PRODAF - Programa de Transtornos Afetivos, Department of Psychiatry, Federal University of Sao Paulo, Rua Major Maragliano, 241. Vila Mariana, Sao Paulo 04017-030, Brazil.
Department of Psychiatry, Federal University of Sao Paulo; Centro Alfa de Humanização, Escola Paulista de Medicina, Federal University of Sao Paulo, Sao Paulo, Brazil.
J Affect Disord. 2021 Jan 1;278:515-518. doi: 10.1016/j.jad.2020.09.056. Epub 2020 Sep 15.
Anhedonia is a symptom associated with poorer outcomes in depression treatment, including resistance to treatment, higher functional impact and suicidality. Few drugs are known to adequately treat anhedonia in both unipolar and bipolar depression. The NMDA antagonist ketamine has been demonstrated to be effective in rapidly ameliorating anhedonia in depressive episodes. The main aim of present study is to evaluate the anti-anhedonic effect of esketamine, the S-enantiomer of ketamine recently approved for treatment-resistant depression, in unipolar and bipolar depression.
70 patients with unipolar or bipolar depression were treated with 6 weekly subcutaneous esketamine infusions (0.5-1mg/kg). Anhedonia was measured through MADRS item 8 before and 24h after each infusion.
A significant reduction in anhedonia severity was observed (p<0.0001) after 6 infusions. The effect was statistically significant 24h after the first infusion (p<0.001) in both unipolar and bipolar groups and increased with repeated infusions. Anti-anhedonic effect of esketamine did not differ between groups.
This is an open-label, real-world study. Lack of blinding and of a placebo arm may limit the interpretation of findings.
Although preliminary, present findings suggest that repeated subcutaneous esketamine infusions are effective for the treatment of anhedonia in both unipolar and bipolar depressed patients. These results need to be confirmed through replication in larger double-blinded controlled trials.
快感缺失是与抑郁症治疗结果较差相关的一种症状,包括对治疗的抵抗、更高的功能影响和自杀倾向。已知很少有药物能够充分治疗单相和双相抑郁症中的快感缺失。NMDA 拮抗剂氯胺酮已被证明在迅速改善抑郁发作中的快感缺失方面有效。本研究的主要目的是评估新近被批准用于治疗难治性抑郁症的氯胺酮 S-对映体依他佐辛在单相和双相抑郁症中的抗快感缺失作用。
70 例单相或双相抑郁症患者接受 6 周皮下依他佐辛输注(0.5-1mg/kg)。在每次输注前后通过 MADRS 项目 8 测量快感缺失。
6 次输注后观察到快感缺失严重程度显著降低(p<0.0001)。在单相和双相组中,第一次输注后 24 小时(p<0.001)的效果具有统计学意义,并且随着重复输注而增加。依他佐辛的抗快感缺失作用在两组之间没有差异。
这是一项开放标签、真实世界的研究。缺乏盲法和安慰剂组可能会限制对研究结果的解释。
尽管初步研究结果表明,重复皮下依他佐辛输注对单相和双相抑郁患者的快感缺失治疗有效。这些结果需要通过更大规模的双盲对照试验进行复制来确认。