Saint Martin Magali, Labeix Pierre, Garet Martin, Thomas Thierry, Barthélémy Jean-Claude, Collet Philippe, Roche Frédéric, Sforza Emilia
Service de Physiologie Clinique et de l'Exercice, CHU Nord, Saint-Etienne, Faculté de Médecine Jacques Lisfranc, PRES de Lyon, Université Jean Monnet, Saint-Etienne, France.
Service de Neurologie, réhabilitation cognitive, centre Hélio Marin, Hyères, France.
J Clin Sleep Med. 2016 Nov 15;12(11):1461-1469. doi: 10.5664/jcsm.6266.
Clinical and epidemiological studies suggest a relation between bone mineral density (BMD) and self-assessment of sleep with an effect on bone formation and osteoporosis (OS) risk in short and long sleepers. This study explores this association in a large sample of older subjects.
We examined 500 participants without insomnia complaints aged 65.7 ± 0.8 y. Each participant had a full evaluation including anthropometric measurement, clinical examination and measurements of BMD at the lumbar spine and femoral sites by dual-energy X-ray absorptiometry. The daily energy expenditure (DEE) was measured by the Population Physical Activity Questionnaire. Sleep duration and quality were evaluated by the Pittsburgh Sleep Quality Index. The subjects were stratified into three groups according to sleep duration, i.e., short (< 6 h), normal (6-8 h), and long (≥ 8 h) sleepers.
Osteopenia was found in 40% of the subjects at the femoral level and 43% at the vertebral level. The prevalence of OS was lower both at femoral (8%) and vertebral (12%) levels. Short, normal, and long sleepers accounted for 29%, 40%, and 31% of subjects, respectively. After adjustments for metabolic, anthropometric, and DEE, multinomial logistic regression analysis indicated that long sleepers were more likely to have femoral neck OS with a slight effect of DEE at vertebral spine.
In a sample of older subjects, self-reported long sleep was the best predictor of OS risk at the femoral level. This finding suggests an association between OS and self-reported sleep duration in older subjects.
NCT 00759304 and NCT 00766584.
临床和流行病学研究表明,骨密度(BMD)与睡眠自我评估之间存在关联,对短期和长期睡眠者的骨形成和骨质疏松症(OS)风险有影响。本研究在大量老年受试者样本中探讨这种关联。
我们检查了500名年龄为65.7±0.8岁且无失眠主诉的参与者。每位参与者都进行了全面评估,包括人体测量、临床检查以及通过双能X线吸收法测量腰椎和股骨部位的骨密度。通过人群身体活动问卷测量每日能量消耗(DEE)。通过匹兹堡睡眠质量指数评估睡眠时间和质量。根据睡眠时间将受试者分为三组,即短睡眠者(<6小时)、正常睡眠者(6 - 8小时)和长睡眠者(≥8小时)。
在股骨水平,40%的受试者存在骨量减少,在椎体水平为43%。OS在股骨(8%)和椎体(12%)水平的患病率均较低。短睡眠者、正常睡眠者和长睡眠者分别占受试者的29%、40%和31%。在对代谢、人体测量和DEE进行调整后,多项逻辑回归分析表明,长睡眠者更有可能患有股骨颈OS,DEE对脊柱有轻微影响。
在老年受试者样本中,自我报告的长睡眠是股骨水平OS风险的最佳预测指标。这一发现表明老年受试者的OS与自我报告的睡眠时间之间存在关联。
NCT 00759304和NCT 00766584。