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Time-of-day and Meal Size Effects on Clinical Lipid Markers
Leilah K Grant1,2, Charles A Czeisler1,2, Steven W Lockley1,2
1Division of Sleep and Circadian Disorders, Departments of Medicine and Neurology, Brigham and Women's Hospital, Boston, Massachusetts.
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 ~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 ~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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