Obesity Clinical Trial
Official title:
Pilot Study: The Effects of Whole Grapes on Markers of Health
Verified date | May 2017 |
Source | University of California, Davis |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators hope to learn about the effects of whole grapes, in the form of
freeze-dried grape powder, on markers of health. Phytochemical rich food consumption is
associated with protection against chronic diseases such as cardiovascular disease (CVD)
demonstrating the ability to modify endothelial function and lipemia, but exact causal
mechanisms are still not well understood. The investigators will examine metabolic and
mechanistic effects of consumption of whole grape powder in chronic as well as acute
settings in response to meal challenges by testing blood samples to determine if markers of
health have improved.
The central hypothesis of this project is that consumption of grapes in the form of a
polyphenol-rich freeze-dried whole grape powder (WGP) will attenuate chronic and meal
induced oxidative stress and inflammatory responses in obese individuals.
Status | Completed |
Enrollment | 20 |
Est. completion date | April 2015 |
Est. primary completion date | October 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Men and women 18 years of age or older in good health - BMI >30 Exclusion Criteria: - Smokers - Chronic disease, such as diabetes, cancer, and renal, liver or thyroid dysfunction - History of gastrointestinal disease - History of cardiovascular events - If pregnant or lactating - Regular users of statin drugs, aspirin, anti-inflammatory medications, antioxidants or botanical supplements - Allergy to grapes |
Country | Name | City | State |
---|---|---|---|
United States | Ragle Human Nutrition Center | Davis | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Davis |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decrease inflammatory markers | High sensitivity C reactive protein, TNF-alpha, IL-1beta, lL-6. Assessed at time 0, 1, 3, 5 hours of acute meal challenge and in fasting samples at the end of the intervention. | After 4 week intervention | |
Primary | Decrease oxidative stress | Oxidized low density lipoprotein, urinary F2-isoprostane. | After 4 week intervention | |
Primary | Increase endothelial function | Blood pressure, intercellular adhesion molecule-1, vascular cell adhesion molecule-1, ESelectin. | After 4 week intervention | |
Primary | Improve lipid profile | Total cholesterol, low density lipoprotein cholesterol, high density lipoprotein cholesterol, triglyceride level, apolipoproteinA1, apolipoproteinB100. | After 4 week intervention | |
Primary | Decrease in mononuclear cell production | TLR4, SOCS-3, NADPH oxidase subunit p47phox, Nrf-2, p50 subunit, IL-1ß, MMP-9, MCP-1. | After 4 week intervention |
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