Bukowska-Damska Agnieszka, Reszka Edyta, Kaluzny Pawel, Wieczorek Edyta, Przybek Monika, Zienolddiny Shanbeh, Peplonska Beata
a Department of Environmental Epidemiology , Nofer Institute of Occupational Medicine , Lodz , Poland.
b Department of Molecular Genetics and Epigenetics , Nofer Institute of Occupational Medicine , Lodz , Poland.
Chronobiol Int. 2018 Jan;35(1):122-131. doi: 10.1080/07420528.2017.1376219. Epub 2017 Nov 16.
Chronic sleep restriction may affect metabolism, hormone secretion patterns and inflammatory responses. Limited reports suggest also epigenetic effects, such as changes in DNA methylation profiles. The study aims to assess the potential association between poor sleep quality or sleep duration and the levels of 5-methylcytosine in the promoter regions of selected tumor suppressor genes. A cross-sectional study was conducted on 710 nurses and midwives aged 40-60 years. Data from interviews regarding sleep habits and potential confounders were used. The methylation status of tumor suppressor genes was determined via qMSP reactions using DNA samples derived from leucocytes. No significant findings were observed in the total study population or in the two subgroups of women stratified by the current system of work. A borderline significance association was observed between a shorter duration of sleep and an increased methylation level in CDKN2A among day working nurses and midwives. Further studies are warranted to explore this under-investigated topic.
长期睡眠受限可能会影响新陈代谢、激素分泌模式和炎症反应。有限的报告也表明存在表观遗传效应,如DNA甲基化谱的变化。本研究旨在评估睡眠质量差或睡眠时间与所选肿瘤抑制基因启动子区域5-甲基胞嘧啶水平之间的潜在关联。对710名年龄在40至60岁之间的护士和助产士进行了一项横断面研究。使用了关于睡眠习惯和潜在混杂因素的访谈数据。通过使用来自白细胞的DNA样本进行qMSP反应来确定肿瘤抑制基因的甲基化状态。在整个研究人群或按当前工作系统分层的两个女性亚组中均未观察到显著结果。在日间工作的护士和助产士中,观察到睡眠时间较短与CDKN2A甲基化水平升高之间存在临界显著关联。有必要进行进一步研究以探索这个研究不足的主题。