阿尔茨海默病的昼夜节律中断和睡眠障碍:机制见解和治疗潜力。

IF 0.6
Neuro endocrinology letters Pub Date : 2025-09-02
Kechen Liu
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引用次数: 0

摘要

阿尔茨海默病(AD)是世界范围内痴呆症的主要原因,其严重的认知和行为障碍使个人及其家庭遭受重创。队列水平的研究结果表明,睡眠和昼夜节律紊乱(SCRD)在阿尔茨海默病中具有更广泛的人群水平的影响,并强调了早期干预的必要性,强调了及时行动的重要性。然而,其机制尚不清楚。SCRD损害淋巴系统,该系统在慢波睡眠期间负责清除淀粉样蛋白-β和tau等神经毒性蛋白,加速神经变性。此外,SCRD通过破坏免疫反应的昼夜节律调节来加剧神经炎症,主要是通过调节小胶质细胞活性和促炎细胞因子的释放,从而进一步促进神经元损伤。本文综述了目前对AD中SCRD的认识,概述了机制联系,动物模型证据,针对AD中SCRD的新兴治疗方法,以及临床前研究中出现的有希望的新药物靶点。昼夜节律调节可能是治疗AD的一种新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circadian Rhythm Disruption and Sleep Disorders in Alzheimer's Disease: Mechanistic Insights and Therapeutic Potentials.

Alzheimer's Disease (AD) is the leading cause of dementia worldwide, with significant cognitive and behavioural impairments that devastate individuals and their families. Cohort-level findings, demonstrate the broader population-level implications of Sleep and Circadian Rhythm Disruption (SCRD) in AD and underscore the need for early interventions, emphasizing the importance of timely action. However, the mechanism remains unclear. SCRD impairs the glymphatic system, which is responsible for the clearance of neurotoxic proteins such as amyloid-β and tau during slow-wave sleep, accelerating neurodegeneration. Moreover, SCRD exacerbates neuroinflammation by disrupting the circadian regulation of immune responses, mainly through the dysregulation of microglial activity and pro-inflammatory cytokine release, which further promotes neuronal damage. This review summarizes the current understanding of SCRD in AD, outlining the mechanistic links, evidence from animal models, and emerging treatments targeting SCRD in AD, as well as promising new drug targets emerging from preclinical studies. Circadian modulation may represent a novel therapeutic avenue for AD.

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