Department of Epidemiology, Mailman School of Public Health, Columbia University Irving Medical Center, New York, NY, USA.
Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Ann Behav Med. 2023 Jan 2;57(1):93-97. doi: 10.1093/abm/kaac042.
The timing and regularity of eating patterns could play a role in systemic inflammation, as circadian clocks responsible for daily rhythms of inflammatory signaling are entrained by food intake.
To evaluate associations of intra-weekly and weekday-weekend differences in eating timing patterns with high-sensitivity C-reactive protein (hsCRP).
A community-based sample of 103 U.S. women from the American Heart Association Go Red for Women Strategically Focused Research Network completed a meal-timing questionnaire and provided a blood sample for measurement of hsCRP. Differences in weekday versus weekend eating start time, eating end time, and nightly fasting duration were calculated as eating jetlag metrics. Intra-weekly variability in eating timing patterns was defined by the standard deviation (SD) of these variables. Multivariable linear regression models were used to evaluate cross-sectional associations of eating timing variability metrics with hsCRP.
Each additional 30-min difference in weekday-weekend eating end time was related to 13% higher hsCRP (p = .023). Similarly, every 30-min increase in eating end time SD, reflecting greater variability in timing of last eating occasion, was associated with 29% higher hsCRP. Per 1-hr weekday-weekend difference in nightly fasting duration, there was a 45% elevation in hsCRP (p = .003). Every 30-min increase in nightly fasting duration SD, representing greater variability in span of the daily fasting/eating periods, was associated with 46% higher hsCRP.
Variable eating timing patterns were associated with higher hsCRP. Intervention studies are needed to determine whether stabilizing the timing of eating occasions may represent a novel strategy to reduce chronic inflammation.
饮食模式的时间和规律性可能在全身炎症中发挥作用,因为负责炎症信号日节律的生物钟会被食物摄入所调节。
评估每周内和工作日-周末差异的进食时间模式与高敏 C 反应蛋白(hsCRP)之间的相关性。
美国心脏协会 Go Red for Women 战略重点研究网络的 103 名美国女性参与了一项基于社区的研究,完成了一份饮食时间问卷,并提供了一份血液样本,用于测量 hsCRP。工作日与周末的进食起始时间、进食结束时间和夜间禁食时间的差异计算为进食时差指标。饮食时间模式的每周内变异性由这些变量的标准差(SD)定义。多变量线性回归模型用于评估饮食时间变异性指标与 hsCRP 的横断面相关性。
工作日-周末进食结束时间每相差 30 分钟,hsCRP 就会增加 13%(p =.023)。同样,进食结束时间 SD 每增加 30 分钟,反映最后一次进食时间的变异性增加,hsCRP 就会增加 29%。每周工作日-周末夜间禁食时间相差 1 小时,hsCRP 升高 45%(p =.003)。夜间禁食时间 SD 每增加 30 分钟,代表每日禁食/进食期间跨度的变异性增加,hsCRP 就会增加 46%。
可变的进食时间模式与较高的 hsCRP 有关。需要进行干预研究,以确定稳定进食时间是否可能是减少慢性炎症的一种新策略。