首页> 外文期刊>Journal of psychopharmacology >Effects of bupropion augmentation on pro-inflammatory cytokines in escitalopram-resistant patients with major depressive disorder.
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Effects of bupropion augmentation on pro-inflammatory cytokines in escitalopram-resistant patients with major depressive disorder.

机译:安非他酮的增强对依西普仑耐药的重度抑郁症患者促炎细胞因子的影响。

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Studies so far have provided contradictory results on immune system markers during use of antidepressants. There are no data on changes in immune parameters after treatment augmentation. The present study aimed to clarify whether the addition of bupropion in escitalopram-resistant patients with major depression causes changes in the immune system and whether treatment response could be predicted by baseline levels of cytokines. We recruited 28 depressive patients (11 men and 17 women) who did not respond to 12-week treatment with escitalopram (20 mg/d) for an augmentation trial with bupropion (150-300 mg/day). The levels of soluble interleukin-2 receptor, interleukin-8 (IL-8) and tumor-necrosis factor-alpha were measured before and 6 weeks after addition of bupropion. For a control group, we recruited 45 healthy volunteers (19 men and 26 women). The results indicated that the baseline levels of studied cytokines did not predict treatment response to bupropion augmentation. Concentration of IL-8 increased during the treatment similarly in both responder and non-responder groups. Although bupropion augmentation had increased the response rate in escitalopram-resistant patients, this clinical improvement was not accompanied by specific changes in studied cytokine levels.
机译:迄今为止的研究已经在使用抗抑郁药期间对免疫系统标志物提供了矛盾的结果。没有关于增强治疗后免疫参数变化的数据。本研究旨在阐明对依西普仑耐药的重度抑郁患者中安非他酮的添加是否会引起免疫系统的改变,以及是否可以通过基线细胞因子来预测治疗反应。我们招募了28名抑郁患者(11名男性和17名女性),他们对使用依他普仑(20 mg / d)的12周治疗无反应,进行了安非他酮(150-300 mg /天)的增强试验。在加入安非他酮之前和之后6周测量可溶性白细胞介素2受体,白细胞介素8(IL-8)和肿瘤坏死因子-α的水平。对于对照组,我们招募了45名健康志愿者(19名男性和26名女性)。结果表明,研究细胞因子的基线水平不能预测对安非他酮增强的治疗反应。在有反应者和无反应者组中,在治疗过程中,IL-8的浓度均升高。尽管安非他酮的增加增加了依西酞普兰耐药患者的反应率,但这种临床改善并未伴随研究的细胞因子水平的具体变化。

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