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发作性睡病的近期获批及即将推出的治疗方法。

Recently Approved and Upcoming Treatments for Narcolepsy.

作者信息

Thorpy Michael J

机构信息

Sleep-Wake Disorders Center, Montefiore Medical Center, 111 East 210th Street, Bronx, NY, 10467-2509, USA.

出版信息

CNS Drugs. 2020 Jan;34(1):9-27. doi: 10.1007/s40263-019-00689-1.

Abstract

Narcolepsy is a chronic, disabling neurologic disorder characterised by excessive daytime sleepiness (EDS) and, in up to 60% of patients, cataplexy. Treatments for narcolepsy are aimed at improving wakefulness (e.g. modafinil, armodafinil, stimulants), reducing cataplexy attacks (e.g. sodium oxybate, venlafaxine), and treating the symptoms of disturbed nocturnal sleep, sleep paralysis and sleep-related hallucinations (e.g. sodium oxybate). In general, medications that increase the release, or inhibit the reuptake, of norepinephrine or dopamine have wake-promoting effects and are useful in managing EDS, whereas medications that inhibit serotonin or norepinephrine reuptake have anticataplectic effects. Modulation of γ-aminobutyric acid B (GABA) receptors or histamine H receptors (H3Rs) has effects on both EDS and cataplexy. Pitolisant, an H3R antagonist, and solriamfetol, a dopamine and norepinephrine reuptake inhibitor, are the most recently approved treatments for EDS associated with narcolepsy in the European Union (pitolisant) and the USA (pitolisant and solriamfetol). Several new agents are being developed and tested as potential treatments for EDS and cataplexy associated with narcolepsy; these agents include novel oxybate formulations (once-nightly [FT218]; low sodium [JZP-258]), a selective norepinephrine reuptake inhibitor (AXS-12), and a product combining modafinil and an astroglial connexin inhibitor (THN102). This review summarises the mechanisms of action, pharmacokinetics, efficacy, and safety/tolerability of recently approved and emerging treatments for narcolepsy.

摘要

发作性睡病是一种慢性致残性神经系统疾病,其特征为日间过度嗜睡(EDS),高达60%的患者伴有猝倒。发作性睡病的治疗旨在改善觉醒状态(如莫达非尼、阿莫达非尼、兴奋剂),减少猝倒发作(如羟丁酸钠、文拉法辛),并治疗夜间睡眠障碍、睡眠瘫痪和与睡眠相关幻觉的症状(如羟丁酸钠)。一般来说,增加去甲肾上腺素或多巴胺释放或抑制其再摄取的药物具有促醒作用,有助于治疗EDS,而抑制5-羟色胺或去甲肾上腺素再摄取的药物具有抗猝倒作用。调节γ-氨基丁酸B(GABA)受体或组胺H3受体(H3Rs)对EDS和猝倒均有影响。H3R拮抗剂匹托利生和多巴胺及去甲肾上腺素再摄取抑制剂索利那非是欧盟(匹托利生)和美国(匹托利生和索利那非)最近批准的用于治疗与发作性睡病相关的EDS的药物。几种新型药物正在研发和测试,作为发作性睡病相关EDS和猝倒的潜在治疗药物;这些药物包括新型羟丁酸钠制剂(每晚一次[FT218];低钠[JZP-258])、选择性去甲肾上腺素再摄取抑制剂(AXS-12),以及一种将莫达非尼和星形胶质连接蛋白抑制剂组合的产品(THN102)。本综述总结了最近批准的和正在出现的发作性睡病治疗药物的作用机制、药代动力学、疗效以及安全性/耐受性。

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