Acute and two-week effects of neotame, stevia rebaudioside M and sucrose-sweetened biscuits on postprandial appetite and endocrine response in adults with overweight/obesity-a randomised crossover trial from the SWEET consortium.

Appetite Endocrine response Glycaemia Solid food Sweeteners Sweetness enhancers

Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
25 Mar 2024
Historique:
received: 02 10 2023
revised: 26 01 2024
accepted: 28 01 2024
medline: 30 3 2024
pubmed: 30 3 2024
entrez: 29 3 2024
Statut: aheadofprint

Résumé

Sweeteners and sweetness enhancers (S&SE) are used to replace energy yielding sugars and maintain sweet taste in a wide range of products, but controversy exists about their effects on appetite and endocrine responses in reduced or no added sugar solid foods. The aim of the current study was to evaluate the acute (1 day) and repeated (two-week daily) ingestive effects of 2 S&SE vs. sucrose formulations of biscuit with fruit filling on appetite and endocrine responses in adults with overweight and obesity. In a randomised crossover trial, 53 healthy adults (33 female, 20 male) with overweight/obesity in England and France consumed biscuits with fruit filling containing 1) sucrose, or reformulated with either 2) Stevia Rebaudioside M (StRebM) or 3) Neotame daily during three, two-week intervention periods with a two-week washout. The primary outcome was composite appetite score defined as [desire to eat + hunger + (100 - fullness) + prospective consumption]/4. Each formulation elicited a similar reduction in appetite sensations (3-h postprandial net iAUC). Postprandial insulin (2-h iAUC) was lower after Neotame (95% CI (0.093, 0.166); p < 0.001; d = -0.71) and StRebM (95% CI (0.133, 0.205); p < 0.001; d = -1.01) compared to sucrose, and glucose was lower after StRebM (95% CI (0.023, 0.171); p < 0.05; d = -0.39) but not after Neotame (95% CI (-0.007, 0.145); p = 0.074; d = -0.25) compared to sucrose. There were no differences between S&SE or sucrose formulations on ghrelin, glucagon-like peptide 1 or pancreatic polypeptide iAUCs. No clinically meaningful differences between acute vs. two-weeks of daily consumption were found. In conclusion, biscuits reformulated to replace sugar using StRebM or Neotame showed no differences in appetite or endocrine responses, acutely or after a two-week exposure, but can reduce postprandial insulin and glucose response in adults with overweight or obesity. The present study was funded by the Horizon 2020 program: Sweeteners and sweetness enhancers: Impact on health, obesity, safety and sustainability (acronym: SWEET, grant no: 774293).

Sections du résumé

BACKGROUND BACKGROUND
Sweeteners and sweetness enhancers (S&SE) are used to replace energy yielding sugars and maintain sweet taste in a wide range of products, but controversy exists about their effects on appetite and endocrine responses in reduced or no added sugar solid foods. The aim of the current study was to evaluate the acute (1 day) and repeated (two-week daily) ingestive effects of 2 S&SE vs. sucrose formulations of biscuit with fruit filling on appetite and endocrine responses in adults with overweight and obesity.
METHODS METHODS
In a randomised crossover trial, 53 healthy adults (33 female, 20 male) with overweight/obesity in England and France consumed biscuits with fruit filling containing 1) sucrose, or reformulated with either 2) Stevia Rebaudioside M (StRebM) or 3) Neotame daily during three, two-week intervention periods with a two-week washout. The primary outcome was composite appetite score defined as [desire to eat + hunger + (100 - fullness) + prospective consumption]/4.
FINDINGS RESULTS
Each formulation elicited a similar reduction in appetite sensations (3-h postprandial net iAUC). Postprandial insulin (2-h iAUC) was lower after Neotame (95% CI (0.093, 0.166); p < 0.001; d = -0.71) and StRebM (95% CI (0.133, 0.205); p < 0.001; d = -1.01) compared to sucrose, and glucose was lower after StRebM (95% CI (0.023, 0.171); p < 0.05; d = -0.39) but not after Neotame (95% CI (-0.007, 0.145); p = 0.074; d = -0.25) compared to sucrose. There were no differences between S&SE or sucrose formulations on ghrelin, glucagon-like peptide 1 or pancreatic polypeptide iAUCs. No clinically meaningful differences between acute vs. two-weeks of daily consumption were found.
INTERPRETATION CONCLUSIONS
In conclusion, biscuits reformulated to replace sugar using StRebM or Neotame showed no differences in appetite or endocrine responses, acutely or after a two-week exposure, but can reduce postprandial insulin and glucose response in adults with overweight or obesity.
FUNDING BACKGROUND
The present study was funded by the Horizon 2020 program: Sweeteners and sweetness enhancers: Impact on health, obesity, safety and sustainability (acronym: SWEET, grant no: 774293).

