MK4MDD

Study Report

Reference
CitationMusil, 2011 PubMed
Full InfoMusil, R., Schwarz, M.J., Riedel, M., Dehning, S., Cerovecki, A., Spellmann, I., Arolt, V. and Muller, N. (2011) Elevated macrophage migration inhibitory factor and decreased transforming growth factor-beta levels in major depression--no influence of celecoxib treatment. J Affect Disord, 134, 217-225.

Study
Hypothesis or Background The involvement of an immune process in the pathophysiology of major depression disorder (MDD) was substantiated by studies demonstrating elevated levels of proinflammatory cytokines and prostaglandin E(2) (PGE(2)). Cyclooxygenase-2 (COX-2) inhibitors lead to a reduced production of PGE(2) and have been shown to improve depressive symptoms. We investigated the three immune parameters macrophage migration inhibitory factor (MIF), transforming growth factor-beta (TGF-beta) and soluble CD14 (sCD14) in a randomized, placebo-controlled trial of the COX-2 inhibitor celecoxib as add-on therapy in patients with MDD treated with reboxetine.
Sample InformationThirty-two patients with depression and 20 healthy controls participated in the study.
Method DetailThe patients were treated with reboxetine and celecoxib or placebo. Immune parameters were measured from serum at baseline, after three and five weeks using ELISA.
Method Keywordsblood analysis
ResultCelecoxib as add-on strategy resulted in a significant reduction of Hamilton Depression Scale scores compared to placebo. Depressed patients showed significantly elevated MIF (p < 0.001) and reduced TGF-beta (p = 0.006) concentrations at baseline. There was no difference in sCD14-concentrations. There was no difference between the placebo and the celecoxib group and no change over time.
ConclusionsMIF is a promising new candidate in the neuro-immune interplay that may link depressive symptoms, altered immune state and HPA-axis dysregulation. Reduced levels of TGF-beta replicate previous findings and support the importance of this regulatory cytokine in major depressive disorder.
RemarkLIMITATIONS: Limitations of the study are the relatively small sample size and lack of functional assessment of HPA axis in parallel.

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