Jung Youngsin, St Louis Erik K
Center for Sleep Medicine and Departments of Neurology and Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Curr Treat Options Neurol. 2016 Nov;18(11):50. doi: 10.1007/s11940-016-0433-2.
REM sleep behavior disorder (RBD) is a common parasomnia disorder affecting between 1 and 7 % of community-dwelling adults, most frequently older adults. RBD is characterized by nocturnal complex motor behavior and polysomnographic REM sleep without atonia. RBD is strongly associated with synucleinopathy neurodegeneration. The approach to RBD management is currently twofold: symptomatic treatment to prevent injury and prognostic counseling and longitudinal follow-up surveillance for phenoconversion toward overt neurodegenerative disorders. The focus of this review is symptomatic treatment for injury prevention. Injury occurs in up to 55 % of patients prior to treatment, even when most behaviors seem to be infrequent or minor, so patients with RBD should be treated promptly following diagnosis to prevent injury risk. A sound evidence basis for symptomatic treatment of RBD remains lacking, and randomized controlled treatment trials are needed. Traditional therapeutic mainstays with relatively robust retrospective case series level evidence include melatonin and clonazepam, which appear to be equally effective, although melatonin is more tolerable. Melatonin also has one small randomized controlled crossover trial supporting its use for RBD treatment. Melatonin dosed 3-12 mg at bedtime should be considered as the first-line therapy, followed by clonazepam 0.25-2.0 mg at bedtime if initial melatonin is judged ineffective or intolerable. However, neither agent is likely to completely stop dream enactment behaviors, so choosing a moderate target dosage of melatonin 6 mg or clonazepam 0.5 mg, or the highest tolerable dosage that reduces attack frequency and avoids adverse effects from overtreatment, is currently the most reasonable strategy. Alternative second- and third-line therapies with anecdotal efficacy include temazepam, lorazepam, zolpidem, zopiclone, pramipexole, donepezil, ramelteon, agomelatine, cannabinoids, and sodium oxybate. A novel non-pharmacological approach is a bed alarm system, although this may be most useful in patients who also report sleep walking or a history of leaving their bed during dream enactment episodes. The benefit of hypnosis, especially in those with psychiatric RBD, also requires further study. RBD is an attractive target for future neuroprotective treatment trials to prevent evolution of overt parkinsonism or memory decline, but currently, there are no known effective treatments and future trials will be necessary to determine if RBD is an actionable time point in the evolution of overt synucleinopathy.
快速眼动睡眠行为障碍(RBD)是一种常见的异态睡眠障碍,影响着1%至7%的社区成年居民,其中老年人最为常见。RBD的特征是夜间出现复杂的运动行为以及多导睡眠图显示快速眼动睡眠时无肌张力缺失。RBD与α-突触核蛋白病神经退行性变密切相关。目前RBD的管理方法有两个方面:进行对症治疗以预防损伤,以及提供预后咨询并进行纵向随访监测,以观察是否会向明显的神经退行性疾病发生表型转换。本综述的重点是预防损伤的对症治疗。在治疗前,高达55%的患者会发生损伤,即使大多数行为似乎不频繁或较轻微,因此RBD患者在确诊后应立即接受治疗,以预防受伤风险。RBD对症治疗仍缺乏充分的证据基础,需要进行随机对照治疗试验。具有相对可靠的回顾性病例系列水平证据的传统治疗支柱药物包括褪黑素和氯硝西泮,它们似乎同样有效,不过褪黑素的耐受性更好。褪黑素还有一项小型随机对照交叉试验支持其用于RBD治疗。睡前服用3至12毫克褪黑素应被视为一线治疗方法,如果最初使用褪黑素被判定无效或无法耐受,则可在睡前服用0.25至2.0毫克氯硝西泮。然而,这两种药物都不太可能完全阻止梦境行为的发生,因此选择中等剂量的褪黑素6毫克或氯硝西泮0.5毫克,或者选择能降低发作频率且避免过度治疗产生不良反应的最高耐受剂量,目前是最合理的策略。具有轶事疗效的二线和三线替代疗法包括替马西泮、劳拉西泮、唑吡坦、佐匹克隆、普拉克索、多奈哌齐、雷美替胺、阿戈美拉汀、大麻素和γ-羟丁酸钠。一种新的非药物方法是床警报系统,不过这可能对那些还报告有梦游或在梦境行为发作期间有离床史的患者最为有用。催眠的益处,尤其是对患有精神性RBD的患者,也需要进一步研究。RBD是未来神经保护治疗试验预防明显帕金森病或记忆力下降进展的一个有吸引力的靶点,但目前尚无已知的有效治疗方法,未来的试验对于确定RBD是否是明显α-突触核蛋白病进展过程中的一个可干预时间点是必要的。