Physiological Effects of Stevia Consumption in Humans
Study Details
Study Description
Brief Summary
This study will evaluate whether long-term consumption of the low calorie sweetener stevia affects glucose tolerance in healthy participants. With regard to this aim, we will recruit 2 study groups, the stevia group where participants will be required to add stevia drops twice daily in their habitual drinks and the control group where participants will be asked not to change anything in their diet and lifestyle.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Excess consumption of caloric sweeteners contributes to the alarming rates of overweight and obesity, whereas non-nutritive sweeteners (NNS) are non-caloric alternatives offering sensory and health benefits. NNS are widely used to moderate energy intake and postprandial glycaemia, but there is controversial evidence about their role and effects. Stevia, a natural NNS, has been suggested to assist with glucose regulation but data on glucose tolerance after daily consumption of stevia are lacking. The investigators plan to undertake a pilot randomized 2-parallel arm open-label 12-week trial, where participants will start consuming stevia with their habitual drinks. Thirty healthy volunteers (not habitual consumers of stevia or other NNS) will be recruited. The intervention group (n=15) will consume 5 drops of stevia with their habitual drinks twice daily whereas the control group (n=15) will not be required to change anything in their diet, but avoid consuming NNS or diet beverages for the study duration.
Key measures in glucose homeostasis including glucose response to an oral glucose tolerance test will be performed before and after the intervention period. Serum and plasma samples will be stored for potential analysis of insulin and gut hormones levels.
Participants will have to attend 3 study visits, visit week 0, visit week 6 and visit week 12, but the primary outcome will be assessed in visit week 0 and visit week 12.
Participants will be weighed; dietary intake, physical activity and appetite will be also assessed. Faecal samples will be collected and gut microbiome analysis may be performed. Gut microbiome has been considered to be a key linked topic, since it has been suggested that saccharin consumption may induce glucose intolerance in humans through alterations in gut microbiota in humans.
The trial will assess whether regular use of stevia in realistic amounts has any effects on glucose homeostasis, and aims to elucidate our understanding of long-term physiological effects of NNS.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Stevia arm stevia drops |
Dietary Supplement: stevia
This arm will be required to consume 5 stevia drops twice daily in habitual drinks
|
| No Intervention: Control arm No change in diet |
Outcome Measures
Primary Outcome Measures
- Glucose response to an oral glucose tolerance test (OGTT) measured as incremental area under the curve (iAUC) [Week 0 and week 12]
blood glucose levels will be measured at baseline (0) and at 15, 30, 45, 60, 90 and 120 min after the consumption of a 75 g glucose load and iAUC will be calculated
Secondary Outcome Measures
- Change in body weight [Week 0, visit week 6 and week 12]
body weight will be measured on visit week 0, visit week 6 and visit week 12
- Change in dietary intake [Week 0, visit week 6 and week 12]
participants will fill out 3 days of diet recalls before coming to all 3 study visits using Intake24
- Change in waist circumference [Week 0, visit week 6 and week 12]
waist circumference will be measured on visit week 0, visit week 6 and visit week 12
- Change in appetite [Week 0 and week 12]
Appetite questionnaires (three factor eating questionnaire, sweet food frequency questionnaire, Satiety, hunger, and food cravings - using the Control of Eating Questionnaire ) will be completed on visit week 0 and visit week 12
- Change in fasting blood glucose [Week 0 and week 12]
Fasting blood glucose will be measured on visit week 0 and visit week 12.
- Change in the 75-OGTT 2-hour blood glucose [Week 0 and week 12]
75g OGTT 2-h blood glucose will be measured on visit week 0 and visit week 12.
Other Outcome Measures
- Physical activity [Week 0, visit week 6 and week 12]
Total MET-minutes per week measured via the International Physical Activity Questionnaire (IPAQ).
- Physical activity [Week 0, week 6, week 12]
Number of steps per day. 3 days before visit week 0, visit week 6 and visit week 12
- Blood pressure [Week 0, visit week 6 and week 12]
Blood pressure will be measure on visit week 0, visit week 6 and visit week 12
- Composition of gut microbiome [Week 0 and week 12]
Changes in gut microbiota will be measured by 16S rRNA gene sequencing. This outcome is optional and will be decided by the investigators based on the findings in the primary outcome.
- Fasting plasma insulin [Week 0 and week 12]
This outcome is optional and will be decided by the investigators based on the findings in the primary outcome
- 75g OGTT derived iAUC plasma insulin [Week 0 and week 12]
This outcome is optional and will be decided by the investigators based on the findings in the primary outcome.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age 18-40 years
-
BMI 18.5-25 kg/m2
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No or low NNS consumers (up to 1 can of diet soda per week or 1 sachet of NNS per week)
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DEBQ for restraint eating ≤ 3
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Healthy - general good health
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Not taking medications that affect metabolism or appetite (i.e. thiazide diuretics, glucocorticoids or beta blockers)
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Stable weight, ≤ 5 kg last 12 months
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Fasting blood glucose ≤6.0 mmol/L
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Willing to comply with the study protocol
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No self-reported food allergy or intolerance to foods supplied during the study
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The participant is capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
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The participant is able to read, comprehend and record information written in English.
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A signed and dated written informed consent is obtained from the participant.
Exclusion Criteria:
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Age under 18 years or over 40 years old.
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BMI >25 kg/m2 and <18.5kg/m2
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Participants who are not willing to comply with study procedures (including expression of dislike for NNS)
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Habitual NNS consumers, >1 can of diet beverage or >1 sachet of low calorie sweeteners per week.
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Fasting blood glucose measured > 6 mmol/L
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Subjects who are currently dieting and having ceased a diet in < 4 weeks
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DEBQ score for restraint eating > 3
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Subjects who follow special diets for weight maintenance, such as Atkins Diet, Weight Watchers, gluten-free diet, The Zone diet, Vegetarian Diet, Raw Food Diet etc.
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Vegetarians, vegans
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Subjects who take recreational substances such as cannabis.
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Presence of any chronic condition requiring medication that might affect our results (e.g. diabetes, mental diseases, gastrointestinal diseases)
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Subjects with eating disorders (binge eating disorder, bulimia etc)
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Subjects who are currently experiencing anxiety or depression
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Participants who drink alcohol more than the NHS guidelines (14 units per week)
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10 h of vigorous physical activities per week and/or planning to increase/decrease physical activity levels in the next months.
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Having ceased smoking in the last six months
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Female participants who are, or may be, pregnant, or currently lactating.
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Subjects who regularly consume dietary supplements for weight loss, muscle building etc.
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Subjects with food allergies or intolerances related to the study.
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Subjects who have given blood elsewhere within the last month.
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The participant cannot read, comprehend and record information written in English.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Manchester | Manchester | United Kingdom | M13 9PG |
Sponsors and Collaborators
- University of Manchester
- Lancaster University
Investigators
- Principal Investigator: John McLaughlin, University of Manchester
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 4812