Moderate Hypercholesterolemia
Conditions
Keywords
Probiotics, AB-Life, LDL-cholesterol, Hypercholesterolemia
Brief summary
This study aims to demonstrate the effect of the chronic consumption of AB-Life probiotic blend on blood LDL cholesterol level in volunteers with moderate hypercholesterolemia.
Interventions
DIETARY_SUPPLEMENTPlacebo
DIETARY_SUPPLEMENTProbiotics bacterial strains
Sponsors
AB Biotics, SA
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
To be eligible to the study, male and female volunteers will have to fulfill the following criteria (assessment based on the medical examination performed at V1 with a checking at V3): * Age between 18 and 65 years (limits included). * BMI between 18,5 and 30 kg/m² ((limits excluded). * For women : Non menopausal with reliable contraception since at least two cycles before the beginning of the study and agreeing to keep it during the entire duration of the study (condom alone without spermicide gel and oestrogenic contraceptive excluded) or menopausal without oestrogenic replacement therapy. * Good general and mental health with in the opinion of the investigator: no clinically significant and relevant abnormalities of medical history or physical examination. * Able and willing to participate to the study by complying with the protocol procedures as evidenced by his dated and signed informed consent form. * Affiliated with a social security scheme. * Agree to be registered on the volunteers in biomedical research file. After V1 biological analysis the subjects will be eligible to the visit V2 on the following criteria: \- Fasting plasma LDLc level (Friedewald estimation method) between 1,3 and 1,89 g/L (3,35 - 4,92 mmol/L, limits included with ± 2% tolerated around). After V2 biological analysis the subjects will be eligible to the study on the following criteria: \- Fasting plasma LDLc level (Friedewald estimation method) between 1,3 and 1,89 g/L (3,35 - 4,92 mmol/L, limits included with ± 2% tolerated around). A re-screening can occur from 2 months after the exit of study for failure to comply with the one or more of the eligibility criteria listed above.
Exclusion criteria
Volunteers with the following criteria will be considered as non eligible to the study (assessment based on the medical examination performed at V1 with a checking at V3): * Suffering from a metabolic disorder such as diabetes, uncontrolled thyroidal trouble or other chronic severe disease. * Suffering from a severe chronic disease (e.g. cancer, HIV, renal failure, hepatic or biliary disorders ongoing, chronic inflammatory digestive disease, arthritis or other chronic respiratory trouble, etc.) or gastrointestinal disorders found to be inconsistent with the conduct of the study by the investigator (e.g. celiac disease). * With a history of ischemic cardiovascular event or, during the previous 6 months a surgical procedure. * With a known or suspected food allergy or intolerance or hypersensitivity to any of the study products' ingredient. * Suffering from an uncontrolled hypertension (systolic blood pressure ≥ 160 mmHg and diastolic blood pressure ≥ 100 mmHg). * Pregnant or lactating women or intending to become pregnant within 5 months ahead. * Under lipid-lowering treatment (e.g. statins, fibrates, ezetimibe, bile acid sequestrants, niacin, etc.) or stopped less than 4 months before the randomization. * Under medication which could affect blood lipid parameters (e.g. long-term corticosteroid systemic drug, systemic antibodies, androgens or phenytoin, etc.) or stopped less than 1 month before the randomization (stable long-term treatment with beta blocker or thiazide diuretics tolerated). * Regular intake of dietary supplements or functional foods which may interfere with lipid absorption and/or metabolism (e.g. rich in plant stanol or sterol like PRO-ACTIV or DANACOL products, red yeast rice, policosanol, omega-3 fatty acids like fish oils, ST HUBERT OMEGA 3 or PRIMEVERE products, soya protein, oat fiber like QUAKER OATS, psyllium, chitosan, guar gum, inulin, etc.) or stopped less than 3 months before the randomization. * Under treatment which could disturb microbiota balance or stopped in a too short period before the randomization (e.g. less than one month for laxatives, less than 6 weeks for antibiotics). * Regular intake of dietary supplements or functional foods containing prebiotics, probiotics or symbiotics (e.g. BION 3, LACTIBIANE, ACTIMEL, ACTIVIA, etc.) or stopped less than 1 month before the randomization. * Under treatment or dietary supplement which could significantly affect parameter(s) followed during the study according to the investigator or stopped in a too short period before the randomization. * With significant change in food habits or in physical activity in the 3 months before randomization or not agreeing to keep them unchanged throughout the study. * With reported body weight variation \> 5% in the 3 months prior the randomization or with a hyper or hypocaloric diet planned in the next 5 months. * With a personal history of anorexia nervosa, bulimia or significant eating disorders according to the investigator. * Consuming more than 3 standard drinks of alcoholic beverage daily for men or 2 standard drinks daily for women or not agreeing to keep his alcohol consumption habits unchanged throughout the study. * Smoking more than 10 cigarettes daily or not agreeing to keep his smoking habits unchanged throughout the study. * Recent history of chronic alcohol or drug abuse (in the last 2 years). * Having a lifestyle deemed incompatible with the study according to the investigator including high level physical