Department of Psychiatry, University of British Columbia, Room 2C7-2255 Wesbrook Mall, Vancouver, BC, V6T 2A1, Canada.
Department of Psychiatry, University of Montréal, 2900 boul. Édouard-Montpetit, Montreal, QC, Canada.
Drugs. 2023 Jul;83(10):843-863. doi: 10.1007/s40265-023-01872-x. Epub 2023 May 25.
Depression is the most commonly experienced mood state over the life span in individuals with bipolar disorder (BD) and is the primary driver of functional impairment and suicidality in BD. Despite this, there are few effective treatments for BD depression, with only a handful of atypical anti-psychotics and inconsistent evidence for traditional mood stabilizing agents. There have been few major 'breakthroughs' in the treatment of BD depression, and until recently, few agents that work via novel mechanisms of action to exert therapeutic effects. Here, we review treatments for BD depression which are emergent or on the horizon. Included are new atypical anti-psychotics, glutamate modulators (ketamine and cycloserine/lurasidone), neurosteroid modulators (zuranolone), anti-inflammatories and mitochondrial modulators, cannabidiol (CBD) and psilocybin. New atypical anti-psychotics lumateperone and cariprazine have demonstrated efficacy in large-scale, placebo-controlled, double-blind randomized controlled trials (RCT) in treatment of BD depression. Non-racemic amisulpride showed potential therapeutic benefit in one RCT which requires replication. Three small RCTs examined the efficacy of intravenous ketamine in BD depression and showed rapid antidepressant and anti-suicidal effects after a single infusion. Anti-inflammatory and mitochondrial modulators show inconsistent evidence for efficacy. There are currently no adequately powered RCTs of zuranolone, psilocybin or CBD in BD depression to support their use. While there are potentially efficacious, mechanistically novel agents on the horizon, they require further study and validation. Further investigation on how these agents may impact specific subgroups of patients will also advance the field.
抑郁症是双相情感障碍(BD)患者一生中最常见的情绪状态,也是导致 BD 患者功能障碍和自杀的主要原因。尽管如此,BD 抑郁症的有效治疗方法却很少,只有少数几种非典型抗精神病药和传统心境稳定剂的证据不一致。BD 抑郁症的治疗鲜有重大“突破”,而且直到最近,几乎没有通过新型作用机制发挥治疗作用的药物。在此,我们回顾了新兴或即将出现的 BD 抑郁症治疗方法。包括新型非典型抗精神病药、谷氨酸调节剂(氯胺酮和环丝氨酸/鲁拉西酮)、神经甾体调节剂(唑尼沙酮)、抗炎药和线粒体调节剂、大麻二酚(CBD)和裸盖菇素。新型非典型抗精神病药鲁拉西酮和卡利培嗪在治疗 BD 抑郁症的大型安慰剂对照双盲随机对照试验(RCT)中已显示出疗效。一种 RCT 显示非对映异构体阿米舒必利具有潜在的治疗益处,这需要进一步验证。三项小型 RCT 研究了静脉内氯胺酮在 BD 抑郁症中的疗效,单次输注后迅速产生抗抑郁和抗自杀作用。抗炎和线粒体调节剂的疗效证据不一致。目前尚无足够规模的 RCT 研究唑尼沙酮、裸盖菇素或 CBD 在 BD 抑郁症中的应用,无法支持其使用。虽然有一些潜在有效的、机制新颖的药物即将问世,但它们需要进一步的研究和验证。进一步研究这些药物如何影响特定患者亚群也将推动该领域的发展。