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米氮平可诱发年轻健康男性睡眠时周期性肢体运动。

Mirtazapine provokes periodic leg movements during sleep in young healthy men.

机构信息

Max Planck Institute of Psychiatry, Munich, Germany.

出版信息

Sleep. 2013 May 1;36(5):661-9. doi: 10.5665/sleep.2622.

Abstract

STUDY OBJECTIVES

Recent evidence suggests that certain antidepressants are associated with an increase of periodic leg movements (PLMS) that may disturb sleep. So far, this has been shown in patients clinically treated for depression and in cross-sectional studies for various substances, but not mirtazapine. It is unclear whether antidepressants induce the new onset of PLMS or only increase preexisting PLMS, and whether this is a general property of the antidepressant or only seen in depressed patients. We report here the effect of mirtazapine on PLMS in young healthy men.

DESIGN

Open-labeled clinical trial (NCT00878540) including a 3-week preparatory phase with standardized food, physical activity, and sleep-wake behavior, and a 10-day experimental inpatient phase with an adaptation day, 2 baseline days, and 7 days with mirtazapine.

SETTING

Research institute.

PARTICIPANTS

Twelve healthy young (20-25 years) men.

INTERVENTIONS

Seven days of nightly intake (22:00) of 30 mg mirtazapine.

MEASUREMENTS AND RESULTS

Sleep was recorded on 2 drug-free baseline nights, the first 2 drug nights, and the last 2 drug nights. Eight of the 12 subjects showed increased PLMS after the first dose of mirtazapine. Frequency of PLMS was highest on the first drug night and attenuated over the course of the next 6 days. Three subjects reported transient restless legs symptoms.

CONCLUSIONS

Mirtazapine provoked PLMS in 67% of young healthy males. The effect was most pronounced in the first days. The possible role of serotonergic, noradrenergic and histaminergic mechanisms in mirtazapine-induced PLMS is discussed.

摘要

研究目的

最近的证据表明,某些抗抑郁药与周期性腿部运动(PLMS)的增加有关,这可能会干扰睡眠。到目前为止,这在接受临床抑郁症治疗的患者和各种物质的横断面研究中已经得到证实,但米氮平除外。尚不清楚抗抑郁药是引起 PLMS 的新发病还是仅增加了先前存在的 PLMS,以及这是否是抗抑郁药的普遍特性,还是仅在抑郁症患者中可见。我们在此报告米氮平对年轻健康男性 PLMS 的影响。

设计

开放性临床试验(NCT00878540),包括为期 3 周的预备阶段,期间进行标准化的饮食、身体活动和睡眠-觉醒行为,以及为期 10 天的实验住院阶段,包括适应日、2 个基线日和 7 天的米氮平治疗期。

地点

研究所。

参与者

12 名健康的年轻男性(20-25 岁)。

干预措施

每晚 22:00 服用 30 mg 米氮平,共 7 天。

测量和结果

在 2 个无药物基线夜间、第 1 个和第 2 个药物夜间以及最后 2 个药物夜间记录睡眠。在米氮平的第 1 次给药后,有 8 名受试者出现 PLMS 增加。PLMS 的频率在第 1 个药物夜间最高,并在接下来的 6 天内逐渐减弱。3 名受试者报告短暂的不安腿症状。

结论

米氮平引起 67%的年轻健康男性出现 PLMS。该作用在最初几天最为明显。讨论了米氮平引起的 PLMS 可能涉及 5-羟色胺能、去甲肾上腺素能和组胺能机制。

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