activity (defined as more than 10 hours of significant physical activity a week, walking excluded). * Who made a blood donation in the 3 months before the randomization or intending to make it within 4 months ahead. * Taking part in another clinical trial or being in the exclusion period of a previous clinical trial. * Having received, during the last 12 months, indemnities for clinical trial higher or equal to 4500 Euros. * Under legal protection (guardianship, wardship) or deprived from his rights following administrative or judicial decision. * Presenting a psychological or linguistic incapability to sign the informed consent. * Impossible to contact in case of emergency. After V1 biological analysis the subjects will be considered as non eligible to the study on the following criteria : * Fasting plasma glucose level \> 1,26 g/L (6,99 mmol/L). * Fasting plasma triglycerides \> 3,5 g/L (3,95 mmol/L). * Fasting plasma TC, HDLc or insulin with an abnormality judged as clinically significant according to the investigator. After V2 biological analysis the subjects will be considered as non eligible to the study on the following criteria: * Fasting plasma TC, HDL or TG with an abnormality judged as clinically significant according to the investigator. * Serum AST, ALT, GGT, ALP or bilirubin with an abnormality judged as clinically significant according to the investigator. * Serum urea or creatinine with an abnormality judged as clinically significant according to the investigator. * Complete blood count with clinically significant abnormality according to the investigator. Volunteers with the following criteria at the V3 will be considered as non eligible to the study: * Capsules' consumption less than 80% of capsules during the run-in period (since V1) according to the quantities returned. * Gastroenteritis history finished less than 2 weeks before the randomization. The included subjects who cannot be randomized at V3 because of a too short wash out period related to the non inclusion criteria E8, E10, E12 or E34 can delay their visit V3 without to exceed 28 days from the visit V2. A re-screening can occur from 2 months after the exit of study for failure to comply with the one or more of the eligibility criteria listed above (except for E33 criteria).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of the fasting blood LDL cholesterol concentration | 12 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Systolic Blood Pressure | 4 weeks |
| Change in fasting blood total cholesterol concentration | 4 weeks |
| Change in fasting blood LDLc concentration | 4 weeks |
| Change in fasting blood HDLc concentration | 4 weeks |
| Change in fasting blood ratio total cholesterol / HDLc concentrations | 4 weeks |
| Change in fasting blood ratio LDLc / HDLc concentrations | 4 weeks |
| Change in fasting blood triglycerides concentration | 4 weeks |
| Change in fasting blood Apo A1 concentration | 4 weeks |
| Change in fasting blood Apo B100 concentration | 4 weeks |
| Change in fasting blood insulin concentration | 4 weeks |
| Change in fasting blood glucose concentration | 12 weeks |
| Change in fasting blood acetate concentration | 12 weeks |
| Change in fasting blood propionate concentration | 12 weeks |
| Change in fasting blood acetate / propionate concentrations | 12 weeks |
| Change in SCORE - European Low Risk Chart of fatal cardiovascular disease | 4 weeks |
| Change in fasting blood hsCRP concentration | 12 weeks |
| Complete blood count | 12 weeks |
| Blood Alkaline Phosphatase | 12 weeks |
| Blood Alanine Amino Transferase | 12 weeks |
| Blood Aspartate Amino Transferase | 12 weeks |
| Blood Gamma Glutamyl Transpeptidase | 12 weeks |
| Blood total bilirubin | 12 weeks |
| Blood urea | 12 weeks |
| Blood creatinine | 12 weeks |
| Heart rate | 4 weeks |
| Diastolic Blood Pressure | 4 weeks |
| Body weight | 4 weeks |
| Physical Activity Score | 12 weeks |
| Total energy intake | 12 weeks |
| Percentage of energy intake from fat | 12 weeks |
| Dietary fiber intake | 12 weeks |
| Saturated Fatty Acids intake | 12 weeks |
Other
| Measure | Time frame |
|---|---|
| Urinary density level | 12 weeks |
| Urinary bilirubin level | 12 weeks |
| Urinary urobilirubinogen level | 12 weeks |
| Urinary protein level | 12 weeks |
| Urinary glucose level | 12 weeks |
| Urinary ketones level | 12 weeks |
| Urinary nitrites level | 12 weeks |
| Urine sediment | 12 weeks |
| Urine osmolality | 12 weeks |
| Urine pH | 12 weeks |
| Urinary red cells level | 12 weeks |
| Urinary white cells level | 12 weeks |
| Fasting blood potassium concentration | 12 weeks |
| Fasting blood bicarbonates concentration | 12 weeks |
| Fasting blood calcium concentration | 12 weeks |
| Fasting blood inorganic phosphate concentration | 12 weeks |
| Fasting blood PCSK9 concentration | 12 weeks |
| Fasting blood FGF-19 concentration | 12 weeks |
| Fasting blood LDLox concentration | 12 weeks |
| Fasting blood fibrinogen concentration | 12 weeks |
| Fasting blood biliary acids concentrations | 12 weeks |
| Fecal concentrations of neutral sterol including cholesterol and its secondary metabolites | 12 weeks |
| Fecal concentrations of phytosterols | 12 weeks |
| Fecal concentrations of volatil fatty acids | 12 weeks |
| Fecal concentrations of branched chain fatty acids | 12 weeks |
| Fecal concentrations of biliary acids | 12 weeks |
| Fecal concentrations of AB-Life probiotic strains | 12 weeks |
| Fecal concentration of calprotectin | 12 weeks |
| Fasting blood sodium concentration | 12 weeks |
| Urine aspect | 12 weeks |
| Urine color | 12 weeks |
Countries
France
Outcome results
None listed