The Effect of a Bifidobacterium and Polydextrose on Body Fat Mass

Obesity is a major problem worldwide, and it is related to abnormalities in glucose and lipid metabolism. Preclinical studies have shown that weight gain and insulin resistance may be prevented by oral administration of the probiotic Bifidobacterium animalis ssp. lactis 420. Furthermore, the prebiotic polydextrose has shown efficacy on satiety in clinical settings. The purpose of this study is to investigate the effects of these products, individually and combined, on change in body fat mass in a double-blind, randomized, placebo-controlled intervention trial. The study is conducted at four research clinics in southern Finland. The supplement is provided in a sachet, mixed into a fruit smoothie and ingested once per day for the duration of six months. One month from the end of the intervention participants will attend a follow-up visit. The study will enroll 232 participants, who will be randomized into blocks using a computerized procedure.

After the screening visit, there will be seven study visits (once per month) and one follow-up visit. Visits at months 0, 2, 4, 6 and follow-up are clinic visits, and visits at months 1, 3 and 5 are phone contacts to check compliance and any adverse events.

Clinic visits include the following measurements and samples:

• weight
• blood pressure and heart rate
• blood samples
• returning of food diaries (only during intervention)
• returning of exercise questionnaires and food choice questionnaires (only beginning and end of treatment)
• returning of fecal samples, taken at home by participant
• DXA for body composition analysis
• hip and waist circumference
• brief physical examination (only beginning and end of treatment)
• recording of adverse events and concomitant medication

For compliance check, unused sachets are returned to the clinic and counted. At the follow-up visit participants will receive guidance on exercise and a healthy diet.

The primary variable of this study is relative change from baseline to end-of-treatment in body fat mass. Comparisons between each of the active groups against the placebo group will be performed if the global P-value is significant. Secondary variables will be analyzed in a similar fashion. The relative and absolute changes in body fat mass will also be analyzed. To explore the mechanism of potential treatment benefits, post-hoc responder analyses may optionally be performed. Also, correlations between the response variables may be examined in exploratory analyses. Post-hoc analyses may be conducted to compare e.g. different time points or to analyze differences from end-of-treatment to follow-up.

Inclusion criteria

• BMI between 28.0-34.9
• Waist to hip ratio: males ≥0.88, females ≥0.83
• Age 18-65 years
• Signed informed consent
• Available for all study visits and phone calls
• Follows a regular diet that is in agreement with the national dietary recommendations

Exclusion criteria

• Diagnosed type 1 or type 2 diabetes (i.e. fasting plasma glucose ≥ 7 mmol/l and HbA1C ≥ 6.5%)
• Use of medication for diabetes, dyslipidemia or hypertension
• Use of laxatives or fiber supplements in the past 6 weeks
• History of diagnosed coronary heart disease, other significant cardiovascular disease or artificial heart valve
• History of chronic active inflammatory disorders
• History of bariatric surgery
• Use of anti-obesity drugs in the last 3 months
• Use of anticoagulants
• Regular use of non-steroidal anti-inflammatory drugs, systemic or inhaled corticosteroids, or systemic immunomodulatory drugs
• Recent (last 2 months) or ongoing antibiotic use
• Immunosuppression or ongoing therapy causing immunosuppression
• Use of probiotics more than once a week during the previous 6 weeks
• Use of vitamin D supplementation:

• > 50 - <100 µg/day during the previous 2 weeks
• ≥ 100 - <150 µg/day during the previous 2 months
• ≥150 µg/day or above during the previous 12 months
• Active or recent (last 3 months) participation in a weight loss program or weight change (increase or loss) of 3 kg during the past 3 months
• Pregnant or planning pregnancy within 6 months or breastfeeding women
• Participation in a clinical trial with an investigational product or drug within 60 days prior to screening
• Likeliness to be noncompliant with the protocol
• Drug or alcohol abuse
• Allergy to any of the ingredients used in the study
• Other reasons that, in the opinion of the Investigator makes the subject unsuitable for enrolment