Peripheral cytokine and chemokine alterations in depression: a meta‐analysis of 82 studies

Cristiano A. Köhler(Universidade Federal do Ceará), Thiago Holanda Freitas(Universidade Federal do Ceará), Michaël Maes(Universidade Estadual de Londrina), Nayanna Quezado de Andrade(Universidade Federal do Ceará), C. S. Liu(Sunnybrook Health Science Centre), Brisa S. Fernandes(Universidade Federal do Rio Grande do Sul), Brendon Stubbs(King's College London), Marco Solmi(University of Padua), Nicola Veronese(University of Padua), Nathan Herrmann(Sunnybrook Health Science Centre), Charles L. Raison(University of Wisconsin–Madison), Brian J. Miller(Augusta University), Krista L. Lanctôt(Sunnybrook Health Science Centre), André F. Carvalho(Universidade Federal do Ceará)
Acta Psychiatrica Scandinavica
January 25, 2017
Cited by 1,417Open Access
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Abstract

Objective To conduct a systematic review and meta‐analysis of studies that measured cytokine and chemokine levels in individuals with major depressive disorder ( MDD ) compared to healthy controls ( HC s). Method The PubMed/MEDLINE, EMBASE , and PsycINFO databases were searched up until May 30, 2016. Effect sizes were estimated with random‐effects models. Result Eighty‐two studies comprising 3212 participants with MDD and 2798 HC s met inclusion criteria. Peripheral levels of interleukin‐6 ( IL ‐6), tumor necrosis factor ( TNF )‐alpha, IL ‐10, the soluble IL ‐2 receptor, C‐C chemokine ligand 2, IL ‐13, IL ‐18, IL ‐12, the IL ‐1 receptor antagonist, and the soluble TNF receptor 2 were elevated in patients with MDD compared to HC s, whereas interferon‐gamma levels were lower in MDD (Hedge's g = −0.477, P = 0.043). Levels of IL ‐1β, IL ‐2, IL ‐4, IL ‐8, the soluble IL ‐6 receptor ( sIL ‐6R), IL ‐5, CCL ‐3, IL ‐17, and transforming growth factor‐beta 1 were not significantly altered in individuals with MDD compared to HC s. Heterogeneity was large ( I 2 : 51.6–97.7%), and sources of heterogeneity were explored (e.g., age, smoking status, and body mass index). Conclusion Our results further characterize a cytokine/chemokine profile associated with MDD . Future studies are warranted to further elucidate sources of heterogeneity, as well as biosignature cytokines secreted by other immune cells.


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