4.7 Article

Time-of-day and Meal Size Effects on Clinical Lipid Markers

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 106, 期 3, 页码 E1373-E1379

出版社

ENDOCRINE SOC
DOI: 10.1210/clinem/dgaa739

关键词

circadian; chrononutrition; meal timing; lipids; triglyceride

资金

  1. National Space Biomedical Research Institute through NASA [HPF01301, NCC 9-58]
  2. National Center for Research Resources [NCRR M01 RR02635]
  3. Harvard Clinical and Translational Science Center (NCRR) [UL1 RR025758]

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Eating at night can lead to an increase in triglyceride levels, which may contribute to the dyslipidemia and elevated cardiovascular disease risk observed in shift workers. This time-of-day dependency on postprandial lipid metabolism highlights the importance of meal timing in maintaining a healthy lipid profile.
Context: Dyslipidemia and cardiovascular disease are common in shift workers and eating at night may contribute to this pathophysiology. Objective: To examine the effects of eating at different times of day on lipid profiles. Design: Two 24-hour baseline days with 8 hours of sleep, 3 meals (breakfast, lunch, dinner) and a snack, followed by a 40-hour constant routine (CR) with hourly isocaloric meals. Setting: Intensive Physiological Monitoring Unit, Brigham and Women's Hospital. Participants: Twenty-one healthy adults [23.4 2.7 years, 5F] Intervention: Forty-hour CR. Main Outcome Measures: A standard clinical lipid panel, consisting of total cholesterol, triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C), was assayed in blood samples collected 4-hourly across similar to 4 days. Results: When participants ate at night, levels of TG were similar to eating during the day, however, these levels at night were reached with consuming approximately half the calories. Additionally, 24-hour levels of TG were 10% higher when meals were consumed hourly across 24 hours compared to consuming a typical 3-meal schedule while awake during the day and sleeping at night. The endogenous circadian rhythms of TG, which peaked at night, were shifted earlier by similar to 10 hours under baseline conditions, whereas the rhythms in total cholesterol, HDL-C, and LDL-C remained unchanged and peaked in the afternoon. Conclusions: The time-of-day dependency on postprandial lipid metabolism, which leads to hypersensitivity in TG responses when eating at night, may underlie the dyslipidemia and elevated cardiovascular disease risk observed in shift workers.

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