Ding Yitong, Wang Zhengye, Huang Jing, Yi Yanzi, Wu Zhouquan
Department of Anesthesiology, Nanjing Medical University, Jiangning, Nanjing, 211166, People's Republic of China.
Department of Anesthesiology, The Second People's Hospital of Changzhou, The Third Affiliated Hospital of Nanjing Medical University, Changzhou, Jiangsu, 213164, People's Republic of China.
Neuropsychiatr Dis Treat. 2025 Jul 12;21:1409-1423. doi: 10.2147/NDT.S530265. eCollection 2025.
Although Dexmedetomidine (DEX) can induce sleep that resembles natural sleep, it has demonstrated limited efficacy in patients with comorbid insomnia and depression. On the other hand, Esketamine (ESK) has shown a potent antidepressant effect. Herein, we aimed to establish whether esketamine could enhance the therapeutic efficacy of DEX in treating patients with comorbid insomnia and depression.
We recruited 84 patients with comorbid insomnia and depression who were randomized into two groups for a 1-month follow-up study: the DE group (receiving dexmedetomidine and esketamine) and the DS group (receiving dexmedetomidine and saline). Outcome measures included polysomnographic monitoring (PSG), Montgomery-Åsberg Depression Rating Scale (MADRS), Pittsburgh Sleep Quality Index (PSQI), Sleep Numeric Rating Scale (SNRS), and serum brain-derived neurotrophic factor (BDNF) concentrations. The primary outcome was a comparison of PSG parameters recorded at baseline (D) and on treatment day 3 (D).
After 3 days of treatment, patients in DE group had a significant increase in total sleep duration, duration and proportion of N3 sleep ( < 0.05), a significant decrease in proportion of N2 sleep and proportion of REM sleep ( < 0.05), and a significant decrease in depression score and sleep numeric rating scale score ( < 0.05), as compared with DS group. Improvements in sleep were associated with improvements in MADRS score and increases in BDNF. Oral dryness was the most frequent adverse event (AE).
When combined with ESK, DEX improved patients' depression scores, further extended total sleep time, increased the N3 sleep proportion, and enhanced deep sleep continuity, with few AEs.
尽管右美托咪定(DEX)可诱导出类似自然睡眠的状态,但在伴有失眠和抑郁的患者中其疗效有限。另一方面,艾司氯胺酮(ESK)已显示出强大的抗抑郁作用。在此,我们旨在确定艾司氯胺酮是否能增强右美托咪定治疗伴有失眠和抑郁患者的疗效。
我们招募了84例伴有失眠和抑郁的患者,将其随机分为两组进行为期1个月的随访研究:DE组(接受右美托咪定和艾司氯胺酮)和DS组(接受右美托咪定和生理盐水)。观察指标包括多导睡眠图监测(PSG)、蒙哥马利-阿斯伯格抑郁量表(MADRS)、匹兹堡睡眠质量指数(PSQI)、睡眠数字评分量表(SNRS)以及血清脑源性神经营养因子(BDNF)浓度。主要结局是比较基线时(D)和治疗第3天(D)记录的PSG参数。
治疗3天后,与DS组相比,DE组患者的总睡眠时间、N3睡眠时长和比例显著增加(<0.05),N2睡眠比例和快速眼动睡眠比例显著降低(<0.05),抑郁评分和睡眠数字评分量表评分显著降低(<0.05)。睡眠改善与MADRS评分改善和BDNF增加相关。口干是最常见的不良事件(AE)。
与艾司氯胺酮联合使用时,右美托咪定改善了患者的抑郁评分,进一步延长了总睡眠时间,增加了N3睡眠比例,并增强了深度睡眠连续性,且不良事件较少。