24-h energy expenditure in people with type 1 diabetes: impact on equations for clinical estimation of energy expenditure

Eur J Clin Nutr. 2024 Aug;78(8):718-725. doi: 10.1038/s41430-024-01446-4. Epub 2024 May 14.

Abstract

Background/objectives: Type 1 diabetes (T1D) is associated with an increase in resting metabolic rate (RMR), but the impact of T1D on other components of 24-h energy expenditure (24-h EE) is not known. Also, there is a lack of equations to estimate 24-h EE in patients with T1D. The aims of this analysis were to compare 24-h EE and its components in young adults with T1D and healthy controls across the spectrum of body mass index (BMI) and derive T1D-specific equations from clinical variables.

Subjects/methods: Thirty-three young adults with T1D diagnosed ≥1 year prior and 33 healthy controls matched for sex, age and BMI were included in this analysis. We measured 24-h EE inside a whole room indirect calorimeter (WRIC) and body composition with dual x-ray absorptiometry.

Results: Participants with T1D had significantly higher 24-h EE than healthy controls (T1D = 2047 ± 23 kcal/day vs control= 1908 ± 23 kcal/day; P < 0.01). We derived equations to estimate 24-h EE with both body composition (fat free mass + fat mass) and anthropometric (weight + height) models, which provided high coefficients of determination (R2 = 0.912 for both). A clinical model that did not incorporate spontaneous physical activity yielded high coefficients of determination as well (R2 = 0.897 and R2 = 0.880 for body composition and anthropometric models, respectively).

Conclusion: These results confirm that young adults with established T1D have increased 24-h EE relative to controls without T1D. The derived equations from clinically available variables can assist clinicians with energy prescriptions for weight management in patients with T1D.

MeSH terms

  • Absorptiometry, Photon
  • Adolescent
  • Adult
  • Basal Metabolism
  • Body Composition*
  • Body Mass Index*
  • Calorimetry, Indirect*
  • Case-Control Studies
  • Diabetes Mellitus, Type 1* / metabolism
  • Diabetes Mellitus, Type 1* / physiopathology
  • Energy Metabolism* / physiology
  • Female
  • Humans
  • Male
  • Young Adult