Combination of AB-LIFE Probiotic Plus Monacolin K to Reduce Blood Cholesterol

Hypercholesterolemia Clinical Trial

Official title:

Effect of a Nutritional Supplement (AB-LIFE Plus Monacolin K) to Reduce Total and LDL Cholesterol Levels

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04677335
• Other study ID #: PRIMACOL01
• Status: Completed
• Phase: N/A
• Start date: October 1, 2014
• Est. completion date: September 19, 2017

Study information

• Verified date: January 2021
• Source: AB Biotics, SA
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This randomized study evaluates the effectiveness of a nutraceutical combining billion colony forming units (cfu) of three L. plantarum strains (CECT7527, CECT7528 and CECT7529) and 10 mg of monacolin K in reducing blood cholesterol.

Description:

Cardiovascular diseases (CVDs) are the number 1 cause of death globally, and retention of low-density lipoprotein cholesterol (LDL-C) and similar cholesterol-rich lipoproteins containing apolipoprotein B (ApoB) within the arterial wall is a key initiating event in CVDs. Statins are the mainstay of pharmacological cholesterol-reduction therapy. However, a significant proportion of patients report some degree of statin intolerance, which typically fade away when the statin is switched, discontinued or the dosage reduced. A growing attention has been devoted to the correction of increased LDL-C levels through the use of dietary supplements, either because some patients have milder forms of hypercholesterolemia or as an alternative to statins in patients who may have experienced or are worried of side effects. Nutraceutical combinations are increasingly used in clinical practice. In this pilot randomized study, we sought to evaluate of the effect on LDL-C and other blood lipid parameters of a nutraceutical combining Red Yeast Rice extract (also known by its scientific name Monascus purpureus) containing 10 mg of monacolin K, plus 1 billion colony forming units (cfu) of the AB-LIFE probiotic formula. The later is composed of three L. plantarum strains, namely CECT7527 (also known as KABP011™), CECT7528 (also known as KABP012™) and CECT7529 (also known as KABP013™).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: September 19, 2017
• Est. primary completion date: April 15, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Total cholesterol (TC) =200 mg/dL and statin-naïve or having recently stopped statin treatment because of statin intolerance.

Exclusion Criteria:

• History of cardiovascular events or alcohol abuse, presence of diabetes, chronic advanced kidney disease, thyroid disorders, hepatic disorders, familial hypercholesterolemia or immunosuppression

• Body mass index (BMI) = 18.5 or =40 Kg/m2

• Use of antibiotics within 4 weeks of study initiation, current use of other probiotics, lipid-lowering medications, corticoids, beta-blockers or calcium channel blockers, thiazide diuretics, estrogen replacement therapy

• Pregnant or lactating women

• Patients with other severe disease that could interfere with the results of the study.

• Patients not agreeing to maintain their usual physical activity throughout the study.

Related Conditions & MeSH terms

• Hypercholesterolemia

Intervention

Dietary Supplement:
• AB-LIFE with Monacolin K
Red yeast rice extract (also known by its scientific name, Monascus purpureus) certified to contain 10 mg of monacolin K, plus 1 billion total cfu of AB-LIFE probiotic formula, which is composed of 3 Lactoplantibacillus plantarum (formerly known as Lactobacillus plantarum) strains: CECT7527 (also known as KABP011™), CECT7528 (also known as KABP012™) and CECT7529 (also known as KABP013™), all in a maltodextrin carrier. Capsules are of vegetable origin (hydroxypropylmethyl cellulose).

Other:
• Placebo
Placebo capsules containing maltodextrin carrier only. Capsules are of vegetable origin (hydroxypropylmethyl cellulose).

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
AB Biotics, SA	University of Extremadura

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in low density lipoprotein cholesterol (LDL-C)	Fasting serum levels of low density lipoprotein cholesterol (LDL-C), assessed by repeated measures analysis at three timepoints (baseline, mid of intervention and end of intervention).	0, 6 and 12 weeks
Secondary	Change in total cholesterol (TC)	Fasting serum levels of total cholesterol (TC), assessed by repeated measures analysis at three timepoints (baseline, mid of intervention and end of intervention).	0, 6 and 12 weeks
Secondary	Change in high density lipoprotein cholesterol (HDL-C)	Fasting serum levels of high density lipoprotein cholesterol (HDL-C), assessed by repeated measures analysis at three timepoints (baseline, mid of intervention and end of intervention).	0, 6 and 12 weeks
Secondary	Change in triglycerides (TG)	Fasting serum levels of triglycerides (TG), assessed by repeated measures analysis at three timepoints (baseline, mid of intervention and end of intervention).	0, 6 and 12 weeks
Secondary	Change in Body Mass Index (BMI)	Body Mass Index, calculated as body weight (in kilograms) divided by squared height (in meters), assessed by repeated measures analysis at two timepoints (baseline and end of intervention).	0 and 12 weeks
Secondary	Change in body weight	Body weight in kilograms, assessed by repeated measures analysis at two timepoints (baseline and end of intervention).	0 and 12 weeks
Secondary	Change in percent body fat	Percent of body fat (as determined with a MC780 Body Analyzer), assessed by repeated measures analysis at two timepoints (baseline and end of intervention).	0 and 12 weeks
Secondary	Patient satisfaction with treatment	Rated with a Likert-type scale ranging 0 (very dissatisfied) to 4 (very satisfied), assessed at the end of the intervention.	12 weeks
Secondary	Treatment-emergent adverse effects	Incidence of adverse effects (type and number) and relatedness to study product (using a 5 category system: certain, likely related, possibly related, conditionally related, unknown), as documented according to the Spanish Medicine and Medical Device Agency (AEMPS) pharmacovigilance system	12 weeks