Olivola Miriam, Mazzoni Filippo, Tarantino Barbara, Guffanti Alessandro, Marcatili Matteo, Motta Federico Luigi, Cornaggia Ranieri Domenico, Martiadis Vassilis, Prodi Tiziano, Politi Pierluigi, Brondino Natascia, Martinotti Giovanni, Clerici Massimo, Dell'Osso Bernardo
Department of Brain and Behavioural Sciences, University of Pavia, 27100 Pavia, Italy; Department of Mental Health and Addiction Services, ASST Fatebenefratelli-Sacco, Milan, Italy.
Department of Brain and Behavioural Sciences, University of Pavia, 27100 Pavia, Italy.
J Affect Disord. 2026 Jan 1;392:120231. doi: 10.1016/j.jad.2025.120231. Epub 2025 Sep 2.
Treatment-Resistant Depression (TRD) remains a major challenge in the management of Major Depressive Disorder (MDD). Esketamine, the S-enantiomer of ketamine and a glutamatergic modulator, has been approved by the FDA and EMA for TRD in 2019. Beyond its rapid antidepressant effects, esketamine may enhance neuroplasticity, facilitating the reconnection with emotional and cognitive processes, improving mentalization, social cognition and promoting resilience.
This prospective multicenter observational study aimed to evaluate esketamine's therapeutic impact on depressive symptoms and explore whether psychological and clinical factors-including mentalization, psychache, social cognition, suicidality, and cognitive-emotional rigidity-could predict treatment response, enabling a more personalized approach to TRD management.
Thirty-six TRD patients treated with esketamine were assessed over a six-month follow-up period using psychometric measures of depression severity, suicidality, mentalization, social cognition, psychache, and cognitive-emotional rigidity.
A significant association emerged between mentalization deficits and depressive symptoms. Specifically, patients with poor baseline mentalization abilities exhibited higher Montgomery-Åsberg Depression Rating Scale (MADRS) scores both at baseline and throughout follow-up. In contrast, greater cognitive rigidity appeared to have a protective role, potentially mitigating negative thinking and providing emotional stability, which may enhance resilience to stressors.
These findings highlight the importance of a personalized treatment approach in TRD. Esketamine may be particularly beneficial in reducing cognitive rigidity, improving mentalization, and breaking the cognitive inflexibility that contributes to sustained negative depressive thinking patterns. Further research is needed to refine patient stratification and optimize treatment strategies for individuals with TRD.
难治性抑郁症(TRD)仍是重度抑郁症(MDD)治疗中的一项重大挑战。艾氯胺酮是氯胺酮的S-对映体,作为一种谷氨酸能调节剂,于2019年获得美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准用于治疗TRD。除了具有快速抗抑郁作用外,艾氯胺酮还可能增强神经可塑性,促进与情绪和认知过程的重新连接,改善心理化、社会认知并提升恢复力。
这项前瞻性多中心观察性研究旨在评估艾氯胺酮对抑郁症状的治疗效果,并探讨心理和临床因素——包括心理化、精神痛苦、社会认知、自杀倾向以及认知-情绪僵化——是否能够预测治疗反应,从而实现对TRD治疗更具个性化的方法。
对36例接受艾氯胺酮治疗的TRD患者进行了为期六个月的随访,使用抑郁严重程度、自杀倾向、心理化、社会认知、精神痛苦和认知-情绪僵化的心理测量指标进行评估。
心理化缺陷与抑郁症状之间出现了显著关联。具体而言,基线心理化能力较差的患者在基线时以及整个随访期间的蒙哥马利-Åsberg抑郁评定量表(MADRS)得分均较高。相比之下,更强的认知僵化似乎具有保护作用,可能减轻消极思维并提供情绪稳定性,这可能增强对应激源的恢复力。
这些发现凸显了TRD个性化治疗方法的重要性。艾氯胺酮在降低认知僵化、改善心理化以及打破导致持续消极抑郁思维模式的认知不灵活性方面可能特别有益。需要进一步研究以完善患者分层并优化TRD患者的治疗策略。