotherapy (n = 29) or combination therapy (n = 32) and from healthy controls (n = 26). Lithium response was assessed using the Alda scale. Lithium in monotherapy was associated with hypomethylation (F = 4.63, p = 0.036). Lithium + valproate showed a hypermethylated pattern compared to lithium alone (F = 7.27, p = 0.011). Lithium response was not associated with DNA methylation levels. These data suggest that the choice of treatment in BD may lead to different levels of global DNA methylation. However, further research is needed to understand its clinical significance.
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