Association between sleep duration and osteoporosis risk in middle-aged and elderly women: A systematic review and meta-analysis of observational studies

医学 骨质疏松症 荟萃分析 优势比 队列研究 前瞻性队列研究 观察研究 睡眠(系统调用) 人口 相对风险 队列 内科学 置信区间 环境卫生 计算机科学 操作系统
作者
Sajjad Moradi,Sakineh Shab‐Bidar,Shahab Alizadeh,Kurosh Djafarian
出处
期刊:Metabolism-clinical and Experimental [Elsevier]
卷期号:69: 199-206 被引量:72
标识
DOI:10.1016/j.metabol.2017.01.027
摘要

Objective Increasing evidence has suggested an association between sleep duration and osteoporosis risk, although the results of previous studies have been inconsistent. To our knowledge, this is the first meta-analysis of the literature and quantitative estimates of the association between sleep duration and risk of osteoporosis in population-based studies of middle aged and elderly women. Methods Pertinent studies were identified by searching PubMed and EMBASE databases up to February 2016. Five out of six included studies were cross-sectional and one was a prospective cohort study. They included 72,326 participants from three different countries. We extracted 31,625 individuals in these studies for our meta-analysis. Results A pooled odds ratio analysis in women between 40 to 86 years indicated that there is an inverse relationship between sleep duration and osteoporosis (overall OR =1.07 95% CI: 1.00–1.15). The negative association of long sleep duration (8 h or more per day) with osteoporosis risk was observed in middle aged and elderly women (OR =1.22, 95% CI: 1.06–1.38) but not in women with short sleep duration (7 h or less per day) (OR =0.98, 95% CI: 0.90–1.05). Conclusion This meta-analysis suggests that long sleep duration (8 h or more per day) may be associated with a higher risk of osteoporosis in middle-aged and elderly. Further prospective cohort studies with longer follow-up periods, valid instruments for measurement of sleep duration and dynamic sleep quality are warranted to support the possible relationship between sleep duration and osteoporosis risk in women.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
小李的李完成签到,获得积分10
刚刚
fangruofuyun完成签到,获得积分10
刚刚
科目三应助无奈的书琴采纳,获得10
刚刚
老唐老唐完成签到 ,获得积分10
2秒前
自觉的丹珍完成签到,获得积分10
2秒前
闪闪的金鱼完成签到 ,获得积分10
3秒前
3秒前
4秒前
大模型应助草莓大果汁采纳,获得10
5秒前
hjc完成签到 ,获得积分10
6秒前
科研通AI6.2应助Mortisssssssss采纳,获得10
6秒前
李明月完成签到,获得积分10
7秒前
123完成签到,获得积分10
7秒前
开朗的千雁完成签到 ,获得积分10
7秒前
8秒前
稳重墨镜发布了新的文献求助10
9秒前
10秒前
追寻澜完成签到 ,获得积分10
10秒前
Sxq完成签到,获得积分10
10秒前
11秒前
李爱国应助康康采纳,获得10
11秒前
hotmail发布了新的文献求助10
12秒前
小田儿发布了新的文献求助10
13秒前
15秒前
15秒前
爆米花应助lllkate采纳,获得10
16秒前
彭于晏应助Clara6208采纳,获得10
17秒前
Smithjiang发布了新的文献求助10
19秒前
19秒前
19秒前
gwfew发布了新的文献求助10
20秒前
何必在乎发布了新的文献求助10
24秒前
不喝蒙牛发布了新的文献求助10
25秒前
空白完成签到 ,获得积分10
26秒前
空空完成签到,获得积分10
26秒前
28秒前
WenHao发布了新的文献求助10
28秒前
29秒前
善学以致用应助唐唐采纳,获得10
30秒前
呆萌紊完成签到 ,获得积分10
30秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Modern Epidemiology, Fourth Edition 5000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Digital Twins of Advanced Materials Processing 2000
Propeller Design 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 化学工程 生物化学 物理 计算机科学 内科学 复合材料 催化作用 物理化学 光电子学 电极 冶金 细胞生物学 基因
热门帖子
关注 科研通微信公众号,转发送积分 6015269
求助须知:如何正确求助?哪些是违规求助? 7591856
关于积分的说明 16148330
捐赠科研通 5162928
什么是DOI,文献DOI怎么找? 2764236
邀请新用户注册赠送积分活动 1744789
关于科研通互助平台的介绍 1634673