Irregular sleep-wake rhythm disorder: From the pathophysiologic perspective to the treatment.

Q2 Medicine
Aleksandar Videnovic, Alice Cai
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引用次数: 0

Abstract

Irregular sleep-wake rhythm disorder (ISWRD) is an intrinsic circadian rhythm disorder caused by loss of the brain's circadian regulation, through changes of the input and/or output to the suprachiasmatic nucleus (SCN), or of the SCN itself. Although there are limited prevalence data for this rare disease, ISWRD is associated with neurodegenerative disorders, including the Alzheimer disease (AD) and the Parkinson disease (PD), which will become increasingly prevalent in an aging population. It additionally presents in childhood developmental disorders, psychiatric disorders, and traumatic brain injury (TBI). Patients present with unpredictable, short sleep periods over a 24-h period, with significant day-to-day and weekly variability. Symptoms manifest as insomnia and excessive daytime sleepiness. Sleep logs and actigraphy monitoring capture rest-activity patterns required for diagnosis. Treatment aims to enhance external circadian cues through timed light therapy, behavioral activity regimens, and melatonin, but efficacy remains quite limited. Pathophysiology of ISWRD in association with various diseases and their specific management are discussed. There is a need for further investigation of disease pathophysiology, development of widely applicable tools for diagnosis, and development of treatments.

睡眠-觉醒节律失调:从病理生理学角度看治疗。
不规则睡眠-觉醒节律障碍(ISWRD)是一种内在的昼夜节律障碍,由大脑的昼夜节律调节丧失引起,通过改变输入和/或输出到视交叉上核(SCN)或SCN本身。尽管这种罕见疾病的患病率数据有限,但ISWRD与神经退行性疾病有关,包括阿尔茨海默病(AD)和帕金森病(PD),这两种疾病将在老龄化人口中变得越来越普遍。它还出现在儿童发育障碍、精神障碍和创伤性脑损伤(TBI)中。患者在24小时内出现不可预测的短睡眠时间,并且每天和每周都有显著的可变性。症状表现为失眠和白天过度嗜睡。睡眠日志和活动记录仪监测捕捉到诊断所需的休息-活动模式。治疗的目的是通过定时光疗、行为活动方案和褪黑激素来增强外部昼夜节律线索,但疗效仍然相当有限。本文讨论了ISWRD与多种疾病相关的病理生理机制及其具体治疗方法。有必要进一步研究疾病的病理生理学,开发广泛适用的诊断工具,并开发治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Handbook of clinical neurology
Handbook of clinical neurology Medicine-Neurology (clinical)
CiteScore
4.10
自引率
0.00%
发文量
302
期刊介绍: The Handbook of Clinical Neurology (HCN) was originally conceived and edited by Pierre Vinken and George Bruyn as a prestigious, multivolume reference work that would cover all the disorders encountered by clinicians and researchers engaged in neurology and allied fields. The first series of the Handbook (Volumes 1-44) was published between 1968 and 1982 and was followed by a second series (Volumes 45-78), guided by the same editors, which concluded in 2002. By that time, the Handbook had come to represent one of the largest scientific works ever published. In 2002, Professors Michael J. Aminoff, François Boller, and Dick F. Swaab took on the responsibility of supervising the third (current) series, the first volumes of which published in 2003. They have designed this series to encompass both clinical neurology and also the basic and clinical neurosciences that are its underpinning. Given the enormity and complexity of the accumulating literature, it is almost impossible to keep abreast of developments in the field, thus providing the raison d''être for the series. The series will thus appeal to clinicians and investigators alike, providing to each an added dimension. Now, more than 140 volumes after it began, the Handbook of Clinical Neurology series has an unparalleled reputation for providing the latest information on fundamental research on the operation of the nervous system in health and disease, comprehensive clinical information on neurological and related disorders, and up-to-date treatment protocols.
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