GLP-1 Analog Modulates Appetite, Taste Preference, Gut Hormones, and Regional Body Fat Stores in Adults with Obesity.
Adipose Tissue
/ drug effects
Adolescent
Adult
Aged
Appetite
/ drug effects
Body Composition
/ drug effects
Double-Blind Method
Female
Food Preferences
/ drug effects
Gastrointestinal Hormones
/ blood
Glucagon-Like Peptide 1
/ analogs & derivatives
Humans
Hypoglycemic Agents
/ pharmacology
Liraglutide
/ pharmacology
Male
Middle Aged
Obesity
/ drug therapy
Placebos
Satiation
/ drug effects
Taste
/ drug effects
Young Adult
GLP-1 analog
appetite
body fat
liraglutide
obesity
taste preference
Journal
The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362
Informations de publication
Date de publication:
01 05 2020
01 05 2020
Historique:
received:
28
06
2019
accepted:
23
10
2019
pubmed:
31
10
2019
medline:
10
2
2021
entrez:
31
10
2019
Statut:
ppublish
Résumé
Obesity is associated with alterations in appetite, gastrointestinal hormone levels and excessive fat mass. We previously published a double-blind, placebo-controlled, randomized, 16-week trial on effects of once-daily glucagon-like peptide-1 (GLP-1) analog, liraglutide on weight, satiation, and gastric functions in obese volunteers. The aim of this substudy is to compare to placebo the effects of liraglutide on appetite, taste preference, regional body fat stores, and anthropometric measurements. Forty obese adults received standard instruction for weight management, monthly behavioral intervention utilizing motivational interviews, and 16-week treatment of once-daily liraglutide (escalated to 3 mg SQ daily). At baseline and 16 weeks, the following were measured: appetite and taste preferences rated every 30 min for 5 h after ingesting 300 mL Ensure®; maximal tolerated volume (MTV) with a nutrient drink test; fasting and postprandial bioactive GLP-1 (7-36) and peptide YY (PYY) levels; total and regional body fat with dual-energy X-ray absorptiometry, and waist and hip circumference. Thirty-five participants (17 liraglutide; 18 placebo) completed the trial. Compared to placebo group, liraglutide group had significant reductions in MTV; prospective food consumption score; desire to eat something sweet, salty, savory or fatty; and an increase in perceived fullness. Postprandial plasma levels of GLP-1 decreased and PYY levels increased with liraglutide relative to baseline. Significant reductions in total body, trunk, and upper and lower body fat without reduction in lean body mass were observed. Liraglutide 3 mg SQ modulates appetite, taste preference, gut hormones, and regional body fat stores in adults with obesity without reduction in lean body mass.
Identifiants
pubmed: 31665455
pii: 5609015
doi: 10.1210/clinem/dgz140
pmc: PMC7105351
pii:
doi:
Substances chimiques
Gastrointestinal Hormones
0
Hypoglycemic Agents
0
Placebos
0
Liraglutide
839I73S42A
Glucagon-Like Peptide 1
89750-14-1
Banques de données
ClinicalTrials.gov
['NCT02647944']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK067071
Pays : United States
Organisme : NIDDK NIH HHS
ID : R56 DK067071
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000135
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002377
Pays : United States
Informations de copyright
© Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
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