Zhou Jiaojiao, Chen Xu, Xiao Le, Zhou Jingjing, Feng Lei, Wang Gang
The National Clinical Research Center for Mental Disorders and Beijing Key Laboratory of Mental Disorders, Beijing Anding Hospital, The Advanced Innovation Center for Human Brain Protection, Capital Medical University, Beijing, China.
Front Psychiatry. 2021 Nov 11;12:754921. doi: 10.3389/fpsyt.2021.754921. eCollection 2021.
Insomnia is a common clinical manifestation in patients with depression. Insomnia is not only a depression symptom but also an independent risk factor for recurrence. () is thought to have the potential to treat insomnia. This study aimed to examine the efficacy and safety of duloxetine with in improving sleep symptoms in patients with depression. This study was a single-center, randomized, double-blind, placebo-controlled study that recruited outpatients admitted to Beijing Anding hospital from January 2018 to January 2019. Major depressive disorder (MDD) with insomnia was diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) criteria and Mini-International Neuropsychiatric Interview (M.I.N.I.). Eligible subjects will be randomly assigned to two treatment groups in a 1:1 ratio, and receive treatment and follow-up of about 6 weeks of duloxetine plus or placebo, respectively. The severity of depression and insomnia was evaluated at baseline and at 1, 2, 4, and 6 weeks using the 17-item Hamilton Depression Scale (HAMD-17) and Athens Insomnia Scale (AIS). A total of 59 subjects were included in the study (31 in the placebo group and 28 in the group). 11 (18.6%) participants withdrew during the study period, 5 (17.9%) in the group, and 6 (19.3%) in the placebo group. Depressive and sleep symptoms in all patients reduced over time. We found that the total scores of AIS and its subscales decreased more in the placebo group compared to the group ( < 0.05). Secondary outcome revealed that there were no significant differences between the two groups in total HAMD-17 and its sleep factor scores ( > 0.05) at 1, 2, 4, and 6 weeks after treatment initiation. The incidences of adverse events were not significantly different between the two groups (all > 0.05). at the current dose and duration did not improve sleep symptoms in patients with depression, but it is safe with rare side effects.
失眠是抑郁症患者常见的临床表现。失眠不仅是一种抑郁症状,也是复发的独立危险因素。()被认为有治疗失眠的潜力。本研究旨在探讨度洛西汀联合(此处原文缺失信息)改善抑郁症患者睡眠症状的疗效和安全性。本研究为单中心、随机、双盲、安慰剂对照研究,招募了2018年1月至2019年1月在北京安定医院就诊的门诊患者。根据《精神疾病诊断与统计手册》(DSM-IV-TR)标准和迷你国际神经精神病学访谈(M.I.N.I.)诊断伴有失眠的重度抑郁症(MDD)。符合条件的受试者将按1:1的比例随机分配到两个治疗组,分别接受约6周的度洛西汀联合(此处原文缺失信息)或安慰剂治疗及随访。在基线以及治疗1、2、4和6周时,使用17项汉密尔顿抑郁量表(HAMD-17)和雅典失眠量表(AIS)评估抑郁和失眠的严重程度。本研究共纳入59名受试者(安慰剂组31名,(此处原文缺失信息)组28名)。11名(18.6%)参与者在研究期间退出,(此处原文缺失信息)组5名(17.9%),安慰剂组6名(19.3%)。所有患者的抑郁和睡眠症状随时间推移均有所减轻。我们发现,与(此处原文缺失信息)组相比,安慰剂组AIS及其各子量表的总分下降得更多(P<0.05)。次要结果显示,治疗开始后1、2、4和6周时,两组在HAMD-17总分及其睡眠因子评分方面无显著差异(P>0.05)。两组不良事件的发生率无显著差异(均P>0.05)。当前剂量和疗程的(此处原文缺失信息)并未改善抑郁症患者的睡眠症状,但安全性良好,副作用罕见。