Effect of Lemborexant on Daytime Functioning in Adults With Insomnia: Patient-Reported Outcomes From a Phase 3 Clinical Trial.

Q4 Medicine
Craig Chepke, Kimberly A Cote, Kate Pinner, Jane Yardley, Christie Lundwall, Margaret Moline
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引用次数: 0

Abstract

Objective: Insomnia and some insomnia treatments can impact an individual's daytime functioning. Here, we performed post hoc analyses of patient-reported outcomes from a phase 3 clinical trial to assess the impact of lemborexant (LEM), a dual orexin receptor antagonist, on daytime functioning.

Methods: Adults with insomnia were randomized 1:1:1 to receive placebo, LEM 5 mg (LEM5) or LEM 10 mg (LEM10) for 6 months. Treatment impact on subjects' perceptions of their insomnia symptoms and daytime functioning was assessed by the Insomnia Severity Index (ISI) and Fatigue Severity Scale (FSS) questionnaires. Safety assessments included monitoring of treatment emergent adverse events.

Results: Compared with placebo, LEM5 and LEM10 treatment significantly improved ISI Total Score (ISI-TS) (LEM5, P < .01; LEM10, P < .0001) and ISI Daytime Functioning Score (ISI-DFS) (LEM5, P < .05; LEM10, P < .01) at 1 month; these improvements were maintained at the end of 6 months (P < .0001 for LEM5 and LEM10, both scores). In separate analyses, baseline ISI-TS or ISI-DFS was used to classify subjects' symptom severity into 1 of 4 categories. At 1 and 6 months, greater proportions of subjects treated with LEM5 and LEM10 shifted to a category associated with less severe symptoms (P < .01 for all comparisons vs placebo). FSS score also improved with LEM treatment vs placebo as assessed at month 3; improvements were maintained at month 6 (P < .05). LEM5 and LEM10 treatment was well tolerated.

Conclusion: Improved insomnia symptoms with LEM treatment may translate into improved daytime functioning, suggesting LEM may be appropriate for adults experiencing daytime impairment with their nighttime symptoms.

Trial Registration: ClinicalTrials.gov identifier: NCT02952820.

Prim Care Companion CNS Disord 2025;27(1):24m03810.

Author affiliations are listed at the end of this article.

Lemborexant对成人失眠患者日间功能的影响:一项3期临床试验中患者报告的结果
目的:失眠和一些失眠治疗会影响一个人的白天功能。在这里,我们对患者报告的3期临床试验结果进行了事后分析,以评估双食欲素受体拮抗剂lemborexant (LEM)对白天功能的影响。方法:成人失眠症患者以1:1:1的比例随机分为安慰剂、LEM5 mg (LEM5)或LEM10 mg (LEM10),疗程6个月。通过失眠严重程度指数(ISI)和疲劳严重程度量表(FSS)问卷评估治疗对受试者失眠症状和日间功能的影响。安全性评估包括监测治疗中出现的不良事件。结果:与安慰剂相比,LEM5和LEM10治疗显著提高了ISI总分(ISI- ts) (LEM5, P < 0.01;LEM10, P < 0.0001)和ISI日间功能评分(ISI- dfs) (LEM5, P < 0.05;1个月时LEM10, P < 0.01);这些改善在6个月后保持不变(LEM5和LEM10的评分P < 0.0001)。在单独的分析中,使用基线ISI-TS或ISI-DFS将受试者的症状严重程度分为4类中的1类。在第1个月和第6个月,接受LEM5和LEM10治疗的受试者中,更大比例的受试者转移到症状较轻的类别(与安慰剂相比,所有比较的P < 0.01)。在第3个月时,与安慰剂相比,LEM治疗组的FSS评分也有所改善;改善在第6个月维持(P < 0.05)。LEM5和LEM10治疗耐受性良好。结论:LEM治疗失眠症状的改善可能转化为白天功能的改善,这表明LEM可能适用于有白天障碍和夜间症状的成年人。试验注册:ClinicalTrials.gov标识符:NCT02952820。中枢神经系统疾病诊治[j]; 2015;27(1):24m03810。本文末尾列出了作者所属单位。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
300
期刊介绍: Founded in 1998, The Primary Care Companion for CNS Disorders (ISSN 2155-7780), formerly The Primary Care Companion to The Journal of Clinical Psychiatry, is an international, peer-reviewed, online-only journal, and its articles are indexed by the National Library of Medicine. PCC seeks to advance the clinical expertise of primary care physicians and other health care professionals who treat patients with mental and neurologic illnesses. PCC publishes research from disciplines such as medicine, nursing, pharmacy, and psychology, especially as it pertains to integrated delivery systems and interdisciplinary collaboration. PCC focuses on providing information of direct clinical utility and giving a voice to clinician researchers. Practice-based research from individuals and groups with clinical expertise is particularly welcome. Pertinent manuscript types include: -Original research -Systematic reviews -Meta-analyses -Case reports and series -Commenting letters to the editor Articles published in PCC typically cover attention-deficit/hyperactivity disorder, depression, bipolar disorder, anxiety, addiction, sleep disorders, pain, Alzheimer’s disease, multiple sclerosis, and Parkinson’s disease.
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