Thomaz Tania G, McBenedict Billy, Meireles Dennys K, Farias Giovanna F, Almeida Luiz C, de Almeida Leitão Marina C, Hauwanga Wilhelmina N, Lima Pessôa Bruno, do Nascimento Maria Isabel
Physiology and Pharmacology, Fluminense Federal University, Niterói, BRA.
Neurosurgery, Fluminense Federal University, Niterói, BRA.
Cureus. 2024 Dec 31;16(12):e76692. doi: 10.7759/cureus.76692. eCollection 2024 Dec.
Narcolepsy is a rare, chronic neurological disorder characterized by excessive daytime sleepiness (EDS). Narcolepsy type 1 is probably caused by an autoimmune-mediated loss of orexin-producing neurons. Type 2 patients retain the physiological functioning of orexigenic neurons. The basis for treating narcolepsy type 1 with orexin-A is that if narcolepsy develops because of a loss of orexigenic neurons, then administering orexin should be able to eliminate, reduce, or prevent the impact of this loss. The aim of this review was to capture and analyze studies to elucidate the efficacy of orexin-A in the treatment of narcolepsy type 1 in humans. The search strategy included the following descriptors: "narcolepsy," "orexin," and "treatment," with filters for randomized clinical trials (RCT) and human studies. A total of 70 publications were retrieved from the databases. Duplicate records were removed before screening (n = 13), and 54 were then excluded for the following reasons: off-topic (n = 18), reviews (n = 14), use of a different intervention other than orexin (n = 14), non-human studies (n = 4), out-of-population selection criteria (n = 2), and case report (n = 2). Thus, the studies included in the review were three. Treatment of narcolepsy with orexin decreases the number of wake-REM (rapid eye movement) transitions and total time of REM sleep, although it does not increase wake time. The failure of orexin to alleviate daytime sleepiness suggests that orexin deficiency is not the only factor involved in the pathophysiology of type I narcolepsy.
发作性睡病是一种罕见的慢性神经疾病,其特征为日间过度嗜睡(EDS)。1型发作性睡病可能是由自身免疫介导的产生食欲素的神经元缺失所致。2型患者保留了促食欲神经元的生理功能。用食欲素-A治疗1型发作性睡病的依据是,如果发作性睡病是由于促食欲神经元缺失而发生的,那么给予食欲素应该能够消除、减少或预防这种缺失的影响。本综述的目的是收集和分析相关研究,以阐明食欲素-A治疗人类1型发作性睡病的疗效。检索策略包括以下描述词:“发作性睡病”“食欲素”和“治疗”,并对随机临床试验(RCT)和人体研究进行筛选。从数据库中总共检索到70篇出版物。在筛选前删除了重复记录(n = 13),然后因以下原因排除了54篇:主题不相关(n = 18)、综述(n = 14)、使用了除食欲素以外的其他干预措施(n = 14)、非人体研究(n = 4)、不符合人群选择标准(n = 2)以及病例报告(n = 2)。因此,本综述纳入的研究有三项。用食欲素治疗发作性睡病可减少觉醒-快速眼动(REM)转换次数和REM睡眠总时长,尽管它不会增加觉醒时间。食欲素未能缓解日间嗜睡表明,食欲素缺乏并非1型发作性睡病病理生理学中唯一涉及的因素。