The objective of the trial is to study how a synbiotic treatment will affect weight loss and management in individuals enrolled in weight loss diet Profile®. The investigators propose to follow up 2 cohorts of Profile® subjects during 6 months. One group will receive a synbiotic treatment supplement (Bifidobacterium spp plus bimuno- galacto-oligosaccharides (B-GOS)) while the other group will receive placebo capsules. Anthropomorphic and metabolic analysis will be performed by-monthly. Fecal samples will be obtained before and after the dietary intervention and samples will be sequenced trough next generation DNA sequencing to analyze the gut microbiota. Because dietary interventions with high protein and low glycemic index have been shown to be effective in reducing weight, but has also been linked to potential colon harm due to increased fermentation of undigested protein on the colon, the investigators expect supplementation of Profile® with a synbiotic product will lead to an increased overall wellbeing without compromising weight management.
The investigators intend to recruit 40 new Profile® members and to randomly divide them into 2 groups; Group A will follow the conventional coaching and diet plan, while group B will also receive a daily dose of the synbiotic treatment (group A will receive a placebo supplement similar in appearance and caloric content to the synbiotic treatment). Volunteers will be followed for 6 months, and weight loss, waist circumference, BMI and glucose and cholesterol levels will be assessed monthly. Dual-energy x-ray absorptiometry (DXA) will be used to analyze body composition at the beginning and end of the dietary interventions. Fecal samples will be obtained at the beginning and the end of the study. Because both our pre- and probiotic supplements have been reported to increase the concentration of satiating bacteria-derived metabolites, we expect that the individuals on the group B (synbiotic supplement) will experience a higher weight loss as well as more significant drops in glucose and cholesterol levels. Because synbiotic treatments have been reported to facilitate GI passage, the investigators expect volunteers in group B will also report improved bowels movements and general wellbeing.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
40
Volunteers will be asked to take one probiotic capsule and one prebiotic satchel daily.
Volunteers will be asked to take one placebo capsule and one placebo satchel daily.
South Dakota State University
Brookings, South Dakota, United States
RECRUITINGChanges in Gut microbiota associated to the synbiotic treatment
Stools samples will be collected and analyzed before and after the intervention and compared between groups
Time frame: 3 months
Changes in weight associated to the synbiotic treatment
Weight (kg) will be monitored every 6 weeks
Time frame: 3 months
Changes in glucose levels associated to the synbiotic treatment
A1C (Glycated hemoglobin) levels will be monitored every 6 weeks
Time frame: 3 months
Changes in body density associated to the synbiotic treatment
body density . A DXA body scan will be performed at the beginning and end of the intervention
Time frame: 3 months
Changes in waist circumference associated to the synbiotic treatment
Waist circumference (cm) will be measured every 6 weeks
Time frame: 3 months
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