New York Obesity Nutrition Research Center, Department of Medicine, Columbia University Medical Center, New York, NY, USA.
Institute of Human Nutrition, Columbia University Medical Center, New York, NY, USA.
Eur J Clin Nutr. 2019 Jul;72(Suppl 1):76-82. doi: 10.1038/s41430-018-0312-x.
Studies associate sleeping and eating late in the day with poor dietary quality and higher obesity risk but differences in sleep duration confound this association. We aimed to determine whether sleep and meal timing, independent of sleep duration, influenced food intake in healthy adults.
This was a controlled, 2 × 2 inpatient crossover study with normal (0000-0800 h) or late (0330-1130 h) sleep and normal (1, 5, 11, and 12.5 h after awakening) or late (4.5, 8.5, 14.5, and 16 h after awakening) meals. Food intake was controlled while blood samples were obtained for determination of appetite-regulating hormones on days 3-4. Self-selected food intake was assessed on day 5. Data were analyzed using linear mixed model analysis with sleep, meal, and sleep x meal interaction as dependent variables.
Five participants completed all phases (mean age 25.1 ± [SD] 3.9 y, body mass index 29.2 ± 2.7 kg/m). There was a significant sleep x meal interaction on energy intake (P = 0.035) and trends on fat and sodium intakes (P < 0.10). Overnight ghrelin concentrations were higher under normal sleep and meal conditions relative to late (P < 0.005) but lower when both were combined (P < 0.001). Overnight leptin concentrations were higher under normal meal conditions (P = 0.012). There was a significant sleep x meal interaction on ghrelin (P = 0.032) and glucagon-like peptide 1 (P = 0.041) concentrations, but not leptin (P = 0.83), in response to a test meal.
Our results suggest that alignment of sleep and meals may influence food choice and energy balance. Additional research is necessary to expand and confirm our findings.
研究表明,白天晚睡晚起与较差的饮食质量和更高的肥胖风险有关,但睡眠持续时间的差异使这种关联变得复杂。我们旨在确定睡眠和用餐时间是否会影响健康成年人的食物摄入,而与睡眠持续时间无关。
这是一项对照的、2×2 住院交叉研究,参与者的睡眠时间分别为正常(0000-0800 h)或延迟(0330-1130 h),用餐时间分别为正常(1、5、11 和 12.5 h 后醒来)或延迟(4.5、8.5、14.5 和 16 h 后醒来)。在第 3-4 天采集血液样本以确定食欲调节激素时,控制食物摄入量。在第 5 天评估自我选择的食物摄入量。使用线性混合模型分析,将睡眠、用餐和睡眠 x 用餐交互作用作为因变量进行数据分析。
共有 5 名参与者完成了所有阶段(平均年龄 25.1±3.9 岁,体重指数 29.2±2.7 kg/m)。能量摄入存在显著的睡眠 x 用餐交互作用(P=0.035),脂肪和钠摄入量也存在趋势(P<0.10)。与延迟睡眠和用餐条件相比,正常睡眠和用餐条件下 overnight ghrelin 浓度更高(P<0.005),但两者结合时浓度更低(P<0.001)。正常用餐条件下 overnight leptin 浓度更高(P=0.012)。ghrelin(P=0.032)和胰高血糖素样肽 1(P=0.041)浓度存在显著的睡眠 x 用餐交互作用,但 leptin 浓度没有(P=0.83),对测试餐的反应也是如此。
我们的结果表明,睡眠和用餐时间的一致可能会影响食物选择和能量平衡。需要进一步的研究来扩展和证实我们的发现。