1 Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
2 Department of Psychiatry, Dokuz Eylül University, Izmir, Turkey.
J Psychopharmacol. 2019 Feb;33(2):177-184. doi: 10.1177/0269881118822167. Epub 2019 Feb 11.
Tamoxifen is an oral medication that has been proposed as a potential treatment for bipolar disorder. Tamoxifen acts to inhibit the intracellular action of protein kinase C, which is also an action of well-established treatments such as lithium and valproate. Here we aimed to identify randomised controlled trials (RCTs) of tamoxifen in the treatment of bipolar disorder and synthesise their results using meta-analysis.
RCTs were identified by searching of electronic databases and from discussion with experts in the field. Data were extracted, and meta-analyses performed in R.
Five placebo-controlled RCTs of tamoxifen in the treatment of acute mania were identified. There were no trials in the treatment of episodes of bipolar depression, or for relapse prevention. The studies of mania treatment were of between three and six weeks duration. Tamoxifen was studied either as monotherapy (two trials) or as augmentation of lithium or valproate (three trials). Change in mania scale scores favoured tamoxifen over placebo: SMD -2.14 (95% CI -3.39 to -0.89; 4 trials), as did endpoint mania scale scores SMD 1.23 (95% CI 0.60-1.87; 5 trials). Response rates were also higher: RR 4.35 (1.99-9.50; 4 trials). Acceptability was similar to placebo: RR 1.03 (0.94-1.13; 5 trials).
Tamoxifen appears to be a promising potential treatment for episodes of mania. Future studies could investigate its effects as an adjunct to dopamine antagonists for improved anti-manic efficacy, and establish its longer term effects on mood, particularly depression and relapse.
他莫昔芬是一种口服药物,已被提议作为双相情感障碍的潜在治疗方法。他莫昔芬的作用是抑制蛋白激酶 C 的细胞内作用,这也是锂和丙戊酸盐等经过充分验证的治疗方法的作用机制。在这里,我们旨在确定他莫昔芬治疗双相情感障碍的随机对照试验 (RCT),并使用荟萃分析综合其结果。
通过搜索电子数据库和与该领域专家讨论,确定 RCT。提取数据,并在 R 中进行荟萃分析。
确定了五项关于他莫昔芬治疗急性躁狂的安慰剂对照 RCT。没有关于双相情感障碍发作或预防复发的试验。这些躁狂症治疗研究的持续时间为三至六周。他莫昔芬作为单药治疗(两项试验)或作为锂或丙戊酸盐的增效剂(三项试验)进行了研究。躁狂量表评分的变化表明他莫昔芬优于安慰剂:SMD-2.14(95%CI-3.39 至-0.89;四项试验),终点躁狂量表评分 SMD1.23(95%CI0.60-1.87;五项试验)也有同样的结果。反应率也更高:RR4.35(1.99-9.50;四项试验)。可接受性与安慰剂相似:RR1.03(0.94-1.13;五项试验)。
他莫昔芬似乎是一种有前途的潜在治疗躁狂发作的方法。未来的研究可以探讨其作为多巴胺拮抗剂的辅助治疗作用,以提高抗躁狂疗效,并确定其对情绪的长期影响,特别是抑郁和复发。