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早期疗效可预测难治性抑郁症患者对依他佐辛治疗的反应轨迹。

Early effects predict trajectories of response to esketamine in treatment-resistant depression.

机构信息

Clinique des Maladies Mentales et de l'Encéphale (CMME), GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte-Anne, Paris, France.

Pôle Hospitalo-Universitaire Psychiatrie Paris 15, GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte-Anne, Paris, France; Université Paris Cité, Paris, France; Institut Pasteur, Université Paris Cité, CNRS UMR 3571, Perception and Memory Unit, F-75015 Paris, France.

出版信息

J Affect Disord. 2023 Dec 1;342:166-176. doi: 10.1016/j.jad.2023.09.030. Epub 2023 Sep 20.

Abstract

BACKGROUND

The efficacy of esketamine in treatment-resistant depression (TRD) has been confirmed. However, its administration is expensive and restrictive, with limited knowledge on how long the treatment should be continued. Predicting the treatment outcome would benefit patients and alleviate the global treatment cost. We aimed to define distinct trajectories of treatment response and assess their predictability.

METHODS

In this longitudinal study, two independent samples of patients with unipolar or bipolar TRD were treated with esketamine in real-world settings. Depression severity was assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) before each esketamine administration. Latent class analyses were used to define trajectories of response.

RESULTS

In the original sample (N = 50), we identified two classes whose trajectories depicted response and non-response, respectively. The model was validated in the confirmatory sample (N = 55). Class membership was influenced by a few baseline characteristics such as concomitant benzodiazepine medication, number of depressive episodes or polarity. On the other hand, after only two esketamine administrations, the MADRS score predicted the 90-day trajectory of response with an accuracy of 80 %.

LIMITATIONS

This observational study is not placebo-controlled. Therefore, its results and their generalizability need to be confirmed in experimental settings.

CONCLUSIONS

After the first administrations of esketamine, the MADRS score has a good capacity to predict the most plausible trajectory of response. While thresholds and their predictive values need to be confirmed, this finding suggests that clinicians could base on MADRS scores their decision to discontinue treatment because of poor remaining chances of treatment response.

摘要

背景

氯胺酮治疗抵抗性抑郁症(TRD)的疗效已得到证实。然而,其使用成本高昂且受限,对于治疗应持续多久的相关知识有限。预测治疗效果将使患者受益并减轻全球治疗成本。我们旨在定义不同的治疗反应轨迹,并评估其可预测性。

方法

在这项纵向研究中,两个独立的单相或双相 TRD 患者样本在真实环境中接受氯胺酮治疗。在每次氯胺酮给药前,使用蒙哥马利-阿斯伯格抑郁评定量表(MADRS)评估抑郁严重程度。使用潜在类别分析来定义反应轨迹。

结果

在原始样本(N=50)中,我们确定了两个类别的轨迹分别代表反应和无反应。该模型在验证性样本(N=55)中得到验证。类别的归属受到一些基线特征的影响,例如同时使用苯二氮䓬类药物、抑郁发作次数或极性。另一方面,在仅接受两次氯胺酮给药后,MADRS 评分可准确预测 90 天的反应轨迹,准确率为 80%。

局限性

这项观察性研究没有安慰剂对照。因此,其结果及其普遍性需要在实验环境中得到证实。

结论

在首次使用氯胺酮后,MADRS 评分具有很好的预测反应最可能轨迹的能力。虽然需要确认阈值及其预测值,但这一发现表明,临床医生可以根据 MADRS 评分来决定是否因治疗反应不佳而停止治疗。

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