Identifiants

pubmed: 38553262
pii: S2352-3964(24)00040-9
doi: 10.1016/j.ebiom.2024.105005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105005

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests JCGH and JAH are in receipt of research funding from the American Beverage Association. ARA has received honoraria from Nestle, Unilever and the International Sweeteners Association. University of Liverpool has received income from International Food Information Council by CH. CH has received honoraria for work with Food Standards Agency Advisory Committee on Social Sciences. MW was previously contracted to research funded by AstraZeneca through funding paid to University of Liverpool. CS is a paid employee of Cargill, Inc. The University of Leeds has received income from consultancy for Mars Inc by JCGH. EAR has received honoraria for manuscript writing from Institute of Life Sciences (ILSI-Europe).

Auteurs

Catherine Gibbons (C)

School of Psychology, Faculty of Medicine & Health, University of Leeds, UK. Electronic address: c.gibbons@leeds.ac.uk.

Kristine Beaulieu (K)

School of Psychology, Faculty of Medicine & Health, University of Leeds, UK.

Eva Almiron-Roig (E)

University of Navarra, Faculty of Pharmacy and Nutrition, Dept. of Food Science and Physiology, Center for Nutrition Research, Pamplona, Spain; Navarra Institute for Health Research (IdiSNa), Pamplona, Spain.

Santiago Navas-Carretero (S)

University of Navarra, Faculty of Pharmacy and Nutrition, Dept. of Food Science and Physiology, Center for Nutrition Research, Pamplona, Spain; Navarra Institute for Health Research (IdiSNa), Pamplona, Spain; Spanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition (CIBERobn), Institute of Health Carlos III, Madrid, Spain.

J Alfredo Martínez (JA)

University of Navarra, Faculty of Pharmacy and Nutrition, Dept. of Food Science and Physiology, Center for Nutrition Research, Pamplona, Spain; Spanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition (CIBERobn), Institute of Health Carlos III, Madrid, Spain.

Beverley O'Hara (B)

School of Psychology, Faculty of Medicine & Health, University of Leeds, UK.

Dominic O'Connor (D)

School of Psychology, Faculty of Medicine & Health, University of Leeds, UK.

Julie-Anne Nazare (JA)

Human Nutrition Research Center Rhône-Alpes, Lyon 1 Claude Bernard University, France.

Alain Le Bail (A)

ONIRIS - UMR CNRS GEPEA 6144, Oniris, France.

Cécile Rannou (C)

ONIRIS - UMR CNRS GEPEA 6144, Oniris, France.

Charlotte Hardman (C)

Department of Psychology, Institute of Population Health, University of Liverpool, UK.

Moon Wilton (M)

Department of Psychology, Institute of Population Health, University of Liverpool, UK.

Louise Kjølbæk (L)

Department of Nutrition, Exercise and Sports, University of Copenhagen, Denmark.

Corey Scott (C)

Core Research and Development, Cargill, Inc, USA.

Hariklia Moshoyiannis (H)

International Reference Laboratory Services, Bioiatriki S.A., Athens, Greece.

Anne Raben (A)

Department of Nutrition, Exercise and Sports, University of Copenhagen, Denmark; Clinical Research, Copenhagen University Hospital - Steno Diabetes Center Copenhagen, Herlev, Denmark.

Joanne A Harrold (JA)

Department of Psychology, Institute of Population Health, University of Liverpool, UK.

Jason C G Halford (JCG)

School of Psychology, Faculty of Medicine & Health, University of Leeds, UK.

Graham Finlayson (G)

School of Psychology, Faculty of Medicine & Health, University of Leeds, UK.

Classifications MeSH