Circadian Rhythm Disruption in Alzheimer's Disease: Mechanistic Insights, Diagnostic Implications, and Emerging Chronotherapeutic Strategies: A Narrative Review.

IF 3
Jasleen Kaur, Ritu Kainth, Roopal Mittal, Arshpreet Kaur, Ajay Singh Kushwah
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Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disease with a complex etiology that involves environmental, genetic, and metabolic components. Among these, circadian rhythm disruption has been seen critical but underexplored component in the pathogenesis of Alzheimer's disease. The suprachiasmatic nucleus (SCN), the central pacemaker of circadian regulation, coordinates all the physiological processes, such as sleep-wake cycles, metabolism, and neuroendocrine signalling. Tau-pathology, neuroinflammation, amyloid-β build-up, and cognitive decline in Alzheimer's disease are all becoming gradually linked to dysregulation of the system. A detailed review of literature was performed to study the role of circadian disruption in Alzheimer's disease. Alzheimer's disease-related circadian rhythm dysregulation is expressed through decreased melatonin secretion, sleep disturbances, and modified SCN signalling. Neuronal dysfunction could be caused by mutations in important clock genes (BMAL1, PER, CRY, and CLOCK). Sleep deprivation increases the buildup of amyloid-β and impairs glymphatic clearance. Also, tau pathology interrupts the circadian clock, further speeding up cognitive decline. Chronotherapies involving melatonin supplementation, light therapy, environment, and sleep hygiene provide promising effects in restoring circadian regulation and enhancing cognitive performance. According to the research from both experimental and clinical studies, there is a link between circadian rhythm abnormalities and Alzheimer's disease. Non-invasive biomarkers for the early identification of circadian nonalignment may aid in preventative measures. Researchers are currently looking into new treatment options that could slow down the progression of Alzheimer's disease. The integration of circadianbased therapies into individualised therapy paradigms for Alzheimer's disease patients should be the main focus of future research.

阿尔茨海默病的昼夜节律中断:机制见解,诊断意义和新兴的时间治疗策略:叙述性回顾。
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其病因复杂,涉及环境、遗传和代谢因素。其中,昼夜节律紊乱被认为是阿尔茨海默病发病机制的关键因素,但尚未得到充分研究。视交叉上核(SCN)是昼夜节律调节的中心起搏器,协调所有生理过程,如睡眠-觉醒周期、代谢和神经内分泌信号。tau病理、神经炎症、β淀粉样蛋白积累和阿尔茨海默病的认知能力下降都逐渐与该系统的失调联系在一起。详细回顾了文献,研究了昼夜节律紊乱在阿尔茨海默病中的作用。阿尔茨海默病相关的昼夜节律失调通过褪黑激素分泌减少、睡眠障碍和SCN信号改变来表达。神经元功能障碍可能由重要时钟基因(BMAL1、PER、CRY和clock)的突变引起。睡眠不足会增加β淀粉样蛋白的积累,损害淋巴细胞的清除。此外,tau蛋白病理会扰乱生物钟,进一步加速认知能力的下降。包括褪黑激素补充、光疗、环境和睡眠卫生在内的时间疗法在恢复昼夜节律调节和提高认知能力方面有很好的效果。根据实验和临床研究,昼夜节律异常与阿尔茨海默病之间存在联系。用于早期识别昼夜节律不一致的非侵入性生物标志物可能有助于预防措施。研究人员目前正在寻找新的治疗方案,以减缓阿尔茨海默病的进展。将基于昼夜节律的治疗整合到阿尔茨海默病患者的个体化治疗范例中应该是未来研究的主要重点。
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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