Food timing, circadian clock, and metabolic health
Contact: PD Dr. Olga Ramich
A number of metabolic processes and hormones show pronounced 24-hour rhythms. These rhythms are driven by so-called clock genes which “autonomously” control their own synthesis via linked cycles of up- and downregulation. Clock genes regulate different metabolic processes and could be in turn entrained by the light and food intake (Fig.1). The main aim of our project is to understand how the circadian clock affects metabolism in humans and which role they play in the metabolic response to the food intake.

We have demonstrated diurnal oscillations of key genes of glucose, lipid and energy metabolism as well as inflammatory genes in human blood cells and adipose tissue. Moreover, we found that the expression of clock genes in human adipose tissue is regulated by body weight changes. Even isocaloric changes in carbohydrate and fat intake and the time of the food intake affect circadian rhythms in humans. In our recent Diabetes study, we demonstrated the direct effects of insulin on the circadian clock in adipose tissue, which might, at least in part, explain how the food intake affect circadian clock.
We have further shown that the consumption of carbohydrates and fat at different times of the day induces different metabolic effects, especially the daily glucose levels. We further observed that levels of blood glucose, plasma lipidome, inflammatory markers, substrate oxidation, as well as postprandial hormone secretion was strongly dependent on the day time. Indeed, the postprandial glucose level in the afternoon was markedly higher than postprandial levels after the same meal in the morning which suggests a decrease in glucose tolerance as the day progresses. Notably, the afternoon decline in glucose tolerance was more pronounced in subjects with impaired glucose metabolism (Fig.2).

In summary, our data shows that both meal timing and food composition can alter circadian rhythms in humans and in this way affect dietary-induced metabolic response in humans. In the ongoing human study, we investigate effects of intermittent fasting on the glucose metabolism and other metabolic parameters in subjects with an increased diabetes risk.