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Review
. 2016;14(7):732-42.
doi: 10.2174/1570159x14666151208113700.

Inflammation in Depression and the Potential for Anti-Inflammatory Treatment

Affiliations
Review

Inflammation in Depression and the Potential for Anti-Inflammatory Treatment

Ole Kohler et al. Curr Neuropharmacol. 2016.

Abstract

Accumulating evidence supports an association between depression and inflammatory processes, a connection that seems to be bidirectional. Clinical trials have indicated antidepressant treatment effects for anti-inflammatory agents, both as add-on treatment and as monotherapy. In particular, nonsteroidal anti-inflammatory drugs (NSAIDs) and cytokine-inhibitors have shown antidepressant treatment effects compared to placebo, but also statins, poly-unsaturated fatty acids, pioglitazone, minocycline, modafinil, and corticosteroids may yield antidepressant treatment effects. However, the complexity of the inflammatory cascade, limited clinical evidence, and the risk for side effects stress cautiousness before clinical application. Thus, despite proof-of-concept studies of anti-inflammatory treatment effects in depression, important challenges remain to be investigated. Within this paper, we review the association between inflammation and depression together with the current evidence on use of anti-inflammatory treatment in depression. Based on this, we address the questions and challenges that seem most important and relevant to future studies, such as timing, most effective treatment lengths and identification of subgroups of patients potentially responding better to different anti-inflammatory treatment regimens.

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References

    1. Smith R.S. The macrophage theory of depression. Med. Hypotheses. 1991;35(4):298–306. [http://dx.doi.org/10.1016/0306-9877(91)90272-Z]. [PMID: 1943879]. - PubMed
    1. Howren M.B., Lamkin D.M., Suls J. Associations of depression with C-reactive protein, IL-1, and IL-6: a meta-analysis. Psychosom. Med. 2009;71(2):171–186. [http://dx.doi.org/10.1097/PSY.0b013e3181907c1b]. [PMID: 19188531]. - PubMed
    1. Müller N., Schwarz M.J., Dehning S., Douhe A., Cerovecki A., Goldstein-Müller B., Spellmann I., Hetzel G., Maino K., Kleindienst N., Möller H.J., Arolt V., Riedel M. The cyclooxygenase-2 inhibitor celecoxib has therapeutic effects in major depression: results of a double-blind, randomized, placebo controlled, add-on pilot study to reboxetine. Mol. Psychiatry. 2006;11(7):680–684. [http://dx.doi.org/10.1038/sj.mp.4001805]. [PMID: 16491133]. - PubMed
    1. Tyring S., Gottlieb A., Papp K., Gordon K., Leonardi C., Wang A., Lalla D., Woolley M., Jahreis A., Zitnik R., Cella D., Krishnan R. Etanercept and clinical outcomes, fatigue, and depression in psoriasis: double-blind placebo-controlled randomised phase III trial. Lancet. 2006;367(9504):29–35. [http://dx.doi.org/10.1016/S0140-6736(05)67763-X]. [PMID: 16399150]. - PubMed
    1. Akhondzadeh S., Jafari S., Raisi F., Nasehi A.A., Ghoreishi A., Salehi B., Mohebbi-Rasa S., Raznahan M., Kamalipour A. Clinical trial of adjunctive celecoxib treatment in patients with major depression: a double blind and placebo controlled trial. Depress. Anxiety. 2009;26(7):607–611. [http://dx.doi.org/10.1002/ da.20589]. [PMID: 19496103]. - PubMed

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