Effect of Non-nutritive Sweeteners of High Sugar Sweetened Beverages on Metabolic Health and Gut Microbiome

Sponsor
Laval University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03259685
Collaborator
(none)
66
1
3
73.4
0.9

Study Details

Study Description

Brief Summary

Increasing evidence suggest that artificial sweeteners such as saccharin, aspartame and sucralose may not be as metabolically safe as they first appeared, and it has been proposed that their consumption may be linked to important disturbances in the gut microbiome. Some in vitro and in vivo studies suggest that the recently approved sugar substitute Stevia (eg. steviol glycosides) can also influence intestinal homeostasis. However, it is not clear whether this natural non-nutritive sweetener (NNS) could also cause metabolic and microbiome disturbances as proposed for their synthetic counterparts. In fact, steviol glycosides may even have a beneficial impact on glucose homeostasis and lipid metabolism possibly through a positive action on intestinal health and gut microbiome, but this has yet to be experimentally tested in a rigorous study.

The main objective of this project is to evaluate whether steviol glycosides sweetened beverages (SGSB) or aspartame/acesulfame K sweetened beverages (AASB) exert beneficial, neutral or detrimental effects on metabolic health of regular consumers of sugar-sweetened beverages (SSBs), and whether modulation of the gut microbiome is involved in the resulting impact of these NNSs on metabolic health.

As chronic overconsumption of SSBs is clearly associated with an increased cardiometabolic risk, this study will be the first to determine the metabolic impact of replacing SSBs by potentially "healthier alternatives" such as the increasingly popular stevia-based soft drinks and aspartame-based soft drinks. The investigators will further investigate whether these NNS can cause pernicious effects on intestinal health and the gut microbiome. It is a crucial concern since the importance of this unsuspected key "organ" has been ignored for too long and its important implication in many chronic societal diseases has just been discovered.

Results of this study could have a direct influence on health, nutrition and even agricultural policies as well as dietary guidelines around the world. This project is also critically important as an increasing amount of health professionals such as physicians, nurses and registered dietitians seek to provide evidenced-based guidance to individuals looking for healthier alternatives to SSBs including stevia-based or aspartame-based soft drinks.

Condition or Disease Intervention/Treatment Phase
  • Other: 710 ml of regular soft drinks, taken daily for 10 weeks
  • Other: 710 ml of diet soft drinks, taken daily for 10 weeks
  • Other: 710 ml of stevia-sweetened soft drinks, taken daily for 10 weeks
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
66 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effect of Free Sugar Replacement With Non-nutritive Sweeteners on Metabolic Health of High Sugar Sweetened Beverages Consumers: Potential Role of the Gut Microbiome
Actual Study Start Date :
Oct 18, 2017
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Regular beverages

Sugar sweetened soft drinks

Other: 710 ml of regular soft drinks, taken daily for 10 weeks
Subjects will consume regular soft drinks to test if there is a significant difference on the impact on gut microbiota composition and metabolic syndrome parameters between this treatment and the active treatments (diet and stevia beverages).

Experimental: Diet beverages

Soft drinks sweetened with artificial non-nutritive sweeteners (i.e. aspartame, acesulfame-K)

Other: 710 ml of diet soft drinks, taken daily for 10 weeks
Subjects will consume diet soft drinks during 10 weeks to test the possible effects of aspartame/acesulfame-K sweetened beverages on gut microbiota composition and on metabolic syndrome parameters.

Experimental: Stevia beverages

Soft drinks sweetened with natural non-nutritive sweeteners (i.e. steviol glycosides)

Other: 710 ml of stevia-sweetened soft drinks, taken daily for 10 weeks
Subjects will consume soft drinks containing stevia during 10 weeks to test the possible effects of steviol glycosides sweetened beverages on gut microbiota composition and on metabolic syndrome parameters.

Outcome Measures

Primary Outcome Measures

  1. Changes in metabolic syndrome parameters including insulin/glucose homeostasis and lipid/lipoprotein metabolism in sugar-sweetened beverages (SSB) consumers following regular, diet or stevia-sweetened beverages intakes for 10 weeks. [18-24 months]

Secondary Outcome Measures

  1. Changes in intestinal homeostasis of SSB consumers following regular, diet or stevia-sweetened beverages intakes for 10 weeks. [4-6 months]

  2. Changes in gut microbiota composition of SSB consumers following regular, diet or stevia-sweetened beverages intakes for 10 weeks. [4-6 months]

Other Outcome Measures

  1. Changes in key molecular signaling pathways and metabolic regulatory networks identified through transcriptomics and metabolomics of SSB consumers following regular, diet or stevia-sweetened beverages intakes for 10 weeks. [6-12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Men and women in good health

  • Soft drinks consumers (between 4 cans/week to 4 cans/day)

Exclusion Criteria:
  • Metabolic disorders (hypertension, diabetes, hypercholesterolemia)

  • Daily consumption of more than 4 cans of soft drinks

  • Regular use of medication affecting study parameters

  • Change of medication (type or dose) in the last year

  • Use of antibiotics in the last 3 months

  • Change in natural health product use in the last 3 months

  • More than 2 alcohol drinks par day

  • Weight change of more than 5% in the last 3 months

  • Surgery in the last 3 months or planed during the study

  • Allergy or intolerance for products contained in soft drinks

Contacts and Locations

Locations

Site City State Country Postal Code
1 Laval University Québec Canada G1V0A6

Sponsors and Collaborators

  • Laval University

Investigators

  • Principal Investigator: Marie-Claude Vohl, Laval University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marie-Claude Vohl, Professor, Laval University
ClinicalTrials.gov Identifier:
NCT03259685
Other Study ID Numbers:
  • SBG 2017-136
First Posted:
Aug 24, 2017
Last Update Posted:
Jul 7, 2021
Last Verified:
Jul 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Marie-Claude Vohl, Professor, Laval University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2021