Mousavi Seyed Yaser, Khezri Rasoul, Karkhaneh-Yousefi Mohammad-Ali, Mohammadinejad Payam, Gholamian Faezeh, Mohammadi Mohammad Reza, Zeinoddini Atefeh, Akhondzadeh Shahin
Psychiatric Research Center, Roozbeh Hospital, Tehran University of Medical Sciences , Tehran, Iran .
J Child Adolesc Psychopharmacol. 2017 Aug;27(6):494-500. doi: 10.1089/cap.2016.0207. Epub 2017 Apr 14.
Recent studies have focused on the role of inflammatory cascades as one of the possible etiologic factors of bipolar disorder. We hypothesize that celecoxib, through its anti-inflammatory properties, may have a therapeutic role in acute bipolar mania.
Forty-two adolescent inpatients with the diagnosis of acute bipolar mania participated in a parallel, randomized, double-blind controlled trial, and 40 patients underwent an 8-week treatment with either celecoxib (100 mg twice daily) or placebo as an adjunctive treatment to lithium and risperidone. Patients were evaluated using Young Mania Rating Scale (YMRS) at baseline and weeks 2, 4, and 8. The primary outcome measure was to assess the efficacy of celecoxib compared with placebo in improving mania symptoms.
General linear model repeated measures showed significant effect for time × treatment interaction on YMRS scores [F (2.54, 96.56) = 3.21, p = 0.03]. Significantly greater improvement was observed in YMRS scores in the celecoxib group compared with the placebo group from baseline YMRS score at week 8 (p = 0.04). Although a 35% greater response to treatment (considering a Clinical Global Impressions-Improvement score of ≤2, very much/much improved) was observed in the celecoxib group compared with the placebo group, the difference did not reach the statistical significance level (p = 0.09). No serious adverse event was reported.
Celecoxib may be an effective adjuvant therapy in treatment of manic episodes (without psychotic features) of adolescents with bipolar mood disorder. The mood-stabilizing role of this drug might be mediated through its action on inflammatory cascades.
近期研究聚焦于炎症级联反应作为双相情感障碍可能病因之一的作用。我们假设塞来昔布因其抗炎特性,可能在急性双相躁狂发作中具有治疗作用。
42例诊断为急性双相躁狂发作的青少年住院患者参与了一项平行、随机、双盲对照试验,40例患者接受了为期8周的治疗,分别使用塞来昔布(每日两次,每次100毫克)或安慰剂作为锂盐和利培酮的辅助治疗。在基线以及第2、4和8周使用青年躁狂评定量表(YMRS)对患者进行评估。主要结局指标是评估塞来昔布与安慰剂相比改善躁狂症状的疗效。
重复测量的一般线性模型显示,时间×治疗交互作用对YMRS评分有显著影响[F(2.54, 96.56) = 3.21,p = 0.03]。与安慰剂组相比,塞来昔布组在第8周时YMRS评分较基线有显著更大程度的改善(p = 0.04)。尽管与安慰剂组相比,塞来昔布组观察到对治疗的反应高出35%(考虑临床总体印象改善评分≤2,显著改善/改善很多),但差异未达到统计学显著水平(p = 0.09)。未报告严重不良事件。
塞来昔布可能是治疗双相情感障碍青少年躁狂发作(无精神病性特征)的有效辅助疗法。该药物的情绪稳定作用可能通过其对炎症级联反应的作用来介导。