A review of the relationship between proinflammatory cytokines and major depressive disorder

促炎细胞因子 重性抑郁障碍 神经影像学 萧条(经济学) 医学 发病机制 细胞因子 病因学 生物信息学 心理学 炎症 免疫学 内科学 精神科 扁桃形结构 生物 宏观经济学 经济
作者
Juan Young,Davide Bruno,Nunzio Pomara
出处
期刊:Journal of Affective Disorders [Elsevier BV]
卷期号:169: 15-20 被引量:416
标识
DOI:10.1016/j.jad.2014.07.032
摘要

Determining etiological factors and reviewing advances in diagnostic modalities sensitive and specific to Major Depressive Disorder (MDD) is of importance in its evaluation and treatment. The inflammatory hypothesis is one of the most prevalent topics concerning MDD and may provide insight into the pathogenesis of depression, development of biomarkers, and ultimately production of more effective depression therapies.We reviewed several studies to evaluate contemporary concepts concerning proinflammatory cytokines and their relationship to various depressive disorders, the use of anti-inflammatory therapies in MDD treatment, and the application of neuroimaging in conjunction with cytokine profiles from both plasma and CSF as possible diagnostic tools.Proinflammatory cytokines in both plasma and CSF have been found to influence the progression and severity of depressive disorders in different populations. Studies have shown elevated serum levels of IL-1, IL-6, TNF-α, CRP, and MCP-1 in depressed patients, but have presented mixed results with IL-8 serum levels, and with IL-6 and MCP-1 CSF levels. Anti-inflammatory treatment of MDD may have adjuvant properties with current depression medications. MRI and NIRS neuroimaging confirm neurological abnormalities in the presence of elevated proinflammatory cytokines in depressed or stressed patients.Heterogeneity of MDD and limited CSF cytokine research complicate the study of MDD pathogenesis.There is significant evidence that inflammatory processes influence the development and progression of MDD. Future studies with larger arrays of cytokine profiles aided by neuroimaging may provide more sensitive and specific modes of diagnostics in determining MDD etiology and provide guidance in individual therapies.
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