- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04066816
Ellagic Acid, Urolithin and Colonic Microbial Communities Affected by Walnut Consumption
November 24, 2021 updated by: Daniel Rosenberg, UConn Health
Briefly, this is a 28-day dietary intervention study participants will be asked to eat 2 ounces (52 grams) of walnuts every day for 3 weeks, and at the end of the study period they will come in for a colonoscopy.
Participants will first start a 1-week run-in period where they will be asked to avoid foods high in ellagic acid.
In addition, they will be asked to complete food surveys and two sets of 3-day dietary records, and to provide colon biopsies for this study during their routine colonoscopy, as well as a blood, and two urine and stool samples.
Urine samples will be used for analysis of urolithin, ellagic acid metabolites.
Stool samples will be used to assess gut microbiota changes after walnut consumption.
Dietary records will be used for compliance and Food Frequency Questionnaire will be used to assess dietary habits.
Lastly, the biopsy samples will be used for analysis of biomarkers and anti-inflammatory in the colon, as well as adherent microbiome to the colonic tissue.
Data will be analyzed based on the urolithin phenotypes.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The investigators propose to address the influence of ellagic acid obtained from walnuts and its microbial-derived metabolites (urolithin) on the gut microbiome and inflammation-related biomarkers in a human clinical study.
Patients will be enrolled and detailed demographic and dietary information, biopsy specimens through colonoscopies, as well as fecal, blood and urine samples will be collected.
The wide range of gut urolithin levels provides the rationale for our proposed studies.
Will the specific urolithin phenotypes show a disparate range of chemopreventive (anti-inflammatory) response to walnut consumption?
The hypothesis is that walnut ingestion in "Phenotype A" participants (producing the highest levels of urolithin) will be associated with a beneficial anti-inflammatory response as tested in colonic mucosa and a higher abundance of bacterial species associated with ellagic acid metabolism.
Although 16S ribosomal ribonucleic acid gene (rRNA) sequencing allows inexpensive bacterial identification at the genus/species level, a whole genome sequencing (mWGS) will be employed to achieve finer classification (strain level), and identify other microbes (e.g., viruses, fungi, small eukaryotes).
Furthermore, mWGS targets the entire genome of each microbe (not just the 16S rRNA gene), allowing for construction of a microbial gene catalogue, including a metabolic pathway description for each sample.
This will characterize the functional potential of the microbial community.
Ultimately, the proposed studies will inform the application of prebiotic to enhance the formation of urolithin metabolites from ellagic acid for the prevention of inflammation-associated Colorectal Cancer, a development that would have significant translational implications.
Study Type
Interventional
Enrollment (Actual)
47
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
-
Farmington, Connecticut, United States, 06030
- University of Connecticut Health Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
46 years to 61 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Men or women between the ages of 50-65 years old who are scheduled to undergo a routine screening colonoscopy
- English speaking/reading patients willing and able to provide written informed consent for study participation
- Patients willing to consume walnuts for 3 weeks
- Willingness to comply with all study requirements
Exclusion Criteria:
- Current active malignancy, previous history of gastrointestinal malignancy, or altered gastrointestinal anatomy
- Current evidence or previous history of ulcerative colitis or Crohn's disease
- HIV infection, chronic viral hepatitis
- Allergy to walnuts or hypersensitivity to tree nuts
- Use of antibiotics within the past month
- Individuals with blood coagulation disorders or on anti-coagulant therapy
- Treated with steroids, immunosuppressive agents or other anti-inflammatory drugs one week prior to starting intervention
- Non-English-speaking patients who require an interpreter to give consent
- Patients residing in the Department of Correction
- Inability to comply with the protocol requirements
- Any other condition that, in the opinion of the PI, might interfere with study objectives
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Walnut Consumption
After screening, participants will avoid foods high in ellagic acid.
These foods include pomegranates, hazelnuts, pistachios, strawberries, raspberries, blackberries, oak-aged wines, spirits, and walnuts (besides the ones given by researchers); a complete list will be provided to the subjects.
Participants will then return to research facility and provide urine and stool samples, as well as a set of 3-day dietary records.
Then, they will start to consume 2 ounces of walnuts per day for 21 days with their usual diet.
At the end, they will collect another urine and stool sample as well as another set of dietary records, and then come in for the scheduled colonoscopy where they will be asked to provide biopsy specimens.
That completes the intervention and participation in the study.
|
Participants will consume 2 ounces of walnuts for 21 days
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Leve of Urolithin of this Population
Time Frame: 28 days post walnuts
|
Urolithin will be measure in urine using a mass spectrometer to characterize this population into three know urolithin phenotypes, Uro-A, Uro-B and Uro-0, after walnut consumption.
|
28 days post walnuts
|
|
Urolithin Phenotype and Colonic Health
Time Frame: 28 days post walnuts
|
Assess biomarkers in colonic mucosa from biopsy samples collected at colonoscopy that are associated with the three different urolithin metabotype following walnut consumption.
This biomarkers is a total of 287 genes involved in cellular apoptosis and proliferation, inflammation and senescence, including TIMP1 (used for power calculations), cytokine and T cell and B cell signaling genes, as well as markers of lymphocyte subsets and immune checkpoint pathways and targets, providing a wide range of functional annotation groups.
|
28 days post walnuts
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Identify Changes in Microbiota and Microbes Responsible for Urolithin Formation Followed by Walnuts Consumption using Metagenomics Sequencing
Time Frame: Day 7 to Day 28
|
Microbiome will be analyzed before and after walnut consumption with the goal to identify microbes responsible for urolithins production.
DNA will be extracted from fecal samples and the V1-3 hyper-variable region of bacterial 16S rRNA genes will be sequenced to analyze bacterial community structure.
Although 16S rRNA gene sequencing allows inexpensive bacterial identification to the genus/species level, mWGS will be employed in order to achieve finer classification (strain level), and identify other microbes, including viruses, fungi and small eukaryotes.
|
Day 7 to Day 28
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: JOHN BIRK, MD, UConn Health
- Principal Investigator: DANIEL W ROSENBERG, PhD, UConn Health
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 20, 2019
Primary Completion (Actual)
April 8, 2021
Study Completion (Actual)
April 8, 2021
Study Registration Dates
First Submitted
August 20, 2019
First Submitted That Met QC Criteria
August 22, 2019
First Posted (Actual)
August 26, 2019
Study Record Updates
Last Update Posted (Actual)
November 26, 2021
Last Update Submitted That Met QC Criteria
November 24, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 19-121JS-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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