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老年人血浆蛋白质组学特征与继发性睡眠之间的关联。

Associations between plasma proteomic signatures and secondary sleep in older adults.

作者信息

Madhawa Kaushalya, Svensson Thomas, Nt Hoang, Chung Ung-Il, Svensson Akiko Kishi

机构信息

Precision Health, Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.

Graduate School of Health Innovation, Kanagawa University of Human Services, Kawasaki-ku, Kawasaki-shi, Kanagawa, 210-0821, Japan.

出版信息

Geroscience. 2025 Apr 8. doi: 10.1007/s11357-025-01565-1.

DOI:10.1007/s11357-025-01565-1
PMID:40198463
Abstract

Sleep disturbances are prevalent among elderly populations and are linked to various health complications. Understanding the underlying biological mechanisms contributing to sleep disorders is crucial for developing targeted interventions. In this study, we measured 355 plasma proteins in an elderly Japanese cohort (n=77) using a high-throughput proteomic platform. Additionally, we collected over 25,000 person-days of physical activity and sleep behavior data from wrist-worn wearable devices, focusing on total sleep time (TST) across 24 h and daytime sleep. Fragmented sleep was observed as one of the most prevalent sleep disturbances in this population. In protein expression analysis, we identified 9 protein biomarkers associated with increased secondary sleep TST, defined as additional sleep episodes outside of the main sleep episode within 24 h. These findings may suggest disruptions in circadian rhythms or underlying health conditions. Functional analysis revealed that biological processes related to inflammation play a significant role in regulating sleep behavior. Further analysis showed an association of 12 proteins with daytime sleep and 5 proteins with afternoon sleep. Overall, this study identified inflammatory biomarkers and biological processes associated with sleep behavior in the elderly, presenting promising opportunities for developing diagnostic tools and targeted clinical interventions.

摘要

睡眠障碍在老年人群中普遍存在,且与各种健康并发症相关。了解导致睡眠障碍的潜在生物学机制对于制定针对性干预措施至关重要。在本研究中,我们使用高通量蛋白质组学平台对一组日本老年人群(n = 77)的355种血浆蛋白进行了测量。此外,我们从腕戴式可穿戴设备收集了超过25000人日的身体活动和睡眠行为数据,重点关注24小时内的总睡眠时间(TST)和日间睡眠。片段化睡眠被观察到是该人群中最普遍的睡眠障碍之一。在蛋白质表达分析中,我们鉴定出9种与继发性睡眠TST增加相关的蛋白质生物标志物,继发性睡眠TST定义为24小时内主要睡眠时段之外的额外睡眠时段。这些发现可能表明昼夜节律或潜在健康状况受到干扰。功能分析显示,与炎症相关的生物学过程在调节睡眠行为中起重要作用。进一步分析表明,12种蛋白质与日间睡眠相关,5种蛋白质与午后睡眠相关。总体而言,本研究确定了与老年人睡眠行为相关的炎症生物标志物和生物学过程,为开发诊断工具和针对性临床干预提供了有前景的机会。

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