TY - JOUR
T1 - Twice as High Diet-Induced Thermogenesis After Breakfast vs Dinner On High-Calorie as Well as Low-Calorie Meals
AU - Richter, Juliane
AU - Herzog, Nina
AU - Janka, Simon
AU - Baumann, Thalke
AU - Kistenmacher, Alina
AU - Oltmanns, Kerstin M.
N1 - Funding Information:
Financial Support: This work was supported by the
Publisher Copyright:
© 2020 Endocrine Society 2020.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/1/8
Y1 - 2020/1/8
N2 - Background: The question of whether there is daytime time variation in diet-induced thermogenesis (DIT) has not been clearly answered. Moreover, it is unclear whether a potential diurnal variation in DIT is preserved during hypocaloric nutrition. Objective: We hypothesized that DIT varies depending on the time of day and explored whether this physiological regulation is preserved after low-calorie compared with high-calorie intake. Design: Under blinded conditions, 16 normal-weight men twice underwent a 3-day in-laboratory, randomized, crossover study. Volunteers consumed a predetermined low-calorie breakfast (11% of individual daily kilocalorie requirement) and high-calorie dinner (69%) in one condition and vice versa in the other. DIT was measured by indirect calorimetry, parameters of glucose metabolism were determined, and hunger and appetite for sweets were rated on a scale. Results: Identical calorie consumption led to a 2.5-times higher DIT increase in the morning than in the evening after high-calorie and low-calorie meals (P <. 001). The food-induced increase of blood glucose and insulin concentrations was diminished after breakfast compared with dinner (P <. 001). Low-calorie breakfast increased feelings of hunger (P <. 001), specifically appetite for sweets (P =. 007), in the course of the day. Conclusions: DIT is clearly higher in the morning than in the evening, irrespective of the consumed calorie amount; that is, this physiological rhythmicity is preserved during hypocaloric nutrition. Extensive breakfasting should therefore be preferred over large dinner meals to prevent obesity and high blood glucose peaks even under conditions of a hypocaloric diet.
AB - Background: The question of whether there is daytime time variation in diet-induced thermogenesis (DIT) has not been clearly answered. Moreover, it is unclear whether a potential diurnal variation in DIT is preserved during hypocaloric nutrition. Objective: We hypothesized that DIT varies depending on the time of day and explored whether this physiological regulation is preserved after low-calorie compared with high-calorie intake. Design: Under blinded conditions, 16 normal-weight men twice underwent a 3-day in-laboratory, randomized, crossover study. Volunteers consumed a predetermined low-calorie breakfast (11% of individual daily kilocalorie requirement) and high-calorie dinner (69%) in one condition and vice versa in the other. DIT was measured by indirect calorimetry, parameters of glucose metabolism were determined, and hunger and appetite for sweets were rated on a scale. Results: Identical calorie consumption led to a 2.5-times higher DIT increase in the morning than in the evening after high-calorie and low-calorie meals (P <. 001). The food-induced increase of blood glucose and insulin concentrations was diminished after breakfast compared with dinner (P <. 001). Low-calorie breakfast increased feelings of hunger (P <. 001), specifically appetite for sweets (P =. 007), in the course of the day. Conclusions: DIT is clearly higher in the morning than in the evening, irrespective of the consumed calorie amount; that is, this physiological rhythmicity is preserved during hypocaloric nutrition. Extensive breakfasting should therefore be preferred over large dinner meals to prevent obesity and high blood glucose peaks even under conditions of a hypocaloric diet.
UR - http://www.scopus.com/inward/record.url?scp=85080843023&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgz311
DO - 10.1210/clinem/dgz311
M3 - Journal articles
C2 - 32073608
AN - SCOPUS:85080843023
SN - 0021-972X
VL - 105
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 3
M1 - dgz311
ER -