4.7 Article

Effects of infliximab on brain neurochemistry of adults with bipolar depression

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 281, 期 -, 页码 61-66

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ELSEVIER
DOI: 10.1016/j.jad.2020.11.128

关键词

bipolar disorder; neurochemistry; magnetic resonance spectroscopy; infliximab; inflammation; cognition

资金

  1. Stanley Medical Research Institute [13T-012]
  2. Canadian Institutes of Health Research [142255]

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The study found that treatment with infliximab did not significantly affect prefrontal NAA concentration in adults with BD. However, there was a significant effect on Glx levels, with an interaction between treatment and time indicating a decrease in Glx levels in infliximab-treated patients. Furthermore, the reduction in Glx levels in infliximab-treated participants was associated with cognitive improvement, as measured by neurocognitive tests.
Objectives: To explore the relationship between inflammation and neuronal metabolism in bipolar disorder (BD) by evaluating the neurochemical effects of the tumor necrosis factor-alpha (TNF-alpha) antagonist infliximab among individuals with bipolar depression Methods: This is a post-hoc, exploratory analysis from a 12-week, randomized, double-blind, placebo-controlled trial with infliximab for adults with bipolar depression. We assessed the effects of infliximab on concentration of metabolites in the prefrontal cortex, using proton-magnetic resonance spectroscopy (1H-MRS), as well as its association with clinical outcomes (i.e. depressive symptom severity and cognitive function). Results: Eighteen participants in the placebo and 15 in the infliximab group were included in this analysis. In the pre-specified primary outcome, there were no significant effects of treatment on prefrontal concentrations of Nacetylaspartate (NAA; p = 0.712). In the secondary analyses, there was a significant treatment by time interaction for glutamate (Glx; p = 0.018), indicating that Glx levels decreased in infliximab-treated patients, relative to placebo. Treatment group significantly moderated the association between changes in Glx levels and changes in a neurocognitive test (i.e. Digit Symbol Substitution Test; p = 0.014), indicating that in infliximab-treated participants reductions in Glx were associated with cognitive improvement. Conclusions: Treatment with infliximab did not affect prefrontal NAA concentration in adults with BD. Exploratory analysis suggested a potential effect of treatment on the glutamate system, a finding that should be confirmed and validated by additional studies.

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