Abstract

BackgroundThis study aimed to examine whether inflammatory gene expression was a trait or a state marker in patients with bipolar disorder (BD).Methods69 healthy controls (HC), 82 euthymic BD patients and 8 BD patients with a mood episode (7 depressed, 1 manic) were included from the MOODINFLAME study. Six of the eight patients who had a mood episode were also investigated when they were euthymic (6 of the 82 euthymic patients). Of these participants the expression of 35 inflammatory genes was determined in monocytes using quantitative-polymerase chain reaction, of which a total gene expression score was calculated as well as a gene expression score per sub-cluster.ResultsThere were no significant differences in inflammatory monocyte gene expression between healthy controls and euthymic patients. Patients experiencing a mood episode, however, had a significantly higher total gene expression score (10.63 ± 2.58) compared to healthy controls (p = .004) and euthymic patients (p = .009), as well as when compared to their own scores when they were euthymic (p = .02). This applied in particular for the sub-cluster 1 gene expression score, but not for the sub-cluster 2 gene expression score.ConclusionsOur study indicates that in BD inflammatory monocyte, gene expression is especially elevated while in a mood episode compared to being euthymic.

Highlights

  • This study aimed to examine whether inflammatory gene expression was a trait or a state marker in patients with bipolar disorder (BD)

  • We found no significant differences between healthy controls (HC) (2.58 ± 0.88) and BP-Eu (3.48 ± 0.84), or BD patients with a mood episode (BD-Ep) patients when they were euthymic (1.17 ± 0.94)

  • For the means of sub-cluster 1 score, again no significant differences were found between HC (1.13 ± 0.41), euthymic bipolar disorder patients (BD-Eu) (1.59 ± 0.39) and BD-Ep patients when they were euthymic (0.50 ± 1.38)

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Summary

Introduction

This study aimed to examine whether inflammatory gene expression was a trait or a state marker in patients with bipolar disorder (BD). The results are heterogeneous, with studies reporting on normal (Guloksuz et al 2010) or even lower cytokine levels (Boufidou et al 2004) in BD compared to HC. This may be due to the fact that peripheral cytokines are strongly influenced by lifestyle and disease factors (O’Connor et al 2009). Studies from our group focusing on gene expression of circulating monocytes found a discriminating pro-inflammatory gene expression in BD patients compared to HC (Drexhage et al 2010; Padmos et al 2008)

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