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SSRIs 对广泛性焦虑障碍患者外周炎性细胞因子的影响。

Effects of SSRIs on peripheral inflammatory cytokines in patients with Generalized Anxiety Disorder.

机构信息

Department of Psychiatry, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, UK.

Suzhou Psychiatric Hospital, Suzhou, Jiangsu, China.

出版信息

Brain Behav Immun. 2019 Oct;81:105-110. doi: 10.1016/j.bbi.2019.06.001. Epub 2019 Jun 1.

Abstract

BACKGROUND

Extensive research into psychoneuroimmunology has led to substantial advances in our understanding of the reciprocal interactions between the central nervous system and the immune system in neuropsychiatric disorders. To date, inflammation has been implicated in the pathogenesis of depression and anxiety. The immunomodulating effects of antidepressants on depression have been reported, however, there is no evidence of the similar effects of antidepressants on anxiety. The aim of the study was to investigate the effects of selective serotonin reuptake inhibitors (SSRIs) on peripheral inflammatory cytokines in patients with first episode generalized anxiety disorder (GAD).

METHODS

A prospective cohort design was employed: 42 patients with first episode GAD were treated with either escitalopram or sertraline for 12 weeks. Anxiety was measured by the Generalized Anxiety Disorder Scale and the State Trait Anxiety Inventory, serum pro-inflammatory cytokine levels were measured by the enzyme-linked immunosorbent assay (ELISA), and CRP determined by an immunoturbidimetric method before and after SSRIs treatment RESULTS: Baseline levels of anxiety and pro-inflammatory cytokines including IL-1α, IL-6, IL-8, IL-12, IFN-γ, and CRP were significantly reduced after treatment of SSRIs (p < 0.05 in all cases). In addition, the change of anxiety measures co-vary with the change of peripheral cytokine levels (p < 0.05 in all cases). The regression model revealed that log transformed baseline levels of CRP and IL-6 predicted treatment response (p < 0.05 in both cases).

CONCLUSIONS

This study is the first to investigate the effects of SSRIs on pro-inflammatory cytokines in patients with first episode GAD. The findings indicate moderate acute anti-inflammatory effects of SSRIs in GAD, and suggest that these anti-inflammatory effects may underlie anxiolytic effects of SSRIs. The study also indicates that serum levels of CRP and IL-6 may predict treatment response. However, data from randomized controlled trials is warranted to confirm these findings.

摘要

背景

神经精神免疫学的广泛研究极大地促进了我们对神经精神障碍中中枢神经系统与免疫系统之间相互作用的理解。迄今为止,炎症已被认为与抑郁和焦虑的发病机制有关。据报道,抗抑郁药具有调节免疫的作用,可以治疗抑郁,但尚无抗抑郁药对焦虑具有类似作用的证据。本研究旨在探讨选择性 5-羟色胺再摄取抑制剂(SSRIs)对首发广泛性焦虑症(GAD)患者外周炎症细胞因子的影响。

方法

采用前瞻性队列设计:42 例首发 GAD 患者分别接受艾司西酞普兰或舍曲林治疗 12 周。采用广泛性焦虑症量表(GAD)和状态特质焦虑量表(STAI)评估焦虑,酶联免疫吸附试验(ELISA)检测血清促炎细胞因子水平,免疫比浊法检测 CRP。在 SSRIs 治疗前后测量这些指标。

结果

SSRIs 治疗后,焦虑和促炎细胞因子(包括 IL-1α、IL-6、IL-8、IL-12、IFN-γ 和 CRP)的基线水平显著降低(所有情况下均 p<0.05)。此外,焦虑指标的变化与外周细胞因子水平的变化呈正相关(所有情况下均 p<0.05)。回归模型显示,CRP 和 IL-6 的基线水平与治疗反应呈对数相关(两种情况下均 p<0.05)。

结论

本研究首次探讨了 SSRIs 对首发 GAD 患者促炎细胞因子的影响。研究结果表明 SSRIs 对 GAD 具有中度的急性抗炎作用,并提示这些抗炎作用可能是 SSRIs 的抗焦虑作用的基础。研究还表明,血清 CRP 和 IL-6 水平可能预测治疗反应。但是,需要随机对照试验的数据来证实这些发现。

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