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本文引用的文献

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Bone Turnover Markers After Sleep Restriction and Circadian Disruption: A Mechanism for Sleep-Related Bone Loss in Humans.睡眠限制和昼夜节律紊乱后的骨转换标志物:人类睡眠相关性骨质流失的一种机制
J Clin Endocrinol Metab. 2017 Oct 1;102(10):3722-3730. doi: 10.1210/jc.2017-01147.
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Napping Characteristics and Restricted Participation in Valued Activities Among Older Adults.老年人小睡特征与参与重要活动受限
J Gerontol A Biol Sci Med Sci. 2018 Mar 2;73(3):367-373. doi: 10.1093/gerona/glx166.
3
Melatonin at pharmacological concentrations suppresses osteoclastogenesis via the attenuation of intracellular ROS.药理浓度的褪黑素通过抑制细胞内 ROS 来抑制破骨细胞的形成。
Osteoporos Int. 2017 Dec;28(12):3325-3337. doi: 10.1007/s00198-017-4127-8. Epub 2017 Sep 27.
4
Melatonin promotes osteoblast differentiation by regulating Osterix protein stability and expression.褪黑素通过调节成骨细胞特异性转录因子 2(Osterix)蛋白稳定性和表达促进成骨细胞分化。
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Suppression of Osteoclastogenesis by Melatonin: A Melatonin Receptor-Independent Action.褪黑素对破骨细胞生成的抑制作用:一种不依赖褪黑素受体的作用。
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Relationship between sleep parameters, insulin resistance and age-adjusted insulin like growth factor-1 score in non diabetic older patients.非糖尿病老年患者的睡眠参数、胰岛素抵抗与年龄校正后的胰岛素样生长因子-1评分之间的关系。
PLoS One. 2017 Apr 6;12(4):e0174876. doi: 10.1371/journal.pone.0174876. eCollection 2017.
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High Evening Cortisol Level Is Associated With Low TBS and Increased Prevalent Vertebral Fractures: OsteoLaus Study.夜间皮质醇水平高与 TBS 低和高发椎体骨折相关:OsteoLaus 研究。
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Association between sleep apnea and low bone mass in adults: a systematic review and meta-analysis.成年人睡眠呼吸暂停与低骨量的相关性:系统评价和荟萃分析。
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Napping and associated factors: a Japanese nationwide general population survey.午睡及相关因素:一项日本全国性普通人群调查。
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Is daytime napping associated with inflammation in adolescents?青少年白天小睡与炎症有关吗?
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日间小睡特征与老年泰国家庭妇女骨密度的关系:骨质疏松症病例对照研究。

The Association between Daytime Napping Characteristics and Bone Mineral Density in Elderly Thai Women without Osteoporosis.

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.

Division of Endocrinology, Diabetes and Metabolism, University of Illinois at Chicago, Chicago, IL, USA.

出版信息

Sci Rep. 2018 Jul 3;8(1):10016. doi: 10.1038/s41598-018-28260-w.

DOI:10.1038/s41598-018-28260-w
PMID:29968782
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6030206/
Abstract

Low bone mass is more prevalent with increasing age. Studies have found associations between sleep duration, sleep quality and obstructive sleep apnea and bone mineral density (BMD). However, less is known about the relationship between daytime napping and BMD. We aimed to investigate the association between daytime napping and BMD in elderly Thai women. Demographic data, lifestyle information and sleep characteristics were obtained by interviewing 387 elderly women. Weight and height were measured. Serum 25-hydroxyvitamin D [25(OH)D] was measured by radioimmunoassay. BMD was measured by dual-energy X-ray absorptiometry (DXA). Higher BMI and having type 2 diabetes (T2DM) were correlated with higher lumbar spine 2-4 (L2-4) BMD, while younger age, higher BMI and higher serum 25(OH)D level were correlated with higher femoral neck (FN) and total hip (TH) BMD. After adjusting for age, age at menopause, BMI, 25(OH)D level and T2DM, a higher frequency of weekly daytime napping was associated with lower FN and TH BMD but not at L2-4 BMD. Additionally, longer daytime napping duration was negatively associated with BMD at TH. In summary higher frequency and longer duration of daytime napping are associated with lower femoral BMD in elderly women. Mechanisms underlying these associations should be further explored.

摘要

骨量减少随着年龄的增长而更为普遍。研究发现,睡眠时间、睡眠质量与阻塞性睡眠呼吸暂停和骨矿物质密度(BMD)之间存在关联。然而,日间小睡与 BMD 之间的关系则知之甚少。我们旨在调查日间小睡与老年泰国女性 BMD 之间的关系。通过访谈 387 名老年女性获得人口统计学数据、生活方式信息和睡眠特征。测量体重和身高。通过放射免疫测定法测量血清 25-羟维生素 D [25(OH)D]。通过双能 X 射线吸收法(DXA)测量 BMD。更高的 BMI 和患有 2 型糖尿病(T2DM)与更高的腰椎 2-4(L2-4)BMD 相关,而年龄较小、更高的 BMI 和更高的血清 25(OH)D 水平与更高的股骨颈(FN)和全髋(TH)BMD 相关。在调整年龄、绝经年龄、BMI、25(OH)D 水平和 T2DM 后,每周日间小睡频率更高与 FN 和 TH BMD 降低相关,但与 L2-4 BMD 无关。此外,日间小睡时间延长与 TH 处的 BMD 呈负相关。综上所述,较高的日间小睡频率和较长的日间小睡持续时间与老年女性的股骨 BMD 降低相关。应进一步探讨这些关联的潜在机制。