Leukocyte and brain DDR1 hypermethylation is altered in psychosis and is correlated with stress and inflammatory markers.
Beatriz Garcia-RuizLorena MorenoGerard MuntanéVanessa Sánchez-GistauAlfonso Gutiérrez-ZotesLourdes MartorellJavier LabadElisabet VilellaPublished in: Epigenomics (2020)
Aim: To investigate DDR1 methylation in blood and brain DNA in psychosis and its relationship with stress markers. Materials & methods: Saliva cortisol, blood neutrophil and lymphocyte counts, leukocyte DNA and psychological variables were collected from 60 patients with nonaffective psychosis and 40 healthy controls (HC). Brain dorsolateral prefrontal cortex DNA from 35 patients with schizophrenia and 34 HC was studied. DDR1 methylation at 43 CpG sites was measured using the MassARRAY EpiTYPER platform. Results: We describe leukocyte DDR1 hypermethylation in patients with psychosis compared with HC; this hypermethylation is associated with psychological stress, neutrophil-to-lymphocyte ratios, and, in the dorsolateral prefrontal cortex, DDR1 methylation correlated with DDR1 isoform expression. Conclusion: We confirmed a relationship between stress and blood and brain DDR1 methylation in psychosis.
Keyphrases
- prefrontal cortex
- peripheral blood
- resting state
- dna methylation
- white matter
- circulating tumor
- genome wide
- single molecule
- cell free
- functional connectivity
- stress induced
- cerebral ischemia
- poor prognosis
- gene expression
- multiple sclerosis
- high throughput
- long non coding rna
- heat stress
- transcranial direct current stimulation
- working memory
- blood brain barrier
- sleep quality
- transcranial magnetic stimulation
- binding protein