Abstract

Mental health issues, including major depressive disorder, which can lead to suicidal behavior, are considered by the World Health Organization as a major threat to global health. Alterations in neurotransmitter signaling, e.g., serotonin and glutamate, or inflammatory response have been linked to both MDD and suicide. Phosphodiesterase 8A (PDE8A) gene expression is significantly decreased in the temporal cortex of major depressive disorder (MDD) patients. PDE8A specifically hydrolyzes adenosine 3′,5′-cyclic monophosphate (cAMP), which is a key second messenger involved in inflammation, cognition, and chronic antidepressant treatment. Moreover, alterations of RNA editing in PDE8A mRNA has been described in the brain of depressed suicide decedents. Here, we investigated PDE8A A-to-I RNA editing-related modifications in whole blood of depressed patients and suicide attempters compared to age-matched and sex-matched healthy controls. We report significant alterations of RNA editing of PDE8A in the blood of depressed patients and suicide attempters with major depression, for which the suicide attempt took place during the last month before sample collection. The reported RNA editing modifications in whole blood were similar to the changes observed in the brain of suicide decedents. Furthermore, analysis and combinations of different edited isoforms allowed us to discriminate between suicide attempters and control groups. Altogether, our results identify PDE8A as an immune response-related marker whose RNA editing modifications translate from brain to blood, suggesting that monitoring RNA editing in PDE8A in blood samples could help to evaluate depressive state and suicide risk.

Highlights

  • Suicidal behavior and suicide are a major public health issue worldwide; suicide is one of the primary causes of death, with an estimated 1 million deaths every year[1]

  • We have investigated alterations of Phosphodiesterase 8A (PDE8A) RNA editing in the blood of controls, depressed patients and suicide attempters with major depression and identified specific combinations to discriminate between these groups

  • A recent work shown that PDE8A RNA editing is altered in both hepatitis C virus (HCV) patients following interferon alpha treatment and in IFN-alpha-treated SHSY-5Y neuroblastoma cells[32]

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Summary

Introduction

Suicidal behavior and suicide are a major public health issue worldwide; suicide is one of the primary causes of death, with an estimated 1 million deaths every year[1]. Alterations of inflammatory response have been linked to both MDD and suicide A close interaction between immune system activation and changes in brain circuits related to mood and behavior has been described[8]. Deterioration of the normal structure and function of microglia, possibly caused by inflammatory signals, can lead to depression[9]. It is admitted that depressed individuals display dysregulation of immune system An association between pro-inflammatory cytokines and brain activation has been identified in patients with MDD and vulnerability to suicide[11]. A significant increase in depressive symptoms was observed in subjects injected with

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