Effect of a phase advance and phase delay of the 24-h cycle on energy metabolism, appetite, and related hormones

Am J Clin Nutr. 2012 Oct;96(4):689-97. doi: 10.3945/ajcn.112.037192. Epub 2012 Aug 22.

Abstract

Background: The disruption of the circadian system has been associated with the development of obesity.

Objective: We examined the effects of circadian misalignment on sleep, energy expenditure, substrate oxidation, appetite, and related hormones.

Design: Thirteen subjects [aged 24.3 ± 2.5 (mean ± SD) y; BMI (in kg/m²): 23.6 ± 1.7 (mean ± SD)] completed a randomized crossover study. For each condition, subjects stayed time blinded in the respiration chamber during 3 light-entrained circadian cycles that resulted in a phase advance (3 × 21 h) and a phase delay (3 × 27 h) compared with during a 24-h cycle. Sleep, energy expenditure, substrate oxidation, and appetite were quantified. Blood and saliva samples were taken to determine melatonin, glucose, insulin, ghrelin, leptin, glucagon-like peptide 1 (GLP-1), and cortisol concentrations.

Results: Circadian misalignment, either phase advanced or phase delayed, did not result in any changes in appetite or energy expenditure, whereas meal-related blood variables (glucose, insulin, ghrelin, leptin, and GLP-1) followed the new meal patterns. However, phase-advanced misalignment caused flattening of the cortisol-secretion pattern (P < 0.001), increased insulin concentrations (P = 0.04), and increased carbohydrate oxidation (P = 0.03) and decreased protein oxidation (P = 0.001). Phase-delayed misalignment increased rapid eye movement sleep (P < 0.001) and the sleeping metabolic rate (P = 0.02), increased glucose (P = 0.02) and decreased GLP-1 (P = 0.02) concentrations, and increased carbohydrate oxidation (P = 0.01) and decreased protein oxidation (P = 0.003).

Conclusions: The main effect of circadian misalignment, either phase advanced or phase delayed, is a concomitant disturbance of the glucose-insulin metabolism and substrate oxidation, whereas the energy balance or sleep is not largely affected. Chronically eating and sleeping at unusual circadian times may create a health risk through a metabolic disturbance. This trial was registered at the International Clinical Trials Registry Platform (http://apps.who.int/trialsearch/) as NTR2926.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Algorithms
  • Appetite Regulation*
  • Blood Glucose / analysis
  • Chronobiology Disorders / blood
  • Chronobiology Disorders / etiology
  • Chronobiology Disorders / metabolism*
  • Circadian Rhythm*
  • Cross-Over Studies
  • Energy Metabolism*
  • Female
  • Glucagon-Like Peptide 1 / blood*
  • Humans
  • Hydrocortisone / blood*
  • Insulin / blood*
  • Male
  • Meals
  • Netherlands
  • Oxygen Consumption
  • Single-Blind Method
  • Sleep
  • Young Adult

Substances

  • Blood Glucose
  • Insulin
  • Glucagon-Like Peptide 1
  • Hydrocortisone