Chronobiological disruptions: unravelling the interplay of shift work, circadian rhythms, and vascular health in the context of stroke risk.

IF 3.2 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Clinical and Experimental Medicine Pub Date : 2024-11-14 DOI:10.1007/s10238-024-01514-w
Xiaohong Li, Yanjin He, Dawu Wang, Mohammad Reza Momeni
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Abstract

Shift work, particularly night shifts, disrupts circadian rhythms and increases stroke risk. This manuscript explores the mechanisms connecting shift work with stroke, focusing on circadian rhythms, hypertension, and diabetes. The circadian system, controlled by different mechanisms including central and peripheral clock genes, suprachiasmatic nuclei (SCN), and pineal gland (through melatonin production), regulates body functions and responds to environmental signals. Disruptions in this system affect endothelial cells, leading to blood pressure issues. Type 2 diabetes mellitus (T2DM) is significantly associated with night shifts, with circadian disturbances affecting glucose metabolism, insulin sensitivity, and hormone regulation. The manuscript examines the relationship between melatonin, insulin, and glucose balance, highlighting pathways that link T2DM to stroke risk. Additionally, dyslipidemia, particularly reduced HDL-c levels, results from shift work and contributes to stroke development. High lipid levels cause oxidative stress, inflammation, and endothelial dysfunction, increasing cerebrovascular risks. The manuscript details the effects of dyslipidemia on brain functions, including disruptions in blood flow, blood-brain barrier integrity, and neural cell death. This comprehensive analysis emphasizes the complex interplay of circadian disruption, hypertension, diabetes, and dyslipidemia in increasing stroke risk among shift workers. Understanding these mechanisms is essential for developing targeted interventions to reduce stroke susceptibility and improve cerebrovascular health in this vulnerable population.

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时间生物学干扰:从中风风险的角度揭示轮班工作、昼夜节律和血管健康之间的相互作用。
轮班工作,尤其是夜班,会扰乱昼夜节律,增加中风风险。本手稿以昼夜节律、高血压和糖尿病为重点,探讨了轮班工作与中风的关联机制。昼夜节律系统由不同的机制控制,包括中枢和外周时钟基因、副上核(SCN)和松果体(通过分泌褪黑激素),调节身体功能并对环境信号做出反应。这一系统的紊乱会影响内皮细胞,导致血压问题。2 型糖尿病(T2DM)与夜班密切相关,昼夜节律紊乱会影响葡萄糖代谢、胰岛素敏感性和激素调节。手稿研究了褪黑激素、胰岛素和葡萄糖平衡之间的关系,强调了 T2DM 与中风风险之间的联系途径。此外,轮班工作导致血脂异常,尤其是高密度脂蛋白-c 水平降低,也是导致中风的原因之一。高血脂会导致氧化应激、炎症和内皮功能障碍,增加脑血管风险。手稿详细阐述了血脂异常对大脑功能的影响,包括血流紊乱、血脑屏障完整性和神经细胞死亡。这一全面分析强调了昼夜节律紊乱、高血压、糖尿病和血脂异常在增加倒班工人中风风险方面复杂的相互作用。了解这些机制对于制定有针对性的干预措施以降低中风易感性和改善这一弱势群体的脑血管健康至关重要。
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来源期刊
Clinical and Experimental Medicine
Clinical and Experimental Medicine 医学-医学:研究与实验
CiteScore
4.80
自引率
2.20%
发文量
159
审稿时长
2.5 months
期刊介绍: Clinical and Experimental Medicine (CEM) is a multidisciplinary journal that aims to be a forum of scientific excellence and information exchange in relation to the basic and clinical features of the following fields: hematology, onco-hematology, oncology, virology, immunology, and rheumatology. The journal publishes reviews and editorials, experimental and preclinical studies, translational research, prospectively designed clinical trials, and epidemiological studies. Papers containing new clinical or experimental data that are likely to contribute to changes in clinical practice or the way in which a disease is thought about will be given priority due to their immediate importance. Case reports will be accepted on an exceptional basis only, and their submission is discouraged. The major criteria for publication are clarity, scientific soundness, and advances in knowledge. In compliance with the overwhelmingly prevailing request by the international scientific community, and with respect for eco-compatibility issues, CEM is now published exclusively online.
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Chronobiological disruptions: unravelling the interplay of shift work, circadian rhythms, and vascular health in the context of stroke risk. Clinical characteristics and prognosis analysis of pseudomonas aeruginosa bloodstream infection in adults: a retrospective study. A systematic review and meta-analysis of the endothelial-immune candidate biomarker endoglin in rheumatic diseases. Analysis of METTL14 expression in pancreatic cancer and adjacent tissues and its prognostic value for patient outcomes. Tumor-immune hybrid cells evade the immune response and potentiate colorectal cancer metastasis through CTLA4.
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