search
Back to results

Bioavailability and Beneficial Properties of Coffee and Cocoa Bioactive Compounds (P4L)

Primary Purpose

Diet Modification, Cardiovascular Risk Factor, Nutritional and Metabolic Diseases

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
cup of espresso coffee
cocoa-based products containing coffee
Sponsored by
University of Parma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diet Modification focused on measuring coffee, cocoa, bioavailability, pharmacokinetics, cardiometabolic risk factors, caffeoylquinic acids, flavan-3-ol, caffeine, trigonelline, diterpene

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • adult
  • both genders
  • healthy
  • normal weight (BMI 18-25)
  • regular coffee consumers of 1-5 cups per day

Exclusion Criteria:

  • younger than 18 y.o. or older than 60 y.o.
  • clinically diagnosis for metabolic, renal or digestive disorders
  • regular consumption of medication
  • antibiotic therapy taken within the last 3 months
  • intense physical activity
  • pregnancy or lactation
  • underweight or overweight/obese
  • no regular consumption of coffee or regular intake exceeding 5 coffees/day

Sites / Locations

  • Department of Food and Drug, University of Parma

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

low consumers

high consumers

medium consumers

Arm Description

1 cup of espresso coffee/day at 9.00 A.M. for 1 month

3 cup of espresso coffee/day at 9.00 A.M. 12.00 P.M. and 3.00 P.M. for 1 month

1 cup of espresso coffee at 9.00 A.M. + cocoa-based products containing coffee at 12.00 P.M. and 3.00 P.M. for 1 month

Outcomes

Primary Outcome Measures

Daily mean concentration of phenolic metabolites
Assessment of the daily mean concentration of coffee derived plasma circulating phenolic metabolites

Secondary Outcome Measures

Coffee-derived plasma circulating bioactives
Profile of metabolites coming from coffee phytochemicals (phenolic compounds, trigonelline, caffeine, and diterpenes) in plasma
Coffee-derived bioactives in urine
Profile of metabolites coming from coffee phytochemicals (phenolic compounds, trigonelline, caffeine, and diterpenes) in urine
Cocoa-derived plasma circulating bioactives
Profile of metabolites coming from cocoa phytochemicals (phenolic compounds and theobromine) in plasma
Cocoa-derived bioactives in urine
Profile of metabolites coming from cocoa phytochemicals (phenolic compounds and theobromine) in urine
Blood Pressure
Systolic and diastolic blood pressure
Body Mass Index (BMI)
Weight (in kg) and height (in m) will be combined to report BMI in kg/m2
Waist circumference
Trimethyl-ammine-N-oxide (TMAO) in plasma
Trimethyl-ammine-N-oxide (TMAO) in urine
Nitric oxide (NO) in plasma
Blood lipids
Total cholesterol, HDL, LDL, triglycerides
Glucose and Insulin
Fasting glucose and fasting insulin
DNA damage
Assessed by using the Comet assay
DNA catabolites
Assessed by using LC-MS for individual detection and quantification
Nutri-metabolomics in plasma
Metabolomics will be carried out in fasting plasma to unravel the potential metabolic pathways of molecules present in the food matrix
Nutri-metabolomics in urine
Metabolomics will be carried out in urine to unravel the potential metabolic pathways of molecules present in the food matrix
Eicosanoids in urine
Inflammatory markers in plasma
Main inflammatory markers associated with coffee consumption

Full Information

First Posted
May 21, 2017
Last Updated
October 24, 2017
Sponsor
University of Parma
search

1. Study Identification

Unique Protocol Identification Number
NCT03166540
Brief Title
Bioavailability and Beneficial Properties of Coffee and Cocoa Bioactive Compounds
Acronym
P4L
Official Title
Bioavailability and Beneficial Properties of Espresso Coffee and Confectionery Derived Coffee Bioactive Compounds
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
May 10, 2017 (Actual)
Primary Completion Date
October 20, 2017 (Actual)
Study Completion Date
October 20, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Parma

