Stanford University School of Medicine, USA.
Expert Opin Emerg Drugs. 2010 Mar;15(1):139-58. doi: 10.1517/14728210903559852.
Narcolepsy is a chronic sleep disorder, characterized by excessive daytime sleepiness (EDS), cataplexy, hypnagogic hallucinations, sleep paralysis and nocturnal sleep disruption. Non-pharmacological treatments (i.e., behavioral modification) are often helpful for the clinical management of narcoleptic patients. As these symptoms are often disabling, most patients need life-long treatments. Over 90% of diagnosed narcoleptic patients are currently prescribed medications to control their symptoms; however, available treatments are merely symptomatic.
This review presents a description of the clinical symptoms of narcolepsy, followed by a discussion of the state-of-the-art knowledge regarding the disorder and related emerging treatments. In preparing this review, an extensive literature search was conducted using Pubmed. Only selected references from 1970 to 2008 are cited.
This review focuses on emerging treatments for human narcolepsy, and the reader will gain significant knowledge of current and future treatment for this and related disorders. Traditionally, amphetamine-like stimulants (i.e., dopaminergic release enhancers) have been used for clinical management to improve EDS, and tricyclic antidepressants have been used as anticataplectics. However, treatments have recently evolved which utilize better tolerated compounds, such as modafinil (for EDS) and adrenergic/serotonergic selective reuptake inhibitors (as anticataplectics). In addition, night time administration of a short-acting sedative, gamma-hydroxybutyrate, has been used for the treatment for EDS and cataplexy. As a large majority of human narcolepsy is hypocretin peptide deficient, hypocretin replacement therapy may also be a new therapeutic option; yet, this option is still unavailable. In addition to the hypocretin-based therapy, a series of new treatments are currently being tested in animal and/or humans models. These potential options include novel stimulant and anticataplectic drugs as well as immunotherapy, based on current knowledge of the pathophysiology of narcolepsy with cataplexy.
We expect that more pathophysiology-based treatments, capable of curing and/or preventing narcolepsy and related diseases, will be available in near future. As cases of EDS, associated with other neurological conditions (i.e., symptomatic narcolepsy or narcolepsy due to medical conditions), are often linked with hypocretin deficiency, these novel therapeutic options may also be applied to treatment of these disabling conditions.
发作性睡病是一种慢性睡眠障碍,其特征是白天过度嗜睡(EDS),猝倒,催眠幻觉,睡眠瘫痪和夜间睡眠中断。非药物治疗(即行为修正)往往有助于临床管理发作性睡病患者。由于这些症状常常使人丧失能力,大多数患者需要终身治疗。超过 90%的诊断为发作性睡病的患者目前被开处药物来控制他们的症状;然而,现有的治疗方法仅仅是对症治疗。
本文介绍了发作性睡病的临床症状描述,接着讨论了该疾病的最新知识状态和相关新兴治疗方法。在准备这篇综述时,使用 Pubmed 进行了广泛的文献检索。仅引用了 1970 年至 2008 年的精选参考文献。
这篇综述侧重于人类发作性睡病的新兴治疗方法,读者将获得有关这种疾病和相关疾病的当前和未来治疗的重要知识。传统上,安非他命样兴奋剂(即多巴胺释放增强剂)已被用于临床管理以改善 EDS,三环类抗抑郁药已被用作抗猝倒药。然而,最近的治疗方法已经发展到利用耐受性更好的化合物,如莫达非尼(用于 EDS)和肾上腺素能/血清素选择性再摄取抑制剂(作为抗猝倒药)。此外,γ-羟基丁酸的短期作用镇静剂在夜间给药已用于治疗 EDS 和猝倒。由于大多数人类发作性睡病是下丘脑分泌素肽缺乏症,下丘脑分泌素替代疗法也可能是一种新的治疗选择;然而,这个选择还不可用。除了基于下丘脑分泌素的治疗之外,一系列新的治疗方法目前正在动物和/或人类模型中进行测试。这些潜在的选择包括新型兴奋剂和抗猝倒药物以及免疫疗法,基于发作性睡病伴猝倒的病理生理学的当前知识。
我们期望在不久的将来,能够有更多基于病理生理学的治疗方法,能够治愈和/或预防发作性睡病和相关疾病。由于与其他神经状况相关的 EDS 病例(即症状性发作性睡病或由于医疗条件引起的发作性睡病)常常与下丘脑分泌素缺乏有关,这些新的治疗选择也可能应用于这些使人丧失能力的病症的治疗。