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抑郁症的药物单药治疗:现状与未来——一篇叙述性综述

Pharmacological Monotherapy for Depressive Disorders: Current and Future-A Narrative Review.

作者信息

Gao Keming, Oruc Evrim Bayrak, Koparal Buket

机构信息

Department of Mind and Body Medicine, Sichuan Lansheng Brian Hospital, Chengdu 610036, China.

Department of Psychiatry, University Hospitals Cleveland Medical Center, Cleveland, OH 44106, USA.

出版信息

Medicina (Kaunas). 2025 Mar 21;61(4):558. doi: 10.3390/medicina61040558.

Abstract

: To narratively review currently available antidepressants and future potential antidepressants as monotherapy for the treatment of depressive disorders. : Selective serotonin reuptake inhibitors (SSRIs), serotonin norepinephrine reuptake inhibitors (SNRIs), dopamine reuptake inhibitor (bupropion), tricyclic antidepressants (TCAs), and monoamine oxidase inhibitors (MAOIs) were reviewed according to the results from Sequenced Treatment Alternatives to Relieve Depression (STARD) Study and systematic reviews. For the rest of the antidepressants, a PubMed/Medline search was conducted with priority for systematic reviews. For drugs in development for depressive disorders, PubMed, Google, and Clinicaltrials.gov databases were used. : The STARD Study demonstrated that sertraline, venlafaxine, and bupropion monotherapy had similar efficacy in patients with major depressive disorder (MDD) who failed citalopram. A network meta-analyses of randomized, placebo-controlled trials found that SSRIs, SNRIs, bupropion, TCAs, mirtazapine, and agomelatine had similar relative efficacy compared to placebo, but had different acceptability. Gepirone had more failed/negative studies and smaller effect size relative to placebo compared to other antidepressants. The combination of dextromethorphan and bupropion, ketamine infusion, and intranasal esketamine had faster onset of action but similar effect size compared to monoamine-based antidepressants as monotherapy. Brexanolone and zuranolone are effective in postpartum depression (PPD), but the effect size of zuranolone in MDD as monotherapy or adjunctive therapy was very small. Psychedelics, glutamate receptor-related agents, kappa opioid receptor antagonists, orexin receptor antagonists, new anti-inflammatory agents, and biomarker-based antidepressant therapy have been under investigation for depressive disorders. Psychedelics showed faster onset of action, large effect size, and long durability. : Monoamine-based antidepressants likely continue to be the mainstream antidepressants for depressive disorder. NMDA receptor antagonists and neurosteroid antidepressants will play a bigger role with the improvement of accessibility. Psychedelics may become a game changer if phase III studies validate their efficacy and safety in depressive disorders.

摘要

目的

对目前可用的抗抑郁药以及未来可能用于治疗抑郁症的单药治疗抗抑郁药进行叙述性综述。

方法

根据缓解抑郁症的序贯治疗替代方案(STAR*D)研究结果和系统评价,对选择性5-羟色胺再摄取抑制剂(SSRIs)、5-羟色胺去甲肾上腺素再摄取抑制剂(SNRIs)、多巴胺再摄取抑制剂(安非他酮)、三环类抗抑郁药(TCAs)和单胺氧化酶抑制剂(MAOIs)进行综述。对于其余抗抑郁药,优先检索PubMed/Medline进行系统评价。对于正在研发用于治疗抑郁症的药物,使用PubMed、谷歌和Clinicaltrials.gov数据库。

结果

STAR*D研究表明,舍曲林、文拉法辛和安非他酮单药治疗对西酞普兰治疗失败的重度抑郁症(MDD)患者具有相似的疗效。一项随机、安慰剂对照试验的网络荟萃分析发现,与安慰剂相比,SSRIs、SNRIs、安非他酮、TCAs、米氮平和阿戈美拉汀具有相似的相对疗效,但可接受性不同。与其他抗抑郁药相比,吉哌隆有更多失败/阴性研究,相对于安慰剂的效应量更小。右美沙芬与安非他酮联合用药、氯胺酮输注和鼻内艾司氯胺酮作为单药治疗起效更快,但与基于单胺的抗抑郁药效应量相似。布雷沙诺龙和祖拉诺龙对产后抑郁症(PPD)有效,但祖拉诺龙作为单药治疗或辅助治疗在MDD中的效应量非常小。致幻剂、谷氨酸受体相关药物、κ阿片受体拮抗剂、食欲素受体拮抗剂、新型抗炎药和基于生物标志物的抗抑郁治疗已在抑郁症研究中。致幻剂起效更快,效应量大,持续时间长。

结论

基于单胺的抗抑郁药可能仍是抑郁症治疗的主流抗抑郁药。随着可及性的提高,N-甲基-D-天冬氨酸(NMDA)受体拮抗剂和神经甾体类抗抑郁药将发挥更大作用。如果III期研究验证其在抑郁症中的疗效和安全性,致幻剂可能会成为改变局面的药物。

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