Daily stressors, past depression, and metabolic responses to high-fat meals: a novel path to obesity

Biol Psychiatry. 2015 Apr 1;77(7):653-60. doi: 10.1016/j.biopsych.2014.05.018. Epub 2014 Jul 14.

Abstract

Background: Depression and stress promote obesity. This study addressed the impact of daily stressors and a history of major depressive disorder (MDD) on obesity-related metabolic responses to high-fat meals.

Methods: This double-blind, randomized, crossover study included serial assessments of resting energy expenditure (REE), fat and carbohydrate oxidation, triglycerides, cortisol, insulin, and glucose before and after two high-fat meals. During two separate 9.5-hour admissions, 58 healthy women (38 breast cancer survivors and 20 demographically similar control subjects), mean age 53.1 years, received either a high saturated fat meal or a high oleic sunflower oil meal. Prior day stressors were assessed by the Daily Inventory of Stressful Events.

Results: Greater numbers of stressors were associated with lower postmeal REE (p = .008), lower fat oxidation (p = .04), and higher insulin (p = .01), with nonsignificant effects for cortisol and glucose. Women with prior MDD had higher cortisol (p = .008) and higher fat oxidation (p = .004), without significant effects for REE, insulin, and glucose. Women with a depression history who also had more stressors had a higher peak triglyceride response than other participants (p = .01). The only difference between meals was higher postprandial glucose following sunflower oil compared with saturated fat (p = .03).

Conclusions: The cumulative 6-hour difference between one prior day stressor and no stressors translates into 435 kJ, a difference that could add almost 11 pounds per year. These findings illustrate how stress and depression alter metabolic responses to high-fat meals in ways that promote obesity.

Keywords: Cortisol; Daily stressors; Depression; Insulin; Resting energy expenditure; Triglycerides.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Breast Neoplasms / physiopathology
  • Breast Neoplasms / therapy
  • Cross-Over Studies
  • Depressive Disorder / physiopathology*
  • Dietary Fats / administration & dosage*
  • Double-Blind Method
  • Energy Metabolism / physiology*
  • Female
  • Humans
  • Hydrocortisone / blood
  • Middle Aged
  • Obesity / physiopathology*
  • Oleic Acid / administration & dosage
  • Oxidation-Reduction
  • Postprandial Period / physiology*
  • Stress, Psychological / physiopathology*
  • Triglycerides / blood

Substances

  • Dietary Fats
  • Triglycerides
  • Oleic Acid
  • Hydrocortisone