Energy Metabolism and Nutritional Status in Hospitalized Patients with Chronic Heart Failure.
Chronic heart failure
Energy metabolism
Indirect calorimetry
Leptin
Nutritional status
Journal
Annals of nutrition & metabolism
ISSN: 1421-9697
Titre abrégé: Ann Nutr Metab
Pays: Switzerland
ID NLM: 8105511
Informations de publication
Date de publication:
2020
2020
Historique:
received:
23
08
2019
accepted:
19
03
2020
pubmed:
8
4
2020
medline:
9
1
2021
entrez:
8
4
2020
Statut:
ppublish
Résumé
Malnutrition is a factor that defines vital prognosis in chronic heart failure. This study investigated nutritional and metabolic disorders in patients with heart failure by examining the association of severity of heart failure with inflammatory cytokines, appetite-regulating hormones, and energy metabolism. Subjects were 50 patients with heart failure. On admission, nutritional status was assessed, and biochemical blood tests were performed, including for serum tumor necrosis factor-α, interleukin-6, ghrelin, and leptin levels. Resting energy expenditure (REE) was also measured by indirect calorimetry to examine its association with severity of heart failure and levels of inflammatory cytokines and appetite-regulating hormones. There were significant associations between serum brain natriuretic peptide (BNP) level and nutrition indices, indicating that nutritional status was worse when heart failure was more severe. Inflammatory cytokine levels showed significant positive correlations with BNP level. Measured REE/bodyweight was not associated with severity of heart failure, but was negatively correlated with body fat percentage and leptin levels. Energy metabolism was not associated with serum BNP level among patients with heart failure with New York Heart Association functional class up to III. Body fat percentage and leptin levels may be a good predictor of energy metabolism in patients with heart failure.
Identifiants
pubmed: 32259814
pii: 000507355
doi: 10.1159/000507355
doi:
Substances chimiques
Cytokines
0
Leptin
0
Natriuretic Peptide, Brain
114471-18-0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
129-139Informations de copyright
© 2020 S. Karger AG, Basel.