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环氧化酶-2抑制剂塞来昔布对重度抑郁症有治疗作用:一项针对瑞波西汀的双盲、随机、安慰剂对照、附加试验性研究的结果

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.

作者信息

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

机构信息

Hospital for Psychiatry and Psychotherapy, Ludwig-Maximilians-Universität, München, Germany.

出版信息

Mol Psychiatry. 2006 Jul;11(7):680-4. doi: 10.1038/sj.mp.4001805. Epub 2006 Feb 21.

Abstract

Signs of an inflammatory process, in particular increased pro-inflammatory cytokines and increased levels of prostaglandine E(2) (PGE(2)), have repeatedly been described in major depression (MD). As cyclooxygenase-2 (COX-2) inhibitors inhibit the PGE(2) production and the production of pro-inflammatory cytokines, we performed a therapeutic trial with the COX-2 inhibitor celecoxib. In a prospective, double-blind, add-on study, 40 patients suffering from an acute depressive episode were randomly assigned to either reboxetine and celecoxib or to reboxetine plus placebo. After a wash-out period, 20 patients received 4-10 mg reboxetine plus placebo and 20 received reboxetine plus 400 mg celecoxib for 6 weeks. The treatment effect was calculated by analysis of variance. There were no significant differences between groups in age, sex, duration or severity of disease or psychopathology, or reboxetine dose or plasma levels. Over 6 weeks, both groups of patients showed significant improvement in scores of the Hamilton Depression Scale. However, the celecoxib group showed significantly greater improvement compared to the reboxetine-alone group. Additional treatment with celecoxib has significant positive effects on the therapeutic action of reboxetine with regard to depressive symptomatology. Moreover, the fact that treatment with an anti-inflammatory drug showed beneficial effects on MD indicates that inflammation is related to the pathomechanism of the disorder, although the exact mechanisms remain to become elucidated.

摘要

炎症过程的迹象,特别是促炎细胞因子增加和前列腺素E(2)(PGE(2))水平升高,在重度抑郁症(MD)中已被反复描述。由于环氧合酶-2(COX-2)抑制剂可抑制PGE(2)的产生以及促炎细胞因子的产生,我们进行了一项使用COX-2抑制剂塞来昔布的治疗试验。在一项前瞻性、双盲、附加研究中,40名患有急性抑郁发作的患者被随机分配至瑞波西汀加塞来昔布组或瑞波西汀加安慰剂组。经过洗脱期后,20名患者接受4 - 10毫克瑞波西汀加安慰剂治疗,20名患者接受瑞波西汀加400毫克塞来昔布治疗,为期6周。通过方差分析计算治疗效果。两组患者在年龄、性别、疾病持续时间或严重程度、精神病理学、瑞波西汀剂量或血浆水平方面无显著差异。在6周的时间里,两组患者的汉密尔顿抑郁量表评分均有显著改善。然而,与单独使用瑞波西汀的组相比,塞来昔布组的改善更为显著。塞来昔布的附加治疗在抑郁症状学方面对瑞波西汀的治疗作用具有显著的积极影响。此外,一种抗炎药物治疗对MD显示出有益效果这一事实表明,炎症与该疾病的发病机制有关,尽管确切机制仍有待阐明。

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