- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05488886
Bioavailability of Aronia Berry Polyphenols
Optimizing the Bioavailability and Metabolism of Aronia Berry Polyphenols for Improving Gut Health
Study Overview
Status
Conditions
Detailed Description
Inflammatory bowel diseases (IBD): Crohn's disease and ulcerative colitis are two conditions of IBD that are characterized by chronic inflammation and damage of the gastrointestinal tract. In the United States alone, IBD are estimated to affect as many as 1.6 million people. IBD are associated with high morbidity, decreased quality of life, as well as substantial health care costs. IBD currently have no known cure, and treatment of IBD often requires the use of potent immunosuppressors which may lead to side effects or surgery.
Berries and prevention of chronic inflammation: Anthocyanins and other polyphenols are promising dietary agents to prevent and treat IBD by improving intestinal barrier dysfunction, inhibiting differentiation of pro-inflammatory T cells, reducing production of proinflammatory cytokines, and preventing oxidative stress. While preliminary studies are promising, translational human intervention studies are needed to refine delivery of polyphenol-rich foods and to confirm anti-inflammatory mechanisms.
Berries are rich dietary sources of polyphenols and essential nutrients. Polyphenol intake varies significantly by dietary patterns, but mean intake is estimated ~900 mg/day. Among berries, the polyphenol-dense aronia berry is one of the richest sources of fruit polyphenols.
Challenges associated with aronia berry consumption: In spite of its beneficial nutritional properties, the consumption of large amounts of whole aronia berry is not practical because of significant sorbitol and fiber content, which could lead to gastrointestinal discomfort for some individuals. Particularly, IBD patients often are required to limit fiber and whole fruit intake. The investigator's research group recently developed a novel method to extract polyphenols from fruit juice using food-grade lecithin which overcomes this problem.
The investigators hypothesize the resulting phospholipid-polyphenol (PLP) enriched material can improve the delivery of anthocyanins to the gut relative to a purified extract, and similar to that of whole berry. The aim of this study is to determine the comparative metabolism and bioavailability of aronia berry PLP intervention to extract, whole berry, and control food.
Consumption of Intervention Foods: In the morning of the day of each intervention and sampling period (days 6, 13, 20, and 27 i), participants will be asked to visit the Bolling Laboratory at the Department of Food Science fasted. Participants will then be asked to empty their bladders and then consume one serving of the applesauce (≤200 g). Then, in the next 24 h, participants will be asked to only consume commercially available frozen and shelf-stable low-polyphenol meals and snacks provided by study personnel. Insulated bags will be provided to participants for transport of frozen meals. The low-polyphenol diet and snacks will consist of dairy products, meat, low-phenolic snacks (e.g., banana, potato chips) and starch sources (e.g. white bread, rice, and plain bagels). Water will be available to participants over the time course, and its intake is not restricted.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Wisconsin
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Madison, Wisconsin, United States, 53706
- University of Wisconsin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- willing to consume low-anthocyanin diets during the last days of wash-in and wash-out periods
- willing to consume intervention foods during the sampling periods
- willing to provide 24-hour urine and fecal samples during the sampling periods.
Exclusion Criteria:
- people who do not consider themselves healthy
- anyone with a self-reported previous diagnosis of a gastrointestinal disease (e.g. inflammatory bowel disease, irritable bowel syndrome)
- undergoing current cancer treatment (i.e., chemotherapy, radiation therapy)
- are pregnant, lactating, or trying to become pregnant
- unwilling to consume study foods, or are allergic to sunflower, food colorants, berry ingredients, or any other component of the study foods.
- taking medication that contraindicates grapefruit juice consumption
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: A: Whole Aronia Berry Powder
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The food will be designed to be a berry-flavored applesauce.
The food will include applesauce, sweeteners, citric acid, natural flavors and food colorants.
Applesauce A will additionally contain whole aronia berry powder (Milne MicroDried, Nampa, ID).
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Experimental: B: Aronia Berry Extract
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The food will be designed to be a berry-flavored applesauce.
The food will include applesauce, sweeteners, citric acid, natural flavors and food colorants.
Applesauce B will additionally contain aronia berry extract (Artemis International, Fort Wayne, IN).
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Experimental: C: Phospholipid-Polyphenol
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The food will be designed to be a berry-flavored applesauce.
The food will include applesauce, sweeteners, citric acid, natural flavors and food colorants.
Applesauce C will additionally contain PLP which will be prepared with commercially-available aronia juice concentrate (Greenwood Associates, Niles, IL) and soy lecithin (Whole Foods, Austin, TX).
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Experimental: D: Low-Polyphenol Control
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The food will be designed to be a berry-flavored applesauce.
The food will include applesauce, sweeteners, citric acid, natural flavors and food colorants.
Applesauce D will not contain additional polyphenol-rich ingredients and is thus considered a low-polyphenol control.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Urinary Polyphenol Catabolite Concentration
Time Frame: sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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Targeted analysis of free urinary polyphenol metabolites will be performed by ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS).
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sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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Urinary Anthocyanin Concentration
Time Frame: sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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C18 solid-phase extraction (SPE) clean-up methods will be used to isolate anthocyanins and non-anthocyanin low-molecular weight polyphenol metabolites.
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sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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Fecal Polyphenol Catabolite Concentration
Time Frame: sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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C18 solid-phase extraction (SPE) clean-up methods will be used to isolate anthocyanins and non-anthocyanin low-molecular weight polyphenol metabolites.
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sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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Fecal Anthocyanin Concentration
Time Frame: sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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C18 solid-phase extraction (SPE) clean-up methods will be used to isolate anthocyanins and non-anthocyanin low-molecular weight polyphenol metabolites.
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sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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Urine Creatinine Content
Time Frame: sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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The urine creatinine content will be measured by a urinary creatinine colorimetric assay kit (Cayman Chemical).
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sampled on day 6, 13, 20, and 27 (participant randomized to different interventions each visit)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2022-0702
- Protocol Version 07/01/2022 (Other Identifier: UW Madison)
- A074000 (Other Identifier: UW Madison)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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