4. Oversight

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

5. Study Description

Brief Summary
The aim of this study will be to define the bioavailability and the beneficial properties of coffee bioactive compounds. Moreover, the contribution of cocoa-based products containing coffee to the pool of circulating metabolites will be investigated with the aim of evaluating the effect of the combination of bioactives from different sources. To study the bioavailability of coffee/cocoa bioactive compounds and their effects in cardiometabolic health, the objectives will be: i) Assessing the bioavailability of the four main groups of phytochemicals in roasted coffee (methylxanthines, phenolic compounds, trigonelline, and diterpenes), its modulation by the level of consumption, and establishing the daily average concentration of coffee-derived plasma circulating metabolites; ii) Investigating the effect of different levels of coffee consumption on cardiometabolic risk factors; iii) Evaluating circulating metabolites and their putative bioactivity when substituting coffee consumption with the intake of cocoa-based products containing coffee. A 3-arm, crossover, randomized trial will be conducted. Twenty-one volunteers will be randomly assigned to consume three treatments in a random order for 1 month: 1 cup of espresso coffee/day, 3 cups of espresso coffee/day, 1 cup of espresso coffee at breakfast and 2 cocoa-based products containing coffee two times per day. The last day of the treatment subjects will refer to the ambulatory where blood and urine samples will be collected at specific time points up to 24 hours following the consumption of the testing coffee or of the cocoa-based products containing coffee. In addition to the bioavailability of the bioactive compounds, the effect of the coffee consumption on several cardiometabolic risk factors (blood pressure, anthropometric measures, inflammatory markers, nitric oxide, blood lipids, fasting indices of glucose/insulin metabolism, DNA damage, eicosanoids, nutri-metabolomics) will be investigated. At the end of the treatment, the same protocol will be repeated, switching the allocation group.
Detailed Description
A human bioavailability study will be carried out to achieve the above-described goals. The human intervention study will consist of a short-term randomized cross-over trial, addressed at measuring the daily mean concentrations of each coffee/cocoa-derived circulating metabolite (CCDCM) for the four main groups of coffee/cocoa phytochemicals (methylxanthines, trigonelline, phenolics, diterpenes). On the basis of different patterns of consumption, this free-living study (although some minimal dietary restrictions will be provided two days before sampling times) will also take into consideration the effects of repeated doses on the bioavailability of coffee/cocoa bioactives. The study will follow a repeat-dose, 3-arm, cross-over design. This design has been chosen according to ILSI's guidelines for intervention trials with dietary products. Subjects were assigned to consume the following treatments in a random order for 1 month: 1 cup of espresso coffee/day ("low consumers") at 9.00 A.M. 3 cups of espresso coffee/day ("high consumers") at 9.00 A.M., 12.00 P.M.noon and 3.00 P.M. 1 cup of espresso coffee at breakfast 9.00 A.M. and 2 cocoa-based products containing coffee two times per day (at 12.00 P.M.noon and 3.00 P.M.). The group will be named "medium consumers", considering the caffeine content of the cocoa-based products containing coffee. Minimal recommendations to avoid other sources of coffee/cocoa phytochemicals besides what introduced through the assigned treatment, and to standardise the time of coffee consumption, will be provided for the two days prior to each sampling day and on the sampling day. Dinner timing and composition will also be standardised the day before the sampling day. Only water could be drunk during the night. At the sampling day (i.e. the last day of each intervention period), the subjects will refer in the morning at the ambulatory where fasting baseline blood and urine samples will be collected. Then, low and high consumers will drink one or three cups of espresso coffee, respectively (without sugar, sweeteners, and milk for the first coffee; with 5 g of sugar for the last two coffees), while medium consumers will drink a cup of espresso coffee and 2 cocoa-based products containing coffee twice during the day, following the above-described timing. After ingestion of the first coffee together with a phytochemical-free breakfast (a pastry), blood and urine samples will be collected at selected time points along the following 24-h. Five hours after the consumption of the first coffee, participants will receive a standardised mixed meal (sandwich with ham and cheese) free of coffee/cocoa phytochemical-related compounds. Water will be available ad libitum. Twenty-four hours after receiving the treatment, blood and urine samples will also be taken in order to assess return to baseline. In addition, anthropometric characteristics and blood pressure (BP) will be measured. Socio-demographic variables will be assessed through a generic questionnaire filled at recruitment. The questionnaire will also contain questions useful to identify possible exclusion criteria (e.g. diagnosis for diseases, regular consumption of medication, food allergy). Dietary habits of volunteers will also be evaluated during the enrollment, through a semi-quantitative food frequency questionnaire (FFQ) for the assessment of dietary total antioxidant capacity. In addition, participants' food intakes and compliance with the study requirements will be assessed by means of 3-day dietary records, administered throughout each intervention period at two time points: i) in the middle of each intervention period during two weekdays and a weekend day, and ii) at the end of each intervention period, 2 days prior to the sampling day and the sampling day. The habitual physical activity level of each participant will be measured through a validated International Physical Activity Questionnaires. Blood sample collection will be carried out in the ambulatory unit of the Department of Medicine and Surgery. Blood collection will be carried out by a physician. A venous catheter will be inserted into the antecubital vein and blood samples from each subject will be collected in specific tubes over 24 hours. Blood sampling at time-point 24h after first coffee consumption will be done by venipuncture. Urine samples will be collected during different periods of time using urine collectors. Blood samples will be centrifuged and plasma, serum and peripheral blood mononuclear cells (PBMCs) will be collected, aliquoted, and stored at -80 °C for further processing. Urine samples will be aliquoted and stored at -80°C for further processing. The primary selected endpoint of the study is the quantification of the daily mean concentration of coffee-derived plasma circulating phenolic metabolites, whereas the study of the bioavailability of other coffee-derived circulating bioactives, the bioavailability of cocoa-derived circulating phytochemicals, and the assessment of cardiometabolic markers will be considered secondary endpoints.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diet Modification, Cardiovascular Risk Factor, Nutritional and Metabolic Diseases
Keywords
coffee, cocoa, bioavailability, pharmacokinetics, cardiometabolic risk factors, caffeoylquinic acids, flavan-3-ol, caffeine, trigonelline, diterpene

