Resting Energy Expenditure and Substrate Oxidation in Malnourished Patients With Type 1 Glycogenosis

J Clin Endocrinol Metab. 2019 Nov 1;104(11):5566-5572. doi: 10.1210/jc.2019-00585.

Abstract

Context: Type 1a and 1b glycogenosis [glycogen storage disorder (GSD)1a, GSD1b] are rare diseases generally associated with malnutrition. Although abnormal substrate oxidation rates and elevated energy expenditures might contribute to malnutrition, this issue has not been investigated.

Objective: To investigate whether abnormal resting energy expenditure (REE) and substrate oxidation rate characterize patients with GSD1.

Design: Cross-sectional study.

Setting: Outpatient referral center for rare diseases and laboratory of clinical nutrition at the University Hospital of Palermo.

Patients: Five consecutive patients with GSD1 (4 type a, 1 type b; 3 men, 2 women; age range, 19 to 49 years).

Main outcome measures: The usual clinical procedures for patients with malnutrition, including REE and basal substrate oxidation rate (both indirect calorimetry), body composition (bioimpedance method), muscle strength (hand-grip test), and the usual laboratory tests, were performed.

Results: Malnutrition was clearly diagnosed in 2 patients (1 GSD1a and 1 GSD1b), with REE elevated in all five patients, and especially, in the two malnourished patients (+124% and +32.1% vs predictive values using Harris-Benedict equations). The two malnourished patients also exhibited lower basal protein oxidation rates (7.7% and 6.6%) than the nourished patients (range, 12.1% to 24.7%), with higher carbohydrate or lipid oxidation rates. Additionally, the two malnourished patients exhibited higher blood concentrations of lactic acid than the nourished patients.

Conclusions: According to data obtained from our small sample of patients with GSD1, elevated REEs seem to be a common characteristic that might contribute to malnutrition. Low basal protein oxidation rates and elevated blood lactic acid concentrations appear to be associated with malnutrition.

MeSH terms

  • Adult
  • Body Composition / physiology
  • Calorimetry, Indirect
  • Cross-Sectional Studies
  • Energy Metabolism / physiology*
  • Female
  • Glycogen Storage Disease Type I / metabolism*
  • Humans
  • Male
  • Malnutrition / metabolism*
  • Middle Aged
  • Oxidation-Reduction
  • Oxygen Consumption / physiology
  • Young Adult