Energy and substrate metabolism in patients with active Crohn's disease

Citation
B. Schneeweiss et al., Energy and substrate metabolism in patients with active Crohn's disease, J NUTR, 129(4), 1999, pp. 844-848
Citations number
24
Categorie Soggetti
Food Science/Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF NUTRITION
ISSN journal
00223166 → ACNP
Volume
129
Issue
4
Year of publication
1999
Pages
844 - 848
Database
ISI
SICI code
0022-3166(199904)129:4<844:EASMIP>2.0.ZU;2-Z
Abstract
The aim of the study was to evaluate the possible contribution of changes i n energy metabolism and substrate oxidation rates to malnutrition in Crohn' s disease and to assess the effect of enteral nutrition on these parameters . Energy metabolism was evaluated by indirect calorimetry in 32 patients wi th active Crohn's disease and 19 age- and sex-matched healthy individuals. Measurements were done in the postabsorptive state. Seven out of 32 patient s received enteral nutrition via a nasogastric tube. In these patients, res ting energy metabolism was determined at d 0 (postabsorptive), 7, 14(during full enteral nutrition) and 15 (postabsorptive), Resting energy expenditur e was not significantly different between patients and controls, whereas th e respiratory quotient (RQ) was lower in patients (0.78 +/- 0.05 vs, 0.86 /- 0.05; P < 0.05), During enteral nutrition in 7 patients with Crohn's dis ease, the RQ increased on d 7 compared with d 0 and remained high even afte r cessation of enteral nutrition (d 0, 0.78 +/- 0.03; d 7, 0.91 +/- 0.04; d 15, 0.84 +/- 0.05; P < 0.05; d 7 and 15 vs. d 0), No effects of enteral nu trition on resting energy expenditure were found, Active Crohn's disease is associated with changes in substrate metabolism that resemble a starvation pattern. These changes appear not to be specific to Crohn's disease but to malnutrition and are readily reversed by enteral nutrition. Enteral nutrit ion did not affect resting energy expenditure. Wasting is a consequence of malnutrition but not of hypermetabolism in Crohn's disease.