Mirtazapine for chronic insomnia in older adults: a randomised double-blind placebo-controlled trial-the MIRAGE study.

IF 6 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Patrick V-Q Nguyen, Thien T Dang-Vu, Geneviève Forest, Sophie Desjardins, Marie-France Forget, Thien T Vu, Quoc D Nguyen, Edouard Kouassi, Philippe Desmarais
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引用次数: 0

Abstract

Background: Mirtazapine promotes sleep by blocking serotonin and histaminergic receptors and is often used off-label to treat chronic insomnia. However, its efficacy remains to be demonstrated in a clinical trial. The MIRAGE study aims to determine the efficacy and safety of mirtazapine in older patients with chronic insomnia.

Methods: This was a double-blind, randomised, placebo-controlled trial in a geriatric outpatient clinic of a teaching hospital. Adults aged 65 years and older with chronic insomnia were included. Sixty participants were randomised in a 1:1 ratio to receive mirtazapine 7.5 mg or a matching placebo for 28 days. The primary efficacy endpoint was the mean change in the Insomnia Severity Index (ISI) score from baseline to 28 days post-treatment. The primary safety endpoints included any adverse events reported during the clinical trial and all adverse events leading to premature discontinuation.

Results: Mirtazapine was superior to placebo on the primary outcome measure, subjective wake after sleep onset, total sleep time and sleep efficiency. After 28 days, the mean change in ISI score was significantly greater in the mirtazapine group (-6.5 [95%CI; -8.3 to -4.8]) compared to the placebo group (-2.9 [95%CI; -4.4 to -1.4]), with a p-value of 0.003. No participant experienced severe adverse events. A total of 6 participants in the mirtazapine group and 1 participant in the placebo group discontinued their treatment due to adverse events.

Conclusion: Mirtazapine reduces chronic insomnia symptoms in older people. However, its use may be limited by mild but clinically relevant adverse events. (clinicaltrials.gov NCT05247697).

Impact statement: This is the first randomised, double-blind, placebo-controlled trial on the efficacy and safety of Mirtazapine in older adults with chronic insomnia. Our findings show that a 28-day treatment with mirtazapine, compared to placebo, significantly reduces insomnia severity, as measured by the Insomnia Severity Index. Despite the current lack of robust evidence, mirtazapine is widely prescribed by clinicians to treat insomnia in older adults with chronic insomnia. Publishing our study will facilitate the broad dissemination of this critical information, helping clinicians more effectively treat their older patients.

米氮平治疗老年人慢性失眠:一项随机双盲安慰剂对照试验- MIRAGE研究。
背景:米氮平通过阻断5 -羟色胺和组胺能受体促进睡眠,常用于治疗慢性失眠。然而,其有效性仍有待临床试验证明。MIRAGE研究旨在确定米氮平对老年慢性失眠症患者的疗效和安全性。方法:这是一项双盲、随机、安慰剂对照试验,在一家教学医院的老年门诊进行。研究对象为65岁及以上患有慢性失眠症的成年人。60名参与者按1:1的比例随机分配,接受7.5 mg米氮平或匹配的安慰剂,持续28天。主要疗效终点是失眠严重指数(ISI)评分从基线到治疗后28天的平均变化。主要安全终点包括临床试验期间报告的任何不良事件和所有导致过早停药的不良事件。结果:米氮平在主要结局指标、睡眠后主观清醒、总睡眠时间和睡眠效率上优于安慰剂。28天后,米氮平组ISI评分的平均变化显著大于对照组(-6.5 [95%CI;-8.3至-4.8]),与安慰剂组相比(-2.9 [95%CI;-4.4 ~ -1.4]), p值为0.003。没有参与者出现严重的不良事件。米氮平组共有6名参与者和安慰剂组1名参与者因不良事件停止治疗。结论:米氮平可减轻老年人慢性失眠症状。然而,它的使用可能受到轻微但临床相关的不良事件的限制。(clinicaltrials.gov NCT05247697)。影响声明:这是首个关于米氮平治疗老年慢性失眠症疗效和安全性的随机、双盲、安慰剂对照试验。我们的研究结果表明,与安慰剂相比,使用米氮平治疗28天可以显著降低失眠的严重程度,这是由失眠严重程度指数衡量的。尽管目前缺乏强有力的证据,米氮平被临床医生广泛用于治疗老年人慢性失眠症。发表我们的研究将促进这一关键信息的广泛传播,帮助临床医生更有效地治疗老年患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Age and ageing
Age and ageing 医学-老年医学
CiteScore
9.20
自引率
6.00%
发文量
796
审稿时长
4-8 weeks
期刊介绍: Age and Ageing is an international journal publishing refereed original articles and commissioned reviews on geriatric medicine and gerontology. Its range includes research on ageing and clinical, epidemiological, and psychological aspects of later life.
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