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Masking Description
Sample codification, done by the PI, will be hidden to the researchers analysing the samples.
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
low consumers
Arm Type
Experimental
Arm Description
1 cup of espresso coffee/day at 9.00 A.M. for 1 month
Arm Title
high consumers
Arm Type
Experimental
Arm Description
3 cup of espresso coffee/day at 9.00 A.M. 12.00 P.M. and 3.00 P.M. for 1 month
Arm Title
medium consumers
Arm Type
Experimental
Arm Description
1 cup of espresso coffee at 9.00 A.M. + cocoa-based products containing coffee at 12.00 P.M. and 3.00 P.M. for 1 month
Intervention Type
Other
Intervention Name(s)
cup of espresso coffee
Intervention Description
Subjects will consume the assigned treatment for one month. Espresso coffee will be prepared by using coffee capsules. Serving size: approximately 45 mL. The last day of the intervention is the sampling day.
Intervention Type
Other
Intervention Name(s)
cocoa-based products containing coffee
Intervention Description
Subjects will consume the assigned treatment (2 products per serving) for one month. Serving size: approximately 37 g. The last day of the intervention is the sampling day.
Primary Outcome Measure Information:
Title
Daily mean concentration of phenolic metabolites
Description
Assessment of the daily mean concentration of coffee derived plasma circulating phenolic metabolites
Time Frame
24 hours (0 -overnight fasting-, 30, 60, 120, 180, 240, 300, 360, 420, 480, 540, 1440 -overnight fasting- minutes)
Secondary Outcome Measure Information:
Title
Coffee-derived plasma circulating bioactives
Description
Profile of metabolites coming from coffee phytochemicals (phenolic compounds, trigonelline, caffeine, and diterpenes) in plasma
Time Frame
24 hours (0 -overnight fasting-, 30, 60, 120, 180, 240, 300, 360, 420, 480, 540, 1440 -overnight fasting- minutes)
Title
Coffee-derived bioactives in urine
Description
Profile of metabolites coming from coffee phytochemicals (phenolic compounds, trigonelline, caffeine, and diterpenes) in urine
Time Frame
24 hours (0 -overnight fasting-, 180, 360, 540, 1440 -overnight fasting- minutes)
Title
Cocoa-derived plasma circulating bioactives
Description
Profile of metabolites coming from cocoa phytochemicals (phenolic compounds and theobromine) in plasma
Time Frame
24 hours (0 -overnight fasting-, 30, 60, 120, 180, 240, 300, 360, 420, 480, 540, 1440 -overnight fasting- minutes)
Title
Cocoa-derived bioactives in urine
Description
Profile of metabolites coming from cocoa phytochemicals (phenolic compounds and theobromine) in urine
Time Frame
24 hours (0 -overnight fasting-, 180, 360, 540, 1440 -overnight fasting- minutes)
Title
Blood Pressure
Description
Systolic and diastolic blood pressure
Time Frame
two time (0 -overnight fasting-, 1 month-fasting-)
Title
Body Mass Index (BMI)
Description
Weight (in kg) and height (in m) will be combined to report BMI in kg/m2
Time Frame
two time (0 -overnight fasting-, 1 month-fasting-)
Title
Waist circumference
Time Frame
two time (0 -overnight fasting-, 1 month-fasting-)
Title
Trimethyl-ammine-N-oxide (TMAO) in plasma
Time Frame
24 hours (0 -overnight fasting-, 30, 60, 120, 180, 240, 300, 360, 420, 480, 540, 1440 -overnight fasting- minutes)
Title
Trimethyl-ammine-N-oxide (TMAO) in urine
Time Frame
24 hours (0 -overnight fasting-, 180, 360, 540, 1440 -overnight fasting- minutes)
Title
Nitric oxide (NO) in plasma
Time Frame
1440 -overnight fasting- minutes
Title
Blood lipids
Description
Total cholesterol, HDL, LDL, triglycerides
Time Frame
1440 -overnight fasting- minutes
Title
Glucose and Insulin
