Effect of NNS on Metformin/GDF15, Pilot
Study Details
Study Description
Brief Summary
Metformin use for diabetes has the benefit of causing weight loss in some. The investigators preclinical trial, demonstrated that mice consuming non-nutritive sweetened (NNS) drinks had worse glucose improvements and weight loss than mice consuming sugar drinks or water. This study will conduct a pilot to determine if this translates into pediatric clinical practice. The hypothesis is that NNS drinks impair metformin-induced satiation, weight loss, and glucose tolerance.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
This study will enroll 40 children ages 10-21 years (will be recruited from the UF Pediatric Obesity& Metabolic clinic in Gainesville) and randomize eligible participants into a 2-arm, 12-week Metformin (500mg BID) intervention (n=20/group) in which one arm will be randomized to receive education and counseling to avoid all sweetened drinks (drink water only) and the other to avoid drinks sweetened with sugar (can have diet drinks sweetened with NNS). Participants will be asked to consume minimum of 3 drinks/day In the initial visit (baseline visit) the investigators will do a complete evaluations of physical health and eating behaviors. The investigators will draw lab work including A1c and GDF15 levels. The investigators will also get anthropometric measurements of height and weight to calculate BMI. For assessment of beverage intake, the investigators reviewed questionnaires validated in children and adolescents in the past 10 years to better reflect currently available beverages. The investigators combined data from BEVQ-15 (that was validated in children aged 6-18 years) and BFQ(17 items questionnaire validated in young adults, aged 16-30 years),and edited further to make the important distinction between unsweetened and artificially sweetened drinks while adding several examples to each category to help improve correct selection. The investigators will also limit to weekly intake assessments. Will collect data biweekly. Following completion of the 12-week intervention, participants will return fasting to assess the effectiveness of the metformin treatment on the following: A1c, GDF15, with BMI and 24-hour dietary recall, including questions about change in hunger while on metformin. The investigators predict that metformin-induced GDF15 levels will be blunted in participants consuming NNS beverages. To improve compliance and decrease attrition, The investigators will provide performance feedback and interpretation of physiological parameters.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Experimental: Avoid Sugary Drinks and Artificially Sweetened Drinks ( plus Metformin) Counseling on Beverage Intake to avoid sugary sweetened and NNS (non-nutritive sweetened) drinks plus Metformin therapy (subjects will be given 12-week Metformin (500mg BID) as standard of care therapy). |
Behavioral: avoid sugary and NNS drinks plus start Metformin
Subjects will receive education and counseling to avoid all sweetened drinks (drink water only). Participants will be asked to consume minimum of 3 drinks/day
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Active Comparator: Avoid sugary drinks only, allowed water and drinks with NNS (plus Metformin) Counseling on Beverage Intake to avoid sugary drinks (allowed water and drinks sweetened with NNS) plus Metformin therapy (subjects will be given 12-week Metformin (500mg BID) as standard of care therapy). |
Behavioral: avoid sugary drinks (allowed water and drinks sweetened with NNS) plus start Metformin
Subjects will avoid drinks sweetened with sugar (can have diet drinks sweetened with NNS). Participants will be asked to consume minimum of 3 drinks/day
|
Outcome Measures
Primary Outcome Measures
- change in BMI z-score between the two groups at 12 weeks [12 weeks]
Compare post-intervention (metformin) body weight between participants randomized to receive education and counseling to either a) avoid all sweetened drinks (drink water only) or b) avoid drinks sweetened with sugar (can have diet drinks sweetened with NNS)
Secondary Outcome Measures
- improvement of A1C due to metformin between the 2 groups at 12 weeks [12 weeks]
Compare post-intervention change in glycemic control between participants randomized to receive education and counseling to either a) avoid all sweetened drinks (drink water only) or b) avoid drinks sweetened with sugar (can have diet drinks sweetened with NNS)
Other Outcome Measures
- metformin-induced rise in GDF15 in both groups at 12 weeks [12 weeks]
Compare post-intervention rise in GDF15 between participants randomized to receive education and counseling to either a) avoid all sweetened drinks (drink water only) or b) avoid drinks sweetened with sugar (can have diet drinks sweetened with NNS)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Eligible patients will have already been prescribed Metformin as part of their normal clinical care
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Must also be aged 10-21 years
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Have a diagnosis of obesity (BMI > 95th%ile or >30 kg/m2 - whichever is lower) and pre-diabetes (A1c between 5.7 and 6.4%)
Exclusion Criteria:
- Previous treatment with oral hypoglycemic medications, (2) resting SBP>180 mm/Hg or DBP>100mm/Hg, (3) self-reported pregnancy
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- University of Florida
Investigators
- Principal Investigator: Angelina Bernier, MD, University of Florida
- Principal Investigator: Esraa Ismail, MD, University of Florida
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- IRB202102435