Impact of Non Digestible Carbohydrate on Production of Phenolic Acids From Strawberry Juice

NCT ID: NCT03383809

Last Updated: 2019-07-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-04-28

Study Completion Date

2019-07-06

Brief Summary

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This is an acute human bioavailability study in self-reported healthy participants aged 20-70 years old. We hypothesize that combination of dietary polyphenolics and non-digestible carbohydrates (NDC) will increase the production of phenolic acids by bacteria in the human colon and these will be detected in urine. Participants will attend for three arms in a randomised order: Strawberry juice (a high polyphenol food), Inulin (NDC) or Mixture of strawberry juice and inulin.

Detailed Description

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Polyphenol rich plant foods have been associated with several health benefits but their bioavailability is generally low. The majority of plant polyphenols are poorly absorbed in the small intestine and enter the colon where the colonic microbiota metabolise them to release a range of phenolic acids, which are now thought to be the main bioactive components related to the reduction in disease risk. Very little is known about the impact of other constituents of the diet on the metabolism and bacterial catabolism of these polyphenols. The colonic microbiota are key agents in the release of the bioactive molecules from polyphenols but also ferment non-digestible carbohydrates (NDC) such as dietary fibre to short chain fatty acids. It is likely that there are key interactions in the colonic bacteria metabolism of fibre and phenolics. We hypothesize that combination of polyphenolics and non-digestible carbohydrates (NDC) will increase the urinary output of bioactive phenolic acids.

This study will enable a better understanding of how to deliver combinations of ingredients and nutrients to achieve maximum nutritional value and health benefits.

Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Acute human bioavailability studies with a cross-over design will be given to subjects in the form of a drink in one of three combinations

1. Strawberry juice alone
2. Inulin alone
3. Mixture of strawberry juice and inulin
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Strawberry juice with inulin

One dose of 300 g of strawberry with 10 g of inulin will be given to subjects in the form of juice

Group Type EXPERIMENTAL

Strawberry juice with Inulin

Intervention Type DIETARY_SUPPLEMENT

Mixture of polyphenols and non digestible carbohydrates

Strawberry juice

One dose of 300 g of strawberry juice will be given to subjects in the form of juice

Group Type EXPERIMENTAL

Strawberry Juice

Intervention Type DIETARY_SUPPLEMENT

Source of Polyphenols

Inulin

One dose of 10 g of inulin will be given to subjects in the form of a drink

Group Type EXPERIMENTAL

Inulin

Intervention Type DIETARY_SUPPLEMENT

Source of non digestible carbohydrate

Interventions

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Strawberry juice with Inulin

Mixture of polyphenols and non digestible carbohydrates

Intervention Type DIETARY_SUPPLEMENT

Strawberry Juice

Source of Polyphenols

Intervention Type DIETARY_SUPPLEMENT

Inulin

Source of non digestible carbohydrate

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

Self-reported healthy adults

Exclusion Criteria

Antibiotic use within the last 3 months, identified gastro-intestinal diseases, on prescribed medication other than the contraceptive pill, individuals who are pregnant or breastfeeding. Individuals who have been diagnosed as anaemic, as well as those who are allergic to any food, or paracetamol.
Minimum Eligible Age

20 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Scottish Universities Environmental Research Centre

OTHER

Sponsor Role collaborator

University of Glasgow

OTHER

Sponsor Role lead

Responsible Party

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Christine Edwards

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Prof. Edwards

Role: PRINCIPAL_INVESTIGATOR

University of Glasgow

Locations

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School of Medicine, Nursing and Dentistry, College of MVLS, University of Glasgow

Glasgow, Lanarkshire, United Kingdom

Site Status

Countries

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United Kingdom

References

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Russell W, Duthie G. Plant secondary metabolites and gut health: the case for phenolic acids. Proc Nutr Soc. 2011 Aug;70(3):389-96. doi: 10.1017/S0029665111000152.

Reference Type BACKGROUND
PMID: 21781364 (View on PubMed)

Roowi S, Mullen W, Edwards CA, Crozier A. Yoghurt impacts on the excretion of phenolic acids derived from colonic breakdown of orange juice flavanones in humans. Mol Nutr Food Res. 2009 May;53 Suppl 1:S68-75. doi: 10.1002/mnfr.200800287.

Reference Type BACKGROUND
PMID: 19415668 (View on PubMed)

Henning SM, Wang P, Abgaryan N, Vicinanza R, de Oliveira DM, Zhang Y, Lee RP, Carpenter CL, Aronson WJ, Heber D. Phenolic acid concentrations in plasma and urine from men consuming green or black tea and potential chemopreventive properties for colon cancer. Mol Nutr Food Res. 2013 Mar;57(3):483-93. doi: 10.1002/mnfr.201200646. Epub 2013 Jan 14.

Reference Type BACKGROUND
PMID: 23319439 (View on PubMed)

Czank C, Cassidy A, Zhang Q, Morrison DJ, Preston T, Kroon PA, Botting NP, Kay CD. Human metabolism and elimination of the anthocyanin, cyanidin-3-glucoside: a (13)C-tracer study. Am J Clin Nutr. 2013 May;97(5):995-1003. doi: 10.3945/ajcn.112.049247.

Reference Type BACKGROUND
PMID: 23604435 (View on PubMed)

Morrison DJ, O'Hara JP, King RF, Preston T. Quantitation of plasma 13C-galactose and 13C-glucose during exercise by liquid chromatography/isotope ratio mass spectrometry. Rapid Commun Mass Spectrom. 2011 Sep 15;25(17):2484-8. doi: 10.1002/rcm.5139.

Reference Type BACKGROUND
PMID: 21818809 (View on PubMed)

Other Identifiers

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BB/MO27724/1-1

Identifier Type: -

Identifier Source: org_study_id

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