Description
Fasting glucose and fasting insulin
Time Frame
1440 -overnight fasting- minutes
Title
DNA damage
Description
Assessed by using the Comet assay
Time Frame
24 hours (0 -overnight fasting-, 60, 240, 420, 1440 -overnight fasting- minutes)
Title
DNA catabolites
Description
Assessed by using LC-MS for individual detection and quantification
Time Frame
24 hours (0 -overnight fasting-, 60, 240, 420, 1440 -overnight fasting- minutes)
Title
Nutri-metabolomics in plasma
Description
Metabolomics will be carried out in fasting plasma to unravel the potential metabolic pathways of molecules present in the food matrix
Time Frame
1440 -overnight fasting- minutes
Title
Nutri-metabolomics in urine
Description
Metabolomics will be carried out in urine to unravel the potential metabolic pathways of molecules present in the food matrix
Time Frame
24 hours (0 -overnight fasting-, 180, 360, 540, 1440 -overnight fasting- minutes)
Title
Eicosanoids in urine
Time Frame
24 hours (0 -overnight fasting-, 180, 360, 540, 1440 -overnight fasting- minutes)
Title
Inflammatory markers in plasma
Description
Main inflammatory markers associated with coffee consumption
Time Frame
1440 -overnight fasting- minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: adult both genders healthy normal weight (BMI 18-25) regular coffee consumers of 1-5 cups per day Exclusion Criteria: younger than 18 y.o. or older than 60 y.o. clinically diagnosis for metabolic, renal or digestive disorders regular consumption of medication antibiotic therapy taken within the last 3 months intense physical activity pregnancy or lactation underweight or overweight/obese no regular consumption of coffee or regular intake exceeding 5 coffees/day
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniele Del Rio, Ph.D.
Organizational Affiliation
University of Parma
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pedro M Mena Parreño, Ph.D.
Organizational Affiliation
University of Parma
Official's Role
Study Director
Facility Information:
Facility Name
Department of Food and Drug, University of Parma
City
Parma
ZIP/Postal Code
43125
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34582552
Citation
Mena P, Bresciani L, Tassotti M, Rosi A, Martini D, Antonini M, Cas AD, Bonadonna R, Brighenti F, Del Rio D. Effect of different patterns of consumption of coffee and a cocoa-based product containing coffee on the nutrikinetics and urinary excretion of phenolic compounds. Am J Clin Nutr. 2021 Dec 1;114(6):2107-2118. doi: 10.1093/ajcn/nqab299.
Results Reference
derived
PubMed Identifier
32728879
Citation
Martini D, Rosi A, Tassotti M, Antonini M, Dall'Asta M, Bresciani L, Fantuzzi F, Spigoni V, Dominguez-Perles R, Angelino D, Ricci C, Del Pozo-Luengo S, Tornel PL, Scazzina F, Gil-Izquierdo A, Dei Cas A, Brighenti F, Bonadonna R, Del Rio D, Mena P. Effect of coffee and cocoa-based confectionery containing coffee on markers of cardiometabolic health: results from the pocket-4-life project. Eur J Nutr. 2021 Apr;60(3):1453-1463. doi: 10.1007/s00394-020-02347-5. Epub 2020 Jul 29.
Results Reference
derived
PubMed Identifier
29121975
Citation
Mena P, Tassotti M, Martini D, Rosi A, Brighenti F, Del Rio D. The Pocket-4-Life project, bioavailability and beneficial properties of the bioactive compounds of espresso coffee and cocoa-based confectionery containing coffee: study protocol for a randomized cross-over trial. Trials. 2017 Nov 9;18(1):527. doi: 10.1186/s13063-017-2271-2.
Results Reference
derived

Learn more about this trial

Bioavailability and Beneficial Properties of Coffee and Cocoa Bioactive Compounds

We'll reach out to this number within 24 hrs