Disturbed eating at high altitude: influence of food preferences, acute mountain sickness and satiation hormones

Eur J Nutr. 2013 Mar;52(2):625-35. doi: 10.1007/s00394-012-0366-9. Epub 2012 May 10.

Abstract

Purpose: Hypoxia has been shown to reduce energy intake and lead to weight loss, but the underlying mechanisms are unclear. The aim was therefore to assess changes in eating after rapid ascent to 4,559 m and to investigate to what extent hypoxia, acute mountain sickness (AMS), food preferences and satiation hormones influence eating behavior.

Methods: Participants (n = 23) were studied at near sea level (Zurich (ZH), 446 m) and on two days after rapid ascent to Capanna Margherita (MG) at 4,559 m (MG2 and MG4). Changes in appetite, food preferences and energy intake in an ad libitum meal were assessed. Plasma concentrations of cholecystokinin, peptide tyrosine-tyrosine, gastrin, glucagon and amylin were measured. Peripheral oxygen saturation (SpO(2)) was monitored, and AMS assessed using the Lake Louis score.

Results: Energy intake from the ad libitum meal was reduced on MG2 compared to ZH (643 ± 308 vs. 952 ± 458 kcal, p = 0.001), but was similar to ZH on MG4 (890 ± 298 kcal). Energy intake on all test days was correlated with hunger/satiety scores prior to the meal and AMS scores on MG2 but not with SpO(2) on any of the 3 days. Liking for high-fat foods before a meal predicted subsequent energy intake on all days. None of the satiation hormones showed significant differences between the 3 days.

Conclusion: Reduced energy intake after rapid ascent to high altitude is associated with AMS severity. This effect was not directly associated with hypoxia or changes in gastrointestinal hormones. Other peripheral and central factors appear to reduce food intake at high altitude.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Altitude Sickness / physiopathology*
  • Altitude*
  • Appetite
  • Body Mass Index
  • Cholecystokinin / blood
  • Dexamethasone / pharmacology
  • Dipeptides / blood
  • Eating / physiology*
  • Energy Intake*
  • Feeding Behavior*
  • Female
  • Food Preferences / physiology*
  • Gastrins / blood
  • Glucagon / blood
  • Humans
  • Hunger
  • Islet Amyloid Polypeptide / blood
  • Male
  • Middle Aged
  • Satiation
  • Surveys and Questionnaires
  • Weight Loss
  • Young Adult

Substances

  • Dipeptides
  • Gastrins
  • Islet Amyloid Polypeptide
  • tyrosyltyrosine
  • Dexamethasone
  • Glucagon
  • Cholecystokinin