Department of Translational Research and of New Surgical and Medical Technologies, University of Pisa, via Savi 10, 56126, Pisa, Italy.
Department of Translational Research and of New Surgical and Medical Technologies, University of Pisa, via Savi 10, 56126, Pisa, Italy; Department of Developmental Neuroscience, IRCCS Stella Maris Foundation, Viale del Tirreno, 341/A/B/C, 56128, Calambrone, Pisa, Italy.
J Psychiatr Res. 2023 Sep;165:96-104. doi: 10.1016/j.jpsychires.2023.07.008. Epub 2023 Jul 11.
The present study evaluates the effect of exogenous melatonin (exo-MEL) on sleep and circadian parameters in patients with bipolar disorder (BD) and delayed sleep-wake phase disorder (DSWPD). BD euthymic patients (n = 83, mean age = 45.13 ± 13.68, males 56%) were evaluated for chronotype (reduced Morningness-Eveningness Questionnaire [rMEQ]), sleep quality (Pittsburgh Sleep Quality Index), sleep and circadian parameters (actigraphic monitoring). Patients that fulfilled criteria for DSWPD (n = 25) were treated for three months with exo-MEL 2 mg administered approximately 4 h before the sleep onset time (SOT) actigraphically-determined at baseline. Sleep and circadian parameters at baseline (T0) and after the exo-MEL treatment (T1) were compared using paired Wilcoxon test. In patients that completed the treatment (n = 19), the rMEQ score increased between T0 (median = 8.0 [IQR = 7.0, 11.0]) and T1 (median = 13.5 [IQR = 9.3, 15.0], p-value = 0.006), the SOT was advanced between T0 (median = 00:55 [IQR = 00:25, 01:39] and T1 (median = 00:09 [IQR = 23:41, 01:04], p-value = 0.039), the sleep efficiency and total sleep time increased (T0: median = 84.4 [IQR = 81.3, 89.4]; T1 (median = 90.3 [IQR = 85.5, 92.9] %, p-value = 0.01, and T0: median = 7.20 [IQR = 6.15, 8.15]; T1: median = 7.7 [IQR = 7.0, 9.3] hours, p-value = 0.04, respectively). These results indicate that in BD with comorbid DSWPD, the self-reported chronotype, the sleep onset time, and sleep efficiency and duration were modified after a personalized treatment with exo-MEL, suggesting its potential efficacy in improving sleep patterns in BD. The absence of proper control groups and of treatment randomization constitute limitations of our study and further randomized controlled trials are required to confirm our results.
本研究评估了外源性褪黑素(exo-MEL)对双相情感障碍(BD)和睡眠时相延迟障碍(DSWPD)患者睡眠和昼夜节律参数的影响。评估了 83 名 BD 病情稳定的患者(平均年龄 45.13 ± 13.68,男性占 56%)的睡眠时型(简化睡眠时型问卷[rMEQ])、睡眠质量(匹兹堡睡眠质量指数)、睡眠和昼夜节律参数(活动记录仪监测)。符合 DSWPD 标准的患者(n=25)接受 exo-MEL 2mg 治疗,在基线时根据活动记录仪确定的睡眠起始时间(SOT)提前约 4 小时给药,治疗持续 3 个月。使用配对 Wilcoxon 检验比较基线(T0)和 exo-MEL 治疗后(T1)的睡眠和昼夜节律参数。在完成治疗的患者(n=19)中,rMEQ 评分在 T0(中位数 8.0[IQR 7.0,11.0])和 T1(中位数 13.5[IQR 9.3,15.0])之间增加(p 值=0.006),SOT 在 T0(中位数 00:55[IQR 00:25,01:39])和 T1(中位数 00:09[IQR 23:41,01:04])之间提前(p 值=0.039),睡眠效率和总睡眠时间增加(T0:中位数 84.4[IQR 81.3,89.4];T1:中位数 90.3[IQR 85.5,92.9]%,p 值=0.01,T0:中位数 7.20[IQR 6.15,8.15];T1:中位数 7.7[IQR 7.0,9.3]小时,p 值=0.04)。这些结果表明,在伴有共病 DSWPD 的 BD 中,经过外源性褪黑素的个体化治疗后,自我报告的睡眠时型、睡眠起始时间以及睡眠效率和持续时间发生了改变,提示其在改善 BD 睡眠模式方面可能具有潜在疗效。本研究的局限性在于缺乏适当的对照组和治疗随机分组,需要进一步的随机对照试验来证实我们的结果。