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Olive Oil Polyphenols and Cardiovascular Health Biomarkers

Primary Purpose

Healthy, Normal Weight, Overweight

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
High-polyphenol olive oil
Low-polyphenol olive oil
Sponsored by
University of California, Davis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Healthy

Eligibility Criteria

20 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Generally healthy male and female subjects within the range of 20-45 years of age and BMI range of 18.5-29.9 kg/m2 for the healthy weight/overweight group and ≥ 30 kg/m2 for the obese group will be recruited.

Exclusion Criteria:

  • Adults unable to consent, individuals who are not yet adults (infants, children, teenagers), pregnant or lactating women, women planning to become pregnant in the next two months and prisoners will be specifically excluded
  • Documented chronic diseases including diabetes, thyroid disease, kidney disease, metabolic syndrome, active cancer, previous cardiovascular events, history of gastric bypass or other GI issues related to fat absorption
  • History of dyslipidemia or abnormal blood glucose levels (total cholesterol >240 mg/dL, elevated fasting blood glucose levels >125 mg/dL)
  • Allergy to olives, inability to tolerate gluten or multiple allergies/intolerances that would significantly limit food intake
  • Smoker or living with a smoker, illicit drug use, consuming >1 alcoholic drink/day, vaporizer and/or electronic cigarette use
  • Extreme dietary or exercise patterns
  • Recent weight fluctuations (>10% in the last 6 months)
  • Taking prescription lipid medications or supplements that may affect lipoprotein metabolism, >1 g of fish oil/day, antioxidant supplements, cannabidiol (CBD) oil
  • Taking exogenous hormones (e.g. hormonal birth control)
  • Poor venous access
  • Unwillingness to comply with study protocol

Sites / Locations

  • Ragle Human Nutrition CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

High-polyphenol olive oil

Low-polyphenol olive oil

Arm Description

Participants will consume 40 mL of high-polyphenol olive oil each day at home for 2 weeks.

Participants will consume 40 mL of low-polyphenol olive oil each day at home for 2 weeks.

Outcomes

Primary Outcome Measures

Assessing the influence of olive oil polyphenols on cholesterol efflux
Cholesterol efflux will be measured by assessing changes in reverse cholesterol transport rate in separated serum at each study time point (baseline, 2 hour, 4 hour) using a commercially available assay kit at each of the 4 study visits.
Assessing the influence of olive oil polyphenols on cholesterol ester transfer protein activity (CETP)
Changes in CETP activity will be measured at each study time point (baseline, 2 hour, 4 hour) in plasma at each of the 4 study visits. The isolated plasma will be co-incubated with donor and acceptor molecules using a commercially available assay kit.
Assessing the influence of olive oil polyphenols on circulating oxidized LDL
Measure for changes in circulating levels of oxidized LDL in separated plasma at each study time point (baseline, 2 hour, 4 hour) using a commercially available ELISA kit; measured in units of U/L at each of the 4 study visits.
Assessing the influence of olive oil polyphenols on blood lipid measurements
Measure for changes in the levels of HDL and LDL in separated plasma; measured in units of mg/dL. Blood will be assessed for the fasting (baseline) sample only at each of the 4 study visits.
Assessing the influence of olive oil polyphenols on paraoxonase-1 (PON-1) activity
Measure for changes in PON-1 activity in separated plasma at each study time point (baseline, 2 hour, 4 hour) at each of the 4 study visits. Activity will be calculated based on linear rates of hydrolysis of phenyl acetate to phenol.
Assessing the influence of olive oil polyphenols on peripheral blood mononuclear cells (PBMC) using ex vivo stimulation assays
Measurement of changes in PBMC derived cytokines as a marker of inflammation at each study time point (baseline, 2 hour, 4 hour) at each of the 4 study visits. Assessment will be based on an increase or decrease in concentration in pg/ml.

Secondary Outcome Measures

Assessing the influence of olive oil polyphenols on gene expression in mirco RNA in PBMCs
Measure level of gene expression in micro RNA from PBMCs at each study time point (baseline, 2 hour, 4 ) at each of the 4 study visits. Assessment will be based on fold change between study arms.

