睡眠与前驱突触病。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Seminars in Neurology Pub Date : 2025-05-01 Epub Date: 2025-03-17 DOI:10.1055/a-2544-1482
Johnson D Pounders, Stuart J McCarter
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引用次数: 0

摘要

α-突触核蛋白病是一组复杂的进行性神经退行性疾病,其前驱期较长,睡眠功能障碍是其标志。前驱突触核蛋白病期间的睡眠障碍,主要是孤立的快速眼动(REM)睡眠行为障碍(iRBD)和白天嗜睡与最近提出的“身体优先”路易体病进展最相关。iRBD是公认最广泛的前驱α-突触核蛋白病,即使在没有认知或运动症状的情况下,iRBD患者在组织和生物体液中也表现出异常的α-突触核蛋白。更重要的是,iRBD患者近期发展为临床可诊断的症状性突触核蛋白病的风险较高。其他睡眠障碍,如嗜睡和昼夜节律障碍也发生在突触核蛋白病谱中,尽管它们的预后意义不如iRBD清楚。最后,孤立的无张力的快速眼动睡眠可能代表前驱突触核蛋白病的更早阶段,但需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep and Prodromal Synucleinopathies.

α-synucleinopathies are a complex group of progressive neurodegenerative disorders with an increasingly recognized long prodromal period, during which sleep dysfunction is a hallmark. Sleep disorders during the prodromal synucleinopathy period, primarily isolated rapid eye movement (REM) sleep behavior disorder (iRBD) and daytime hypersomnolence correlate best with the recently proposed "body-first" Lewy body disease progression. iRBD is the most widely recognized form of prodromal α-synucleinopathy, and patients with iRBD show abnormal α-synuclein in tissues and biofluids even in the absence of cognitive or motor symptoms. More importantly, individuals with iRBD have an elevated risk for near-term development of a clinically diagnosable symptomatic synucleinopathy. Other sleep disorders such as hypersomnia and circadian rhythm dysfunction also occur across the synucleinopathy spectrum, although their prognostic significance is less well understood than iRBD. Finally, isolated REM sleep without atonia may represent an even earlier stage of prodromal synucleinopathy, but further studies are needed.

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来源期刊
Seminars in Neurology
Seminars in Neurology 医学-临床神经学
CiteScore
4.60
自引率
3.70%
发文量
65
审稿时长
6-12 weeks
期刊介绍: Seminars in Neurology is a review journal on current trends in the evaluation, diagnosis, and treatment of neurological diseases. Areas of coverage include multiple sclerosis, central nervous system infections, muscular dystrophy, neuro-immunology, spinal disorders, strokes, epilepsy, motor neuron diseases, movement disorders, higher cortical function, neuro-genetics and neuro-ophthamology. Each issue is presented under the direction of an expert guest editor, and invited contributors focus on a single, high-interest clinical topic. Up-to-the-minute coverage of the latest information in the field makes this journal an invaluable resource for neurologists and residents.
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