Skip to content

Cardio Protective Properties of a Yogurt Enriched With Bioactive Lipids of Olive Oil Products

Cardio Protective Properties of a Yogurt Enriched With Bioactive Lipids of Olive Oil Products

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02259205
Enrollment
100
Registered
2014-10-08
Start date
2014-09-30
Completion date
2015-10-31
Last updated
2015-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases

Keywords

platelet activating factor, inflammatory markers, yogurt, olive oil, platelet aggregation, oxidative stress, endothelial damage, bioactive lipids

Brief summary

This study evaluates the effectiveness of a yogurt enriched with bioactive lipids extracted from olive mill waste in platelet aggregation and other inflammatory and oxidative stress markers. The study will include three groups: the intervention group will receive the enriched yogurt while the other two groups will serve as controls (plain yogurt and no yogurt consumption).

Detailed description

Cardiovascular diseases are the leading cause of mortality worldwide. Data from the investigators research group indicate that platelet activating factor (PAF) is one of the most important inflammatory factors and the main mediator of thrombosis during the formation of atherosclerotic plaque. Thus, dietary interventions aimed at inhibition of PAF is of particular importance in public health level. The aim of the study is to examine the efficacy of administering in humans bioactive lipids extracted from olive mill waste (with proven in vitro anti-thrombotic activity and in vivo anti-atherosclerotic properties in rabbits fed an atherogenic diet) to inhibit the activity of PAF and other inflammatory mediators. Bioactive lipids are isolated by standardized methodology of oil manufacture byproducts. Preliminary studies have been done in animals to establish the safety of administration of these compounds and to clarify the effective dosages of administration for inhibiting formation of atherosclerotic plaques. The effectiveness of these compounds in humans will be examined in a randomized, double-blind clinical trial in subjects aged 40-60 years, lasting eight weeks. Supplementation with the bioactive lipids will be in the form of an enriched yogurt provided daily. The study includes three groups: treatment group, where enriched yogurt will be provided, plain yogurt treatment group and no consumption of yogurt group . Parameters that will be assessed are the inhibition of platelet aggregation (with three different stimuli, including PAF), lipid profile, inflammatory markers such as CRP, IL-6, TNFa, and oxidative stress markers.

Interventions

OTHEREnriched Yogurt

150 g yogurt enriched with bioactive lipids extract from olive oil mill will be provided daily for 8 weeks

OTHERPlain Yogurt

150 g plain yogurt will be provided daily for 8 weeks

Sponsors

National and Kapodistrian University of Athens
CollaboratorOTHER
Competitiveness and Entrepreneurship (OPCE II), NRSF 2007-13
CollaboratorUNKNOWN
Harokopio University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* All individuals, aged 40-60 years, without any of the

Design outcomes

Primary

MeasureTime frameDescription
Changes in Platelet aggregation0 (baseline), end of 4th week and 8th weekThe ability of platelets to aggregate will be measured in platelet rich plasma (PRP) of volunteers using PAF, thrombin and ADP as aggregating factor.

Secondary

MeasureTime frameDescription
Changes in Glucose and Insulin0 (baseline), end of 4th week and 8th weekBlood levels of glucose and insulin
Changes in Gastro-intestinal symptoms0 (baseline), end of 4th week and 8th weekGastro-intestinal symptoms and possible side effects from yogurt consumption will be assessed through validated questionnaires.
Change in Dietary intake0 (baseline), end of 8th weekDietary intake will be assessed through two dietary recalls and a food frequency questionnaire at each time point.
Changes in Blood lipid profile0 (baseline), end of 4th week and 8th weekBlood levels of cholesterol, LDL-cholesterol, HDL-cholesterol and triacylglycerols will be measured.
Changes in Gut microbiota populations0 (baseline), end of 8th weekthe populations of lactobacilli, bifidobacteria and Clostridium histolyticum group will be estimated by real-time PCR using genus specific primers. Furthermore, the metabolic products of the gut microorganisms will be evaluated by measuring the short chain fatty acids profile in fecal samples.
Changes in Inflammation-related markers0 (baseline), end of 4th week and 8th weekC-reactive protein (CRP), IL-6, TNFa, IL-10 levels in fasting blood samples.
Changes in Oxidative stress0 (baseline), end of 4th week and 8th weekEx vivo serum oxidation as a marker for lipid oxidation and protein carbonyls as a marker for protein oxidation will be measured.

Countries

Greece

Contacts

Primary ContactSmaragdi Antonopoulou, PhD
antonop@hua.gr+302109549100
Backup ContactTzortzis Nomikos, PhD
tnomikos@hua.gr+302109549100

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026