Full Information

First Posted
September 30, 2019
Last Updated
September 14, 2023
Sponsor
University of California, Davis
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1. Study Identification

Unique Protocol Identification Number
NCT04149288
Brief Title
Olive Oil Polyphenols and Cardiovascular Health Biomarkers
Official Title
Olive Oil Polyphenols and Cardiovascular Health Biomarkers
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 6, 2021 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
October 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Davis

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research is to investigate whether consuming two different kinds of olive oil will change risk factors related to cardiovascular disease, including levels of good and bad cholesterol, levels of inflammation, and levels of gene expression.
Detailed Description
The purpose of this research is to investigate whether consuming two different kinds of olive oil will change risk factors related to cardiovascular disease, including levels of good and bad cholesterol, levels of inflammation, and levels of gene expression. Healthy individuals aged 20-45 with a BMI over 20 kg/m2 are eligible to participate. The study involves 5 visits (1 initial screening and 4 study visits) and will last about 8 weeks. There is a 2-week run-in period before starting the study, followed by two diet intervention periods each lasting two weeks, separated by a two-week washout period. Participation in this study will involve an initial two-week run in period to become accustomed to the study diet. After this two week period, participants will be randomly selected to start either a high-polyphenol olive oil (extra virgin olive oil) or a low-polyphenol olive oil (refined olive oil); participants will consume the other oil during the second dietary intervention period lasting 2 weeks. During each phase of the study, participants will be asked to come to the University of California, Davis campus after a 10-12 hour overnight fast. At each visit, body measurements will be taken, a serving of olive oil and bread will be eaten, and three urine and blood samples will be collected over the course of 4 hours. Each study visit will involve three blood draws by a trained nurse or phlebotomist. During the 8 weeks of the study, all olive products such as olives, olive oil, and olive containing products will need to be avoided. The study will provide olive oil to be eaten at home for each intervention phase. Additionally, the investigators will ask that nuts and high-polyphenol foods (mostly fruits and vegetables) be avoided in the diet. Detailed food diaries will be filled out and brought to study visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Normal Weight, Overweight, Obese

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
44 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
High-polyphenol olive oil
Arm Type
Active Comparator
Arm Description
Participants will consume 40 mL of high-polyphenol olive oil each day at home for 2 weeks.
Arm Title
Low-polyphenol olive oil
Arm Type
Active Comparator
Arm Description
Participants will consume 40 mL of low-polyphenol olive oil each day at home for 2 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
High-polyphenol olive oil
Intervention Description
High-polyphenol olive oil will be provided to study participants to consume at home. Participants will be asked to consume 40 mL each day for 2 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Low-polyphenol olive oil
Intervention Description
Low-polyphenol olive oil will be provided to study participants to consume at home. Participants will be asked to consume 40 mL each day for 2 weeks.
Primary Outcome Measure Information:
Title
Assessing the influence of olive oil polyphenols on cholesterol efflux
Description
Cholesterol efflux will be measured by assessing changes in reverse cholesterol transport rate in separated serum at each study time point (baseline, 2 hour, 4 hour) using a commercially available assay kit at each of the 4 study visits.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on cholesterol ester transfer protein activity (CETP)
Description
Changes in CETP activity will be measured at each study time point (baseline, 2 hour, 4 hour) in plasma at each of the 4 study visits. The isolated plasma will be co-incubated with donor and acceptor molecules using a commercially available assay kit.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on circulating oxidized LDL
Description
Measure for changes in circulating levels of oxidized LDL in separated plasma at each study time point (baseline, 2 hour, 4 hour) using a commercially available ELISA kit; measured in units of U/L at each of the 4 study visits.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on blood lipid measurements
Description
Measure for changes in the levels of HDL and LDL in separated plasma; measured in units of mg/dL. Blood will be assessed for the fasting (baseline) sample only at each of the 4 study visits.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on paraoxonase-1 (PON-1) activity
Description
Measure for changes in PON-1 activity in separated plasma at each study time point (baseline, 2 hour, 4 hour) at each of the 4 study visits. Activity will be calculated based on linear rates of hydrolysis of phenyl acetate to phenol.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on peripheral blood mononuclear cells (PBMC) using ex vivo stimulation assays
Description
Measurement of changes in PBMC derived cytokines as a marker of inflammation at each study time point (baseline, 2 hour, 4 hour) at each of the 4 study visits. Assessment will be based on an increase or decrease in concentration in pg/ml.
Time Frame
Through study completion, an average of 8 weeks
Secondary Outcome Measure Information:
Title
Assessing the influence of olive oil polyphenols on gene expression in mirco RNA in PBMCs
Description
Measure level of gene expression in micro RNA from PBMCs at each study time point (baseline, 2 hour, 4 ) at each of the 4 study visits. Assessment will be based on fold change between study arms.
Time Frame
Through study completion, an average of 8 weeks
Other Pre-specified Outcome Measures:
Title
Food record analysis
Description
Use a computer program to check for study dietary requirements. Subjects are to avoid olives and olive containing products during study protocol periods. This will be done using a subject self-recorded 3-day food record submitted to study personnel.
Time Frame
Through study completion, an average of 8 weeks
Title
Anthropometric measurements
Description
Measure waist (cm) and hip circumference (cm) before the start of drawing blood on study day protocols.
Time Frame
Through study completion, an average of 8 weeks
Title
Measure for changes in weight
Description
Measure weight (kg) before the start of drawing blood on study day protocols.
Time Frame
Through study completion, an average of 8 weeks
Title
Measure for changes in blood pressure
Description
Measure blood pressure (mmHg) before the start of drawing blood on study day protocols.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on circulating cytokines
Description
Measure circulating cytokines in separated plasma at each study time point (baseline, 2 hour, 4 hour) at each of the 4 study visits. Commercially available ELISA kits will be used: TNF-a, IL-6, IL-1B, MCP-1, and ET-1.
Time Frame
Through study completion, an average of 8 weeks
Title
Assessing the influence of olive oil polyphenols on urine metabolites
Description
Metabolomics will be performed on urine to assess for study compliance of consumption of the polyphenol containing olive oil versus the low-polyphenol containing olive oil at each of the 4 study visits.
Time Frame
Through study completion, an average of 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Generally healthy male and female subjects within the range of 20-45 years of age and BMI range of 18.5-29.9 kg/m2 for the healthy weight/overweight group and ≥ 30 kg/m2 for the obese group will be recruited. Exclusion Criteria: Adults unable to consent, individuals who are not yet adults (infants, children, teenagers), pregnant or lactating women, women planning to become pregnant in the next two months and prisoners will be specifically excluded Documented chronic diseases including diabetes, thyroid disease, kidney disease, metabolic syndrome, active cancer, previous cardiovascular events, history of gastric bypass or other GI issues related to fat absorption History of dyslipidemia or abnormal blood glucose levels (total cholesterol >240 mg/dL, elevated fasting blood glucose levels >125 mg/dL) Allergy to olives, inability to tolerate gluten or multiple allergies/intolerances that would significantly limit food intake Smoker or living with a smoker, illicit drug use, consuming >1 alcoholic drink/day, vaporizer and/or electronic cigarette use Extreme dietary or exercise patterns Recent weight fluctuations (>10% in the last 6 months) Taking prescription lipid medications or supplements that may affect lipoprotein metabolism, >1 g of fish oil/day, antioxidant supplements, cannabidiol (CBD) oil Taking exogenous hormones (e.g. hormonal birth control) Poor venous access Unwillingness to comply with study protocol
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Francene M Steinberg, PhD, RD
Phone
(530) 752-0160
Email
fmsteinberg@ucdavis.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jody Randolph, MS
Phone
(530) 752-7620
Email
jmrandolph@ucdavis.edu
Facility Information:
Facility Name
Ragle Human Nutrition Center
City
Davis
State/Province
California
ZIP/Postal Code
95616
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francene M Steinberg, PhD, RD
Phone
530-752-0160
Email
fmsteinberg@ucdavis.edu

12. IPD Sharing Statement

Links:
URL
https://studypages.com/s/a-study-of-olive-oil-polyphenols-molecules-in-plant-based-food-and-cardiovascular-health-273896/
Description
Learn more or sign up for the study here!

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Olive Oil Polyphenols and Cardiovascular Health Biomarkers

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